CN1308320C - 作为纤溶酶原激活物抑制剂－1(pai－1)的抑制剂的萘基苯并呋喃衍生物 - Google Patents

作为纤溶酶原激活物抑制剂－1(pai－1)的抑制剂的萘基苯并呋喃衍生物 Download PDF

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CN1308320C
CN1308320C CNB028161874A CN02816187A CN1308320C CN 1308320 C CN1308320 C CN 1308320C CN B028161874 A CNB028161874 A CN B028161874A CN 02816187 A CN02816187 A CN 02816187A CN 1308320 C CN1308320 C CN 1308320C
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carbon atom
alkyl
naphthyl
ester
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CN1543456A (zh
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H·M·埃洛克达
G·R·麦克法兰
S·C·迈尔
D·L·克兰达尔
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Wyeth LLC
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    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • A61P19/00—Drugs for skeletal disorders
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    • A61P9/06—Antiarrhythmics
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    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
    • C07D307/79—Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
    • C07D307/80—Radicals substituted by oxygen atoms

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  • Orthopedic Medicine & Surgery (AREA)
  • Neurology (AREA)
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  • Dermatology (AREA)
  • Obesity (AREA)
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  • Biomedical Technology (AREA)
  • Urology & Nephrology (AREA)
  • Child & Adolescent Psychology (AREA)
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  • Vascular Medicine (AREA)
  • Ophthalmology & Optometry (AREA)
  • Emergency Medicine (AREA)
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  • Reproductive Health (AREA)
  • Pulmonology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
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CNB028161874A 2001-06-20 2002-06-18 作为纤溶酶原激活物抑制剂－1(pai－1)的抑制剂的萘基苯并呋喃衍生物 Expired - Fee Related CN1308320C (zh)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US29970201P 2001-06-20 2001-06-20
US60/299,702 2001-06-20

Publications (2)

Publication Number Publication Date
CN1543456A CN1543456A (zh) 2004-11-03
CN1308320C true CN1308320C (zh) 2007-04-04

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CNB028161874A Expired - Fee Related CN1308320C (zh) 2001-06-20 2002-06-18 作为纤溶酶原激活物抑制剂－1(pai－1)的抑制剂的萘基苯并呋喃衍生物

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Country Link
US (1) US6599925B2 (enExample)
EP (1) EP1401822A1 (enExample)
JP (1) JP4476624B2 (enExample)
CN (1) CN1308320C (enExample)
AR (1) AR036100A1 (enExample)
BR (1) BR0210532A (enExample)
CA (1) CA2449844A1 (enExample)
MX (1) MXPA03011400A (enExample)
TW (1) TWI240723B (enExample)
WO (1) WO2003000671A1 (enExample)

