TR199701354A2 - Lökosit adezyonu ve VLA-4-Antagonist'lerinin inhibitörleri. - Google Patents

Lökosit adezyonu ve VLA-4-Antagonist'lerinin inhibitörleri.

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Publication number
TR199701354A2
TR199701354A2 TR97/01354A TR9701354A TR199701354A2 TR 199701354 A2 TR199701354 A2 TR 199701354A2 TR 97/01354 A TR97/01354 A TR 97/01354A TR 9701354 A TR9701354 A TR 9701354A TR 199701354 A2 TR199701354 A2 TR 199701354A2
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TR
Turkey
Prior art keywords
compounds
vla
adhesion
cell
formula
Prior art date
Application number
TR97/01354A
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English (en)
Other versions
TR199701354A3 (tr
Inventor
Heinrich Ulrich Stilz Dr.
Volkmar Wehner Dr.
Jochen Knolle Dr.
Eckard Bartnik Dr.
CHRISTOPH H�LS Dr.
Original Assignee
Hoechst Aktiengesellschaft
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Publication date
Application filed by Hoechst Aktiengesellschaft filed Critical Hoechst Aktiengesellschaft
Publication of TR199701354A2 publication Critical patent/TR199701354A2/tr
Publication of TR199701354A3 publication Critical patent/TR199701354A3/tr

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Abstract

I sayili formülü olan bilesikler, ki bu formülde B, D, E, R, W, Y, Z, b, c, d, e, f, g, ve h istemlerde gösterilmis olan manalara sahiptirler, integrin'ler sinifina giren adezyon reseptörlerinin VLA-4 antagonist'leri ve/veya lökositlerin adezyonu ve migrasyonu enhibitörleridirler. Ihtira I sayili formüle ait bilesiklerin ve bu bilesikleri içeren ispençiyari müstahzarlarin,istenmedik derecedeki bir lökosit adezyonunun ve/veya lökosit migrasyonunun neden oldugu veya bunlara bagli olan veya hücreden hücreye veya hücreden matrise olan karsilikli faaliyetlerin bir rol oynadiklari, yani VLA-4 reseptörlerinin ligand'lariyla karsilikli etkilesmelerine dayanan hastaliklarin, mesala iltihaplanmalarin, reumatoid artritis veya alerjik hastaliklarin tedavisi ve profilaksi için kullanilmalarini ve bu çesit hastaliklarda uygulanacak ilaçlarin üretilmesi için I sayili formüle ait bilesiklerin kullanilmalarini ilgilendirmektedir.
TR97/01354A 1996-11-15 1997-11-13 Lökosit adezyonu ve VLA-4-Antagonist'lerinin inhibitörleri. TR199701354A3 (tr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19647380A DE19647380A1 (de) 1996-11-15 1996-11-15 5-Ring-Heterocyclen als Inhibitoren der Leukozytenadhäsion und VLA-4-Antagonisten

Publications (2)

Publication Number Publication Date
TR199701354A2 true TR199701354A2 (tr) 1998-06-22
TR199701354A3 TR199701354A3 (tr) 1998-06-22

Family

ID=7811830

Family Applications (1)

Application Number Title Priority Date Filing Date
TR97/01354A TR199701354A3 (tr) 1996-11-15 1997-11-13 Lökosit adezyonu ve VLA-4-Antagonist'lerinin inhibitörleri.

Country Status (30)

Country Link
US (1) US20040220148A1 (tr)
EP (1) EP0842943B1 (tr)
JP (1) JPH10147573A (tr)
KR (1) KR19980042457A (tr)
CN (1) CN1135236C (tr)
AR (1) AR010067A1 (tr)
AT (1) ATE233276T1 (tr)
AU (1) AU747789B2 (tr)
BR (1) BR9705727A (tr)
CA (1) CA2220784A1 (tr)
CZ (1) CZ293351B6 (tr)
DE (2) DE19647380A1 (tr)
DK (1) DK0842943T3 (tr)
ES (1) ES2190503T3 (tr)
HR (1) HRP970605B1 (tr)
HU (1) HUP9702035A3 (tr)
ID (1) ID19010A (tr)
IL (1) IL122188A0 (tr)
MX (1) MX9708782A (tr)
MY (1) MY119617A (tr)
NO (1) NO317241B1 (tr)
NZ (1) NZ329178A (tr)
PL (1) PL323128A1 (tr)
PT (1) PT842943E (tr)
RU (1) RU2229296C2 (tr)
SI (1) SI0842943T1 (tr)
SK (1) SK284377B6 (tr)
TR (1) TR199701354A3 (tr)
TW (1) TW496874B (tr)
ZA (1) ZA9710244B (tr)

