[go: up one dir, main page]

AR036876A1 - HETEROCICLIC DERIVATIVES, ITS PREPARATION PROCEDURE AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM - Google Patents

HETEROCICLIC DERIVATIVES, ITS PREPARATION PROCEDURE AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

Info

Publication number
AR036876A1
AR036876A1 ARP020103521A ARP020103521A AR036876A1 AR 036876 A1 AR036876 A1 AR 036876A1 AR P020103521 A ARP020103521 A AR P020103521A AR P020103521 A ARP020103521 A AR P020103521A AR 036876 A1 AR036876 A1 AR 036876A1
Authority
AR
Argentina
Prior art keywords
branched
linear
group
groups
alkyl
Prior art date
Application number
ARP020103521A
Other languages
Spanish (es)
Inventor
Daniel Lesieur
Elodie Blanc-Delmas
Caroline Bennejean
Phillippe Chavatte
Gerald Guillaumet
Catherine Dacquet
Nigel Levens
Jean-Albert Boutin
Pierre Renard
Original Assignee
Servier Lab
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Servier Lab filed Critical Servier Lab
Publication of AR036876A1 publication Critical patent/AR036876A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/06Antihyperlipidemics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Diabetes (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Endocrinology (AREA)
  • Emergency Medicine (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Dermatology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Rheumatology (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Reivindicación 1: Compuestos de la fórmula (1) en la cual: X representa un átomo de oxígeno o de azufre, un grupo CH2 ó CHR'2 (en el cual R'2 forma con R2 una enlace suplementario); Y representa un átomo de oxígeno ó de azufre, R1 y R2, idénticos o diferentes representan un átomo de hidrógeno, un grupo alquilo (C1-6) lineal o ramificado, arilo, arilalquilo (C1-6) lineal o ramificado, ariloxi, arilalquiloxi (C1-6) lineal o ramificado, alcoxi (C1-6) lineal o ramificado, hidroxi, amino, alquilamino (C1-6) lineal o ramificado ó dialquilamino (C1-6) lineal o ramificado, ó R1 y R2 forman juntos un grupo oxo, tioxo ó imino, R2 puede además formar con R'2 un enlace suplementario; A representa una cadena alquileno (C1-6) en la cual uno de sus grupos CH2 puede estar reemplazado por un heteroátomo elegido entre oxígeno o azufre, o por un grupo NRn (donde Rn representa un átomo de hidrógeno ó un grupo alquilo (C1-6) lineal o ramificado), ó por un grupo fenileno ó naftileno, B representa un grupo alquilo (C1-6) lineal o ramificado, ó alquenilo (C2-6) lineal o ramificado, ó alquinileno (C2-6) lineal o ramificado; D y D', idénticos o diferentes, representan un núcleo bencénico ó un núcleo piridínico, esos núcleos son no sustituidos o sustituidos por 1 a 3 grupos, idénticos o diferentes elegidos entre un átomo de halógeno y un grupo ciano, nitro, R, OR, S(O)nR, C(Z)R, -CH(OR)-R', C(Z)OR, NRR', C(Z)NRR', -C(=N-OR')R, -NR-C(Z)R', -NR-C(Z)OR' ó OC(Me)2COOR, (donde R y R' idénticos o diferentes representan un átomo de hidrógeno ó un grupo alquilo (C1-6) lineal o ramificado, alquenilo (C2-6) lineal o ramificado, alquinilo (C2-6) lineal o ramificado, arilo, arilalquilo (C1-6) lineal o ramificado, heteroarilo, heteroarilalquilo (C1-6) lineal o ramificado, cicloalquilo (C3-8) ó cicloalquil (C3-8)-alquilo (C1-6) lineal o ramificado; Z representa un átomo de oxígeno ó de azufre y n representa un número entero comprendido entre 0 y 2 inclusive); R3 y R4, idénticos o diferentes, representan un átomo de hidrógeno, de halógeno, un grupo R, OR ó NRR' (donde R y R' son tal como se los ha definido precedentemente), ó R3 y R4 forman junto con los átomos de carbono que los llevan, cuando son llevados por dos átomos de carbono adyacentes, un ciclo que presenta 5 ó 6 eslabones y que pueden contener un heteroátomo elegido entre oxígeno, azufre y nitrógeno; R5 representa un átomo de hidrógeno, un grupo alquilo (C1-6) lineal o ramificado, alquenilo (C2-6) lineal o ramificado, alquinilo (C2-6) lineal o ramificado, arilo, heteroarilo, alquilcarbonilo (C1-6), arilcarbonilo, ó heteroarilcarbonilo, siendo eventualmente sustituido cada uno de esos grupos: -por uno ó varios grupos R6 tal como R6 representa un grupo -(CH2)t-C(=Z)Z' (donde Z es tal como se ha definido precedentemente, Z' representa un grupo OR ó NRR' con R y R' tal como se los ha