AU3130100A - LHRH antagonist peptides - Google Patents

Description

-1-

AUSTRALIA

PATENTS ACT 1990 COMPLETE SPECIFICATION FOR A STANDARD PATENT

ORIGINAL

.i Name of Applicant: Indiana University Foundation Actual Inventor: Roger W. Roeske Address for Service: BALDWIN SHELSTON WATERS MARGARET STREET .".SYDNEY NSW 2000 Invention Title: 'LHRH ANTAGONIST PEPTIDES' a Details of Original Application No. 61680/96 dated 07 Jun 1996 The following statement is a full description of this invention, including the best method of performing it known to me/us:- File: 28006AUP00 -1A- LHRH ANTAGONIST PEPTIDES Background of the Invention The present invention relates to LHRH antagonist peptides and uses thereof.

Luteinizing hormone (LH) and follicle-stimulating hormone (FSH) are hormones released by the pituitary gland. These hormones regulate the functioning of the gonads and the production and maturation of gametes. LH and FSH are generally released by the pituitary gland upon prior release of triggering hormone from the hypothalamus.

Luteinizing hormone-releasing hormone (LHRH; also known as gonadotropin-releasing hormone or GnRH) is one of the principal hypothalamic hormones which triggers the release of LH. Thus, release of LHRH represents a control point in the physiological regulation of gonadal function. The structure of mammalian LHRH has been determined, and has been found to be a decapeptide: 0V 0.: 15 p-Glu-His-Trp-Ser-Tyr-Gly-Leu-Arg-Pro-Gly-NH 2 (SEQ ID NO: 1) 1 2 3 4 5 6 7 8 9 LH release is necessary for ovulation; thus, compounds which inhibit LH release by blocking the action of LHRH are useful as contraceptive agents. LHRH antagonists are also useful for regulating secretion of gonadotropins in male mammals, and thus can be used as male contraceptives. In addition, LHRH antagonists can be used in the treatment of sex-hormone dependent cancers (for example, prostate cancer), where increased levels of gonadotropins increase the rate of tumor growth.

S. Many modified LHRH analog peptides have been synthesized in an attempt to 25 increase the potency of the antagonists, preferably while also increasing the resistance of the antagonist to enzymatic degradation. For example, synthetic LHRH antagonist peptides which incorporate modified or unnatural amino acids have been tested. Common substitutions include, for example, substitution of 4-Cl-D-Phe for His at position 2, or substitution of D-Ala-NH 2 for Gly-NH 2 at position One problem frequently encountered in LHRH antagonist peptides is the occurrence of histamine-releasing activity. This histamine-releasing activity represents a serious obstacle to the clinical use of such antagonists because histamine release results in adverse side effects such as edema and itching. Thus, LHRH antagonist peptides which have low histamine releasing activity are particularly desirable. Although the LHRH antagonist and histamine-releasing properties are not necessarily related, very few prior art compounds combine low histamine-releasing activity with high LHRH antagonist activity. Many prior art LHRH antagonist peptides also suffer from poor water-solubility, which complicates formulation of the antagonist for administration.

-2- Summary of the Invention The present invention features LHRH antagonist peptides, methods of modulating LHRH activity, and methods of treating a subject with the antagonists of the invention.

In one embodiment, an LHRH antagonist comprises a peptide compound, wherein a residue of the peptide compound corresponding to the amino acid at position 6 of natural mammalian LHRH comprises D-Lys(Imdac), D-Lys(Ppic), D-Lys(Dodac), D-Lys(pGlu), D-Lys(Otac) and D-Lys(Onic) or a moiety selected from the group consisting of a dipolar moiety, a sulfonium moiety, a receptor-modifying moiety and a small polar moiety, such that the peptide compound has LHRH antagonist activity, with the provisos that the dipolar moiety is not a zwitterionic pyridinium and the residue is not D-Cit, D-Hci or a lower alkyl derivative of D-Cit or D-Hci. Preferably, the peptide compound comprises about 8 to about 12 residues.

More preferably, the peptide compound comprises 10 residues.

o* In another embodiment, the invention provides a peptide compound comprising a 15 structure:

A-B-C-D-E-F-G-H-I-J

wherein A is pyro-Glu, Ac-D-Nal Ac-D-Qal, Ac-Sar, or Ac-D-Pal; B is His or 4-Cl-D-Phe; C is Trp, D-Pal, D-Nal, L-Nal, D-Pal(N-O), or D-Trp; S D is Ser; E is N-Me-Ala, Tyr, N-Me-Tyr, Ser, Lys(iPr), 4-Cl-Phe, His, Asn, Met, Ala, Arg or Ile; F is D-Lys(Imdac), D-Lys(Ppic), D-Lys(Dodac), D-Lys(pGlu), D-Lys(Otac), 25 D-Lys(Onic) or a structure: X

Y

R I wherein R and X are, independently, H or alkyl; and Y comprises a moiety selected from the group consisting a dipolar moiety, a sulfonium moiety, a receptor-modifying moiety and a small polar moiety, the provisos that the dipolar moiety is not a zwitterionic pyridinium and F is not D-Cit, D-Hci or a lower alkyl derivative of D-Cit or D-Hci; G is Leu or Trp; H is Lys(iPr), Gin, Met, or Arg; I is Pro; and J is Gly-NH 2 or D-Ala-NH 2 or a pharmaceutically acceptable salt thereof.

The invention also provides pharmaceutical compositions of the LHRH antagonist peptides.

In another aspect, the invention provides a method of inhibiting LHRH activity in a subject, comprising administering to a subject an effective amount of an LHRH antagonist, such that LHRH activity is inhibited.

In another aspect, the invention provides a method of inhibiting LHRH activity in a cell, comprising contacting a cell with an LHRH antagonist, such that LHRH activity is inhibited.

In another aspect, the invention provides a method of inhibiting growth of a hormone-dependent tumor in a subject, comprising administering to a subject an effective amount of an LHRH antagonist, such that tumor growth is inhibited.

In another aspect, the invention provides a method of inhibiting ovulation in a subject, comprising administering to a subject an effective amount of an LHRH antagonist, such that ovulation is inhibited.

15 In another aspect, the invention provides a packaged formulation for treating a S. subject for a disorder associated with LHRH activity, comprising an LHRH antagonist packaged with instructions for using the LHRH antagonist for treating a subject having a disorder associated with LHRH activity.

Brief Description of the Drawings Figure 1 is a graph depicting plasma testosterone levels (in ng/ml) in adult male rats administered eight subcutaneous injections of the LHRH antagonist #3827, one injection every three hours, at doses of 1, 10 or 100 Lg/kg.

Figure 2 is a graph depicting plasma testosterone levels (in ng/ml) in adult male rats subcutaneously administered the LHRH antagonist #3827 via an osmotic pump. Doses were either 300 ug/kg/day for two weeks, followed by 15 Pg/kg/day for an additional two weeks or 1000 pg/kg/day for two weeks, followed by 5, 15 or 50 gg/kg/day for an additional two weeks.

Figure 3 is a graph depicting the plasma testosterone levels (in ng/ml) in adult male rats subcutaneously administered the LHRH antagonist #3827 via an osmotic pump. Doses were either 30 ug/kg/day for two weeks, followed by 5 pg/kg/day for an additional two weeks, 100 ug/kg/day for two weeks, followed by 5 gg/kg/day for an additional two weeks.

or 300 g/kg/day for two weeks, followed by 0 or 5 pg/kg/day for an additional two weeks.

Detailed Description of the Invention In order that the present invention may be more readily understood, certain terms are first defined.

As used herein, "LHRH antagonist peptide" is intended to include peptides and peptide analogs which inhibit LHRH activity has "LHRH antagonist activity") in vivo or in vitro. Candidate LHRH antagonist peptides can be assayed, for example, in the animal model described in Corbin and Beattie, Endocrine Res. Commun. 2:1 (1975) (and see infra). In this assay, the LHRH antagonistic activity of a candidate compound is assayed by measuring the antiovulatory activity (AOA) of the compound in rats.

The term "histamine-releasing activity", as used herein, refers to the tendency of a compound to release histamine when administered to a subject. The histamine-releasing activity of a compound can be measured with an in vitro assay (described in more detail, infra). Preferred LHRH antagonist peptides have high activity in the rat antiovulatory activity assay, but low histamine releasing activity. Preferred LHRH antagonist peptides have an ED 50 in the histamine release assay of at least 3 pg/ml, more preferably at least 5 p g/ml, and still more preferably at least 10 ig/ml.

The term "alkyl", as used herein, refers to a straight or branched chain hydrocarbon group having from about 1 to about 10 carbon atoms. The term "lower alkyl" refers to an alkyl group having from about 1 to about 6 carbon atoms. Exemplary lower alkyl groups 15 include methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, S and n-hexyl. An alkyl group may be unsubstituted, or may be substituted at one or more S:positions, with, halogens, alkyls, cycloalkyls, alkenyls, alkynyls, aryls, heterocycles, hydroxyls, aminos, nitros, thiols, amines, imines, amides, phosphonates, phosphines, carbonyls, carboxyls, silyls, ethers, thioethers, sulfonyls, selenoethers, ketones, aldehydes, esters, -CF 3 -CN, or the like. Preferred alkyls are lower alkyls.

The term "cycloalkyl" refers to a cyclic saturated hydrocarbon group having from 3 to 8 carbon atoms. Exemplary cycloalkyls include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and cyclooctyl. Cycloalkyl groups may be unsubstituted or substituted at one or more ring positions as described for alkyls. Thus, a cycloalkyl may be substituted with, 25 halogens, alkyls, cycloalkyls, alkenyls, alkynyls, aryls, heterocycles, hydroxyls, aminos, nitros, thiols amines, imines, amides, phosphonates, phosphines, carbonyls, carboxyls, silyls, ethers, thioethers, sulfonyls, selenoethers, ketones, aldehydes, esters,

CF

3 -CN, or the like.

The terms "alkenyl" and "alkynyl", as used herein, refer to unsaturated groups analogous in length and possible substitution to the alkyls described above, but which contain at least one carbon-carbon double or triple bond respectively.

The term "aryl" as used herein includes 6- and 7-membered single-ring aromatic groups which may include from zero to four heteroatoms, for example, benzene, pyrrole, furan, thiophene, imidazole, oxazole, thiazole, triazole, tetrazole, pyrazole, pyridine, pyrazine, pyridazine and pyrimidine, and the like. Those aryl groups having heteroatoms in the ring structure may also be referred to as "aryl heterocycle" or "heteroaromatic". The aromatic ring can be substituted at one or more ring positions with such substituents as described above, as for example, halogens, alkyls, cycloalkyls, alkenyls, alkynyls, heterocycles, hydroxyls, aminos. nitros, thiols, amines, imines, amides, phosphonates, phosphines, carbonyls, carboxyls, silyls, ethers, thioethers, sulfonyls, selenoethers, ketones, aldehydes, esters, -CF 3 -CN, or the like. An aromatic ring may also be substituted with another aromatic ring, as in, for example, a biphenyl. Aryl groups also include fused or polycyclic aromatic systems.

The terms "heterocycle" or "heterocyclic group" refer to 4- to I 0-membered ring structures, more preferably 5 to 7 membered rings, which ring structures include one to four heteroatoms. Heterocyclic groups include pyrrolidine, oxolane, thiolane, imidazole, oxazole, piperidine, piperazine, morpholine. The heterocyclic ring can be substituted at one or more positions with such substituents as described above, as for example, halogens, alkyls, cycloalkyls, alkenyls, alkynyls, aryls, other heterocycles, hydroxyl, amino, nitro, thiol, amines, imines, amides, phosphonates, phosphines, carbonyls, carboxyls, silyls, ethers, thioethers, sulfonyls, selenoethers, ketones, aldehydes, esters, -CF 3 -CN, or the like.

Heterocycles may also be bridged or fused to other cyclic groups as described below.

The terms "polycycle" or "polycyclic group" refer to two or more cyclic rings 15 cycloalkyls, cycloalkenyls, cycloalkynyls, aryls and/or heterocycles) in which two or more carbons are common to two adjoining rings, the rings are "fused rings". Rings that are joined through non-adjacent atoms are termed "bridged" rings. Each of the rings of the polycycle can be substituted with such substituents as described above, as for example, halogens, alkyls, cycloalkyls, alkenyls, alkynyls, hydroxyl, amino, nitro, thiol, amines, imines, amides, phosphonates, phosphines, carbonyls, carboxyls, silyls, ethers, thioethers, sulfonyls, selenoethers, ketones, aldehydes, esters, -CF 3 -CN, or the like.

The term "heteroatom" as used herein means an atom of any element other than carbon or hydrogen. Preferred heteroatoms are nitrogen, oxygen, sulfur, phosphorus and selenium.

The term "arylalkyl", as used herein, refers to an aryl group appended to an alkyl group, including, but not limited to, benzyl, naphthylmethyl, pyridyl methyl, and the like.

The term "ylid" is known in the art and refers to a moiety in which a positively charged atom (especially from Groups V and VI of the periodic table) is bonded to a carbon atom which bears an unshared pair of electrons. Thus, an ylid has the resonance forms:

W

W

RI/C R2 RI -R2 in which W is a heteroatom such as S, or P, and R 1 and R2 are, independently, H, alkyl, cycloalkyls, alkenyl, alkynyl, aryl, alkoxy, thioalkoxy, and the like. The heteroatom is substituted with an appropriate number of substituents two for N and S, and three for the substituents are independently alkyl, cycloalkyl, aryl, and the like. Nitrogen ylides do not have a significant contribution from the non-charge-separated resonance form (on the right, above).

-6- The term "dipolar moiety", as used herein, refers to a covalently bonded moiety having both positive and negative charges a zwitterionic moiety). Exemplary dipolar groups include ylids of S, N, or tertiary amine oxides, nitrones, pyridine-N-oxides, nitrile oxides, quaternary amino acids 2 -(N,N,N-trialkylammonium) acetate), amino acids, sulfonium arene oxides (as described in, for example, U.S. Patent 4,111,914), betaines trigonellin), and the like. In certain preferred embodiments, the dipolar moiety is a pyridine-N-oxide. In other preferred embodiments, the dipolar moiety is a zwitterionic pyridinium moiety. In certain other embodiments, the dipolar moiety is not a zwitterionic pyridinium moiety.

As used herein, a "cationic moiety" is a moiety in which at least one atom bears a positive charge, and the moiety has a net positive charge. Thus, for example, an N-alkyl (or N-alkenyl, -alkynyl, or -aryl, collectively referred to herein as "N-substituted pyridinium") pyridinium moiety can be a cationic moiety (and is referred to herein as a "cationic S* pyridinium moiety"), but a pyridine-N-oxide is not, unless it has a net positive charge. As 15 described above, a pyridine-N-oxide can be a dipolar moiety. Other exemplary cationic moieties include quaternary amines, sulfonium salts, phosphonium salts, and the like. In certain preferred embodiments, the cationic moiety is a sulfonium moiety.

*A sulfonium moiety has the following structure:

R

3 S/ R 4 20 in which R 3 and R4 are each, independently, alkyl, cycloalkyl, alkenyl, alkynyl, aryl, and the like.

In other preferred embodiments, the cationic moiety is a cationic pyridinium moiety. A cationic pyridinium moiety has the following structure:

R

16

R

1 5 R 1 7

R

1 4 R12

R

13 wherein R 12 is alkyl or aryl, and R 13

-R

17 are each, independently, hydrogen, halogens, alkyls, cycloalkyls, alkenyls. alkynyls, aryls, other heterocycles, hydroxyl, amino, nitro, thiol, amines, imines, amides, phosphonates, phosphines, carbonyls, carboxyls, silyls, ethers, thioethers, sulfonyls, selenoethers, ketones, aldehydes, esters, -CF 3 -CN, or the like.

Preferred cationic pyridinium moieties include Pal(iPr) and Pal(Bzl). N-methyl pyridinium moieties are not preferred.

Although the above examples describe pyridine (or pyridinium) moieties, it will be apparent to the skilled artisan that other N-heteroaromatic moieties (that is, a moiety in which at least one nitrogen is present in an aromatic ring) may be substituted for the pyridine (or pyridiniumi moieties described herein. Exemplary N-heteroaromatics include -7thiazole, triazole, tetrazole, pyrazole, pyrazine, pyridazine and pyrimidine, and the like.

Thus, N-substituted pyrazines, pyridazines, and the like, are contemplated for use in the present invention.

As used herein, "tertiary amine" includes trialkyl amines, triaryl amines, and amines which have both alkyl and aryl substituents.

As used herein, "zwitterionic pyridinium moiety" refers to a moiety having the form: Rio R Ril R7 in which R 6 comprises an alkyl, cycloalkyl, alkenyl, alkynyl, or aryl moiety and R 7

-R

1 1 10 are each, independently, hydrogen, halogens, alkyls, cycloalkyls, alkenyls, alkynyls, aryls, other heterocycles, hydroxyl, amino, nitro, thiol, amines, imines, amides, phosphonates, phosphines, carbonyls, carboxyls, silyls, ethers, thioethers, sulfonyls, selenoethers, ketones, Saldehydes, esters, -CF3, -CN, or the like, with the proviso that at least one of R 6

-R

1 1 is substituted with an anionic moiety. An "anionic moiety", as used herein, is a moiety which has a net negative charge. The anionic moiety is chosen to be compatible with other moieties, and to form a stable compound. Illustrative anionic moieties include carboxylates, phosphates. phosphonates, sulfates, sulfonates, and the like. In certain preferred embodiments, the anionic moiety is a carboxylate. In other preferred embodiments, the anionic moiety is a sulfonate. In a preferred embodiment, R 6 comprises: 20 co A pyridine N-oxide is a moiety which has the form: RI6

R

15

R

1 7 RI4 O" Rl 3 where R 13

-R

1 7 have the meanings defined above.

