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AR002958A1 - Derivados de acidos alcanoicos o fosfinicos que tienen un sustituyente triciclico, composiciones que los contienen y procedimiento para su preparacion - Google Patents

Derivados de acidos alcanoicos o fosfinicos que tienen un sustituyente triciclico, composiciones que los contienen y procedimiento para su preparacion

Info

Publication number
AR002958A1
AR002958A1 ARP960101275A AR10127596A AR002958A1 AR 002958 A1 AR002958 A1 AR 002958A1 AR P960101275 A ARP960101275 A AR P960101275A AR 10127596 A AR10127596 A AR 10127596A AR 002958 A1 AR002958 A1 AR 002958A1
Authority
AR
Argentina
Prior art keywords
alkyl
alkoxycarbonyl
hydrogen
aralkoxycarbonyl
naphth
Prior art date
Application number
ARP960101275A
Other languages
English (en)
Original Assignee
Syntex Inc
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 Syntex Inc filed Critical Syntex Inc
Publication of AR002958A1 publication Critical patent/AR002958A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/02Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/02Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • 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
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/12Drugs for disorders of the metabolism for electrolyte homeostasis
    • A61P3/14Drugs for disorders of the metabolism for electrolyte homeostasis for calcium homeostasis
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/08Bridged systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6561Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Rheumatology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • Dermatology (AREA)
  • Immunology (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Pain & Pain Management (AREA)
  • Diabetes (AREA)
  • Endocrinology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Indole Compounds (AREA)

Abstract

Compuestos de fórmula (I), como estereoisómero único o como mezcla de estereoisómeros, donde: m es 3,4,5 ó 6; y n es 0, 1, 3 ó 4; de modo que: cuandom es 3 ó 4; y n es 1, 2, 3 ó 4; entonces A es -CH2-, -O-, ó -N(R11)-, donde R11 eshidrógen o o alquilo; R1 es a) -CH2-R4 donde R4 es mercapto, acetiltio,carboxi, hidroxiaminocarbonilo, N-hidroxiformilamino, alcoxicarbonilo, ariloxicarbonilo, aralcoxicarbonilo, benciloxi-aminocarbonilo, ó -P(:O)OHS-R6en el cual R6 esquinol-2-ilo, naft-1-ilo, naft-2-ilo, piridilo o fenilo sustituido o no; b) -CH(R7)-R8 donde R8 es HOOC-, HOHNOC-; R7 es OH, NH2,alquilo, alquil o arilamino, alquilo, arilsulfonilamino, H2NOC-, alcoxi o aminocarbonilo, o -CH2NHR donde Res H, alquil- o aril-, 2-benzoxazol, -SO2Ra,-SO2NHRa, -SO2ORa, -C:ORa, -COORa, -CONHRa donde Ra es alquilo sustituido o no; ó c) -NH-CH(R9)-R10 donde R9 es hidrógeno, alquilo o aralquilo, y R10 escarboxi, alcoxicarbonilo o aralcoxicarbonilo,fosfonilo, dialquilfos fonilo o metoxifosfonilo; R2 es alquilo, trifluormetilalquilo, cicloalquilo,cicloalquilalquilo, arilo, ariloxialquilo o aralquilo; y R3 es hidrógeno, halo, alquilo o alcoxi; o cuando n es 0; y m es 4, 5 ó 6; entonces A es -CH(R12)donde R12 es carb oxi, alcoxicarbonilo u opcionalmente carbamoilo substituido. Son estereoisómeros únicos o mezclas de los mismos y sus salesfarmacéuticamente aceptables que inhiben las metaloproteasas de matriz, tales como colagenasasintersticiales y que son úti les para el tratamiento deenfermedades artríticas o enfermedades de resorción ósea, tales como osteoporosis.
ARP960101275A 1995-02-03 1996-02-05 Derivados de acidos alcanoicos o fosfinicos que tienen un sustituyente triciclico, composiciones que los contienen y procedimiento para su preparacion AR002958A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US08/382,818 US6013792A (en) 1993-08-05 1995-02-03 Matrix metalloprotease inhibitors

Publications (1)

Publication Number Publication Date
AR002958A1 true AR002958A1 (es) 1998-05-27

Family

ID=23510527

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP960101275A AR002958A1 (es) 1995-02-03 1996-02-05 Derivados de acidos alcanoicos o fosfinicos que tienen un sustituyente triciclico, composiciones que los contienen y procedimiento para su preparacion

Country Status (18)