Families Citing this family (55)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19741235A1 (de) 1997-09-18 1999-03-25 Hoechst Marion Roussel De Gmbh Neue Imidazolidinderivate, ihre Herstellung, ihre Verwendung und sie enthaltende pharmazeutische Präparate
DE19741873A1 (de) * 1997-09-23 1999-03-25 Hoechst Marion Roussel De Gmbh Neue 5-Ring-Heterocyclen, ihre Herstellung, ihre Verwendung und sie enthaltende pharmazeutische Präparate
DE19751251A1 (de) 1997-11-19 1999-05-20 Hoechst Marion Roussel De Gmbh Substituierte Imidazolidinderivate, ihre Herstellung, ihre Verwendung und sie enthaltende pharmezeutische Präparate
US6329372B1 (en) 1998-01-27 2001-12-11 Celltech Therapeutics Limited Phenylalanine derivatives
ATE273273T1 (de) 1998-02-26 2004-08-15 Celltech Therapeutics Ltd Phenylalaninderivate als inhibitoren von alpha4 integrinen
GB9805655D0 (en) 1998-03-16 1998-05-13 Celltech Therapeutics Ltd Chemical compounds
US6521626B1 (en) 1998-03-24 2003-02-18 Celltech R&D Limited Thiocarboxamide derivatives
DE19821483A1 (de) 1998-05-14 1999-11-18 Hoechst Marion Roussel De Gmbh Imidazolidinderivate, ihre Herstellung, ihre Verwendung und sie enthaltende pharmazeutische Präparate
GB9811159D0 (en) * 1998-05-22 1998-07-22 Celltech Therapeutics Ltd Chemical compounds
GB9811969D0 (en) * 1998-06-03 1998-07-29 Celltech Therapeutics Ltd Chemical compounds
GB9812088D0 (en) 1998-06-05 1998-08-05 Celltech Therapeutics Ltd Chemical compounds
GB9814414D0 (en) 1998-07-03 1998-09-02 Celltech Therapeutics Ltd Chemical compounds
GB9821061D0 (en) 1998-09-28 1998-11-18 Celltech Therapeutics Ltd Chemical compounds
GB9821222D0 (en) 1998-09-30 1998-11-25 Celltech Therapeutics Ltd Chemical compounds
GB9825652D0 (en) 1998-11-23 1999-01-13 Celltech Therapeutics Ltd Chemical compounds
GB9826174D0 (en) 1998-11-30 1999-01-20 Celltech Therapeutics Ltd Chemical compounds
AU3246600A (en) 1999-03-01 2000-09-21 Elan Pharmaceuticals, Inc. Alpha-aminoacetic acid derivatives useful as alpha 4 beta 7 receptor antagonists
US6723711B2 (en) 1999-05-07 2004-04-20 Texas Biotechnology Corporation Propanoic acid derivatives that inhibit the binding of integrins to their receptors
IL146312A0 (en) * 1999-05-07 2002-07-25 Texas Biotechnology Corp Propanoic acid derivatives that inhibit the binding of integrins to their receptors
DE19922462A1 (de) * 1999-05-17 2000-11-23 Aventis Pharma Gmbh Spiro-imidazolidinderivate, ihre Herstellung ihre Verwendung und sie enthaltende pharmazeutische Präparate
US6518283B1 (en) 1999-05-28 2003-02-11 Celltech R&D Limited Squaric acid derivatives
KR100720907B1 (ko) 1999-08-13 2007-05-25 바이오겐 아이덱 엠에이 인코포레이티드 세포 유착 억제제
US6534513B1 (en) 1999-09-29 2003-03-18 Celltech R&D Limited Phenylalkanoic acid derivatives
US6455539B2 (en) 1999-12-23 2002-09-24 Celltech R&D Limited Squaric acid derivates
JP2003519697A (ja) 1999-12-28 2003-06-24 ファイザー・プロダクツ・インク 炎症性疾患、自己免疫疾患および呼吸器疾患の処置に有用な非ペプチド系のvla−4依存性細胞結合阻害薬
US6518421B1 (en) 2000-03-20 2003-02-11 Bristol-Myers Squibb Company Process for the preparation of epothilone analogs
AU2001248553A1 (en) 2000-04-17 2001-10-30 Celltech R And D Limited Enamine derivatives as cell adhesion molecules
US6545013B2 (en) 2000-05-30 2003-04-08 Celltech R&D Limited 2,7-naphthyridine derivatives
US6403608B1 (en) 2000-05-30 2002-06-11 Celltech R&D, Ltd. 3-Substituted isoquinolin-1-yl derivatives
CA2413418A1 (en) 2000-06-21 2001-12-27 Joseph B. Santella Piperidine amides as modulators of chemokine receptor activity
WO2002004426A1 (en) 2000-07-07 2002-01-17 Celltech R & D Limited Squaric acid derivatives containing a bicyclic heteroaromatic ring as integrin antagonists
JP2004505110A (ja) 2000-08-02 2004-02-19 セルテック アール アンド ディ リミテッド 3位置換イソキノリン−1−イル誘導体
DE10111877A1 (de) 2001-03-10 2002-09-12 Aventis Pharma Gmbh Neue Imidazolidinderivate, ihre Herstellung, ihre Verwendung und sie enthaltende pharmazeutische Präparate
DE10137595A1 (de) 2001-08-01 2003-02-13 Aventis Pharma Gmbh Neue Imidazolidinderivate, ihre Herstellung und ihre Verwendung
CA2494870A1 (en) * 2001-08-06 2003-03-06 The Regents Of The University Of California Methods for inhibiting angiogenesis
JP4901474B2 (ja) 2003-05-30 2012-03-21 ランバクシー ラボラトリーズ リミテッド 置換ピロール誘導体
US9403908B2 (en) 2003-09-29 2016-08-02 The Regents Of The University Of California Method for altering hematopoietic progenitor cell adhesion, differentiation, and migration
DOP2005000123A (es) * 2004-07-02 2011-07-15 Merck Sharp & Dohme Inhibidores de cetp
KR101329112B1 (ko) 2005-11-08 2013-11-14 랜박시 래보러터리스 리미티드 (3r,5r)-7-〔2-(4-플루오로페닐)-5-이소프로필-3-페닐-4-〔(4-히드록시 메틸 페닐 아미노)카르보닐〕-피롤-1-일〕-3,5-디히드록시 헵탄산 헤미 칼슘염의 제조 방법
WO2007092471A2 (en) 2006-02-03 2007-08-16 The Regents Of The University Of California Methods for inhibition of lymphangiogenesis and tumor metastasis
EP2510941A3 (en) 2007-02-20 2013-01-23 Merrimack Pharmaceuticals, Inc. Methods of treating multiple sclerosis by administration of alpha-fetoprotein in combination with an integrin antagonist
EP2860260A1 (en) 2008-04-11 2015-04-15 Merrimack Pharmaceuticals, Inc. Human serum albumin linkers and conjugates thereof
WO2009131958A2 (en) * 2008-04-21 2009-10-29 Institute For Oneworld Health Compounds, compositions and methods comprising triazine derivatives
US20090270398A1 (en) * 2008-04-21 2009-10-29 Institute For Oneworld Health Compounds, Compositions and Methods Comprising Pyridazine Derivatives
US8236838B2 (en) * 2008-04-21 2012-08-07 Institute For Oneworld Health Compounds, compositions and methods comprising isoxazole derivatives
WO2009131957A2 (en) 2008-04-21 2009-10-29 Institute For Oneworld Health Compounds, compositions and methods comprising oxadiazole derivatives
EP2341776A4 (en) * 2008-09-19 2012-05-30 Inst Oneworld Health COMPOUNDS, COMPOSITIONS AND METHODS COMPRISING IMIDAZOL AND TRIAZOL DERIVATIVES
DE102009012314A1 (de) 2009-03-09 2010-09-16 Bayer Schering Pharma Aktiengesellschaft Oxo-heterocyclisch substituierte Alkylcarbonsäuren und ihre Verwendung
US8511216B2 (en) * 2009-03-30 2013-08-20 Kanzaki Kokyukoki Mfg. Co., Ltd. Hydraulic actuator unit
US8343976B2 (en) * 2009-04-20 2013-01-01 Institute For Oneworld Health Compounds, compositions and methods comprising pyrazole derivatives
EP2467159A1 (en) 2009-08-20 2012-06-27 INSERM (Institut National de la Santé et de la Recherche Médicale) Vla-4 as a biomarker for prognosis and target for therapy in duchenne muscular dystrophy
EA027324B1 (ru) 2011-11-11 2017-07-31 Пфайзер Инк. 2-тиопиримидиноны
PE20180503A1 (es) 2015-05-05 2018-03-09 Pfizer 2-tiopirimidinonas
EP3886854A4 (en) 2018-11-30 2022-07-06 Nuvation Bio Inc. PYRROLE AND PYRAZOLE COMPOUNDS AND METHODS OF USE THERE
WO2022162164A1 (en) 2021-01-29 2022-08-04 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods of assessing the risk of developing progressive multifocal leukoencephalopathy in patients treated with vla-4 antagonists