The term "hydrophilic N-acyl moiety", as used herein, refers to a moiety which comprises a nitrogen atom acylated so as to form a hydrophilic moiety. Thus, a hydrophilic N-acyl moiety can have the form: 0 N R43 R42 -8where R41 and R 4 2 are each, independently, H, alkyl, cycloalkyl, aryl and the like; and

R

4 3 is alkyl, cycloalkyl, alkenyl, alkynyl, aryl, and the like; and R 4 1

-R

4 3 are selected to form a hydrophilic moiety. In preferred embodiments, R 4 1 and R 4 2 are not both H.

Relative hydrophilicity can be determined by any of several methods known in the art (Hansch, ed., "Comprehensive Medicinal Chemistry", Vol. 4, Pergamon Press, Oxford, 1990), and can be used to guide the choice of potential hydrophilic moieties for use in the invention. The partition coefficient, P, between I-octanol and water has been used as a reference for measuring the hydrophilicity of a compound. Hydrophilicity can be expressed as log P, the logarithm of the partition coefficient (Hansch et al., Nature 194:178 (1962); Fujita et al., J. Am. Chem. Soc. 86:5175 (1964)). Standard tables of hydrophilicity for many molecules, and lipophilicity (hydrophobicity) substituent constants (denoted 7r) for many functional groups, have-been compiled (see, Hansch and Leo, "Substituent Constants for Correlation Analysis in Chemistry and Biology," Wiley, New York, New York, (1979)). The hydrophilicity of a vast range of candidate hydrophilicity moieties can eae 15 be quite accurately predicted with the aid of these tables. For example, the measured log P S(octanol/water) of naphthalene is 3.45. The substituent constant p for -OH is -0.67.

*Therefore, the predicted log P for p-naphthol is 3.45 2.78. This value is in good agreement with the measured log P for p-naphthol, which is 2.84. In certain preferred embodiments, the hydrophilic N-acyl moiety has a value of log P between -1 and more preferably between -0.5 and Examples of residues incorporating preferred hydrophilic acyl moieties are D-Lys(Imdac), D-Lys(Ppic), D-Lys(Dodac), D-Lys(pGlu), D- Lys(Otac), and D-Lys(Onic). Other preferred residues incorporating hydrophilic acyl moieties include Lys(Imdac), Lys(Ppic), Lys(Dodac), Lys(pGlu), Lys(Otac), and Lys(Onic).

25 The term "small polar moiety" refers to a moiety which has small steric bulk and is relatively polar. In certain embodiments, a small polar moiety is not D-Cit, D-Hci or lower alkyl derivatives thereof. Polarity is measured as hydrophilicity by the P scale described above. In certain preferred embodiments, the small polar moieties have a log P between -1 and In particularly preferred embodiments, the small polar moiety modifies residue 6.

In preferred embodiments, the steric bulk of the small polar moiety is less than the steric bulk of Trp. Examples of residues incorporating preferred small polar moieties are D- or L- Asn, D- or L-Gln, and D- or L-Thr. In preferred embodiments, the small polar moiety is not Glu or a carboxylic ester of Glu. In an especially preferred embodiment, the small polar moiety is D-Asn.

The term "leaving group" is known in the art and, as used herein, refers to a functionality which upon heterolytic bond cleavage departs with an electron pair. In general, good leaving groups are those moieties which are expelled from the substrate as weak bases, whether charged or uncharged. For example, sulfates, sulfonates, sulfides, chloride, bromide, iodide, phosphates, phosphinates, and the like are good leaving groups.

In other words, when, for example, a C-S bond of a sulfonium moiety is cleaved, a sulfide departs (with an electron pair).

The term "receptor-modifying moiety", as used herein, refers to a moiety which can modify, covalently or non-covalently, a receptor for an LHRH antagonist peptide. For example, it has recently been shown Flanagan et al., (1994) J. Biol. Chem.

269:22636) that Glu301 of the mouse LHRH receptor (which corresponds to Asp301 in the human LHRH receptor) interacts with Arg 8 in LHRH agonists. Thus, a carboxylatemodifying reagent (such as an alkylating agent) can modify Glu301 (Asp301) and thus modify the mouse (or human) LHRH receptor. A receptor-modifying moiety may act to bond the LHRH antagonist peptide to the receptor esterifying the antagonist to the receptor by displacement of a-leaving group), or it may modify the receptor without bonding the LRHR antagonist peptide to the receptor by methylation with a methylsulfonium moiety). Other residues of an LHRH receptor can also be modified, and 0* 15 moieties which can modify such residues are also receptor-modifying moieties.

Exemplary receptor-modifying reagents include alkyl and benzyl halides methyl iodide or benzyl bromide), a-haloketones, a-haloesters and a-haloamides (collectively referred to as "a-halocarbonyls"), sulfonium salts, sulfates, alkyl or aryl sulfonates, and other reagents which comprise a good leaving group as described above. Other receptormodifying reagents are described in, for example, A.J. Barrett and G. Salvesen, eds. (1986) "Proteinase Inhibitors", Research Monographs in Cell and Tissue Physiology, Vol. 12, 0'0* Elsevier Press, Amsterdam.

Although in certain embodiments an LHRH antagonist of the invention contains a receptor-modifying moiety, the invention is not intended to be limited to those antagonists 25 that actually modify a receptor residue. An LHRH antagonist comprising a receptormodifying moiety but which does not actually modify the receptor may nonetheless be an effective LHRH antagonist. However, for those antagonists that do modify a receptor residue, one advantage is that such moieties can be designed to selectively modify only the targeted receptor, thereby reducing non-specific reactions and decreasing the probability of toxic side effects.

The term "a peptide having a sidechain modified by" a moiety, as used herein, refers to a peptide (or peptide mimetic, see below) in which at least one residue has a sidechain comprising that moiety. Thus, for example, a "peptide having a sidechain modified by a dipolar moiety" means a peptide in which at least one side chain comprises a dipolar moiety.

The LHRH antagonist peptides of the present invention also include peptide analogs and peptide mimetics. The term "peptide compound" as used herein is intended to encompass peptides, peptide analogs, peptide derivatives and peptide mimetics. The terms "peptide analog", "peptide derivative" and "peptide mimetic" as used herein are intended to include molecules which mimic the chemical structure of a peptide and retain the functional properties of the peptide. A "residue" refers to an amino acid or amino acid mimetic incorporated in the peptide compound by an amide bond or amide bond mimetic.

Approaches to designing peptide analogs are known in the art. For example, see Farmer, P.S. in Drug Design Ariens, ed.) Academic Press, New York, 1980, vol. 10, pp. 119- 143; Ball. J.B. and Alewood, P.F. (1990) J. Mol. Recognition 3:55; Morgan, B.A. and Gainor, J.A. (1989) Ann. Rep. Med. Chem. 24:243; and Freidinger, R.M. (1989) Trends Pharmacol. Sci. 10:270.

An "amino acid mimetic" refers to a moiety, other than a naturally occurring amino acid, that conformationally and functionally serves as a substitute for a particular amino acid in a peptide compound without adversely interfering to a significant extent with the function of the peptide interaction of the peptide with an LHRH receptor). In some circumstances, substitution with an amino acid mimetic may actually enhance properties of the peptide interaction of the peptide with an LHRH receptor). Examples of amino 15 acid mimetics include D-amino acids. LHRH antagonist peptides substituted with one or more D-amino acids may be made using well known peptide synthesis procedures. The effect of amino acid substitutions with D-amino acids or other amino-acid mimetics can be tested using assays, the AOA and histamine-release assays as described below. Other methods of determining the effect of substitution with an amino acid mimetic will be apparent to the skilled artisan.

The peptide analogs or mimetics of the invention include isosteres. The term "isostere" as used herein refers to a sequence of two or more residues that can be •substituted for a second sequence because the steric conformation of the first sequence fits a binding site specific for the second sequence. The term specifically includes peptide back-bone modifications amide bond mimetics) well known to those skilled in the art.

"Such modifications include modifications of the amide nitrogen, the a-carbon, amide carbonyl, complete replacement of the amide bond, extensions, deletions or backbone crosslinks. Several peptide backbone modifications are known, including W[CH 2

S],

V[CH

2 NH], w[C(S)NH 2 y[NHCO], [C(O)CH 2 and or CH=CH]. In the nomenclature used above, indicates the absence of an amide bond. The structure that replaces the amide group is specified within the brackets. Other examples of isosteres include peptides substituted with one or more benzodiazepine molecules (see James, G.L. et al. (1993) Science 260:1937-1942) Other possible modifications include an N-alkyl (or aryl) substitution (w[CONR]), backbone crosslinking to construct lactams and other cyclic structures, or retro-inverso amino acid incorporation (i[NHCO]). By "inverso" is meant replacing L-amino acids of a sequence with D-amino acids, and by "retro-inverso" or "enantio-retro" is meant reversing the sequence of the amino acids ("retro") and replacing the L-amino acids with D-amino acids. For example, if the parent peptide is Thr-Ala-Tyr, the retro modified form is Tyr- -11- Ala-Thr, the inverso form is thr-ala-tyr, and the retro-inverso form is tyr-ala-thr (lower case letters refer to D-amino acids). Compared to the parent peptide, a retro-inverso peptide has a reversed backbone while retaining substantially the original spatial conformation of the side chains, resulting in a retro-inverso isomer with a topology that closely resembles the parent peptide and is able to bind the selected LHRH receptor. See Goodman et al.

"Perspectives in Peptide Chemistry" pp. 283-294 (1981). See also U.S. Patent No.

4,522,752 by Sisto for further description of "retro-inverso" peptides.

In addition to amino acid-substituted LHRH antagonist peptides, the invention also encompasses LHRH antagonist peptide compounds having other modifications. For example, the amino-terminus or carboxy-terminus of the peptide can be modified. The term "amino-derivative group" is intended to include amino-terminal modifications of the peptide compounds of the invention. Examples ofN-terminal modifications include alkyl, cycloalkyl, aryl, arylalkyl, and acyl groups. A preferred N-terminal modification is acetylation. The N-terminal residue may be linked to a variety of moieties other than 15 amino acids such as polyethylene glycols (such as tetraethylene glycol carboxylic acid S monomethyl ether), pyroglutamic acid, succinoyl, methoxy succinoyl, benzoyl, phenylacetyl, or 4-pyridylalkanoyl, aroyl, alkanoyl (including acetyl and cycloalkanoyl cyclohexylpropanoyl), arylalkanoyl, arylaminocarbonyl, alkylaminocarbonyl, cycloalkylaminocarbonyl, alkyloxycarbonyl (carbamate caps), and cycloalkoxycarbonyl, among others.

The term "carboxy-derivative group" is intended to include carboxy-terminal modifications of the peptide compounds of the invention. Examples of modifications of the C-terminus include modification of the carbonyl carbon of the C-terminal residue to form a carboxyterminal amide or alcohol a reduced form). In general, the amide nitrogen, covalently bound to the carbonyl carbon on the C-terminal residue, will have two Ssubstitution groups, each of which can be hydrogen, alkyl or an alkylaryl group (substituted or unsubstituted). Preferably the C-terminal is an amido group, such as -CONH2,

CONHCH

3

-CONHCH

2

C

6

H

5 or -CON(CH 3 2 most preferably -CONH 2 but may also be S* or 4-pyridylmethyl, or 4-pyridylethyl, carboxylic acid, ethers, carbonyl esters, alkyl, arylalkyl, aryl, cyclohexylamide, piperidineamide, other mono or disubstituted amides, ureas, or carbamates. Other moieties that can be linked to the C-terminal residue include piperidine-4-carboxylic acid or amide and cis- or trans- 4-aminocyclohexanecarboxylic acid or amide.

The modified forms of LHRH antagonist peptides of the invention, including L- or D-amino acid substitutions, covalent modification of end termini or side chains, and peptide analogs and mimetics can be selected for desired alterations of the physical or chemical properties of the peptide, for example, increased stability, solubility, bioavailability, increased or decreased immunogenicity, etc. The peptides of the invention can be targeted to particular organs the brain) by methods known in the art, for -12example, the dihydropyridine-pyridinium carrier of Bodor (see, U.S. patent 4,540,564). In an exemplary embodiment, when a side-chain modified by a pyridinium moiety is desired, the corresponding N-alkylated dihydropyridine sidechain is incorporated into the peptide. When the peptide is administered to a subject, the N-alkylated dihydropyridine sidechain is oxidized in vivo to the desired pyridinium moiety.

Preferred LHRH antagonist peptides of the present invention range in length from about 8 to about 12 residues, more preferably from 9 to 11 residues, and most preferably are 10 residues in length.

The LHRH antagonist peptides of the present invention can be prepared by any suitable method for peptide synthesis, including solution-phase and solid-phase chemical synthesis. Preferably, the peptides are synthesized on a solid support. Methods for chemically synthesizing peptides are well known in the art (see, Bodansky, M.

Principles ofPeptide Synthesis, Springer Verlag, Berlin (1993) and Grant, G.A Synthetic Peptides: A User's Guide, W.H. Freeman and Company, New York (1992).

Automated peptide synthesizers are commercially available.

The use of combinatorial libraries to identify ligands is now well established (see, M.A. Gallop et al., (1994) J. Med. Chem. 37:1233; and E.M. Gordon et al., (1994) J.

Med Chem. 37:1385; and references cited therein). Therefore, LHRH antagonist peptides can be identified by chemical solution or solid-phase) synthesis of combinatorial e 20 libraries of peptides or peptoids) and screening of the resulting libraries according to known techniques. Thus, many potential ligands can be synthesized and screened in a short period of time, and the most active ligands selected for further testing or use.

Standard abbreviations and conventions are used throughout this disclosure when describing the peptides of the invention. Peptides are written with the N-terminus on the left, the carboxyl terminus on the right. Amino acids are of the L-form unless stated otherwise, D-Lys means the D-form of lysine. Ac-Xaa means the N-terminal residue Xaa is N-acetylated; C-terminal amides are denoted Xaa-NH 2 In Table 1, only residues which differ from native mammalian LHRH are noted; thus, the notation Met(S+Me) 8 LHRH.TFA means a peptide which differs from native mammalian LHRH only in the substitution of Met(S'Me) for the native Arg at position 8 (TFA indicates the trifluoroacetate salt). Lys(iPr) denotes N-E-2-propyl-lysinyl; other alkylating and acylating moieties are similar indicated. Thus, for example, Met(S+CH 2

C

6

H

5 denotes S-benzyl methionine. Certain other non-standard residues and moieties are abbreviated as follows: 13 Abbreviation pGlu Nal Ada 4-CI-Phe Qal Pal Pal(N-O) Pal(iPr) PaI(Bzl) Pal(CH 2

COO-)

Lys(iPr) Imdac Otac Ppic Dodac Met(S+Me)

PEG

Cit Hci Glu(Taurine) Pyz Pip CNa Dea Onic Gic Orotic Gmn Dap Residue or moiety pyro-glutaniyl 3-(2-naphthyl)alaninyl I-adamantanyl)alaninyl (4'-chlorophenyl)alaninyl 3-(2'-quinolinyl)alaninyl 3-(3'-pyridyl)alaninyl 3-(3'-pyridine-N-oxide)alaninyl 3-(N-(2-propyl)-3'-pyridinium)alaninyl 3-(N-(benzyl)-3'-pyridini um)alaninyl 3-(3'-pyridinium-N-(2-acetate))alaninyl N-E-2-propyl-lysinyl 2-oxo-4-imidazolinyl 2-oxoA-thiazolinyl 3-(piperidin- I -yl)-propanoyl 2,5-dioxo-4-imidazolinyl S-methyl methioninyl polyethylene glycol citrullinyl homocitrullinyl 5-(2-sulfoethylamido)glutamyl 1 ,4-pyrazmnecarbonyl pipecolyl (2-cyano)acetyl diethvlaxnide 3-nicotinyl-N-oxide gluconate orotate ornithine 2,4-diaminopropionyl I. LHRI-I Antag~onist Peptides of the Invention In one aspect, the invention pertains to LHRH antagonist peptides.

In one embodiment, the invention provides an LH-RH antagonist comprising a peptide compound, wherein a residue of the peptide compound corresponding to the amino acid at position 6 of natural mammalian LHRH comprises D-Lys(Imdac), D-Lys(Ppic), D- Lys(Dodac), D-Lys(pGlu), D-Lys(Otac) and D-Lys(Onic) or a moiety selected from the group consisting of a dipolar moiety, a sulfonium moiety, a receptor-modify'ing moiety and -14a small polar moiety, such that the peptide compound has LHRH antagonist activity, with the provisos that the dipolar moiety is not a zwitterionic pyridinium and the residue is not D-Cit, D-Hci or a lower alkyl derivative of D-Cit or D-Hci. Preferably, the peptide compound comprises about 8 to about 12 residues. More preferably, the peptide compound comprises 10 residues.