Country Link
US (1) US6013792A (es)
EP (1) EP0807114A1 (es)
JP (1) JPH11500109A (es)
KR (1) KR100403687B1 (es)
CN (1) CN1066150C (es)
AR (1) AR002958A1 (es)
AU (1) AU705763B2 (es)
BR (1) BR9606998A (es)
CA (1) CA2212236A1 (es)
CZ (1) CZ293868B6 (es)
FI (1) FI113965B (es)
HU (1) HUP9702073A3 (es)
NO (1) NO311257B1 (es)
PL (1) PL321659A1 (es)
RU (1) RU2191779C2 (es)
UA (1) UA67716C2 (es)
WO (1) WO1996023791A1 (es)
ZA (1) ZA96850B (es)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR19990072009A (ko) * 1995-08-12 1999-09-27 게리 이. 프리드만 메탈로프로티나제 방해제, 그를 포함하는 약제 조성물 및 약제로서의 용도, 그리고 그의 제조방법 및 제조에 유용한 중간체
US6500948B1 (en) 1995-12-08 2002-12-31 Agouron Pharmaceuticals, Inc. Metalloproteinase inhibitors-compositions, uses preparation and intermediates thereof
US6174915B1 (en) 1997-03-25 2001-01-16 Agouron Pharmaceuticals, Inc. Metalloproteinase inhibitors, pharmaceutical compositions containing them and their pharmaceutical uses
US6008243A (en) * 1996-10-24 1999-12-28 Agouron Pharmaceuticals, Inc. Metalloproteinase inhibitors, pharmaceutical compositions containing them, and their use
US5985900A (en) * 1997-04-01 1999-11-16 Agouron Pharmaceuticals, Inc. Metalloproteinase inhibitors, pharmaceutical compositions containing them and their pharmaceutical uses
GB9715030D0 (en) 1997-07-18 1997-09-24 British Biotech Pharm Metalloproteinase inhibitors
US6858598B1 (en) 1998-12-23 2005-02-22 G. D. Searle & Co. Method of using a matrix metalloproteinase inhibitor and one or more antineoplastic agents as a combination therapy in the treatment of neoplasia
GB9907055D0 (en) * 1999-03-29 1999-05-19 British Biotech Pharm Antibacterial agents
AR032920A1 (es) * 2001-03-01 2003-12-03 Smithkline Beecham Corp Compuestos inhibidores de las peptido-deformilasas y medios para tratar infecciones bacterianas utilizando dichos inhibidores
UY27813A1 (es) * 2002-05-31 2003-12-31 Smithkline Beecham Corp Inhibidores de la peptido-desformilasa
BR0317715A (pt) * 2002-12-27 2005-11-22 Angiotech Int Ag Composições e processos de uso de collajolie
JP2006516548A (ja) 2002-12-30 2006-07-06 アンジオテック インターナショナル アクツィエン ゲゼルシャフト 迅速ゲル化ポリマー組成物からの薬物送達法
US7927579B2 (en) * 2003-01-17 2011-04-19 Advanced Proteome Therapeutics, Inc Tandem analyses of noncovalently driven effectors for modulatory mapping of activities of protein sites
AU2003902115A0 (en) * 2003-05-02 2003-05-22 The University Of Queensland Method of predicting functional outcome of a stroke using eeg measures
RU2247563C1 (ru) * 2003-06-16 2005-03-10 Пятигорская государственная фармацевтическая академия Способ получения твердой лекарственной формы, содержащей глюкозамина гидрохлорид
CA2533820C (en) * 2003-07-31 2016-12-13 Tranzyme Pharma Spatially-defined macrocycles incorporating peptide bond surrogates
RU2257386C1 (ru) * 2004-05-05 2005-07-27 Пермский государственный университет 20-ароил-12-гидрокси-17,17-диметил-3-фенил-3,10,13- триазапентацикло[10.7.1.01,10.04,9.014,19]эйкоза-4,6,8,14(19)-тетраен- 2,11,15- трионы и способ их получения
KR100753796B1 (ko) 2006-07-28 2007-08-31 주식회사 프로메디텍 데포르밀라제 저해제, 이의 제조방법, 및 이를 포함하는조성물
UA108596C2 (xx) * 2007-11-09 2015-05-25 Інгібітори пептиддеформілази
CN105801530A (zh) * 2016-04-13 2016-07-27 成都拿盛科技有限公司 一种4位取代的手性γ-丁内酯的合成方法
KR20220105061A (ko) 2021-01-19 2022-07-26 (주)월드트렌드 밀착력과 착용감 향상 및 수시 교체가 가능한 안경테와 코 받침의 조립구조

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4761406A (en) * 1985-06-06 1988-08-02 The Procter & Gamble Company Regimen for treating osteoporosis
GB9000846D0 (en) * 1990-01-15 1990-03-14 Beecham Group Plc Novel compounds
GB9022117D0 (en) * 1990-10-11 1990-11-21 Beecham Group Plc Novel compounds
US5189178A (en) * 1990-11-21 1993-02-23 Galardy Richard E Matrix metalloprotease inhibitors
US5183900A (en) * 1990-11-21 1993-02-02 Galardy Richard E Matrix metalloprotease inhibitors
WO1992021360A1 (en) * 1991-05-28 1992-12-10 Merck & Co., Inc. Substituted n-carboxyalkylpeptidyl derivatives as antidegenerative active agents
GB9122859D0 (en) * 1991-10-28 1991-12-11 Smithkline Beecham Plc Novel compounds
NZ246456A (en) * 1991-12-17 1997-03-24 Procter & Gamble Pharma Use of bone active phosphonate and a parathyroid hormone to prepare medicaments for a thirty day treatment regimen for osteoporosis
DK0712403T3 (da) * 1993-08-05 1998-01-26 Syntex Inc Matrix-metalloproteaseinhibitorer

Also Published As

Publication number Publication date
NO973551D0 (no) 1997-08-01
PL321659A1 (en) 1997-12-22
WO1996023791A1 (en) 1996-08-08
NO973551L (no) 1997-10-03
KR100403687B1 (ko) 2004-02-11
AU705763B2 (en) 1999-06-03
AU4863696A (en) 1996-08-21
CN1066150C (zh) 2001-05-23
BR9606998A (pt) 1997-10-28
JPH11500109A (ja) 1999-01-06
HUP9702073A2 (hu) 1998-03-30
FI113965B (fi) 2004-07-15
NO311257B1 (no) 2001-11-05
CA2212236A1 (en) 1996-08-08
HUP9702073A3 (en) 1999-05-28
CN1180358A (zh) 1998-04-29
RU2191779C2 (ru) 2002-10-27
FI973198A0 (fi) 1997-08-01
EP0807114A1 (en) 1997-11-19
CZ293868B6 (cs) 2004-08-18
US6013792A (en) 2000-01-11
UA67716C2 (en) 2004-07-15
CZ243197A3 (cs) 1998-01-14
ZA96850B (en) 1997-11-03
FI973198L (fi) 1997-08-01

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