BR9909322A - Derivados de sulfonilamino que inibem metaloproteinases de degradação de matriz - Google Patents

Derivados de sulfonilamino que inibem metaloproteinases de degradação de matriz

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Publication number
BR9909322A
BR9909322A BR9909322-7A BR9909322A BR9909322A BR 9909322 A BR9909322 A BR 9909322A BR 9909322 A BR9909322 A BR 9909322A BR 9909322 A BR9909322 A BR 9909322A
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Prior art keywords
nitrogen
heterocyclylalkyl
aralkyl
alkyl
heteroarylalkyl
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Application number
BR9909322-7A
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English (en)
Inventor
Paivi Jaana Kukkola
Leslie Anne Robinson
Junichi Sakaki
Motowo Nakajima
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Novartis Ag
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Publication date
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of BR9909322A publication Critical patent/BR9909322A/pt

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    • 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
    • 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
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • 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
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis
    • 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
    • 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
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/15Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C311/16Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
    • C07C311/19Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom to an acyclic carbon atom of a hydrocarbon radical substituted by carboxyl groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/72Two oxygen atoms, e.g. hydantoin
    • C07D233/74Two oxygen atoms, e.g. hydantoin with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to other ring members
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72Quinazolines; Hydrogenated quinazolines
    • C07D239/95Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in positions 2 and 4
    • C07D239/96Two oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D275/00Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
    • C07D275/04Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems
    • C07D275/06Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems with hetero atoms directly attached to the ring sulfur atom
    • 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

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  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Rheumatology (AREA)
  • Urology & Nephrology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pain & Pain Management (AREA)
  • Oncology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Immunology (AREA)
  • Vascular Medicine (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Indole Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Hydrogenated Pyridines (AREA)

Abstract