In another embodiment, the invention provides a peptide compound comprising a structure:

A-B-C-D-E-F-G-H-I-J

wherein A is pyro-Glu, Ac-D-Nal Ac-D-Qal, Ac-Sar, or Ac-D-Pal; B is His or 4-Cl-D-Phe; C is Trp, D-Pal, D-Nal, L-Nal, D-Pal(N-O), or D-Trp; D is Ser; E is N-Me-Ala, Tyr, N-Me-Tyr, Ser, Lys(iPr), 4-Cl-Phe, His, Asn, Met, Ala, Arg or 15 Ile; F is D-Lys(Imdac), D-Lys(Ppic), D-Lys(Dodac), D-Lys(pGlu), D-Lys(Otac), D-Lys(Onic) or a structure: X Y

N

*R A 0 wherein 20 R and X are, independently, H or alkyl; and Y comprises a moiety selected from the group consisting a dipolar moiety, a sulfonium moiety, a receptor-modifying moiety and a small polar moiety, the provisos that the dipolar moiety is not a zwitterionic pyridinium and F is not D-Cit, D-Hci or a lower alkyl derivative of D-Cit or D-Hci; 25 G is Leu or Trp; H is Lys(iPr), Gin, Met, or Arg; SI is Pro; and J is Gly-NH2 or D-Ala-NH 2 or a pharmaceutically acceptable salt thereof.

In a subembodiment, Y comprises a dipolar moiety, with the proviso that the dipolar moiety is not a zwitterionic pyridinium. Preferred dipolar moieties include ylids, tertiary amine oxides, nitrile oxides and pyridine-N-oxides.

In another subembodiment, Y comprises a sulfonium moiety.

In another subembodiment, Y comprises a receptor-modifying moiety. Preferred receptor modifying moieties include ylids, sulfonium moieties, a-halocarbonyls, sulfates, sulfonates, alkyl halides and benzyl halides.

In another subembodiment, F is D-Lys(Imdac), D-Lys(Ppic) and D-Lys(Dodac), D- Lys(pGlu), D-Lys(Otac) or D-Lys(Onic).

In another subembodiment, Y comprises a small polar moiety, with the proviso that F is not D-Cit, D-Hci or a lower alkyl derivative of D-Cit or D-Hci. Preferably, F is selected from the group consisting of D-Asn, D-Gln and D-Thr. More preferably, F is D- Asn.

In another embodiment, the invention provides an LHRH antagonist comprising a peptide compound, wherein a residue of the peptide compound corresponding to the amino acid at position 6 of natural mammalian LHRH comprises a small polar moiety such that the peptide compound has LHRH antagonist activity, with the proviso that the residue is not D-Cit, D-Hci or a lower alkyl derivative of D-Cit or D-Hci. Preferably, the antagonist has an antiovulatory activity of less than about 1 pg per rat in a rat antiovulation assay and/or the antagonist has an ED 50 in a histamine release assay of at least about 5 gg/ml.

Preferably, the peptide compound comprises about 8 to about 12 residues. More 15 preferably, the peptide compound comprises 10 residues.

In another embodiment, the invention provides a peptide compound comprising a structure:

A-B-C-D-E-F-G-H-I-J

wherein A is pyro-Glu, Ac-D-Nal, Ac-D-Qal, Ac-Sar, or Ac-D-Pal B is His or 4-Cl-D-Phe C is Trp, D-Pal, D-Nal, L-Nal, D-Pal(N-O), or D-Trp D is Ser E is N-Me-Ala, Tyr, N-Me-Tyr, Ser, Lys(iPr), 4-Cl-Phe, His, Asn, Met, Ala, Arg or le; F is

R

X L

R

wherein R and X are, independently, H or alkyl; and L comprises a small polar moiety, with the proviso that F is not D- Cit, D-Hci or a lower alkyl derivative of D-Cit or D-Hci; G is Leu or Trp; H is Lys(iPr), Gin. Met, or Arg I is Pro; and J is Gly-NH 2 or D-Ala-NH 2 or a pharmaceutically acceptable salt thereof. Preferably. F is selected from the group consisting of D-Asn. D-Gln and D-Thr.

-16- In another embodiment, the invention provides a peptide compound comprising a structure:

A-B-C-D-E-F-G-H-I-J

wherein A is pyro-Glu, Ac-D-NaI Ac-D-Qal, Ac-Sar, or Ac-D-Pal; B is His or 4-Cl-D-Phe; C is Trp, D-Pal, D-Nal, L-Nal, D-PaI(N-O), or D-Trp; D is Ser; E is N-Me-Ala, Tyr, N-Me-Tyr, Ser, Lys(iPr), 4-Ci-Phe, His, Asn, Met, Ala, Arg or le; F is D-Asn;- G is Leu or Trp; H is Lys(iPr), Gin, Met, or Arg; 1Iis Pro; and J is Gly-NH2) or D-Ala-NH 2 or a pharmaceutically acceptable salt thereof.

In another embodiment, the invention provides a peptide compound comprising a structure: A-B-C-D-E-F-G-H-l-J wherein A is pyro-Glu, Ac-D-Nal Ac-D-QaI, Ac-Sar, or Ac-D-Pal; B is His or 4-C1-D-Phe; C is Trp, D-Pal. D-NaI, L-Nal, D-PaI(N-O). or D-Trp; D is Ser; E is N-M-Ala, Tyr, NMe-Me-Tyr, Ser, Lys(iPr), 4-Ci-Phe, His, Asn, Met,.Ala, Arg or Ile; F is D-Arg, D-Lys(iPr), D-Pal(iPr), D-Cit or Q, wherein Q has a structure x z N

RY

0 wherein R and X are, independently, H or alkyl; and Z comprises a sulfonium moiety; G is Leu or Trp; H is Lys(iPr), Gin, Met, Arg or Q; I is Pro. and J is Gly-NH, or D-Ala-NH 2 -17with the proviso that at least one of F and H is Q; or a pharmaceutically acceptable salt thereof.

In preferred specific embodiments, the invention provides peptide compounds of the following structures: Ac-D-NaI-4-CI-Phe-D-Pal-Ser-Tyr-D-Pa(N-O)-Leu-Lys(Pr)-Pro-D-AlaNH 2 and pharmaceutically acceptable salts thereof.

Ac-D-Nal-4-CI-D-Phe-D-Pal-Ser-Tyr-D-Pal(CH 2 COO-)-Leu-Lys(iPr)-ProD..a.

NE

2 and pharmaceutically acceptable salts thereof.

Ac-Sar-4-CI-D-Phe-D-Nal-Ser-Tyr-D-Pal(Bzl)-Leu-Lys(ipr)-Pro-D-Ala-NH 2 and pharmaceutically acceptable salts thereof.

AcDNl4C--h--r-e-y-DMtSM)LuAgPoDAaN2 and pharmaceutically acceptable salts thereof.

Ac-D-Nal-4-Cl-D-Phe-D-Pal-Ser-Tyr-D-Arg-Leu-Met(S+Me)-Pro-D-Ala.NH 2 and pharmaceutically acceptable salts thereof.

Ac-D-Nal-4-Cl-D-Phe-D-Pal-Ser-Tyr-D-Lys(Imdac)-Leu-Lys(iPr)-Pro-D..Ala-NH 2 .9 and pharmaceutically acceptable salts thereof.

Ac-D-Nal-4-Cl-D-Phe-D)-Pal-Ser-N-Me-Tyr-D-Asn-Leu-Lys(iPr)-Pro-D.Ala.NH 2 and pharmaceutically acceptable salts thereof 20 Ac-D-Nalb4-Cl-D-Phe-D-Pal-Ser-Tyr-D-Asn-LeuLys(iPr)-ProD-Ala-NH 2 and pharmaceutically acceptable salts thereof.

In another embodiment, the invention provides a peptide comprising a structure:

A-B-C-D-E-F-G-H-I-J

9999 wherein A is pyro-Glu, Ac-D-Nal Ac-D-Qal, Ac-Sar, or Ac-D-Pal :B is His or 4-CI-D-Phe C is Trp, D-Pal, D-Nal, L-Nal-D-Pal(N-O), or D-Trp D is Ser E is N-Me-Ala, Tyr, N-Me-Tyr, Ser, Lys(iPr), 4-Cl-Phe, His, Asn, Met, Ala, Arg or Ile; F is x Y R 0 wherein R and X are, independently, H or alkyl; and Y comprises a dipolar moiety; G is Leu or Trp; H is Lys(iPr), Gln, Met, or Arg -18- I is Pro; and J is Gly-NH 2 or D-Ala-NH2; or a pharmaceutically acceptable salt thereof. In preferred embodiments, Y is selected from the group consisting of ylids, tertiary amine oxides, nitrile oxides, pyridine-N-oxides, and pyridinium zwitterions. In particularly preferred embodiments, Y is an ylid, a pyridine-Noxide or a pyridinium zwitterion.

In another aspect, the invention provides a peptide comprising a structure:

A-B-C-D-E-F-G-H-I-J

wherein A is pyro-Glu, Ac-D-Nal Ac-D-Qal, Ac-Sar, or Ac-D-Pal B is His or 4-Cl-D-Phe C is Trp, D-Pal, D-Nal, L-Nal-D-Pal(N-O), or D-Trp D is Ser E is N-Me-Ala, Tyr, N-Me-Tyr, Ser, Lys(iPr), 4-Cl-Phe, His, Asn, Met, Ala, Arg or 15 Ile; F is D-Arg, D-Lys(iPr), D-Pal(iPr), D-Cit or Q, wherein Q has a structure x z xKr wherein R and X are, independently, H or alkyl; and Z comprises a cationic moiety selected from the group consisting of e cationic pyridinium moieties and sulfonium moieties, with the proviso that the cationic moiety is not N-methyl pyridinium; G is Leu or Trp; H is Lys(iPr), Gin, Met, Arg or Q; 0 25 I is Pro; and J is Gly-NH 2 or D-Ala-NH 2 with the proviso that at least one ofF and H is Q; or a pharmaceutically acceptable salt thereof.

In preferred embodiments, F is Q and Z is a cationic pyridinium moiety. In preferred embodiments, Z is an N-benzyl pyridinium moiety. In other preferred embodiments, F is Q and Z is a sulfonium moiety. In yet other preferred embodiments, H is Q and Z is a sulfonium moiety.

In another aspect, the invention provides a peptide comprising a structure:

A-B-C-D-E-F-G-H-I-J

wherein A is p-Glu, Ac-D-Nal, Ac-D-Qal, Ac-Sar, or Ac-D-Pal B is His or 4-CI-D-Phe -19- C is Trp, D-Pal, D-Nal, L-Nal-D-Pal(N-), or D-Trp D is Scr E is N-Mc-Ala, Tyr, N-Mc-Tyr, Ser, Lys(iPr), 4-C-Phe, His, Asn, Met, Ala, Arg or Ile; F is wherein R and X are, independently, H or alkyl; and T comprises a receptor-modifying moiety; G is Leu or Trp; H is Lys(iPr), Gln, Met, or Arg I is Pro; and 1J is Gly-NH-) or D-Ala-NH2; or a pharmaceutically acceptable salt thereof.

i' 15 In preferred embodiments, T is selected from the group consisting of ylids, **see: sulfoniurn moieties, a-halocarbonyls, sulfates, sulfonates. alkyl halides and benzyl halides.

i' a particularly preferred embodiment, T is an a-halocarbonyl.

In another embodiment, the invention provides a peptide comprising a structure: A-B-C-D-E-F-G-H-1-J wherein A is pyro-lu, Ac-D-Nal Ac-D-Qal, Ac-Sar, or Ac-D-Pal B is His or 4-CI-D-Phe C is Trp. D-Pal. D-Nal, L-Nal-D-Pal(N-0). or D-Trp D is Ser E is N-Me-Ala, Tyr, N-Me-Tyr, Ser, Lys(iPr), 4-Cl-Phe, His, Asn, Met, Ala, Arg or Ile; F is N

-K

R

wherein R and X are, independently, H or alkyl; and M comprises an N-acyl hydrophilic moiety; G is Leu or Trp; H is Lys(iPr), Gln, Met. or Arg I is Pro: and J is Gly-NH 2 or D-Ala-NH2; or a pharmaceutically acceptable salt thereof.

In another aspect, the invention provides a peptide comprising a structure:

A-B-C-D-E-F-G-H-I-J

wherein A is pyro-Glu, Ac-D-Nal, Ac-D-Qal, Ac-Sar, or Ac-D-Pal B is His or 4-CI-D-Phe C is Trp, D-Pal, D-Nal, L-Nal-D-Pal(N-0), or D-Trp D is Ser E is N-Me-Ala, Tyr, N-Me-Tyr, Ser, Lys(iPr), 4-CI-Phe, His, Asn, Met, Ala, Arg or Ile; F is X L

N

R

wherein R and X are, independently, H or alkyl; and L comprises a small polar moiety; SG is Leu or Trp; H is Lys(iPr), Gin, Met, or Arg I is Pro; and 20 J is Gly-NH 2 or D-Ala-NH 2 or a pharmaceutically acceptable salt thereof.

In another aspect, the invention provides an LHRH antagonist, comprising a peptide having a sidechain modified by a dipolar moiety forming a modified peptide, such that the modified peptide has LHRH antagonist activity. In preferred embodiments, the dipolar S. moiety is selected from the group consisting of ylids, tertiary amine oxides, nitrile oxides, pyridine-N-oxides, and pyridinium zwitterions. In more preferred embodiments, the dipolar moiety is an ylid, a pyridine-N-oxide or a pyridinium zwitterion. In other preferred embodiments, the peptide comprises about 8 to about 12 residues. In more preferred embodiments, the peptide comprises 10 residues. In certain preferred embodiments, the dipolar moiety modifies residue 6. In certain preferred embodiments, the LHRH antagonist is a peptide mimetic.

In another embodiment, the invention provides an LHRH antagonist, comprising a peptide having a sidechain modified by a cationic moiety selected from the group consisting of cationic pyridinium moieties and sulfonium moieties, with the proviso that the cationic moiety is not N-methyl pyridinium, forming a modified peptide, such that the modified peptide has LHRH antagonist activity. In preferred embodiments, the cationic -21moiety is a cationic pyridinium moiety. In other preferred embodiments, the cationic moiety is a sulfonium moiety. In other preferred embodiments, the peptide comprises about 8 to about 12 residues. In more preferred embodiments, the peptide comprises residues. In other preferred embodiments, the cationic moiety modifies at least one of residue 6 and residue 8. In other preferred embodiments, the LHRH antagonist is a peptide mimetic.

In another embodiment, the invention provides an LHRH antagonist, comprising a peptide having a sidechain modified by a receptor-modifying moiety forming a modified peptide, such that the modified peptide has LHRH antagonist activity. In preferred embodiments, the receptor-modifying moiety is selected from the group consisting of ylids, sulfonium moieties, a-halocarbonyls, sulfates, sulfonates alkyl halides, and benzyl halides.

In preferred embodiments, the-peptide comprises about 8 to 12 residues. In more preferred embodiments, the peptide comprises 10 residues. In preferred embodiments, the receptormodifying moiety modifies residue 6. In preferred embodiments, the LHRH antagonist is a 15 peptide mimetic.

S. In another embodiment, the invention provides an LHRH antagonist, comprising a peptide having a sidechain modified by a hydrophilic N-acyl moiety forming a modified peptide, such that the modified peptide has LHRH antagonist activity. In preferred .0 embodiments, the hydrophilic N-acyl moiety modifies position 6. In preferred embodiments, a residue comprises a hydrophilic acyl moiety is selected from the group consisting of D-Lys(Imdac), D-Lys(Ppic), and D-Lys(Dodac).In preferred embodiments, the hydrophilic N-acyl moiety has a log P between -1 and +2.

In another embodiment, the invention provides an LHRH antagonist, comprising a peptide having a small polar moiety in position 6, such that the peptide has LHRH antagonist activity. In preferred embodiments, the antagonist has an AOA less than about 1 Gg. In preferred embodiments, the antagonist has a histamine-releasing activity of at least about pg.

II. Pharmaceutical Compositions The LHRH antagonist peptides of the invention can be incorporated into pharmaceutical compositions suitable for administration to a subject. In a preferred embodiment, the pharmaceutical composition comprises an LHRH antagonist peptide of the invention and a pharmaceutically acceptable carrier.

A "therapeutically effective amount" refers to an amount effective, at dosages and for periods of time necessary, to achieve the desired result. A therapeutically effective amount of an LHRH antagonist peptide of the present invention may vary according to factors such as the disease state, age, sex, and weight of the individual, and the ability of the antagonist to elicit a desired response in the individual. Dosage regimens may be -22adjusted to provide the optimum therapeutic response. A therapeutically effective amount is also one in which any toxic or detrimental effects of the antagonist are outweighed by the therapeutically beneficial effects. A non-limiting range for a therapeutically effective amount of an LHRH antagonist is 0.01 Lg/kg-10 mg/kg, preferably between about 0.01 and 5 mg/kg. It is to be noted that dosage values may vary with the severity of the condition to be alleviated. It is to be further understood that for any particular subject, specific dosage regimens should be adjusted over time according to the individual need and the professional judgment of the person administering or supervising the administration of the compositions, and that dosage ranges set forth herein are exemplary only and are not intended to limit the scope or practice of the claimed composition.

As used herein, "pharmaceutically acceptable carrier" includes any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents, and the like that are physiologically compatible. Preferably, the carrier is suitable for intravenous, intramuscular, subcutaneous or parenteral administration by 15 injection). Depending on the route of administration, the active compound may be coated in a material to protect the compound from the action of acids and other natural conditions Swhich may inactivate the compound.

A "pharmaceutically acceptable salt" refers to a salt that retains the desired biological activity of the parent compound and does not impart any undesired toxicological effects. Examples of such salts are salts of acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, phosporic acid, nitric acid, and the like; acetic acid, oxalic acid, tartaric acid, succinic acid, malic acid, benzoic acid, pamoic acid, alginic acid, methanesulfonic ~acid, naphthalenesulfonic acid, and the like. Also included are salts of cations such as sodium, potassium, lithium, zinc, copper, barium, bismuth, calcium, and the like; or 25 organic cations such as trialkylammonium. Combinations of the above salts are also useful.