definido precedentemente y t es un entero comprendido entre 0 y 6 inclusive); -por un grupo de fórmula (2), en la cual la línea punteada significa que el enlace es simple ó doble y R7 y R8, idénticos o diferentes, representan un grupo -C(=Z)Z' (donde Z y Z' son tal como se los ha definido precedentemente), ó -por un átomo de halógeno, un grupo hidroxi, nitro, ciano, amino ó alcoxi (C1-6) lineal o ramificado, y se entiende que, salvo indicación en contrario: se entiende por arilo, un grupo fenilo, naftilo ó bifenilo, esos grupos pueden estar parcialmente hidrogenados; se entiende por heteroarilo, cualquier grupo aromático mono ó bicíclico que contiene de 5 a 10 eslabones, que puede ser parcialmente hidrogenado en uno de los ciclos en el caso de los heteroarilos bicíclicos, y que contienen 1 a 3 heteroátomos elegidos entre oxígeno, nitrógeno y azufre, los grupos arilo y heteroarilo pueden ser eventualmente sustituidos por 1 a 3 átomos de halógeno ó grupos alquilo (C1-6) lineal o ramificado, alcoxi (C1-6) lineal o ramificado, carboxi, formilo, amino, alquilamino (C1-6) lineal o ramificado, dialquilamino (C1-6) lineal o ramificado, éster, amido, nitro, ciano, y O-C(Me)2COOR (donde R es tal como se ha definido precedentemente), sus enantiómeros y diastereoisómeros así como sus sales de adición con un ácido o con una base farmacéuticamente aceptables. Reivindicación 9: Compuestos de fórmula (1) de acuerdo con una cualquiera de las reivindicaciones 1 a 8, caracterizados porque es la 3-(2-{4-[(5-benzoil-2-oxo-2,3-dihidro-1H-indol-3-il)metil]fenoxi}etil)-1,3-benzotiazol-2(3H)-ona, así como sus sales de adición con un ácido farmacéuticamente aceptable. Reivindicación 10: Compuestos de fórmula (1) de acuerdo con una cualquiera de las reivindicaciones 1 a 8, caracterizados porque es la 6-benzoil-3-(2-{4-[(2-oxo-2,3-dihidro-1H-indol-3-il)metil]fenoxi}etil)-1,3-benzotiazol-2(3H)-ona, así como sus sales de adición con un ácido farmacéuticamente aceptable. Reivindicación 13: Composiciones farmacéuticas de acuerdo con la reivindicación 12, caracterizadas porque son útiles para la fabricación de un medicamento para el tratamiento y/o profilaxis de las hiperglucemias, de las dislipidemias y más particularmente en el tratamiento de las diabetes no insulinodependientes de tipo II, de la resistencia a la insulina, de la intolerancia a la glucosa, de los desórdenes relacionados con el síndrome X, de las enfermedades arteriales coronarias y otras enfermedades cardiovasculares, de las enfermedades renales, de las retionopatías, de los desórdenes relacionados con la activación de las células endoteliales, de la psoriasis, del síndrome poliquístico de ovario, de la demencia, de la osteoporosis, de las enfermedades inflamatorias intestinales, de las distrofias miotónicas, de las pancreatitis, de la arterioesclerosis, del xantoma , pero también en el tratamiento o la prevención de la diabetes de tipo I, de la obesidad, de la regulación del apetito, de la anorexia, de la bulimia, de la anorexia nerviosa, así como de las patologías cancerosas y en especial de los cánceres hormonodependientes tales como el cáncer de pecho y el cáncer de colon y como inhibidores de angiogénesis.Claim 1: Compounds of the formula (1) in which: X represents an oxygen or sulfur atom, a CH2 or CHR'2 group (in which R'2 forms a supplementary bond with R2); Y represents an oxygen or sulfur atom, R1 and R2, identical or different, represent a hydrogen atom, a linear or branched (C1-6) alkyl group, aryl, linear or branched (C1-6) alkyl, aryloxy, arylaxyloxy (C1-6) linear or branched, linear or branched (C1-6) alkoxy, hydroxy, amino, linear or branched (C1-6) alkylamino or linear or branched (C1-6) dialkylamino, or R1 and R2 together form a oxo, thioxo or imino group, R2 can also form a supplementary bond with R'2; A represents an (C1-6) alkylene chain in which one of its CH2 groups can be replaced by a heteroatom chosen from oxygen or sulfur, or by an NRn group (where Rn represents a hydrogen atom or a (C1-) alkyl group 6) linear or branched), or by a phenylene or naphthylene group, B represents a linear or branched (C1-6) alkyl or linear or branched (C2-6) alkenyl group, or linear or branched (C2-6) alkynylene ; D and D ', identical or different, represent a benzene nucleus or