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US7291639B2 (en) * 2001-06-20 2007-11-06 Wyeth Aryloxy-acetic acid compounds useful as inhibitors of plasminogen activator inhibitor-1 (PAI-1)
ES2290318T3 (es) * 2001-06-20 2008-02-16 Wyeth Derivados sustituidos de acido indolico como inhibidores del inhibidor del activador del plasminogeno-1 (pai-1).
TWI224101B (en) * 2001-06-20 2004-11-21 Wyeth Corp Substituted naphthyl indole derivatives as inhibitors of plasminogen activator inhibitor type-1 (PAI-1)
ES2314289T3 (es) * 2002-12-10 2009-03-16 Wyeth Derivados del acido 1h-indol-3-il glioxilico sustituidos con arilo, ariloxi y alquloxi como inhibidores del inhibidor del activador del plasminogeno-1(pai-1).
ATE331708T1 (de) * 2002-12-10 2006-07-15 Wyeth Corp Substituierte 3-alkyl- und 3-arylalkyl-1h-indol-1-yl-essigsäure-derivate als plasminogen aktivator inhibitor-1 (pai-1) inhibitoren
DK1569900T3 (da) * 2002-12-10 2006-10-23 Wyeth Corp Substituerede 3-carbonyl-1-yl-eddikesyrederivater som inhibitorer af plasminogenaktivator-inhibitor-1 (PAI-1)
UA80453C2 (en) * 2002-12-10 2007-09-25 Derivatives of substituted dyhydropyranoindol-3,4-dion as inhibitors of plasminogen activator inhibitor-1 (pai-1)
US7351726B2 (en) * 2003-09-25 2008-04-01 Wyeth Substituted oxadiazolidinediones
US7265148B2 (en) * 2003-09-25 2007-09-04 Wyeth Substituted pyrrole-indoles
US7163954B2 (en) * 2003-09-25 2007-01-16 Wyeth Substituted naphthyl benzothiophene acids
US7332521B2 (en) * 2003-09-25 2008-02-19 Wyeth Substituted indoles
US7534894B2 (en) * 2003-09-25 2009-05-19 Wyeth Biphenyloxy-acids
US7442805B2 (en) * 2003-09-25 2008-10-28 Wyeth Substituted sulfonamide-indoles
US7582773B2 (en) * 2003-09-25 2009-09-01 Wyeth Substituted phenyl indoles
US7141592B2 (en) * 2003-09-25 2006-11-28 Wyeth Substituted oxadiazolidinediones
US7411083B2 (en) * 2003-09-25 2008-08-12 Wyeth Substituted acetic acid derivatives
US7420083B2 (en) * 2003-09-25 2008-09-02 Wyeth Substituted aryloximes
US7446201B2 (en) * 2003-09-25 2008-11-04 Wyeth Substituted heteroaryl benzofuran acids
US7342039B2 (en) * 2003-09-25 2008-03-11 Wyeth Substituted indole oximes
US7268159B2 (en) * 2003-09-25 2007-09-11 Wyeth Substituted indoles
US20080019910A1 (en) * 2004-03-30 2008-01-24 Romer Maria U Cancer Treatment and Cancer Treatment Efficacy Prediction by Blocking and Detecting Protease Inhibitors
WO2006023866A2 (en) * 2004-08-23 2006-03-02 Wyeth Thiazolo-naphthyl acids as inhibitors of plasminogen activator inhibitor-1
MX2007002178A (es) * 2004-08-23 2007-04-02 Wyeth Corp Acidos de oxazolo-naftilo como moduladores del inhibidor del activador de plasminogeno tipo 1 (pai-1) util en el tratamiento de trombosis y enfermedades cardiovasculares.
AU2005277137A1 (en) * 2004-08-23 2006-03-02 Wyeth Pyrrolo-naphthyl acids as PAI-1 inhibitors
AU2006279496A1 (en) * 2005-08-17 2007-02-22 Wyeth Substituted indoles and use thereof
AR059629A1 (es) * 2006-02-27 2008-04-16 Wyeth Corp Inhibidores del inhibidor del activador de plasminogeno (pai- 1) para el tratamiento de trastornos musculares
JP5253174B2 (ja) 2006-10-12 2013-07-31 株式会社医薬分子設計研究所 Ｎ−フェニルオキサミド酸誘導体
US8044236B2 (en) 2006-10-12 2011-10-25 Institute Of Medicinal Molecular Design, Inc. Carboxilic acid derivatives
JP5470046B2 (ja) 2007-10-23 2014-04-16 株式会社医薬分子設計研究所 Ｐａｉ−１産生抑制剤
RU2010145916A (ru) 2008-04-11 2012-05-20 Инститьют Оф Медисинал Молекьюлар Дизайн, Инк. (Jp) Ингибитор pai-1
US8633245B2 (en) * 2008-04-11 2014-01-21 Institute Of Medicinal Molecular Design, Inc. PAI-1 inhibitor
EP2361093A2 (en) 2008-11-26 2011-08-31 Five Prime Therapeutics, Inc. Compositions and methods for regulating collagen and smooth muscle actin expression by serpine2
EP2427057B1 (en) 2009-05-05 2015-08-12 Sloan-Kettering Institute for Cancer Research Benzofuran-4,5-diones as selective peptide deformylase inhibitors
CN102850451B (zh) * 2011-06-29 2014-05-07 辽宁诺康生物制药有限责任公司 具有抑制纤溶酶活性的重组textilinin-1及其制备方法和应用
CN108778307A (zh) 2015-12-18 2018-11-09 泰伦基国际有限公司 一种预防和治疗糖尿病肾病的方法
CN106890324A (zh) * 2015-12-18 2017-06-27 深圳瑞健生命科学研究院有限公司 一种预防和治疗糖尿病肾病的方法
TWI669130B (zh) 2016-12-15 2019-08-21 深圳瑞健生命科學硏究院有限公司 纖溶酶原在製備用於治療糖尿病的藥物上的用途
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BR0210532A (pt) 2004-06-22
JP2004534824A (ja) 2004-11-18
TWI240723B (en) 2005-10-01
AR036100A1 (es) 2004-08-11
CN1543456A (zh) 2004-11-03
EP1401822A1 (en) 2004-03-31
JP4476624B2 (ja) 2010-06-09
CA2449844A1 (en) 2003-01-03
US6599925B2 (en) 2003-07-29
US20030018067A1 (en) 2003-01-23
MXPA03011400A (es) 2004-04-05

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