An LHRH-R antagonist can be administered by a variety of methods known in the art. In a preferred embodiment, the LHRH-R antagonist is administered in a time release formulation, for example in a composition which includes a slow release polymer, or by depot injection. The active compounds can be prepared with carriers that will protect the compound against rapid release, such as a controlled release formulation, including implants, transdermal patches, and microencapsulated delivery systems. Biodegradable, biocompatible polymers can be used, such as ethylene vinyl acetate, polyanhydrides, polyglycolic acid, collagen, polyorthoesters, polylactic acid and polylactic, polyglycolic copolymers (PLG). Many methods for the preparation of such formulations are patented or generally known to those skilled in the art. See, Sustained and Controlled Release Drug Delivery Systems, J.R. Robinson, ed., Marcel Dekker, Inc., New York, 1978.

Particularly preferred formulations include controlled-release compositions such as are -23known in the art for the administration of leuprolide (trade name: Lupron), e.g., microcapsules Patents 4,652,441 and 4,917,893), injectable formulations Patent 4,849,228), lactic acid-glycolic acid copolymers useful in making microcapsules or injectable formulations Patents 4,677,191 and 4,728,721), and sustained-release compositions for water-soluble polypeptides Patent 4,675,189).

When appropriately formulated, an LHRH-R antagonist may be orally administered, for example, with an inert diluent or an assimilable edible carrier. The LHRH antagonists and other ingredients may also be enclosed in a hard or soft shell gelatin capsule, compressed into tablets, or incorporated directly into the subject's diet. For oral therapeutic administration, the LHRH antagonists may be incorporated with excipients and used in the form of ingestible tablets, buccal tablets, troches, capsules, elixirs, suspensions, syrups, wafers, and the like. The percentage of the LHRH antagonists in the compositions and preparations may, of course, be varied. The amount of the LHRH antagonists in such therapeutically useful compositions is such that a suitable dosage will be obtained.

15 To administer the LHRH antagonists by other than parenteral administration, it may be necessary to coat the compound with, or co-administer the compound with, a material to prevent its inactivation. For example, the LHRH antagonists may be administered to a subject in an appropriate carrier, for example, liposomes, or a diluent. Pharmaceutically acceptable diluents include saline and aqueous buffer solutions. Liposomes include waterin-oil-in-water CGF emulsions as well as conventional liposomes (Strejan et al., (1984) J.

Neuroimmunol. 7:27). Pharmaceutically acceptable carriers include sterile aqueous solutions or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersion. The use of such media and agents for pharmaceutically active substances is well known in the art. Except insofar as any conventional media or agent is incompatible with the active compound, use thereof in the pharmaceutical compositions of the invention is contemplated. Supplementary active compounds can also be incorporated into the compositions.

Therapeutic compositions typically must be sterile and stable under the conditions of manufacture and storage. The composition can be formulated as a solution, microemulsion, liposome. or other ordered structure suitable to high drug concentration.

The carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (for example, glycerol, propylene glycol, and liquid polyetheylene glycol, and the like), and suitable mixtures thereof. The proper fluidity can be maintained, for example, by the use of a coating such as lecithin, by the maintenance of the required particle size in the case of dispersion and by the use of surfactants. In many cases, it will be preferable to include isotonic agents, for example, sugars, polyalcohols such as manitol, sorbitol, or sodium chloride in the composition. Prolonged absorption of the injectable compositions can be brought about by including in the composition an agent which delays absorption, for example, monostearate salts and gelatin.

-24- Sterile injectable solutions can be prepared by incorporating the active compound LHRH antagonist) in the required amount in an appropriate solvent with one or a combination of ingredients enumerated above, as required, followed by filtered sterilization. Generally, dispersions are prepared by incorporating the active compound into a sterile vehicle which contains a basic dispersion medium and the required other ingredients from those enumerated above. In the case of sterile powders for the preparation of sterile injectable solutions, the preferred methods of preparation are vacuum drying and freeze-drying which yields a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof.

Dosage regimens may be adjusted to provide the optimum therapeutic response.

For example, a single bolus may be administered, several divided doses may be administered over time or the-dose may be proportionally reduced or increased as indicated by the exigencies of the therapeutic situation. It is especially advantageous to formulate parenteral compositions in dosage unit form for ease of administration and uniformity of 15 dosage. Dosage unit form as used herein refers to physically discrete units suited as unitary dosages for the mammalian subjects to be treated; each unit containing a predetermined quantity of active compound calculated to produce the desired therapeutic effect in i. association with the required pharmaceutical carrier. The specification for the dosage unit •o forms of the invention are dictated by and directly dependent on the unique characteristics of the active compound and the particular therapeutic effect to be achieved, and the limitations inherent in the art of compounding such an active compound for the treatment of sensitivity in individuals.

III. Methods of Using the LHRH Antagonists of the Invention The LHRH antagonist peptides of the present invention are useful for the treatment of such conditions as precocious puberty, prostate cancer, ovarian cancer, benign prostatic hypertrophy, endometriosis, uterine fibroids, breast cancer, premenstrual syndrome, polycystic ovary syndrome, and diseases which result from excesses of gonadal hormones in humans or animals of either sex. The LHRH antagonist peptides of the invention are also useful for behavior modification "chemical castration"). The LHRH antagonist peptides are also useful for controlling reproduction in both males and females.

Furthermore, the peptides of the invention may be used to treat immunosuppressed patients, as described in, for example, U.S. Patent 5,003,011.

Thus, in one embodiment, the invention provides a method of inhibiting LHRH activity in a subject, comprising administering to a subject an effective amount of an LHRH antagonist of the present invention, such that LHRH activity is inhibited.

In another embodiment, the invention provides a method of inhibiting LHRH activity in a cell, comprising contacting a cell with an LHRH antagonist of the invention, such that LHRH activity is inhibited.

In another embodiment, the invention provides a method of inhibiting growth of a hormone-dependent tumor in a subject, comprising administering to a subject an effective amount of an LHRH antagonist of the invention, such that tumor growth is inhibited. In a preferred embodiment, an LHRH antagonist of the invention is administered to a subject suffering from prostate cancer to inhibit the growth of the prostatic tumor.

In another embodiment, the invention provides a method of inhibiting ovulation in a subject, comprising administering to a subject an effective amount of an LHRH antagonist of the invention, such that ovulation is inhibited.

In another aspect, the invention provides a packaged formulation for treating a subject for a disorder associated with LHRH activity, comprising an LHRH antagonist of the invention packaged with instructions for using the LHRH antagonist for treating a subject having a disorder associated with LHRH activity.

In another aspect, the invention encompasses use of the peptide compounds of the invention in the manufacture of a medicament for the treatment of a disorder in which 15 inhibition of LHRH activity is beneficial. For example, the disorder in which inhibition of S. LHRH activity is beneficial can be selected from the group consisting of precocious puberty, prostate cancer, ovarian cancer, benign prostatic hypertrophy, endometriosis, uterine fibroids, breast cancer, premenstrual syndrome, polycystic ovary syndrome, and diseases which result from excesses of gonadal hormones.

This invention is further illustrated by the following examples which should not be construed as limiting. The contents of all references, patents and published patent applications cited throughout this application are hereby incorporated by reference.

In the examples, the following abbreviations are used: Boc: N-t-butoxycarbonyl HOBt: 1-hydroxybenzotriazole MCPBA: m-chloroperbenzoic acid DCC: dicyclohexylcarbodiimide EXAMPLE 1: Anti-Ovalulatory and Histamine Release Activity of LHRH Antagonists Anti-ovulatory activity (AOA) was measured by an in vivo assay in rats, as described in Corbin and Beattie, Endocrine Res. Commun. 2:1 (1975). In brief, female rats are injected with a candidate LHRH antagonist on the day of proestrus; in general, the candidate LHRH antagonist was dissolved in 0.1% DMSO. The ability of the candidate peptide to inhibit ovulation is measured by determining the number of rats which ovulate.

A candidate peptide is considered to have LHRH antagonist qualities if it inhibits ovulation -26-

S

S S in at least 50% of the treated rats at a dose of 5 jig per rat. Preferred LHRH antagonists inhibit ovulation in at least 50% of rats at a dose of 2 pLg per rat, more preferably at a dose of 1 jag per rat, and still more preferably at a dose of 0.5 gg per rat.

Histamine-releasing activity was assayed by the method described in U.S. Patent 4,851,385 to Roeske. Briefly, a suspension of rat mast cells was added to increasing concentrations of an LHRH antagonist peptide and incubated for 15 minutes at 3 7 0 C. The buffer contained 25 mM PIPES, PH 7.4, NaCl (119 mM), KCl (5 mMv), NaOH glucose (5.6 mlv), CaC1 2 (1 mM) and 0. 1% bovine serum albumin. The reaction was stopped by centrifugation at 400 x g for 15 minutes at 4*C, and the supernatant assayed for histamine content by a published method (Siriganian (1974) Anal Biochem. 57:3 83 and Siriganian and Hook (1986) in "Manual of Clinical Imnmunology", 3rd ed., N.R. Rose, H.

Friedman, and J.L Fahey, eds., p. 808), or by a manual method which gave similar results.

Maximal histamine release occurred rapidly, typically in less than one minute. No evidence of cell toxicity was seen for any of the peptides tested. The histamine-releasing 15 activity of peptides is measured as the ED 50 in gg/ml; a higher ED 50 represents lower histamine release.

The AQA and histamine-releasing activities of several peptides are summnarized in Table 1.

Table I. LHRH Antagonists Compound Sequence AO activity Histamine (AOA) release 3341 Ac-D-Nal 1.4-CI-D-Phe 2 1)-Pal- 3 D-Glnb- 4/10@l jig 106 8 1)-Ala I 0 -LHRH.TFA 2/10@2 g 3342 Ac-D-Nal 1 4-Cl-D-Phe 2 1)-Pal', D-Asn3- 2J10@2 gg 126 Lys(iPr) 8 D-Ala I -LHRH.TFA 3343 Ac-D-Nal I. 4-CI-D-Phe 2 D-Pal 3 D-Th-ro- 5/10@1 pg 62 Lys(iPr) 8 1)-Ala 1 I -LHRH-.TFA 3344 Ac-D-Nal 1 4-CI-D-Phel, 1)-Pal 3 D-C!itb'- 9/10@l 1pg 32 Lys(iPr) 8 Pip 9 -D-Ala' I 0 -LHRI-.TFA 3361 Ac-D-Nal 1 4-CI-D-Phey, 1)-Pal 3 1/8@5 gg 131 Glu(Taurine) 6 -Lys(iPr) 8 D-Ala O- 3362 Ac-D-Nal 1 4-Cl-1-Phe2, D-Pal-', D-CitF_ 4/8@l 1pg 22 8 3363 Ac-D-Nal i. 4-CI-D-Phe 2 1)-Pal 3 D-Cit6- 6/8@ 1 pig Lvs(iPr) 8 Pip 9 -LHRH.TFA 3364 Ac-D-Nal 1 ,4-CI-D-Phe 2 1)Pal 3 D-Phe(4- 6/8@ 1 pg 14 2 6 -Lys(iPr) 8 1-Ala 1 0 -LHRH.TFA 3365 Ac-D-Nal I.4-CI-D-Phe- 2 D-Pal 3 D-Citb- 24 8 ProNHOt-des-Gly 1 I -LHRH.TFA 3366 Ac-D-(or L)-9-anthryl-Ala I, 4-CI-D-Phe, 6/8@~5 g Pal 3 D-Cit 6 -Lys( iPr) 8 1)-Ala 1

I

0 -LHRI-LTFA 3367 Ac-L-(or D)-9-anthryl-Ala I, 4-CI-D-Phe-Z, D- 7/8@5 g 3 D-C it 6 -Lys(iPr) 8 D-Ala 1 0 -LHRH.TFA

S

C

55

S

@0Sg@e 0 0 *00*@e 0 *0 00 0 0 0 -27- 3368 Ac-D-(or L)-Ada-Ail, 4-Cl-D-Phey, 1)-Pal 3 5/8@5 jig 34 3369 Ac-L-(or D)-Ada-Ala I, 4-Cl-D-Phey, 7/8@S jig 93 3423A Ac-D-Nal I 4-Cl-D-Phe 2 z, 1-Pal 3 J,D1- 7/10@0O.5 jig 52 Lys(Glc) 6 -Lys(iPr) 8 D-Ala 1 I -LHRH.TFA 2/1 0@~1 tg 0/10@2_Mg 3428 Ac-D-Nal 1 4-C l-1-Phe2, 1)-Pal- 3 1)-Pal(1 1/8@ 1 jig Bu) 6 Lys(iPr) 8 D-Ala I 3429 Ac-D-NaI 1 4-Cl-D-Phe 2 D-Pal- 3 D- 0/8@ 1 jig 6 Lys(iPr) 8 1)-Ala 1 I -LHRH.TFA 4/8@0.5 g 3430 Ac-D-Nal 1 4-CI-D-Phe 2 1)-Pal 3 Pal-', 3/8@ 1 Mg 6 Lys(iPr) 8 1)-Ala' 0 -LH-RH.T-FA 3431 Ac-D-Nal T,4-CI-D-Phe 2 1)-Pal- 3 Cit-), 6/8@1 Mig C it 6 Lys(iPr) 8 1)-Ala'I 0 -LHRH.TFA 3432 Ac-D-Nal 1 4-CI-D-Phe-Z, 1)-Pal 3 Pal-', D- 7/8@ 1 jg Cit 6 Lys(iPr) 8 D-Ala I 3433 Ac-D-Nal 1 4-Cl-D-Phe2, 1)-Pal 3 Cit-), D- 5/8@1 g Pal 6 Lys(iPr) 8 1)-Ala 1 I -LHRH.TFA______ 3434 Ac-D-Nal 1 4-Cl-D-Phe 2 D-Pal-', Asn 4 4/8@ 1 g Tyr 5 D-Cit 6 Lys(iPr) 8 1)-Ala LHRI-LTFA 3435 AcDNl1 -lDPe2 -aJ i-,D 7/8@l1 g 6 Lys(iPr) 8 1-Ala' 0 -LHRI-LTFA 3436 Ac-D-Nal 1 4-Cl-1)-Phe 2 1)-Pal- 3 D- 7/8@1l g HomoArg(N02) 6 Lys(ipr) 8 1)-Ala' 0 3437 Ac-D-Nal 1 4-CI-1)-Phe 2 D-Pal- 3 D- 7/8@1 jig Lys(Glycolyl) 6 Lys(iPr) 8 1)-Ala' 0 3438 Ac-D-Nal I, 4-CI-D-Phe 2 1)-Pal 3 2/8@1 Mg 5.6 Lvs(iPrPic) 6 Lys(iPr) 8 ,D1-Ala' 0 3439 Ac-D-Nal 1 4-CI-1)-Phe 2 1)-Pal 3 D- 2/8@ 1 Mig Lys(HomoPro) 6 Lys( iPr) 8 D-Ala' 0

LHR}I.TFA_____

2958 Ac-D-Nal, 4-CI-D-Phe 2 D-Pal 3

D)-

Pal( iPr) 6 Lys(iPr) 8 D-Ala' I -LHRHLTFA 3440 Ac-D-Nal 1 4-CI-D-Phe 2 D-Pal 3 1)-Lys(3- 2/8@ 1 jig pyridineacetic) 6 Lys(iPr) 8 1)-Ala' 0.

LHRH.TFA

3441 Ac-D-Nal 1 4-CI-D-Phe 2 z, D-Pal- 3 D-Lys(2- 8/8@ 1 g ClNic) 6 Lys(iPr) 8 1)-Ala' 0

-LHRJ-.TFA

3442 Ac..NcMe-D..Nal 1, 4-CI-D-Phe 2 D-Pal 3 D- 7/8@1 g 6 Lys(iPr) 8 1)-Ala' 0 3502 Ac-D-Na7 1 4-CI-1)-Phe 2 D-Pal 3 6/8@l1 g Lys(Otac) 5 D-Lys(Qtac) 6 Lys(iPr) 8 1)- Ala' 0 -LHRH.TFA 3503 Ac-D-Nai 1 4-CI-1)-Phe 2 1)-Pal- 3 6/8@1 g Lys(ONic) 5 D-Lys(ONic) 6 Lys(iPr) 8 1)- 0

-LHRI-LTFA____

00 0 0 0 0000 0 0000 00 00 0 0 0 a a.

a a. a 28- 3504 Ac-D-Nal 1, 4-Cl-D-Phe2, D-Pal-J, Lys(Pyz).', 4/8@1;tg D-Lys(pyz) 6 Lys(iPr) 8 D-Ala 1 0 LHRH.TFA 3552 Ac-D-NalI 1 4-Cl-D-Phie2, D-PalP, D-GluUb 8 8 @I;tg Lys(iPr) 8 D-Ala 1 I 3505 Ac-D-Nal 1 4-CI-D-Phe- 2 D-PalP, D-Ly-so, 581 8 D-Al I 0 3506 Ac-D-Nal 1 4-Cl-D-Phe 2 D-PalP, D- 4/8@ljgg Lys(Gulonyl) 6 Lys(iPr) 8 D-Alal 0

_______LHRH.TFA

3553 Ac-D-Nal 1 4-CI-D-Phe 2 D-PalP, D- 8 8 @l~g Lys(iPrNic) 5 D-Lys(iPrNic) 6 Lys(iPr) 8

D-

Ala' I -LHRH.T'FA 3507 Ac-D-Nal, 4-Cl-D-Phe 2 D-Pal-J, D- 1/8@ 1 Ag Lys(ONic) 6 Lys(iPr) 8 D-Ala' I -LHRH.TFA 3508 Ac-D-Nal i, -Cl-D-Phe-Z, D-Pal i, D- 01 8 @Ipg Lvs(OTac) 6 Lys(iPr) 8 D-Ala I -LHRH.TFA 6 8 @0.