Patente de Invenção: <B>"DERIVADOS DE SULFONILAMINO QUE INIBEM METALOPROTEINASES DE DEGRADAçãO DE MATRIZ"<D>. Compostos de fórmula I na qual W é -OH ou -NHOH; X é a) um radical heterocíclico não-substituído ou substituído, selecionado do grupo consistindo em pirrolidinila, pirrolila, pirazolila, oxetanila, pirazolinila, imidazolinila, imidazolidinila, oxazolila, oxazolidinila, isoxazolinila, isoxazolila, tiazolila, tiadiazolila, tiazolidinila, isotiazolila, isotiazolidinila, furila, tetrahidrofurila, oxadiazolila, piperidinila, piperazinila, 2-oxopiperazinila, 2-oxopiperidinila, 2-oxopirrolodinila, 2-oxoazepinila, azepinila, 4-piperidinila, piridila, pirazinila, piridazinila, tetrahidropiranila, morfolinila, tiamorfolinila, sulfóxido de tiamorfolinila, sulfona de tiamorfolinila, 1,3-dioxolano, tetrahidro-1,1-dioxotienila, benzotiazolila, benzoxazolila, quinuclidinila, quinolinila, tetrahidroisoquinolinila, isoquinolinila, benzimidazolila, benzopiranila, idolizinila, benzofurila, cromonila, cumarinila, benzopiranila, cinolinila, quinoxalinila, indazolila, pirrolopiridila, furopiridinila, dihidrobenzoisotiazolila, dihidroquinazozolinila, tetrahidroquinazolinil e sistemas de anel tricíclico de 10 a 15 membros, que têm pelo menos um heteroátomo em pelo menos um anel contendo átomo de carbono, no qual cada anel do radical heterocíclico contendo um heteroátomo pode ter 1, 2 ou 3 heteroátomos selecionados dos átomos de nitrogênio, átomos de oxigênio e átomos de súrfur; com a condição de que quando X é um radical heterocíclico contendo nitrogênio, o radical heterocíclico é ligado à porção de (CH~ 2~)~ m~ por um nitrogênio de anel e a condição de que os heteroátomos de nitrogênio e enxofre do radical heterocíclico podem também ser oxidizados; b) -NR~ 1~SO~ 2~R~ 2~, no qual R~ 1~ é hidrogênio, alquila, heterociclialquila, aralquila ou heteroarilalquila e R2 é hidrogênio, alquila, heterociclilalquila, aralquila, heteroarilalquila, arila ou heteroarila; c) heterociclialquiltio; d) -CONR~ 2~R~ 3~, no qual R~ 2~ e R~ 3~ tomados juntos com o átomo de nitrogênio ao qual eles são ligados formam um anel de 5 a 7 membros, que pode opcionalmente conter outro heteroátomo selecionado de oxigênio, nitrogênio e enxofre; ou e) -NR~ 1~COR~ 2~, no qual R~ 1~ é hidrogênio, alquila, heterociclilalquila, aralquila ou heteroarilalquila e R~ 2~ é hidrogênio, heterociclilalquila, aralquila, heteroarilalquila ou arila; Y é carbono, nitrogênio, oxigênio ou enxofre, contanto que quando Y é carbono, n é 2; Z é alquila, arila, alcóxi, arilóxi, aralcoxiarila, aralcoxiheteroarila, heteroarila, heterociclila, heteroarilóxi, -CONR~ 2~R~ 3~, -NR~ 1~COR~ 2~, -NR~ 1~CONR~ 2~R~ 3~, -OCONR~ 2~R~ 3~, -NR~ 1~COOR~ 4~, ou -SO~ 2~R~ 2~, no qual R~ 1~ é hidrogênio, alquila, heterociclilalquila, aralquila ou heteroarilalquila e R~ 2~ e R~ 3~ são independentemente hidrogênio, alquila, heterociclilalquila, aralquila, heteroarilalquila, arila ou heteroarila; ou R~ 2~ e R~ 3~ tomados juntos com o átomo de nitrogênio ao qual eles são ligados formam um anel de 5 a 7 membros, que pode opcionalmente conter outro heteroátomo selecionado de oxigênio, nitrogênio e enxofre; R~ 4~ é alquila, heterociclilalquila, aralquila, arila ou heteroarila; m representa um número inteiro de um a seis; e n representa o número inteiro de um ou dois; e sal farmaceuticamente aceitável destes; composições farmacêuticas compreendendo os referidos compostos e processos para sua preparação; um método de inibição de metaloproteinases de degradação de matriz em mamíferos empregando tais compostos e o uso destes derivados como medicamento. Os compostos de fórmula I são inibidores de metaloproteinases de degradação de matriz e são úteis para o tratamento de condições relacionadas com eles.
BR9909322-7A 1998-02-04 1999-02-02 Derivados de sulfonilamino que inibem metaloproteinases de degradação de matriz BR9909322A (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US1881998A 1998-02-04 1998-02-04
PCT/EP1999/000646 WO1999042443A1 (en) 1998-02-04 1999-02-02 Sulfonylamino derivatives which inhibit matrix-degrading metalloproteinases