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4126277A1 (de) * 1991-08-08 1993-02-11 Cassella Ag Hydantoinderivate
DE4213634A1 (de) * 1992-04-24 1993-10-28 Cassella Ag 2,4-Dioxo-imidazolidin-Derivate
DE4224414A1 (de) * 1992-07-24 1994-01-27 Cassella Ag Phenylimidazolidin-derivate, ihre Herstellung und ihre Verwendung
DE4228717A1 (de) * 1992-08-28 1994-03-03 Cassella Ag Imidazolidin-Derivate
DE4308034A1 (de) * 1993-03-13 1994-09-15 Cassella Ag Neue Heterocyclen, ihre Herstellung und ihre Verwendung
DE4427979A1 (de) * 1993-11-15 1996-02-15 Cassella Ag Substituierte 5-Ring-Heterocyclen, ihre Herstellung und ihre Verwendung
AU693143B2 (en) * 1993-12-06 1998-06-25 Cytel Corporation CS-1 peptidomimetics, compositions and methods of using the same
US6306840B1 (en) * 1995-01-23 2001-10-23 Biogen, Inc. Cell adhesion inhibitors
EP0796855B1 (de) * 1996-03-20 2002-02-06 Hoechst Aktiengesellschaft Inhibitoren der Knochenresorption und Vitronectinrezeptor-Antagonisten
DE19622489A1 (de) * 1996-06-05 1997-12-11 Hoechst Ag Salze des 3-(2-(4-(4-(Amino-imino-methyl)-phenyl)-4- methyl-2,5-dioxo-imidazolidin-1-yl)-acetylamino)-3- phenyl-propionsäure-ethylesters
DE19629817A1 (de) * 1996-07-24 1998-01-29 Hoechst Ag Neue Imino-Derivate als Inhibitoren der Knochenresorption und Vitronectinrezeptor-Antagonisten
DE19647381A1 (de) * 1996-11-15 1998-05-20 Hoechst Ag Neue Heterocyclen als Inhibitoren der Leukozytenadhäsion und VLA-4-Antagonisten
PL323130A1 (en) * 1996-11-15 1998-05-25 Hoechst Ag Application of heterocyclic compounds in production of a pharmaceutic agent, novel heterocyclic compounds and pharmaceutic agent as such
DE19653645A1 (de) * 1996-12-20 1998-06-25 Hoechst Ag Vitronectin - Rezeptorantagonisten, deren Herstellung sowie deren Verwendung
DE19741873A1 (de) * 1997-09-23 1999-03-25 Hoechst Marion Roussel De Gmbh Neue 5-Ring-Heterocyclen, ihre Herstellung, ihre Verwendung und sie enthaltende pharmazeutische Präparate
DE10111877A1 (de) * 2001-03-10 2002-09-12 Aventis Pharma Gmbh Neue Imidazolidinderivate, ihre Herstellung, ihre Verwendung und sie enthaltende pharmazeutische Präparate