5 g 3509 Ac-D-Nal 1, 4-CI-D-Phe 2 D-PaP, D- ____Lys(Pyz) 6 Lys(iPr) 8 D-Ala 1 0

-LHRH.TFA

3510 Ac-D-Nal 1 4-CI-D-Phe 2 D-Pal-3, D- Lys(nBuNic) 6 Lys(iPr) 8 D-Ala 1 0

_______LHRI-LTFA

3511 Ac-D-Nal 1 4-CI-D-Phe 2 D-Pal- 3 7 8 @1 gg 6 Lys(iPr) 8 D-Ala 1 I -LHRH.TFA 3543 Ac-D-Nal 1 4-Cl-D-Phe2, D-PalP, D- 6/8@ 1 pg 6 Lys(iPr) 8 D-Ala I -LHRH.TFA 3563 Ac-D-Nal 1, 4-CI-D-Phe-, D-Pal-3 Lys(pGiu) 5 D-Lys(pGlu) 6 Lys(iPr) 8

D-

1 I -LHR-TEA 3540 Ac-D-Nal 1, 4-CI-D-Phe 2 D-PaI 3 NcLMe- Tyr 5 D-PaI(iPr) 6 Lys(iPr) 8 D-Ala' 0

_______LHRH.TFA

3541 Ac-D-Nal 1 CcLMe-4Cl-Phe 2 D-Pal 3 NaL 1/8@ 1 gg Me-Tyr 5 D-Pal(iPr) 6 Lys(iPr) 8 D.Ala' 0 LHRH4TFA 3554 Ac-D-NaI 1 4-C I-D-Phe2, D-Pal-3, 6 Lys(iPr) 8 D-Ala' I -LHRH-.TFA 3542 Ac-D-Nal 4-CI-D-Phe 2 D-PalP, D- 7 8 @2jpg G Glu(PEG) 6 Lys(iPr) 8 D-Ala 1 I -LHRI-L2TFA______ 3565 AcDNl1 -lD-hT -aD 6 Lys( iPr) 8 D-Ala 1 I -LHRI-L2TFA 3551 AcDNl1 -lD-hl :al) 6 8 @1 gg Lys(CNa) 5 D-Lys(CNa) 6 Lys(iPr) 8

D-

1 0 -LHRH.2TFA 3544 Ac-D-Nal i, 4-CI-D-Phe 2 D-PaIJ,6/@1A Lys(CIN ic) 5 D-Lys(CINic) 6 Lys(iPr) 8

D-

Ala 1 0 -LHRH.2TFA 3555A Ac-D-Nal 1 4-Cl-D-Phe2, D-Pal-3, D- Lys(Ac) 6 Lys(iPr) 8 D-Ala' I -LHRH.2TFA 3564 Ac-D-Nal 1 4-Cl-D-Phe-", D-Pal-3, D- Glu(Tris) 6 Lys(iPr) 8 D-Ala' I -LHRH.2TFA a a a a a a. *a a a a a -29- 3545 Ac-D-Nal 1 4-CI-D-Phe 2 D-Pa1-J, D- 7 1 g G ln(ipr) 6 Lys(iPr) 8 D-Ala I -LHRH.2TFA 3550 Ac-D-Nal 1 4-CI-D-Phe 2 D-PalI 3 D- 6/8@ 1 jig Glu(CSer) 6 Lys(iPr) 8 D-Ala' 0 LHRH.2TFA_____ 3549 Ac-D-Nal 1 4-CI-D-Phe4, D-Pal 3 D- 6/8@ 1 pg 6 Lys(iPr) 8 D-Ala 1 0 3548 Ac-D-Nal 1 4-CI-D-PheA- D-PalP, Lys-*, D- 6/8@lpig 6 Lys(iPr) 8 D-Ala' 1 0 LHRH.4TA 3566 Ac-D-Nal I, 4-Cl-D-Phe2, D-Pa1P, Lys(Nic)-3, D-Pal(iPr) 6 Lys(ipr) 8 D-Ala.

1 0- LHRH.3TFA____ 3567 Ac-D-Nal 1 4-CI-D-Phe2, D-Pal- 3 D-PaI(iPr) 6 Lys(iPr) 8 D-Ala 1 0 3568 Ac-D-Nal 1 4-cI-D-Phe 2 D-Pal-3, D- Glu(DEGA) 6 Lys(iPr) 8 D-Ala 1 0..

_______LHRI-L2TFA 3547 Ac-D-Nal 1 4-CI-D-Phe 2 D-Pal-', Lys(Nic)-5, 6/8@ 1 gg D-PaI(Bzl) 6 Lys(iPr) 8 D-Aa 1 0- _______LHRH.3TFA 3569 Ac-D-Nal 4-CI-D-Phe 2 D-Pai-3, Lys(Ac)- D-PaI(Bzl) 6 Lys(iPr) 8 D-Alal 0..

LHRH.3TFA 3546 Ac-D-NalI, 4-CI-D-Phe 2 D-PaP-, 6/8@ Ijgg Lys(TFAc) 6 Lys(ipr) 8 D-Ala 10 LHRH.2TFA 3570 Ac-D-Nal, 4-Cl-D-Phe2, D-Pal-3, Lys-*, D-Pal(Bzl) 6 Lys(iPr) 8 D-Ala 1 0 LHRI-I3TFA 3571 Ac-D-Nal 1 4-Cl-D-Phe 2 Lys(iPr)3, D-Lys(Nic) 6 Lys(iPr) 8 -D-Ala 1 0 LHRI-I3TFA 3572 Ac-D-NaI 1 4-CI-D-Phe 2 D-PaI-', Lys(iPr), D-Lys(Pic) 6 Lys(iPr) 8 D-A la 1 0 LHRH.3TFA Ac-D-Nal 1 4-Cl-D-Phe 2 Z, D-Pal- 3 Lys(TFAc) 5 D-Lys(TFAc) 6 Lys(iPr) 8

D-

Ala 1 I -LHRI-L2TFA Ac-D-Nal 1 4-CI-D-Phe 2 D-Pal- 3 Lys(iPr)3, 4-C I-D-Phe 6 Lys(iPr) 8 D-Ala 1 0 ________LHRH.3TFA Ac-D-Nal 1 4-CI-D-Phez, D-PaP, Lys(iPr)3, 6 Lys(iPr) 8 D-Ala' I -LHRI-.3TFA Ac-D-Nal 1 4-CI-1-Phe 2 D-Pal 3 -Lys(iPr)-, D-Lys(pGlu) 6 Lys( iPr) 8 D-Ala 1 0 ________LHRI-L3TFA Ac-D-Nal 1 4-CI-D-Phe 2 D-Pal-, Lys(iP'r)' D-Lys(OTac) 6 Lys(iPr) 8 D-Ala 1 0 D-Pal(Bzl) 6 Lys(iPr)g, D-Ala Ac-D-Nar, 4-Cl-D-Phe2, D-Pal-J, Lys(Pic)-), D-PaI(ipr) 6 Lys(iPr) 8 D-Ala 1 0 LHRI-I3TFA 3721 Ac-D-Nal 1 4-CI-D-Phe 2 D-PaIJ D-Lys(3-A 4/8@1.0 -Pro) 6 Lys(iPr) 8 D-Al I 0 -LHRH-TFA 3722 Ac-D-Nal-4-Cl-D-Phel 2 ,D-Pal13,D-Lys(Ac-D- 8/8@5.0 Nal' ,4-CI-D-Phe 2 ,D-PaI 3 ,Ser) 6 ,Lys(iPr) 8

,D-

3723 Ac-D-Qa1 1 ,4-Cl-D-Phe-,D-Pa1,D-7/@.

Lys(pGlu) 6 Lys(ipr) 8 ,D-Ala' I -LHRH.TFA 78 3740 Ac-D-Qal l,4-Cl.D..Phel,D..PaliJ,D..Lys(Ac)b), 6/8@1 .0 Lys(ipr) 8 .D-Alal I -LHRH.TFA______ 3741 Ac..D.Nal 1,4:C1..D.Phe2,D..Pal-3,D- 1/8@ Lys(lmdac) 6 Lys(iPr) 8 ,D-Ala' I -LHR.H.TFA 6/8@0.5 3742 Ac-D-QaI 1 ,-4-Cl-D-Phe'2,D-Pal-',D- 68 6 Lys(iPr) 8 ,D-Ala' I -LHRH.TFA 68 3743 Ac-D-Nal 1,4-Cl-D-Phe 2 ,D-Pal-3,SerP,D- 8/81.0 Pal(iPr) 6 ,Lvs(iPr) 8 ,D-Ala' I -LHRH-.2TFA 3753 Ac-D-Nal 1 ,4-Cl-D-Phez,D-PalJ,D- 7/8@ Lys(iPr) 5 Lys(TFAc) 6 ,Lys(iPr) 8 ,D-Ala LHRH.2TFA 3754 Ac-D-Nal 1,4-CI-D-Phe Z,D-Pa-i .His)D- 5/8@ 6 ,Lys(iPr) 8 ,D-Ala 1 I -LHRH.2TFA 3744 Ac-D-Na 1 ,4-C1-D-Phe2,D-PaIP,Asn),D- 7/8@ Pal(iPr) 6 ,Lys(iPr) 8 ,D-Ala' I 0 -LHR}1.2TFA 3745 Ac-D-Nal 1,4-Cl-D-Phel,D-Pal-',Lys(iPr)-',D- 6/8@ 6 .Lys(iPr) 8 ,D-Ala 1 I -LHRH.2TFA 3755 Ac-D-NaIT,4-CI-D-Phe-,D-Pal',Met 7/821.0 6 ,Lys(iPr) 8 ,D-Ala 1

I

0 -LHRH-.2TFA .3756 Ac-D-NaI' 14-CI-D-Phe2kD-Phe 2 6/8@ Pal 3 ,Ala 5 .D-Pal(iPr) 6 ,Lys(iPr) 8 ,D-Ala LHRI-L2TFA 3757 Ac-D-Nal 1 ,4-CI-D-Phc- 2 ',D-PaP,N-Me- 7/8@ Ala 5 ,D-PaI(iPr) 6 ,Lys(iPr) 8 ,D-Ala 3758 Ac-D-Nal 1 ,4-Cl-D-Phe 2 ,D-Pal:3,D- 5/8@ Lys(Hippic) 6 Lys(iPr) 8 ,D-Ala

LHRI-ITFA

3759 Ac-D-Nal 1 ,4-CI-D-Phe2,D-PalP,D- 5/8@ Lvs(AcGly) 6 Lys(iPr) 8 ,D-Aa' 3760 Ac-D-Nal 1 ,4-CI-D-Phe 2 ,D-PaP-,D- 1/8@ Lys(Ppic) 6 Lys( iPr) 8 ,D-Ala 1 I -LHRI-.TFA 7/8@0.5 3761 Ac-D-Na' 1,4-CI-D-Phe 2 ,D-PaP-,D- 78 6 Lys(iPr)S,D-Ala 1

I

0 -LHRH.TFA 78 3-7-2 Ac-D-Nal 1 .4-C -D-Phe2,D-PalI 6/8@ 6 Lys(iPr) 8 ,D-Ala 1 I -LHRI-1.TFA -31 3763 Ac-Sar 1,4-Cl-D-Pb 2,D-NalP,D-Pa(Bz) 4/8@1 .0 101,6 Lys(iPr) 8 ,D-Ala' I -LHRH.2TFA_____ 3769 Ac-Sar 1 ,4-Cl-D-PheLy, 1-1-Nal-5,D-Pal(-Bzl), 6/8@ Lys(iPr)g,D-Al I 0 -LHRH.2TFA______ 3770 Ac-D-NaI 1 ,4-CI-D-Phe 2 ,D-Pa-i 3 6/8@1.0 PaI(CH 2

COOH)

6 ,Lys(ipr) 8 ,D-Ala 1 0- 0.1DMSO LHRH.TFA__ 3771 Ac-D-Nal' ,4-CJ-D-Phe 2 z,D-PaITD- Lys(Ala) 6 Lys(iPr) 8 ,D-Ala 1 I -LHRJ-LTFA 1.

3772 Ac-Sar' ,4-CI-D-Phe 2 Z,D- 1-.Nali,D.Pal Ir)b, 878@ 8 ,D-Aa I 0 -LHRH.2TFA______ 3773 AcSr,4-CI-D-Phe 2 I -Na] 3 ,D-PaI(iPr)t 0 7/8@ 8 ,D-Ala 1 I -LHRI-.2TFA______ 3785 Ac-D-QalI .4-CI-D-Phe2,D-Pa 3 7/8@ Lys(Gulonyl) 6 ,Lys(iPr) 8 ,D-Ala 1 0 0.1DMSO 3786 AcDNl14C--he,-aJDPlN 4/8@ Lys(iPr) 8 ,D-Ala 1 I -LHRI-LTFA______ 3787 Ac-D-Qa 1 ,4-C1-D-PheL,D-Pa1-3,D- 78 6 Lys(iPr) 8 ,D-Ala 1 I -LHRH.TFA 78 3800 Ac-D-Qa t 1,4-CI-D-Phe 2 z,D-PalI 3 6 Lys(iPr) 8 ,D-Ala' I -LHRH.TFA 78 3801 Ac-D-Qa' 1,4-C1-D-Phe 2 ,D-Pal15,D- 8/8@ 6 Lys(iPr) 8 ,D-Ala' I -LHRH-.TFA 3802 Ac-D-Qa t 1,4-CI-D-Phey,D-PaI 3 6 Lys(iPr) 8 ,D-Ala 1 I -LHRH.TFA 58 3803 Ac-b-Nal 1 ,4-Cl-D-Phey,D-PaI-3,D-2/@.

6 Lys(iPr) 8 ,D-Ala 1 I -LHRH.TFA 28 3804 Ac-D-Pa 1 ,4-CI..D.Phe-Z,D..Pal-,D-Pal(iPr-)b, 8/8@ Lvs(iPr) 8 ,D-Ala 1 I 3827 Ac-D-Nal 1 ,4-CI-D-Phe 2 ,D-Pal-5,N-Me- 4/8@ 6 ,Lys(iPr) 8 ,D-AlI'-LHR.H.TFA 3828 Ac-D-Nal 1,4-CI-D-Phe 2 ,D-PalI',N-Me- 4/8@ 1.0 425,39b Tvr'.D-Lys(Onic) 8 ,Lys(iPr)g,D-Ala 1 0 LHRH.TFA 3829 Ac-D-NaI 1,4-CI-D-Phe2,D-PaI ,N-Me- 8/8@ .D-Lys(Ac) 6 ,Lys(iPr) 8 ,D-Aa' 3852.TF A-NI 1 ,-CI-D-Phe 2 ,D-Pal-' ,Lys(iPr)-),D- 8/8@5.0 His 6 .Trp 7 .0m 8 ,D-Ala 1 I -LHRI-.TFA 3853 Ac-D-Na 1 ,4-CI-D-Phe 2 ,D-PaI-3,His-*,D- 0/8@5.0 Arg 6 Trp 7 ,0m 8 ,D-AlI 0

-LHRH.TFA

3854 Ac-D-Na 1 i,4-C1-D-Phe 2 ,D-PaP~,Arg- 6/8@5.0 His 6 Trp 7 ,0m 8 ,D-Ala 1

I

0 3855 Ac-D-Nal 1 ,4-CI-D-Phe-,D-Pal-j,Lys(iPr)),D- 4/8@ 6 ,Trp 7 .Orn 8 ,D-Ala 1 I -LHRH-.TFA 3851 Ac-D-Na 1 ,4-CI-D-Phe-,D-PaI',4-CI- 0/8@ 1.0 4. 1 a, 5 4 b 6 ,Lys(iPr) 8 ,D-Ala 1 0 6/8@0.5 3882 Ac-D-NaI 4-C1-D-Phe 2 ,D-PaIN-O-3,D- 6/8@ iPr) 6 ,Lysk i Pr) 8 ,D-A la 1 0 LHRH-.2TFA -32- 3880 Ac-D-Nal 1 ,4-Cl-D-Phe 2 -,D-Trp-J,D-Argb, 8/8@1 .0 8 ,D-Ala 1 0

-LHRH.TFA_____

3878 Ac..D.Nal 1,4-C1..D.Phwz,D..TrpJ,D-XArgb, 2.8@ Met(S+Me) 8 ,D-Ala' I -LHRH.2TFA 7/8@0.5 3881 Ac-D-Nal 1 ,4-CI..D.PheJ,D-TrpiJ,D..Metb',D 7/8@1 .0 Ala' 0

-LHRH.TFA

3879 Ac-D-Nal 1 ,4-C1-D-Phe&,D-Trp-3,D- 0/8@ Met(S+Me) 6 D-Ala I -LHRH.2TFA 6/8@0.5 3926 Ac-D-Na 1 ,4-CI..D.Phe 2 ,D..Trp-i,D..Argb, 6/8@1 .0 Lys(COCH 2 Br) 8 ,D-Ala 1 0

-LHRH.TFA_____

3925 Ac-D-Nal 1 ,4-CI-D-PheI,D-Trp-,D- /@10 Met(S+Me) 6 Met(S+Me) 8 ,D-Ala 1 58 10 3

C

3941 Met(S+Me)g-LHRH-.TFA 8/8@50.0 .3942 Lys(COCH 2 Br)8~-LF[RH 8/8@50.0 3948 Ac-D-Na 1 ,4-Cl-D-Phe 2 ,D-Trp- 3 low activity Lys(COCH27Br) 6 ,D-Ala' I 0

-LHRH.TFA

3949* Ac-D-Nal I 4-Cl-D-Phe-Z,D-Pal-3,D- low activity Lys(COCH 2

CH

2 N(Et) 2 6 'D-Ala' 0 _______LHRH.2TFA 3960 Ac-D-Nal 1 ,4-C1-D-Phe2,D-Pal-3,D-Lys(2- 5/8 1.00 pyrim idylthio)acetic) 6 ,Lys(iPr) 8 ,D-Ala 3961 Ac-D-NaI 1 ,4_CI-D-Phe 2 4/8@2.00 Met(S+CH2-C 6

H

5 6 ,D-Ala I 0 -LHR H.2TFA 3/8@ 1.00 3967 Ac-D-Na' 1,4-CI-D-Phek-D-Pal- 3 1 /8@0.5 0.38e,0.- Met(S+CH 3 6 ,D-Ala 1 I -LHRH.2TFA 7/8@0.25 3968* Ac-D-NaI 1 ,4-Cl-D-Phe2,D-Pal-',D-4/@10 Met(s~cH-,COPh) 6 ,D-Ala 1

I

0 -LHR-2TFA 4/@10 3969 Ac-D-NaI 1,4-C l-D.Phe',D..Pali,D- 3/8@ 1.00 2 6 ,D-Ala 1 I -LHRH-.2TFA 3982 Ac-D-Nal i,4-CI-D-Phe 2 .,D-Pal-3.His-)D- 8/8@ 1.00 5 3 c, 3 3 d -Pa(iPr) 6 ,Lys(iPr) 8 ,D-Ala' I-LHRH.2TFA 3983 Ac-D-Nal 1,4-C1-D..Phe-,D..Pali,D-Arg6, 0/8@ 1.00 5.35, 1.32 Met(S+Me) 8 ,D-Ala' I 0 -LHRH-.2TFA 8/8@0.5 h 3984 Ac-D-Nal 1 ,4-CI-D-Phe 2 ,D-Trp 3 i.D- 3/8@ 1.00 Met(S+CH,-CH=CH',) 6 .D-Ala 1 0.