a pyridine nucleus, these nuclei are unsubstituted or substituted by 1 to 3 groups, identical or different, chosen between a halogen atom and a cyano, nitro, R, OR group , S (O) nR, C (Z) R, -CH (OR) -R ', C (Z) OR, NRR', C (Z) NRR ', -C (= N-OR') R, - NR-C (Z) R ', -NR-C (Z) OR' or OC (Me) 2COOR, (where identical and different R and R 'represent a hydrogen atom or a linear (C1-6) alkyl group or branched, linear or branched (C2-6) alkenyl, linear or branched (C2-6) alkynyl, aryl, linear or branched (C1-6) arylalkyl, heteroaryl, straight or branched (C1-6) heteroarylalkyl, (C3-) cycloalkyl 8) or linear or branched (C1-6) cycloalkyl (C1-6) alkyl; Z represents an oxygen or sulfur atom and n represents an integer between 0 and 2 inclusive); R3 and R4, identical or different, represent a hydrogen atom, a halogen, a group R, OR or NRR '(where R and R' are as defined above), or R3 and R4 form together with the atoms of carbon that carry them, when they are carried by two adjacent carbon atoms, a cycle that has 5 or 6 links and can contain a heteroatom chosen from oxygen, sulfur and nitrogen; R5 represents a hydrogen atom, a linear or branched (C1-6) alkyl, linear or branched (C2-6) alkenyl, linear or branched (C2-6) alkynyl, aryl, heteroaryl, (C1-6) alkylcarbonyl group, arylcarbonyl, or heteroarylcarbonyl, each of these groups being eventually substituted: - by one or several groups R6 such as R6 represents a group - (CH2) tC (= Z) Z '(where Z is as defined above, Z 'represents an OR or NRR group' with R and R 'as defined above and t is an integer between 0 and 6 inclusive); -by a group of formula (2), in which the dotted line means that the bond is single or double and R7 and R8, identical or different, represent a group -C (= Z) Z '(where Z and Z' they are as defined above), or - by a halogen atom, a linear or branched hydroxy, nitro, cyano, amino or (C1-6) alkoxy group, and it is understood that, unless otherwise indicated: it is understood by aryl, a phenyl, naphthyl or biphenyl group, these groups may be partially hydrogenated; heteroaryl is understood as any mono or bicyclic aromatic group containing 5 to 10 links, which can be partially hydrogenated in one of the cycles in the case of bicyclic heteroaryls, and containing 1 to 3 heteroatoms chosen from oxygen, nitrogen and sulfur, the aryl and heteroaryl groups may be substituted by 1 to 3 halogen atoms or linear or branched (C1-6) alkyl groups, linear or branched (C1-6) alkoxy, carboxy, formyl, amino, (C1-) alkylamino groups 6) linear or branched, dialkylamino (C1-6) linear or branched, ester, amido, nitro, cyano, and OC (Me) 2COOR (where R is as defined above), its enantiomers and diastereoisomers as well as its salts of addition with a pharmaceutically acceptable acid or base. Claim 9: Compounds of formula (1) according to any one of claims 1 to 8, characterized in that it is 3- (2- {4 - [(5-benzoyl-2-oxo-2,3-dihydro-1H -indole-3-yl) methyl] phenoxy} ethyl) -1,3-benzothiazol-2 (3H) -one, as well as its addition salts with a pharmaceutically acceptable acid. Claim 10: Compounds of formula (1) according to any one of claims 1 to 8, characterized in that it is 6-benzoyl-3- (2- {4 - [(2-oxo-2,3-dihydro-1H -indole-3-yl) methyl] phenoxy} ethyl) -1,3-benzothiazol-2 (3H) -one, as well as its addition salts with a pharmaceutically acceptable acid. Claim 13: Pharmaceutical compositions according to claim 12, characterized in that they are useful for the manufacture of a medicament for the treatment and / or prophylaxis of hyperglycemia, of dyslipidemias and more particularly in the treatment of non-insulin-dependent type II diabetes. , insulin resistance, glucose intolerance, disorders related to syndrome X, coronary artery disease and other cardiovascular diseases, kidney diseases, rethiopathies, disorders related to activation of endothelial cells, psoriasis, polycystic ovary syndrome, dementia, osteoporosis, inflammatory bowel diseases, myotonic dystrophies, pancreatitis, arteriosclerosis, xanthoma, but also in treatment or the prevention of type I diabetes, obesity, regulation Onion of appetite, anorexia, bulimia, anorexia nervosa, as well as cancerous pathologies and especially hormone-dependent cancers such as breast cancer and colon cancer and as angiogenesis inhibitors.