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CN1135236C (zh) 2004-01-21
SK152697A3 (en) 1998-06-03
CN1187490A (zh) 1998-07-15
AU747789B2 (en) 2002-05-23
US20040220148A1 (en) 2004-11-04
HUP9702035A3 (en) 1998-12-28
ATE233276T1 (de) 2003-03-15
CA2220784A1 (en) 1998-05-15
HUP9702035A2 (hu) 1998-07-28
DE19647380A1 (de) 1998-05-20
NO975244L (no) 1998-05-18
HU9702035D0 (en) 1998-01-28
TR199701354A3 (tr) 1998-06-22
AR010067A1 (es) 2000-05-17
AU4515997A (en) 1998-05-21
NO975244D0 (no) 1997-11-14
MY119617A (en) 2005-06-30
IL122188A0 (en) 1998-04-05
DK0842943T3 (da) 2003-06-02
TW496874B (en) 2002-08-01
EP0842943B1 (de) 2003-02-26
PL323128A1 (en) 1998-05-25
EP0842943A2 (de) 1998-05-20
ID19010A (id) 1998-06-04
ZA9710244B (en) 1998-05-15
MX9708782A (es) 1998-05-31
NO317241B1 (no) 2004-09-27
DE59709383D1 (de) 2003-04-03
CZ293351B6 (cs) 2004-04-14
JPH10147573A (ja) 1998-06-02
ES2190503T3 (es) 2003-08-01
RU2229296C2 (ru) 2004-05-27
CZ359997A3 (cs) 1998-06-17
SK284377B6 (sk) 2005-02-04
HRP970605B1 (en) 2003-08-31
EP0842943A3 (de) 1999-02-24
KR19980042457A (ko) 1998-08-17
PT842943E (pt) 2003-07-31
HRP970605A2 (en) 1998-08-31
BR9705727A (pt) 2000-03-21
SI0842943T1 (en) 2003-08-31

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