LHRH.2TiA 3985 AcD-NI 4C..DPhe 2 D.Pal.D.Argb, 0/8@1.00 4.4a,3--U Om(COCH2S+Me 2 8 ,D-Ala I QLHRJ-L2TFA 8/8@0.5 3994 AcDNa ,4_Cl-D-Phe 2 ,D-PaP-,D..ArgO, 6/8@ 1.00 Qr(COCH-,SMe) 8 ,D-AlalO--LHRH.2TFA 3995 Ac-D-Nal 1 4-Cl-D-Phe 2 z,D Pal-3,D-Arg 0 ,Met 5/8@ 1.00 8. D-Ala I 0 -LHRH.TFA -33- 4014 Ac-D-Nal 1,4-Cl-D-Phe,D-Pal 0/8@1.00 Lys(COCH2S+Me 2 6 ,D-Ala1 0 -LHRH.2TFA 4015 Ac-D-Nal 1,4-CI-D-Phe 2 ,D-Pal ,D-Arg

O

1/8@1.00 Lys(COCH2S+Me 2 8 ,D-Ala O-LHRH.2TFA 4016 Ac-D-Nal ,4-Cl-D-Phe 2 ,D-Pal 3 6/8@1.00 Met(S+Me) 6 Met(S+Me) 8 ,D-Alal 0 LHRH.2TFA 4013 Ac-D-Nal ,4-Cl-D-Phe 2 ,D-PalP,D- 0/8@1.00 Om(COCH 2 S+Me 2 6 ,D-Ala 0 -LHRH.2TFA 4023 Ac-D-Nal ,4-Cl-D-PheL,D-Pal3,D-ArgO, 0/8@1.00 Dap(COCH 2 S+Me 2 8 ,D-Ala 1 0 -LHRH.2TFA Mass spectral analysis did not confirm the structure, Nal arg (reference) histamine release values: a=0.11, b=0.14, c=0.28, d=0.11, e=0.1, f=0.02, g=0.1, h=0.02 Sulfonium moieties confer high AOA on peptides when incorporated at position 6 compound 3879) or position 8 compound 3983). Compound 3925 (with two S• sulfonium moieties) showed low histamine release. Both alkyl and a-(sulfonium)carbonyl 10 moieties compound 4023) are effective. Preliminary experiments with LHRH agonists and antagonists suggest that compounds incorporating a bromoacetyl moiety are bound to the receptor and are not removed by repeated washing.

"-Certain peptides which have an N-alkyl pyridinium moiety at position 6 are unexpectedly active compound 3851) in the AOA assay. Some have very little histamine-releasing activity compound 3763) compared to the standard, Nal-Arg.

These results are unexpected in light of the previously reported AOA activity and histamine-releasing qualities of N-methyl pyridinium compounds.

Dipolar moieties generally exhibited modest AOA. Compounds including Lys(Onic) 6 exhibited favorable qualities; one (compound 3828) showed low histamine releasing activity, and compound 3507 showed high AOA.

Several peptides having acylated lysine at position 6 were tested, and showed good AO activity compounds 3741 and 3760).

Compounds having a small polar moiety at position 6 exhibited favorable combinations of AOA and histamine-releasing activity. For example, compound 3827, which has D-Asn (a small, hydrophilic moiety) at position 6 showed moderate AO activity.

Compounds 3341, 3342, and 3343 having D-Gln, D-Asn, and D-Thr, respectively, combined moderate AOA with very low histamine release. Compound 3361, which had the taurine amide of Glu at position 6, also showed very low histamine release. Compound 3369, which had D-Cit at position 6. also showed low histamine release.

All of the analogs listed in Table 1 can by synthesized by the solid phase method using an automated synthesizer Beckman Model 990). The amino acid residues used -34can be purchased from commercial sources Aldrich Chemical Co., Milwaukee, WI), or can be produced from commercially available starting materials according to known methods. For example, pyridinium-N-oxides can be produced by oxidation of the corresponding pyridine with, peroxyacids such as mCPBA (see, Example 3, infra). Pyridinium moieties, for example, N-benzyl pyridinium compounds, can be produced by N-alkylation of the corresponding pyridine, by heating in an inert solvent with benzyl bromide (see Examples 1 and 2, infra). Similarly, sulfonium and phosphonium salts can be produced by S- or P- alkylation of a sulfide or phosphine, respectively, with an alkylating agent such as, for example, methyl iodide. Amino acids which are not obtained commercially can be synthesized in a protected form for coupling, or, if appropriate, can be coupled to form a peptide and subsequently modified to the desired form.

EXAMPLE 2: Synthesis of Boc-D-Pal(Bzl) hydrobromide salt: Boc-D-Pal (1.36g, 6.0 mmol) was suspended in 60 ml of acetonitrile. Benzyl bromide 15 (about 50 mmol) was added and the mixture was warmed to 50°C on a water bath. A cleasr solution resulted, and was stirred at room temperature for 16 hours. A white precipitate formed; TLC after 17 hours showed some starting remaining starting material; stirring continued for a total of 5 days, when the reaction was complete. The solvent was evaporated under reduced pressure, and the residue recrystallized from EtOH/ethyl acetate.

20 Yield: 85%; m.p. 166-170 0

C.

EXAMPLE 3: Synthesis of Boc-D-Pal(iPr) Boc-D-Pal (4.0 g, 17.7 mmol) and Ag20 (8.0 g, 34.4 mmol) in 22 ml water was stirred at room temperature for 4 hours. The reaction vessel was cooled to 0°C, and 2-iodopropane (20.4 g, 120 mmol) in 40 ml 2-propanol was added. After addition was complete, the mixture was allowed to warm to room temperature and stirred for 4 days. Additional (2 g) and 2-iodopropane (2 g) were added after 24 hours and again after 48 hours. The mixture was filtered, and the precipitate was washed with ethanol (2 x 15 ml). The filtrate was evaporated to yield 4.3 g of a yellow oil. Crystallization from ethanol/ethyl acetate gave light yellow crystals (3.0 Yield: 63%; m.p. 182-185 0

C.

EXAMPLE 4: Synthesis of Boc-D-Pal(N-O) Boc-D-Pal (2.0 g, 7.5 mmole) was dissolved in 40 ml acetone and 2.48 g (16.5 mmol) of MCPBA (57-86%; purchased from Aldrich and used as received) in 80 ml acetone was added in one portion. The mixture was stirred at room temperature for 40 hours; a small amount of white precipitate formed as the reaction proceeded. The precipitated was filtered and the mother liquor evaporated to yield a white precipitate. The combined solids were washed with ether (to remove chlorobenzoic acid) and recrystallized from ethyl acetate/hexane. Yield: 1.7 g m.p. 155-157*C.

EXAMPLE 5: Peptide Synthesis A typical coupling cycle for peptide synthesis with Boc-amino acids on a peptide synthesizer (Beckman Model 990) was as follows: Methylbenzyhydramine (MBHA) resin (1.18 g, 0.85 meq amino groups/g resin) was weighed into the reaction vessel and washed with two protions of chloroform (26 ml each).

The resin was prewashed with 22% thioanisole (5 ml)/66% trifluoroacetic acid (TFA) in 14 ml dichloromethane (DCM) for 5 minutes, and then deprotected for 30 minutes with the same thioanisole/TFA mixture. The resin was washed with three portions of chloroform (20 ml each), two portions of 2-propanol (26 ml each) and two portions of DCM (26 ml each). The resin was neutralized with two portions of 12% diisopropylethylamine (DIPEA) (26 ml each), and then washed with four portions of DCM (26 ml each), followed by two i ~portions of 1:1 DCM:dimethylformamide (DMF) (26 ml each). A solution of a Bocprotected amino acid (2.5 mole equivalents) and HOBt (2.5 mole equivalents) was i 15 introduced as a solution in 10 ml DMF, and DCC was added (256 mg in 6 DMF).

Coupling was allowed to proceed for three hours, or overnight. Hindered residues backbone N-methyl amino acids) required longer coupling times. The resin was washed with two 26 ml portions of DMF, followed by two 26 ml portions of 2-propanol and then two 26 ml portions of DCM. Completion of coupling was assessed by Kaiser's test 20 (ninhydrin test). If coupling is not complete, a double coupling was performed the resin was neutralized as above and the coupling step repeated). When complete coupling is achieved, the cycle was repeated with the next amino acid.

Upon completion of the synthesis, the peptide was cleaved from the resin by treatment with liquid hydrofluoric acid (HF) for 45 minutes at 0oC. The HF was evaporated and the the peptide treated with aqueous acetic acid and lyophilized. The crude peptide was then purified by high performance liquid chromatography (HPLC) on a C18 column, Seluting with a mixture of acetonitrile and 0.1% TFA in water. Purified fractions (homogeneous by UV and TLC analysis) were combined and lyophilized. Analytical HPLC was used to determine the purity of the final product; all peptides synthesized were at least 98% pure.

EXAMPLE 6: Suppression of Plasma Testosterone Levels The ability of an LHRH antagonist of the invention to suppress plasma testosterone levels was examined in adult male rats. The rats were administered the LHRH antagonist 3827 (the structure of which is shown in Table In one experiment, a single injection of LHRH antagonist was administered subcutaneously at doses of 300 or 1000 pg/kg.

Animals showed a rapid, pronounced decrease in plasma testosterone to nearly undetectable levels by hours 6 hours post-administration. Testosterone levels returned to normal by 24 hours after the 300 pg/kg dose, but not until 72 hours after the 1000 tg/kg dose.

-36- In another experiment, the LHRH antagonist 3827 was administered in eight intravenous doses of 1, 10 or 100 jg/kg, each every three hours, corresponding respectively to 8, 80 or 800 jg/kg/day: The results are shown graphically in Figure 1. Castrate levels of testosterone were achieved at doses of 10 gg/kg every three hours. A dose as low as 1 jg/kg, equivalent to 8 pg/kg/day, induced a significant decrease in plasma testosterone levels throughout the experimental period.

In another experiment, continuous subcutaneous infusion of the LHRH antagonist 3827 was achieved through use of an osmotic pump. Doses of 300 or 1000 ug/kg/day ("High Dose") were administered subcutaneously for two weeks via Alzet osmotic minipumps in each of five male Sprague-Dawley rats. The animals that received 1000 jtg/kg/day were then maintained for an additional two weeks with 5, 15 or 50 jg/kg/day ("Low Dose") before the purnps were removed completely. The results are shown graphically in Figure 2. Chronic treatment of rats with the LHRH antagonist at initial doses of 300 or 1000 pg/kg/day resulted in castrate levels of testosterone within the first 7 days 15 (and presumably within the first 24 hours) with either initial dose, and were maintained by all three subsequent doses for an additional 21 days. Castration was maintained throughout this period with no apparent "castration response" as has been described with other inhibitors. When the High Dose pumps were replaced with maintenance Low Dose pumps giving doses as low as 5 ig/kg/day, animals remained fully castrated throughout the 20 experiment. Following completion of LHRH antagonist treatment, a dose dependent recovery in plasma testosterone was observed: animals that received the highest maintenance dose appeared to recover more slowly than animals treated with the lower .maintenance doses. Recovery of testosterone levels following pump removal was complete within two weeks. In a follow up study, the results of which are shown graphically in 25 Figure 3, complete suppression of testosterone to castrate levels was achieved by doses as low as 30 pg/kg/day. Castrate levels were again maintained with a dose of LHRH antagonist as low as 5 ig/kg/day

EQUIVALENTS

Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents to the specific embodiments of the invention described herein. Such equivalents are intended to be encompassed by the following claims.

-37- SEQUENCE LISTING GENERAL INFORMATION:

APPLICANT:

NAME: INDIANA UNIVERSITY FOUNDATION STREET: ONE CITY CENTER, SUITE 314 CITY: BLOOMINGTON STATE: INDIANA COUNTRY: USA POSTAL CODE (ZIP): 47401 (ii) TITLE OF INVENTION: LHRH Antagonist Peptides (iii) NUMBER OF SEQUENCES: 1 (iv) CORRESPONDENCE ADDRESS: ADDRESSEE:-LAHIVE COCKFIELD STREET: 60 State Street, Suite 510 CITY: Boston STATE: Massachusetts COUNTRY: USA ZIP: 02109-1875 25 COMPUTER READABLE FORM: MEDIUM TYPE: Floppy disk COMPUTER: IBM PC compatible S OPERATING SYSTEM: PC-DOS/MS-DOS SOFTWARE: PatentIn Release Version #1.25 (vi) CURRENT APPLICATION DATA: APPLICATION NUMBER: 000000 FILING DATE: Herewith

CLASSIFICATION:

(vii) PRIOR APPLICATION DATA: APPLICATION NUMBER: USSN 08/480,494 FILING DATE: 07-JUN-1995 (viii) ATTORNEY/AGENT INFORMATION: NAME: DeConti, Giulio A.

REGISTRATION NUMBER: 31,503 REFERENCE/DOCKET NUMBER: PPI-007CPPC (ix) TELECOMMUNICATION INFORMATION: TELEPHONE: (617)227-7400 TELEFAX: (617)227-5941 INFORMATION FOR SEQ ID NO:1: SEQUENCE CHARACTERISTICS: LENGTH: 10 amino acids TYPE: amino acid TOPOLOGY: linear (ii) MOLECULE TYPE: peptide FRAGMENT TYPE: internal -38- (xi) SEQUENCE DESCRIPTION: SEQ ID NO:1:- Glu His Trp Ser Tyr Gly Leu Arg Pro Gly 1 5 00.0 :-.00 0*

Claims (38)

1. An LHRH antagonist comprising a peptide compound, wherein a residue of the peptide compound corresponding to the amino acid at position 6 of natural mammalian LHRH comprises D-Lys(Imdac), D-Lys(Ppic), D-Lys(Dodac), D-Lys(pGlu), D-Lys(Otac) and D-Lys(Onic) or a moiety selected from the group consisting of a dipolar moiety, a sulfonium moiety, a receptor-modifying moiety and a small polar moiety, such that the peptide compound has LHRH antagonist activity, with the provisos that the dipolar moiety is not a zwitterionic pyridinium and the residue is not D-Cit, D-Hci or a lower alkyl derivative of D-Cit or D-Hci.

2. The LHRH antagonist of claim 1, wherein the peptide compound comprises about 8 to about 12 residues.

3. The LHRH antagonist of claim 1, wherein the peptide compound comprises 10 residues.

4. A peptide compound comprising a structure: A-B-C-D-E-F-G-H-I-J wherein A is pyro-Glu, Ac-D-Nal Ac-D-Qal, Ac-Sar, or Ac-D-Pal; B is His or 4-Cl-D-Phe; C is Trp, D-Pal, D-Nal, L-Nal, D-Pal(N-O), or D-Trp; D is Ser; E is N-Me-Ala, Tyr, N-Me-Tyr, Ser, Lys(iPr), 4-Cl-Phe, His, Asn, Met, Ala, Arg or 25 lie; F is D-Lys(Imdac), D-Lys(Ppic), D-Lys(Dodac), D-Lys(pGlu), D-Lys(Otac), D-Lys(Onic) or a structure: X Y R o wherein R and X are. independently, H or alkyl; and Y comprises a moiety selected from the group consisting a dipolar moiety, a sulfonium moiety, a receptor-modifying moiety and a small polar moiety, the provisos that the dipolar moiety is not a zwitterionic pyridinium and F is not D-Cit, D-Hci or a lower alkyl derivative of D-Cit or D-Hci; G is Leu or Trp; H is Lys(iPr), Gin, Met, or Arg; I is Pro; and J is Gly-NH 2 or D-Ala-NH 2 or a pharmaceutically acceptable salt thereof. The peptide compound of claim 4, wherein Y comprises a dipolar moiety, with the proviso that the dipolar moiety is not a zwitterionic pyridinium.