Publications (1)

Publication Number Publication Date
BR9909322A true BR9909322A (pt) 2000-12-05

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BR9909322-7A BR9909322A (pt) 1998-02-04 1999-02-02 Derivados de sulfonilamino que inibem metaloproteinases de degradação de matriz

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US (1) US6277987B1 (pt)
EP (2) EP1918278A1 (pt)
JP (1) JP4750272B2 (pt)
KR (1) KR20010040698A (pt)
CN (1) CN1195735C (pt)
AU (1) AU747911B2 (pt)
BR (1) BR9909322A (pt)
CA (1) CA2318145C (pt)
HU (1) HUP0101176A3 (pt)
ID (1) ID24957A (pt)
IL (1) IL137465A0 (pt)
NO (1) NO317977B1 (pt)
NZ (1) NZ505968A (pt)
PL (1) PL342009A1 (pt)
RU (1) RU2208609C2 (pt)
SK (1) SK11692000A3 (pt)
TR (1) TR200002224T2 (pt)
WO (1) WO1999042443A1 (pt)

Families Citing this family (50)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2327290A1 (en) * 1998-04-03 1999-10-14 Sankyo Company Limited Sulfonamide derivatives
CZ20013176A3 (cs) * 1999-03-03 2002-04-17 The Procter & Gamble Company Sloučenina vytvářející inhibitor metaloproteinasy, farmaceutický prostředek, způsob přípravy léčiva a léčivo
RU2001126719A (ru) 1999-03-03 2004-02-20 Дзе Проктер Энд Гэмбл Компани (US) Дигетерозамещенные ингибиторы металлопротеазы
GB9918684D0 (en) 1999-08-09 1999-10-13 Novartis Ag Organic compounds
EP1088815A1 (en) * 1999-09-28 2001-04-04 Applied Research Systems ARS Holding N.V. Pharmaceutically active sulfonyl amino acid derivatives
WO2001023363A1 (fr) * 1999-09-29 2001-04-05 Sankyo Company, Limited Derives de sulfonamide
JP2003528082A (ja) 2000-03-21 2003-09-24 ザ プロクター アンド ギャンブル カンパニー ニフッ化酪酸メタロプロテアーゼ阻害物質
KR20020081464A (ko) * 2000-03-21 2002-10-26 더 프록터 앤드 갬블 캄파니 헤테로시클릭 측쇄 함유 메탈로프로테아제 억제제
CA2404131A1 (en) 2000-03-21 2001-09-27 The Procter & Gamble Company Heterocyclic side chain containing, n-substituted metalloprotease inhibitors
AU2001248701A1 (en) * 2000-03-24 2001-10-03 Methylgene, Inc. Inhibitors of histone deacetylase
WO2001083431A1 (fr) * 2000-04-28 2001-11-08 Shionogi & Co., Ltd. Inhibiteurs de mmp-12
EP1174129A1 (en) * 2000-07-17 2002-01-23 Zenner, Hans Peter, Prof. Dr. med. Use of a matrix-metalloprotease inhibitor for the treatment of cancer
GB0103303D0 (en) 2001-02-09 2001-03-28 Novartis Ag Organic compounds
SE0100903D0 (sv) * 2001-03-15 2001-03-15 Astrazeneca Ab Compounds
SE0100902D0 (sv) 2001-03-15 2001-03-15 Astrazeneca Ab Compounds
SE0103710D0 (sv) 2001-11-07 2001-11-07 Astrazeneca Ab Compounds
JP4427328B2 (ja) * 2001-12-14 2010-03-03 エクセリクシス, インク. ヒト−adam−10インヒビター
US20050227994A1 (en) * 2002-03-27 2005-10-13 Shionogi & Co., Ltd. Decomposition inhibitor for extracellular matrix of cartilage
SI1511472T1 (sl) 2002-05-29 2009-08-31 Merck & Co Inc Spojine uporabne pri zdravljenju antraksa in inhibiranju letalnega faktorja
SE0202539D0 (sv) 2002-08-27 2002-08-27 Astrazeneca Ab Compounds
GB0221246D0 (en) * 2002-09-13 2002-10-23 Astrazeneca Ab Compounds
CN1950354A (zh) 2004-05-11 2007-04-18 默克公司 N-磺酰化-氨基酸衍生物的制备方法
GB0412553D0 (en) 2004-06-04 2004-07-07 Univ Aberdeen Therapeutic agents for the treatment of bone conditions
US7648992B2 (en) 2004-07-05 2010-01-19 Astrazeneca Ab Hydantoin derivatives for the treatment of obstructive airway diseases