ARP020103521A 2001-09-21 2002-09-19 HETEROCICLIC DERIVATIVES, ITS PREPARATION PROCEDURE AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM AR036876A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR0112205A FR2830012B1 (en) 2001-09-21 2001-09-21 NOVEL HETEROCYCLIC DERIVATIVES, THEIR PREPARATION PROCESS AND THE PHARAMACEUTICAL COMPOSITIONS CONTAINING THEM

Publications (1)

Publication Number Publication Date
AR036876A1 true AR036876A1 (en) 2004-10-13

Family

ID=8867506

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP020103521A AR036876A1 (en) 2001-09-21 2002-09-19 HETEROCICLIC DERIVATIVES, ITS PREPARATION PROCEDURE AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

Country Status (3)

Country Link
AR (1) AR036876A1 (en)
FR (1) FR2830012B1 (en)
WO (1) WO2003027108A1 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2858321B1 (en) * 2003-07-28 2006-01-20 Servier Lab NOVEL HETEROCYCLIC OXIMIC DERIVATIVES, PROCESS FOR PREPARING THEM AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME
KR20050040746A (en) * 2003-10-27 2005-05-03 주식회사 엘지생명과학 Novel Compounds As Agonist For PPARγ And PPARα, Method For Preparation Of The Same, And Pharmaceutical Composition Containing The Same
DE602005013275D1 (en) * 2004-12-02 2009-04-23 Prosidion Ltd Pyrrolopyridine-2-KARBONSÄUREAMIDE
FR2881137B1 (en) * 2005-01-27 2007-03-02 Servier Lab NOVEL HETEROCYCLIC OXIMIC DERIVATIVES, PROCESS FOR PREPARING THEM AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5089514A (en) * 1990-06-14 1992-02-18 Pfizer Inc. 3-coxazolyl [phenyl, chromanyl or benzofuranyl]-2-hydroxypropionic acid derivatives and analogs as hypoglycemic agents
JP2002515042A (en) * 1997-12-02 2002-05-21 ドクター・レディーズ・リサーチ・ファウンデーション Azolidinedione useful for the treatment of diabetes, dyslipidemia and hypertension, and compositions containing them

Also Published As

Publication number Publication date
FR2830012B1 (en) 2003-10-31
FR2830012A1 (en) 2003-03-28
WO2003027108A1 (en) 2003-04-03