6. The peptide compound of claim 5, wherein Y comprises a moiety selected from the group consisting of ylids, tertiary amine oxides, nitrile oxides and pyridine-N- oxides.

7. The peptide compound of claim 4, wherein Y comprises a sulfonium moiety.

8. The peptide compound of claim 4, wherein Y comprises a receptor- modifying moiety.

9. The peptide compound of claim 8, wherein Y comprises a moiety selected from the group consisting of ylids, sulfonium moieties, a-halocarbonyls, sulfates, sulfonates, alkyl halides and benzyl halides.

10. The peptide compound of claim 9, wherein Y comprises an a-halocarbonyl.

11. The peptide compound of claim 4, wherein F is D-Lys(Imdac), D-Lys(Ppic) and D-Lys(Dodac), D-Lys(pGlu), D-Lys(Otac) or D-Lys(Onic). 25 12. The peptide compound of claim 2, wherein Y comprises a small polar moiety, with the proviso that F is not D-Cit, D-Hci or a lower alkyl derivative of D-Cit or D-Hci.

13. The peptide compound of claim 12, wherein F is selected from the group consisting of D-Asn, D-Gln and D-Thr.

14. An LHRH antagonist comprising a peptide compound, wherein a residue of the peptide compound corresponding to the amino acid at position 6 of natural mammalian LHRH comprises a small polar moiety such that the peptide compound has LHRH antagonist activity, with the proviso that the residue is not D-Cit, D-Hci or a lower alkyl derivative of D-Cit or D-Hci. The LHRH antagonist of claim 14, wherein the antagonist has an antiovulatory activity of less than about 1 jlg per rat in a rat antiovulation assay. -41-

16. The LHRH antagonist of claim 14, wherein the antagonist has an ED 5 0 in a histamine release assay of at least about 5 jg/ml.

17. The LHRH antagonist of claim 14, wherein the peptide compound comprises about 8 to about 12 residues.

18. The LHRH antagonist of claim 14, wherein the peptide compound comprises 10 residues.

19. A peptide compound comprising a structure: A-B-C-D-E-F-G-H-I-J wherein A is pyro-Glu, Ac-D-Nal Ac-D-Qal, Ac-Sar, or Ac-D-Pal B is His or 4-Cl-D-Phe S 15 C is Trp, D-Pal, D-Nal, L-Nal, D-Pal(N-O), or D-Trp D is Ser E is N-Me-Ala, Tyr, N-Me-Tyr, Ser, Lys(iPr), 4-Cl-Phe, His, Asn, Met, Ala, Arg or Ile; F is X L *N R *I 20 O wherein S. R and X are, independently, H or alkyl; and L comprises a small polar moiety, with the proviso that F is not D-Cit, D-Hci or a lower alkyl derivative of D-Cit or D-Hci; G is Leu or Trp; SH is Lys(iPr), Gin, Met, or Arg I is Pro; and J is Gly-NH 2 or D-Ala-NH 2 or a pharmaceutically acceptable salt thereof. The peptide compound of claim 19, wherein F is selected from the group consisting of D-Asn, D-Gln and D-Thr.

21. A peptide compound comprising a structure: A-B-C-D-E-F-G-H-I-J wherein A is pyro-Glu, Ac-D-Nal, Ac-D-Qal, Ac-Sar, or Ac-D-Pal; B is His or 4-Cl-D-Phe; -42- C is Trp, D-Pal, D-Nal, L-NaI, D-Pal(N-O), or D-Trp; D is Ser; E is N-Me-Ala, Tyr, N-Me-Tyr, Ser, Lys(iPr), 4-CI-Phe, His, Asn, Met, Ala, Arg or le; F is D-Asn; G is Leu or Trp; H is Lys(iPr), Gin, Met, or Arg; I s Pro; and J is Gly-NH 2 or D-Ala-NH 2 or a pharmaceutically acceptable salt thereof.

22. A peptide compound comprising a structure: A-B-C-D-E-F-G-H-I-J wherein A is pyro-Glu, Ac-D-Nal Ac-D-Qal, Ac-Sar, or Ac-D-Pal; B is His or 4-CI-D-Phe; C is Trp, D-Pal. D-Nal, L-Nal, D-Pal(N-O), or D-Trp; D is Ser; E is N-Me-Ala, Tyr, N-Me-Tyr, Ser, Lys(iPr), 4-CI-Phe, His, Asn, Met, Ala, Arg or Ile; F is D-Arg, D-Lys(iPr), D-Pal(iPr), D-Cit or Q, wherein Q has a structure x z ~N R 0 :wherein R and X are, independently, H or alkyl; and Z comprises a sulfonium, moiety; G is Leu or Trp; H is Lys(iPr), Gln, Met, Arg or Q I is Pro; and J is Gly-N1- 2 or D-Ala-NH 2 with the proviso that at least one of F and H is Q; or a pharmaceutically acceptable salt thereof.

23. A peptide compound comprising a structure: Ac-D-NaI-4-Cl-Phe-D-Pal-Ser-Tyr-D-Pa(N-O)-Leu-Lys(iPr)-Pro-D-Ala-NH. or a pharmaceutically acceptable salt thereof.

24. A peptide compound comprising a structure Ac-D-Nal-4-Cl-D-Phe-D-Pal-Ser-Tyr-D-Pal(CH 2 COO-)-Leu-Lys(iPr)-ProDAla.NH 2 -43 or a pharmaceutically acceptable salt thereof. A peptide compound comprising a structure AcSr4C--h--a-e-y--alBl-e-y~~)PoDAaN2 or a pharmaceutically acceptable salt thereof.

26. A peptide compound comprising a structure: AcDNl4C--h--r-e-y-DMtSM)LuAgPoDAaN2 or a pharmaceutically acceptable salt thereof.

27. A peptide compound comprising a structure: AcDNl4C--h--a-e-y-DAgLuMtSM)PoDAaN2 or a pharmaceutically acceptable salt thereof.