SE0401762D0 (sv) 2004-07-05 2004-07-05 Astrazeneca Ab Novel compounds
WO2006029173A2 (en) * 2004-09-08 2006-03-16 Boys Town National Research Hospital Treatment of glomerular basement membrane disease involving matrix metalloproteinase-12
US20100003276A1 (en) * 2004-12-07 2010-01-07 Hermes Jeffery D Methods for treating anthrax and inhibiting lethal factor
SE0403085D0 (sv) 2004-12-17 2004-12-17 Astrazeneca Ab Novel componds
SE0403086D0 (sv) 2004-12-17 2004-12-17 Astrazeneca Ab Compounds
US7576222B2 (en) * 2004-12-28 2009-08-18 Wyeth Alkynyl-containing tryptophan derivative inhibitors of TACE/matrix metalloproteinase
US20100247512A1 (en) * 2006-03-31 2010-09-30 The Regents Of The University Of Michigan Pericellular Collagenase Directs the 3-Dimensional Development of White Adipose Tissue
TW200831488A (en) * 2006-11-29 2008-08-01 Astrazeneca Ab Novel compounds
EP1972617A1 (en) * 2007-03-19 2008-09-24 Bracco Imaging, S.P.A. Compounds having aryl-sulphonamidic structure useful as metalloproteases inhibitors
GB0705400D0 (en) 2007-03-21 2007-05-02 Univ Aberdeen Therapeutic compounds andm their use
CA2719457C (en) * 2008-03-24 2017-05-02 Novartis Ag Arylsulfonamide-based matrix metalloprotease inhibitors
EP2147684A1 (en) * 2008-07-22 2010-01-27 Bracco Imaging S.p.A Diagnostic Agents Selective Against Metalloproteases
EP2149568A1 (en) 2008-07-22 2010-02-03 Bracco Imaging S.p.A Aryl-sulphonamidic dimers as metalloproteases inhibitors
GB0817208D0 (en) 2008-09-19 2008-10-29 Pimco 2664 Ltd Therapeutic apsap compounds and their use
GB0817207D0 (en) 2008-09-19 2008-10-29 Pimco 2664 Ltd therapeutic apsac compounds and their use
US20100160322A1 (en) 2008-12-04 2010-06-24 Abbott Laboratories Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
US8557983B2 (en) 2008-12-04 2013-10-15 Abbvie Inc. Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
UA108193C2 (uk) * 2008-12-04 2015-04-10 Апоптозіндукуючий засіб для лікування раку і імунних і аутоімунних захворювань
US8586754B2 (en) 2008-12-05 2013-11-19 Abbvie Inc. BCL-2-selective apoptosis-inducing agents for the treatment of cancer and immune diseases
US8563735B2 (en) 2008-12-05 2013-10-22 Abbvie Inc. Bcl-2-selective apoptosis-inducing agents for the treatment of cancer and immune diseases
PE20120119A1 (es) * 2008-12-05 2012-03-18 Abbvie Inc AGENTES INDUCTORES DE APOPTOSIS CON SELECTIVIDAD POR Bcl-2
ITTO20090648A1 (it) * 2009-08-19 2011-02-20 Istituto Naz Per La Ricerca Sul Cancro Inibitori di adam17 atti a modulare il rilascio di alcam (cd166) solubile in cellule tumorali e loro uso nel trattamento terapeutico del carcinoma ovarico epiteliale (eoc)
US9023318B2 (en) 2011-06-08 2015-05-05 Siemens Medical Solutions Usa, Inc. Compounds with matrix-metalloproteinase inhibitory activity and imaging agents thereof
GB201311361D0 (en) 2013-06-26 2013-08-14 Pimco 2664 Ltd Compounds and their therapeutic use
SI3262028T1 (sl) 2014-12-17 2022-02-28 Pimco 2664 Limited N-(4-hidroksi-4-metil-cikloheksil)-4-fenil-benzensulfonamidne in N-(-4hidroksi-4-metil-cikloheksil)-4-(2-piridil)-benzensulfonamidne spojine in njihova terapevtska uporaba
CN110483437B (zh) * 2018-05-14 2022-12-06 嘉兴维眸生物科技有限公司 一种含五元环的化合物及其制备和应用