Similar Documents

Publication Publication Date Title
CO5580746A2 (en) DERIVATIVES OF PHENYL-PIPERAZINE AS INHIBITORS OF THE REABSORTION OF SEROTONINE
ES2620634T3 (en) Human Pyruvate Kinase Activators
AR064444A1 (en) DERIVATIVES OF AMINO-NICOTINIC AND AMINO-ISONICOTINIC ACIDS. PHARMACEUTICAL COMPOSITIONS
AR037288A1 (en) COMPOUNDS DERIVED FROM SULFONAMIDS, PROCEDURE FOR OBTAINING, PHARMACEUTICAL COMPOSITION AND USE FOR THE PREPARATION OF A MEDICINAL PRODUCT
AR030048A1 (en) HETEROCICLIC DERIVATIVES, ITS PREPARATION PROCEDURE AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
UY29702A1 (en) MACROCYCLIC INHIBITORS OF HEPATITIS C VIRUS
EP3331880A1 (en) N-(pyridin-2-yl)-4-(thiazol-5-yl)pyrimidin-2-amine derivatives as therapeutic compounds
AR061739A1 (en) NEW NAFTALENIC DERIVATIVES, THEIR PREPARATION PROCEDURE AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
AR035892A1 (en) DERIVATIVES OF OXAZOL, PROCESS FOR PREPARATION, PHARMACEUTICAL COMPOSITIONS THAT INCLUDE THEM, AND THE USE OF SUCH COMPOUNDS IN THE PREPARATION OF MEDICINES
AR078163A1 (en) USE OF AMINODIHYDROTIAZINES FOR THE TREATMENT OR PREVENTION OF DIABETES
AR043199A1 (en) USEFUL HETEROCICLIC COMPONENTS FOR THE TREATMENT OF INFLAMMATORY AND ALLERGIC DISEASES, PROCESS FOR OPERATION AND PHARMACEUTICAL COMPOSITION CONTAINING SUCH COMPONENTS
AR008829A1 (en) DERIVATIVES 6,6- OR 6,7 SUBSTITUTED BICYCLES CONTAINING PIRIDO OR PIRIMIDO AS ANTAGONIST AGENTS FOR THE TREATMENT OF GASTROINTESTINAL, INFLAMMATORY AND CNS DISEASES, AND PHARMACEUTICAL COMPOSITION
AR047056A1 (en) DERIVATIVES OF CONDENSED PYRIMIDINS. PHARMACEUTICAL COMPOSITIONS
PE20051112A1 (en) NAPHTHYRIDINE DERIVATIVES SUBSTITUTE AS INHIBITORS OF THE INHIBITOR FACTOR OF MACROPHAGES MIGRATION
AR061835A1 (en) TETRACICLIC DERIVATIVES, ITS PREPARATION PROCEDURE AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
AR057989A1 (en) DERIVATIVES OF INDOL-2-IL-AMIDA 1,5-SUBSTITUTED. PROCESSES OF OBTAINING AND PHARMACEUTICAL COMPOSITIONS
AR036876A1 (en) HETEROCICLIC DERIVATIVES, ITS PREPARATION PROCEDURE AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
CY1105784T1 (en) PIPEPAZINYLACYLPIPEPIDINE DERIVATIVES, THEIR PREPARATION AND THERAPEUTIC APPLICATION
US6034246A (en) 2-arylbenzazole compounds
AR059896A1 (en) STEREOISOMERIC DERIVATIVES OF TETRAHYDRONAFTALENE, METHOD OF PREPARATION, MEDICATIONS CONTAINING THEM, AND USE AS ANTI-INFLAMMATORY AGENTS.
JP2013500946A (en) Composition comprising thalidomide and artemisinin for the treatment of cancer
DE69934027D1 (en) 2- (N-CYANIMINO) THIAZOLIDIN-4-ON DERIVATIVES
ATE290527T1 (en) TETRAHYDROBENZINDOLE DERIVATIVES
CA2475137A1 (en) New heterocyclic oxime derivatives, their preparation process and the pharmaceutical compositions that contain them
AR040605A1 (en) PIPERAZINIL-PIPERAZINONA DERIVATIVES FOR THE TREATMENT OF DISORDERS RELATED TO THE 5-HT2A RECEIVER

Legal Events

Date Code Title Description
FA Abandonment or withdrawal