28. A peptide compound comprising a structure: or a pharmaceutically acceptable salt thereof.

29. A peptide compound comprising a structure: Ac-D-NalIA.CI-D-Phe-D-PalISerN-Tyr-D Asn-Leu.Lysi Pr)PrO..DAla NH 2 or a pharmaceutically acceptable salt thereof. A peptide compound comprising a structure:slce ro h ru consisting of: Ac-D-Nal I .4-CI-D-Phe 2 D-pal 3 D-Gln 6 -Lys(iPr) 8 D-Ala 1 0 -LHRA Ac-D-Nal I. 4-CI-D-Phe 2 D-Pa1 3 D-Asn 6 -Lys(iPr) 8 D-Ala 1 0 -LHRH Ac-D-Nal I. 4-CI-D-Phe 2 D-Pa1 3 D-Thr 6 -Lys(iPr) 8 D-Ala I -LHRH Ac-D-Nall. 4-Cl-D-Phe 2 D-Pa1 3 D-Cit 6 -Lys(iPr) 8 Pip 9 -D-AlJa 10 LHPJ- Ac-D-Nal I. 4-CI-D-Phe 2 D-Pa1 3 D-Glu(Taurine) 6 -Lys(iPr) 8 D-Ala' 0 -LHRH Ac-D-Nal 1 4-CI-D-Phe 2 D-Pa1 3 D-Cit 6 -Lys(iPr) 8 -LHRH Ac-D-Nal 1 4-CI-D-Phe 2 D-Pa1 3 D-Cit 6 -Lys(iPr) 8 Pip 9 -LHRH Ac-D-Nal 1 ,4-Cl-D-Phe 2 D-pal 3 D-Phe(4-NO~,)) 6 -Lys(iPr) 8 D-Ala 1 I -LHRH Ac-D-Nall 1 4-Cl-D-Phe 2 D-pal 3 D-Cit 6 -Lys(iPr) 8 ProNHEt 9 -des-Gly 1 0 -LHR-H Ac-D-(or L)-9-anthr) '-Alal, 4-CI-D-Phe 2 D-pal 3 D-Cit 6 -Lys(iPr) 8 D-Alal 0 LHRH Ac-L-(or D)-9-andhryi-Ala I, 4-CI-D-Phe 2 D-Pa1 3 D-Cit 6 -Lys(iPr) 8 D-Ala 10 LHRH- -44- Ac-D-(or L)-Ada-Ala I, 4-Cl-D-Phe 2 D-pa1 3 D-Cit 6 -Lys(ipr) 8 D-Ala IO-LIJRI Ac-L-(or D}-Ada-Ala I, 4-CI-D-Phe 2 D-pa1 3 D-Cit 6 -Lys(ipr) 8 D-AIO-LHRH- Ac-D-NaI 1 4-CI-D-Phe 2 D-Pal 3 D-Lys(Glc) 6 -Lys(iPr) 8 D-Ala 1 I -LHRII Ac-D-Nal 1 4-Cl-D-Phe 2 D-pal 3 D-PaI( I -BU) 6 Lys(ipr) 8 D-Ala 1 I -LHRH Ac-D-Nal 1 4-Cl-D-Phe 2 D-pal 3 D-Pal(Bzl) 6 Lys(ipr) 8 D-Alal 0 -LHRH Ac-D-Nal I, 4-C1-D-Phe 2 D-pal 3 Pal 5 D-Pal(iPr) 6 Lys(iPr) 8 D-Ala I 0 -LIRH Ac-D-NaI 1 4-Cl-D-Phe 2 D-paI 3 Cit 5 D-Cit 6 Lys(iPr) 8 D-Alal 0 -LHRH Ac-D-Nal 1 4-Cl-D-Phe 2 D-Pal 3 pal 5 D-Cit 6 Lys(iPr) 8 D-Ala I -LHRH Ac-D-Nal 1 4-Cl--D-Phe 2 D-pal 3 Cit 5 D-Pal 6 Lys(iPr) 8 D-Alal 0 -LHRJ Ac-D-Nal 1, 4-Cl-D-Phe 2 D-pal 3 Asn 4 Tyr 5 D-Cit 6 Lys(iPr) 8 D-Ala I -LTYJ- Ac-D-Nal 1 4-CI-D-Phe 2 D-Pal 3 Cit 5 D-PaI(ipr) 6 Lys(iPr) 8 D-Ala I -LHRHd- Ac-D-Nal 1 4-CI-D-Phe 2 D-pal 3 D-HomnoArg(N0 2 6 Lys(iPr) 8 D-Ala 1 0- LHRH- Ac-D-Nal I, 4-C l-D-Phe 2 D-pal 3 D-Lys(Glycolyl) 6 Lys(ipr) 8 D-Ala 1 0 -LH-RH Ac-D-Nal I, 4-Cl-D-Phe 2 D-Pal 3 D-Lys(iPrPic) 6 Lys(iPr) 8 D-Ala I -LHRJI Ac-D-NaI 1 4-Cl-D-Phe 2 D-Pal 3 D-Lys(HomoPro)6, Lys(iPr) 8 D-AlI 0 -LHRH Ac-D-NalI, 4-CI-D-Phe 2 D-PaI1 3 D-Pal(iPr) 6 Lys(iPr) 8 D-Ala I -LHRH- Ac-D-Nal I, 4-Cl-D-Phe 2 D-pal 3 D-Lys(3-pyridineacetic) 6 Lys(iPr) 8 D-Ala 10 LHRH Ac-D-Nall, 4-CI-D-Phe, D-pal 3 D-Lys(2-ClNic) 6 Lys(ipr) 8 D-Alal 0 -LHRH Ac-NaMe-D-NallI, 4-CI-D-Phe 2 D-Pal 3 D-Cit 6 Lys(iPr) 8 D-AlI 0 -LHRH- Ac-D-Nal I, 4-CI-D-Phe 2 D-Pa1 3 Lys(Otac) 5 D-Lys(Otac) 6 Lys(ipr) 8 D-Ala 10 LHRH Ac-D-NaI 1 4-Cl-D-Phe 2 D-Pal 3 Lys(ONic)5, D-Lys(ONic) 6 Lys(iPr) 8 D- Ala 1 0 -LH-RH Ac-D-NalI, 4-Cl-D-Phe 2 D-Pa1 3 Lys(pyz) 5 ,D-Lys(pyz) 6 Lys(iPr) 8 D-Ala 10 LHRH- Ac-D-Nal 1 4-Cl-D-Phe 2 D-pal 3 D-Glu 6 Lys(iPr) 8 D-Ala I -LHRH- ***Ac-D-NaI'1, 4-CI-D-Phe 2 D-Pa1 3 D-Lys 6 Lys(iPr) 8 D-Ala I -LHR- Ac-D-Nall, 4-CI-D-Phe 2 ,-D-Pal 3 D-Lys(Gulonyl) 6 Lys(iPr) 8 D-Ala' 0 -LHRH Ac-D-NalI', 4-CI-D-Phe 2 D-PaI 3 D-Lys(iPrNic) 5 D-Lys(iPrNic) 6 Lys(iPr) 8 D-Afa 10 LHR- Ac-D-NaI 1, 4-CI-D-Phe 2 D-PaI 3 D-Lvs(ONic) 6 Lys(iPr) 8 D-Ala I -LHRH Ac-D-Nal 1 4-Cl-D-Phe 2 D-Pal 3 D-Lys(OTac) 6 Lys(iPr) 8 D-Ala I -LHRH Ac-D-NaI'1, 4-CI-D-Phe 2 D-Pal1 3 D-Lys(pyz) 6 Lys(ipr) 8 D-Alal 0 -LI-RH Ac-D-Nal I, 4-C1-D-Phe 2 D-Pal1 3 D-Lys(nfluNic) 6 Lys(iPr) 8 D-AlI 0 -LI-RH Ac-D-Nal 1 4-CI-D-Phe 2 D-Pa1 3 D-Glu(Amp) 6 Lys(iPr) 8 D-Ala' I -LHR- Ac-D-Nal 1 4-CI-D-Phe 2 D-PaI 3 D-Glu(Dea) 6 Lys(iPr) 8 D-Ala I -LH-RH Ac-D-NaI 1 4-Cl-D-Phe 2 D-Pal1 3 Lys(pGlu) 5 D-Lys(pGlu) 6 Lys(iPr) 8 D- Ala' 0 -LHRH Ac-D-Nal I, 4-Cl-D-Phe 2 D-Pal1 3 NaMe-Tyr5, D-Pal(iPr) 6 Lys(iPr) 8 D-Ala' LHRH Ac-D-Nal 1 CaMe4CI-Phe 2 D-Pa1 3 NaMe.Tyr5, D-Pal(iPr) 6 Lys(iPr) 8 D- Ala' I -LHRH Ac-D-Nal 1 4-C1-D-Phe 2 D-Pal 3 Lys(CNa) 6 Lys(iPr) 8 D-Alal 0 -LHRH Ac-D-Nall, 4-Cl-D-Phe 2 D-PaI 3 D-Glu(PEG) 6 Lys(iPr) 8 D-Ala 10 -LHRFI Ac-D-Nal I, 4-CI-D-Phe 2 D-PaI 3 D-Lys(Oxa) 6 Lys(ipr) 8 D-Alal(-LHRH- Ac-D-NalI, 4-Cl-D-Phe 2 D-Pal 3 Lys(CNa) 5 D-Lys(CNa) 6 Lys(iPr) 8 D-Ala 1 0. LHRH Ac-fl-Nal 1 4-C1-D-Phe 2 D-Pal 3 Lys(CINic) 5 D-Lys(CINic) 6 Lys(iPr) 8 D- Ala 1 0 -LHR}1 Ac-D-Nall, 4-C1-D-Phe 2 D-Pal 3 D-Lys(Ac) 6 Lys(iPr) 8 D-Alal 0 -LHRI Ac-D-Nal I, 4-Cl-D-Phe 2 D-Pal 3 D-Glu(Tris) 6 Lys(iPr) 8 D-Ala I -LRI Ac-fl-Nall, 4-Cl-D-Phe 2 D-PaI 3 D-Gin(ipr) 6 Lys(iPr) 8 D-Al-LHRH Ac-D-Nal I, 4-CI-D-Phe 2 D-Pal 3 D-Glu(CSer) 6 Lys(iPr) 8 D-Ala I -LIH Ac-D-Nal I, 4-CI-D-Phe 2 D-Pal 3 D-Glu(Mop) 6 Lys(iPr) 8 D-Ala I -LHRH- Ac-D-Nal 1 4-CI-D-Phe 2 D-Pal 3 Lys 5 D-Pal(iPr) 6 Lys(ipr) 8 D-Ala I -LHRH Ac-D-Nal 1 4-Cl-D-Phe 2 D-Pal 3 Lys(Nic) 5 D-Pal(iPr) 6 Lys(ipr) 8 D-Alal 0 LHRH Ac-D-NalI, 4-C1-D-Phe 2 D-Pal 3 Lys(Ac) 5 D-Pal(iPr) 6 Lys(iPr) 8 D-Ala 1 0 LI-mN Ac-D-Nal I, 4-CI-D-Phe 2 D-pa1 3 D-Glu(DEGA) 6 Lys(ipr) 8 fl-Ala 1 0 -LHRH Ac-D-Nal I, 4-C1-D-Phe 2 D-pal 3 Lys(Nic) 5 D-Pal(Bzl) 6 Lys(ipr) 8 D-Alal 0 LHR.H Ac-D-Nal I, 4-C1-D-Phe 2 D-Pal 3 Lys(Ac) 5 D-Pal(Bzl) 6 Lys(iPr) 8 D-Ala 10 LH-R}I Ac-D-Nal 1 4-Cl-D-Phe 2 D-Pa1 3 Lys(TFAC) 6 Lys(iPr) 8 D-Ala I -LHRH Ac-D-Nal I, 4-CI-D-Phe 2 D-Pal 3 Lys 5 D-Pal(Bzl) 6 Lys(iPr) 8 D-Alal 0 -LHRH Ac-D-Nall, 4-CI-D-Phe 2 D-Pa1 3 Lys(iPr) 5 D-Lys(Nic) 6 Lys(iPr) 8 D-Ala' 0 LHiR- Ac-D-NaI 1 4-CI-D-Phe 2 D-Pa1 3 Lys(iPr) 5 D-Lys(pic) 6 Lys(iPr) 8 D-Alal 0 LI-RH Ac-D-NaI'1, 4-CI-D-Phe 2 D-Pa1 3 Lys(TFAc) 5 D-Lys(TFAc) 6 Lys(iPr) 8 D- Ala 1 0 -LHRH Ac-D-NaI'1, 4-C1-D-Phe 2 D-Pa1 3 Lys(ipr) 5 4-C I-D-Phe 6 Lys(iPr) 8 D-Ala 10 LHRH Ac-D-Nall, 4-CI-D-Phe 2 D-PaI-, Lys(iPr) 5 D-Na1 6 Lys(iPr) 8 D-Alal 0 -LHRH- Ac-D-NalI 1 4-Cl-D-Phe 2 D-Pa1 3 Lys(iPr) 5 D-Lys(pGlu) 6 Lys(iPr) 8 D-Ala 1 0 LHRH Ac-D-NaI 1 4-Cl-D-Phe 2 D-Pa1 3 Lys(iPr) 5 D-Lys(OTac) 6 Lys(iPr) 8 D-Ala 10 LHRH Ac-D-Nall, 4-CI-D-Phe 2 D-PaI 3 Ile 5 D-Pal(Bzl) 6 Lys(ipr) 8 D-Alal 0 -LHRH Ac-D-Nal 1, 4-C1-D-Phe 2 D-Pal 3 Lys(pic) 5 D-Pal(ipr) 6 Lys(iPr) 8 D-Ala 1 0 LHRH Ac-D-Nall, 4-CI-D-Phe 2 D-Pa1 3 D-Lys(3-A-Pro) 6 Lys(iPr) 8 D-Ala 1 0 -LHRH- TFA Ac-D-NaI-4-CI-D-Phe 2 ,D-PaI-',D-Lys(Ac-D-NaI' ,4-Cl-D-Phe 2 ,D-PaI 3 ,Ser) 6 ,Lys(iPr) 8 ,D-Aa' LHRH Ac-D-Qall ,4-Cl-D-Phe 2 ,D-Pal 3 ,D-Lys(pGlu) 6 Lys(ipr) 8 ,D-Alal 0 -LHRH Ac-D-Qal' ,4-Cl-D-Phe 2 ,D-Pal 3 .D-Lys(Ac) 6 Lys(iPr) 8 ,D-Ala 1 0 -LHR- Ac-D-Nal 1 ,4-Cl-D-Phe 2 ,D-Pal 3 ,D-Lys(lmdac) 6 Lys(ipr) 8 ,D-Ala 1 I -LHRH Ac-D-Qall ,4-C1-D-Phe 2 ,D-paI 3 ,D-Lys(Dodac) 6 Lys(iPr) 8 ,D-Ala 1 0 -LHRH- Ac-D-Na 1 ,4-C1-D-Phe 2 ,D-Pal 3 ,Ser 5 ,D-PaI(iPr) 6 ,Lys(iPr) 8 .D-Alal I -LHRH Ac-D-NaI 1 ,4-Cl-D-Phe 2 ,D-Pal 3 ,D-Lys(iPr)5, D- Lys(TFAc) 6 ,Lys(iPr) 8 ,D-Ala]O- LHRH Ac-D-Nal 1 ,4-C1-D-Phe 2 .D-Pal 3 J-is 5 D-Pal(ipr) 6 Lys(iPr) 8 ,D-AJa 1 0 -LHRH Ac-D-Nal 1 ,4-CI-D-Phe 2 ,D-Pal 3 ,Asn 5 ,D-Pal(iPr) 6 Lys(iPr) 8 ,D-AJal I -LH-RH -46- Ac-D-Nall,- 1 DPh2Dpl3Lsir 0..(4-C6Ly~~),DAaO Ac-D-Nal' ,4-Cl-D-Phe 2 ,D-paP3,Met 5 ,D-PaI(iPr) 6 Lys(ipr) 8 ,D-Alal 0 -LFHR Ac-D-Nal 1 ,4..CI-D.Phe 2 ,D-Phe 2 ,D-paI 3 ,A4la 5 ,D..Pa(iPr) 6 ,Lys(ipr)8,D-Ala LHRH Ac-D-Nal 1 ,4-CI-D-Phe 2 ,D-paI 3 ,N-Me-Ala 5 D-PaI(iPr) 6 ,Lys(ipr),DAlal LIIRH Ac-D-Nal 1 ,4-CI-D-Phe 2 ,D-Pal 3 ,D-Lys(Hippic) 6 Lys(ipr) 8 ,D-Alal 0 -LIRH Ac-D-Na 1 ,4-CI-D-Phe 2 ,D-paI 3 ,D-Lys(AcGly) 6 Lys(iPr) 8 ,D-Alal 0 -LHRH Ac-D-Na 1 ,4-C1-D-Phe 2 ,D-paI 3 ,D-Lys(ppic) 6 Lys(iPr) 8 ,D-Alal I -LHRH Ac-DNal 1 ,4-CI-D-Phe 2 ,D-pal 3 ,D-Lys(Mts) 6 Lys(iPr) 8 ,D-Alal 0 -LHRH- Ac-D-Na 1 ,4-CI-D-Phe 2 ,D-PaI 3 ,D-Lys(Qrotic) 6 Lys(iPr) 8 ,D-Alal I -LH-RH Ac-Sarl,4-C1-D-Phe 2 ,D-Na 3 ,D-Pal(Bzl) 6 Lys(iPr) 8 ,D-Alal 0 -LHRH Ac-Sar' ,4-Cl-D-phe 2 1-1 -Na 3 ,D-Pa1(Bzl) 6 Lys(ipr) 8 ,D-Alal 0 -LHRH Ac-D-Nal' ,4..C1..D.Phe 2 ,D.Pa 3 ,D.Pa(CH 2 COQH) 6 ,Lys(iPr)8,D..Ala 0 -LHRH Ac-D-Nal 1 ,4-C1-D-Phe 2 ,D-pal 3 ,D-Lys(Ala) 6 Lys(iPr) 8 ,D-Alal I -LHRH Ac-Sar 1 ,4-CI-D-Phe 2 ,D-1I-Nal 3 ,D-Pal(iPr) 6 Lys(iPr) 8 ,D-Ala 10 .LHPJI Ac-Sar 1 ,4-Cl-D-Phe 2 I -NaI 3 ,D-PaI(iPr) 6 Lys(iPr) 8 ,D-Alal I -LHRH- Ac-D-Qa' 1,4-CI-D-Phe 2 ,D-paI 3 ,D-Lys(Gulonyl) 6 ,Lys(ipr) 8 ,D-Ala I 0 -LHRH- Ac-D-Na 1 ,4-CI-D-Phe 2 ,D-paI 3 ,D-Pal(N-O) 6 Lys(iPr) 8 ,D-Alal I -LHRH Ac-D-Qa 1 ,4-Cl-D-Phe 2 ,D-paI 3 ,D-Lys(ppic) 6 Lys(ipr) 8 ,D-Ala IO-LHRH Ac-D-Qall,4-CI-D-Phe 2 ,D-paI 3 ,D-Lys(Irndac) 6 Lys(iPr) 8 ,D-Alal I -LHRH Ac-D-Qall ,4-Cl-D-Phe 2 ,D-pal 3 ,D-Lys(Onic) 6 Lys(iPr) 8 ,D-,Alal 0 -LHRH Ac-D-Qall ,4-CI-D-Phe 2 ,D-paI 3 ,D-Lys(Otac) 6 Lys(iPr) 8 ,D-Ala I -LIIRH Ac-D-Na 1 ,4-CI-D-Phe 2 ,D-paI 3 ,D-Lys(Dodac) 6 Lys(iPr) 8 ,D-Alal I -LH-RH- Ac-D-PaJ 1 ,4-CI-D-Phe 2 .D-paI 3 ,D-Pal(iPr) 6 Lys(iPr) 8 ,D-Alai 0 -LHRH Ac-D-NaI 1 ,4-C1-D-Phe 2 ,D-Pal 3 ,N-Me-Tyr 5 Asn 6 ,Lys(iPr) 8 ,D..Alal -LHRH Ac-D-Nal 1 ,4-.CI-D-Phe 2 ,D-pal 3 ,N-Me-Tyr 5 ,D..Lys(Onic) 8 ,Lys(iPr) 8 ,D..AlaI 0.. LHRH Ac-D-NaI 1 ,4-Cl-D-Phe 2 ,D-pal 3 ,N-Me-Tyr 5 ,D-Lys(Ac) 6 ,Lys(iPr) 8 ,D-Alai 0- *R Ac-.D-Nal 1 ,4-Cl-D-Phe 2 ,D-Pal 3 ,Lys(iPr) 5 ,D-His 6 ,Trp 7 ,Orn 8 ,D-Ala 1 0 -LI-RH Ac-D-Nal I,4-CI-D-Phe 2 ,D-pal 3 ,His 5 ,D-Arg 6 Trp 7 ,Orn 8 .D-Ala 1 I -LHRH Ac-D-Nal 1 ,4-CI-D-Phe 2 ,D-Pal 3 ,Arg 5 ,D-His 6 Trp 7 ,0m 8 ,D-Ala 1 I -LHRH Ac-D-NaI 1 ,4-CI-D-Phe 2 ,D-PaI 3 ,Lys(ipr) 5 ,D..Trp 6 ,Trp 7 ,Orn 8 ,D..Alal 0 -LHRH Ac-D-Nal 1 ,4-CI-D-Phe 2 ,D-paI 3 ,4-Cl-Phe 5 D..PaI(iPr) 6 ,Lys(ipr) 8 ,D..Alal 0. LHRH Ac-D-Nal 1 ,4..CI..D.Phe 2 ,D..Pa1(N..O) 3 ,D.Pal(iPr)6,Lys(iPr)8,D-Ala I 0 .LHRJ- Ac-D-Nal 1 ,4-CI-D-Phe 2 ,D-Trp 3 ,D-Arg 6 Met 8 ,D-Ala 1 0 -LHRJI Ac-D-Nal 1 ,4-CI-D-Phe 2 ,D-Trp 3 ,D-Arg 6 Met(S+Me) 8 ,D-Ala 1 0 -LHRH Ac-D-Na 1 ,4-CI-D-Phe 2 ,D-Trp 3 ,D-Met 6 ,D-AIa 1 I -LHRH- Ac-D-Nal 1 ,4-C1-D-Phe 2 ,D-Trp 3 ,D-Met(S+Me) 6 D-Ala 1 0 -LHR- Ac-D-NaI 1 ,4-C1-D-Phe 2 ,D-Ti-p 3 ,D-Arg 6 Lys(COCH 2 Br) 8 .D-Alal I -LHRH Ac-D-Nal 1 ,4-CI-D-Phe 2 ,D-Trp 3 ,D-Met(S+Me) 6 Met(S+Me) 8 ,D-Alai 0 -LI-RH Met(S+Me) 8 -LHRH Lys(COCH 2 Br) 8 -LHRH Ac-D-Na 1 ,4-CI-D-Phe 2 ,D-Trp 3 ,D-Lys(COCH 2 Br) 6 ,D-Alal I -LHRH- Ac-D-NaI 1 ,4-C1-D-Phe 2 ,D-Pal 3 ,D-Lys(COCH9)CH-2N(Et) 2 6 'I-Ala 1 0 -LFHRH -47- Ac-D-Nal ,4-C-D-Phe2,D-Pal3 -Lys(2-pyimidylthio)acetic)6,yysiirr8 P- AlalO- LHRH Ac-D-Na l,4-Cl-D-Phe 2 ,D-Trp 3 ,D-Met(S+CH 2 C 6 J1 5 6 ,D-Ala'-LHRH Ac-D-NaI' ,4-C-D-Phe 2 ,D-Pal 3 D-Met(S+CH 3 ,D-Ala 1 0 -LHRH Ac-D-Nal 1 ,4-Cl-D-Phe 2 ,D-Pa1 D-Met(S+CH 2 COPh) 6 ,D-Alal 0 -LHRI Ac-D-Nal 1 ,4-Cl-D-Phe 2 ,D-Pal3,D-Dap(COCH 2 S+Me 2 6 ,D-Alal 0 -LHRH Ac-D-Nal 1 ,4-C-D-Phe 2 ,D-Pa13 ,His 5 D-Pal(iPr) 6 ,Lys(iPr) 8 ,D-Ala O-LHRH Ac-D-Nall ,4-Cl-D-Phe 2 ,D-Pal 3 ,D-Arg 6 Met(S+Me) 8 ,D-A1al 0 -LHR- Ac-D-Nall ,4-C-D-Phe 2 ,D-Trp3 D-Met(S+CH 2 -CH=CH 2 6 ,D-Alal 0 -LHR} Ac-D-Nall ,4-Cl-D-Phe 2 ,D-Pal 3 ,D-Arg 6 On(COCH 2 S+Me 2 8 ,D-Aal 0 ,HRH Ac-D-Nall ,4-CI-D-Phe 2 ,D-Pal 3 ,D-Arg 6 O,(COCH SMe9",D-Ala 1 LHRH Ac-D-Nall ,4-Cl-D-Phe 2 ,D-Pal 3 ,D-Arg 6 ,Met 8, D-A1; 1 -LHRH Ac-D-Na 1 ,4-C-D-Phe 2 ,D-Pa1 3 ,D-Lys(COCH 2 S+Me 2 6 ,D-Ala, I-LHR Ac-D-Nal 1 ,4-Cl-D-Phe 2 ,D-PaI 3 ,D-Arg 6 Lys(COCH 2 SMe 2 ,D-Alal 0 -LHR Ac-D-Nall ,4-Cl-D-Phe 2 ,D-Pal 3 ,D-Met(S+Me) 6 Met(S+Me) 8 ,D-Alal 0 -LHRH Ac-D-Nall ,4-Cl-D-Phe 2 ,D-Pal 3 ,D-Or(COCH 2 S'Me 2 6 ,D-Alal 0 -LHRH Ac-D-Nall ,4-Cl-D-Phe 2 ,D-PaI 3 ,D-Arg 6 ,Dap(COCH 2 S+Me 2 8 ,D-Ala 1 -LHRH and pharmaceutically acceptable salts thereof.

32. A pharmaceutical composition comprising a peptide compound of claim 1- 31 and a pharmaceutically acceptable carrier.

33. A method of inhibiting LHRH activity in a subject, comprising administering to a subject an effective amount of a peptide compound of claim 1-3 1, such that LHRH activity is inhibited.

34. A method of inhibiting growth of a hormone-dependent tumor in a subject, comprising administering to a subject an effective amount of a peptide compound of claim 1-31, such that growth of the hormone-dependent tumor is inhibited.

35. The method of claim 34, wherein the hormone-dependent tumor is a prostate tumor.

36. A method of inhibiting ovulation in a subject, comprising administering to a subject an effective amount of a peptide compound of claim 1-31, such that ovulation is inhibited.

37. A packaged formulation for treating a subject for a disorder associated with LHRH activity, comprising the peptide compound of claim 1-31 packaged with instructions for using the LHRH antagonist for treating a subject having a disorder associated with LHR- activity. -48

38. A pharmaceutical composition comprising the peptide compound of claim 29 and a pharmaceutically acceptable carrier.

39. The pharmaceutical composition of claim 38, which comprises a slow release polymer. The pharmaceutical composition of claim 38, which is suitable for depot injection.

41. A method of inhibiting LHRH activity in a subject, comprising administering to a subject an effective amount of the peptide compound of claim 29, such that LHRH activity is inhibited.

42. A method of inhibiting growth of a hormone-dependent tumor in a subject, comprising administering to a subject an effective amount of the peptide compound of claim 29, such that growth of the hormone-dependent tumor is inhibited.

43. The method of claim 42, wherein the hormone-dependent tumor is a prostate tumor. S* 44. A packaged formulation for treating a subject for a disorder associated with LHRH activity, comprising the peptide compound of claim 29 packaged with instructions for using the LHRH antagonist for treating a subject having a disorder associated with 25 LHRH activity.

45. Use of the peptide compound of claim 1-31 in the manufacture of a medicament for the treatment of a disorder selected from the group consisting of precocious puberty, prostate cancer, ovarian cancer, benign prostatic hypertrophy, endometriosis, uterine fibroids, breast cancer, premenstrual syndrome, polycystic ovary syndrome, and diseases which result from excesses of gonadal hormones.

46. Use of the peptide of claim 29 in the manufacture of a medicament for the treatment of a disorder selected from the group consisting of precocious puberty, prostate cancer, ovarian cancer, benign prostatic hypertrophy, endometriosis, uterine fibroids, breast cancer, premenstrual syndrome, polycystic ovary syndrome, and diseases which result from excesses of gonadal hormones.

47. The use of claim 46, wherein the disorder is prostate cancer. DATED this 3rd day of May 2000 INDIANA UNIVERSITY FOUNDATION Attorney: IVAN A. RAJKOVIC Fellow Institute of Patent Attorneys of Australia of BALDWIN SHELSTON WATERS