Family Cites Families (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1493665A1 (de) 1964-07-16 1969-02-06 Hoechst Ag Verfahren zur Spaltung von aromatischen Carbonsaeureamiden
EP0639982A1 (en) 1992-05-01 1995-03-01 British Biotech Pharmaceuticals Limited Use of mmp inhibitors
US5646167A (en) * 1993-01-06 1997-07-08 Ciba-Geigy Corporation Arylsulfonamido-substituted hydroxamix acids
US5506242A (en) * 1993-01-06 1996-04-09 Ciba-Geigy Corporation Arylsufonamido-substituted hydroxamic acids
US5552419A (en) 1993-01-06 1996-09-03 Ciba-Geigy Corporation Arylsulfonamido-substituted hydroxamic acids
JPH10501806A (ja) 1994-06-22 1998-02-17 ブリティッシュ バイオテック ファーマシューティカルズ リミテッド 金属タンパク質分解酵素阻害剤
HUP9902083A3 (en) 1995-11-17 2000-06-28 Warner Lambert Co Sulfonamide inhibitors of matrix metalloproteinases
US5753653A (en) 1995-12-08 1998-05-19 Agouron Pharmaceuticals, Inc. Metalloproteinase inhibitors, pharmaceutical compositions containing them and their pharmaceutical uses
ES2195034T3 (es) 1995-12-08 2003-12-01 Agouron Pharma Inhibidor de metaloproteinasas, composicion farmaceutica que contiene este inhibidor y su utilizacion farmaceutica, y procedimientos que sirven para su preparacion.
NZ325939A (en) * 1996-01-23 2000-06-23 Shionogi & Co Sulphonated amino acid derivatives and matrix metalloproteinase inhibitors (MMP) containing these derivatives
DE69707865T2 (de) * 1996-05-17 2002-05-02 Warner Lambert Co Biphenylsulfonamid matrix metalloproteinase inhibitoren
EP0915086A4 (en) 1996-05-24 2001-01-17 Ono Pharmaceutical Co PHENYLSULFONAMIDE DERIVATIVES
EP0923561B1 (en) 1996-08-28 2002-10-23 The Procter & Gamble Company Heterocyclic metalloprotease inhibitors
BR9713185A (pt) 1996-08-28 1999-11-03 Procter & Gamble Inibidores metalo protease heterocìclicos
BR9712792A (pt) 1996-08-28 1999-12-14 Procter & Gamble Inibidores de metaloprotease bidentada.
JP3541043B2 (ja) 1996-08-28 2004-07-07 ザ プロクター アンド ギャンブル カンパニー 置換環状アミンメタロプロテアーゼ阻害剤
DE69730033T2 (de) 1996-08-28 2005-07-21 The Procter & Gamble Company, Cincinnati Spirocyclisch metalloprotease inhibitoren
ATE227274T1 (de) 1996-08-28 2002-11-15 Procter & Gamble 1,3-diheterozyklische metalloprotease inhibitoren
AU737117B2 (en) * 1996-12-17 2001-08-09 Warner-Lambert Company Use of matrix metalloproteinase inhibitors for treating neurological disorders and promoting wound healing
CN1243507A (zh) * 1997-01-17 2000-02-02 法玛西雅厄普约翰美国公司 用作mmp抑制剂的双磺酰胺异羟肟酸类化合物
US5985900A (en) * 1997-04-01 1999-11-16 Agouron Pharmaceuticals, Inc. Metalloproteinase inhibitors, pharmaceutical compositions containing them and their pharmaceutical uses
JP2001521504A (ja) 1997-04-01 2001-11-06 アグロン・ファーマシュウティカルズ・インコーポレーテッド メタロプロテイナーゼ阻害薬、それらを含有する薬剤組成物および薬剤としてのそれらの使用
US5756545A (en) * 1997-04-21 1998-05-26 Warner-Lambert Company Biphenysulfonamide matrix metal alloproteinase inhibitors
DE19719428A1 (de) 1997-05-12 1998-11-19 Hoechst Ag Substituierte Diaminocarbonsäuren
DE19719585A1 (de) 1997-05-09 1998-11-12 Hoechst Ag Substituierte Diaminocarbonsäuren
PT877019E (pt) 1997-05-09 2002-05-31 Hoechst Ag Acidos diaminocarboxilicos substituidos
DE19719621A1 (de) 1997-05-09 1998-11-12 Hoechst Ag Sulfonylaminocarbonsäuren
AU7294098A (en) 1997-05-09 1998-11-27 Agouron Pharmaceuticals, Inc. Metalloproteinase inhibitors, pharmaceutical compositions containing them and their pharmaceutical uses
IL133933A0 (en) 1997-07-22 2001-04-30 Shionogi & Co Composition for treating or preventing glomerulopathy
WO1999006340A2 (en) * 1997-07-31 1999-02-11 The Procter & Gamble Company Sulfonylamino substituted hydroxamic acid derivatives as metalloprotease inhibitors

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RU2208609C2 (ru) 2003-07-20
CN1290250A (zh) 2001-04-04
JP4750272B2 (ja) 2011-08-17
WO1999042443A1 (en) 1999-08-26
CN1195735C (zh) 2005-04-06
EP1918278A1 (en) 2008-05-07
TR200002224T2 (tr) 2000-12-21
NO317977B1 (no) 2005-01-17
IL137465A0 (en) 2001-07-24
EP1053226A1 (en) 2000-11-22
CA2318145A1 (en) 1999-08-26
NO20003565D0 (no) 2000-07-11
SK11692000A3 (sk) 2001-02-12
PL342009A1 (en) 2001-05-07
NO20003565L (no) 2000-10-03
AU2923599A (en) 1999-09-06
NZ505968A (en) 2003-03-28
US6277987B1 (en) 2001-08-21
ID24957A (id) 2000-08-31
JP2002503720A (ja) 2002-02-05
AU747911B2 (en) 2002-05-30
HUP0101176A3 (en) 2002-06-28
HUP0101176A2 (hu) 2001-09-28
KR20010040698A (ko) 2001-05-15

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