DE69915692D1 - Inhibitoren der alpha-4 beta-1 vermittelten zelladhäsion - Google Patents

Inhibitoren der alpha-4 beta-1 vermittelten zelladhäsion

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Publication number
DE69915692D1
DE69915692D1 DE69915692T DE69915692T DE69915692D1 DE 69915692 D1 DE69915692 D1 DE 69915692D1 DE 69915692 T DE69915692 T DE 69915692T DE 69915692 T DE69915692 T DE 69915692T DE 69915692 D1 DE69915692 D1 DE 69915692D1
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Germany
Prior art keywords
beta
alpha
inhibitors
cell adhesion
mediated cell
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Expired - Fee Related
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DE69915692T
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English (en)
Other versions
DE69915692T2 (de
Inventor
R Teegarden
Honnappa Jayakumar
Kenji Matsuki
A Chrusciel
F Fisher
P Tanis
W Thomas
R Blinn
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Tanabe Seiyaku Co Ltd
Pharmacia and Upjohn Co
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Tanabe Seiyaku Co Ltd
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Publication of DE69915692T2 publication Critical patent/DE69915692T2/de
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    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
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    • C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
    • C07D317/50—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to atoms of the carbocyclic ring
    • C07D317/58—Radicals substituted by nitrogen atoms
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    • C07K5/0202—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link containing the structure -NH-X-X-C(=0)-, X being an optionally substituted carbon atom or a heteroatom, e.g. beta-amino acids
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    • C07K5/06—Dipeptides
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    • A—HUMAN NECESSITIES
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    • C07C2602/04—One of the condensed rings being a six-membered aromatic ring
    • C07C2602/10—One of the condensed rings being a six-membered aromatic ring the other ring being six-membered, e.g. tetraline

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DE69915692T 1998-12-22 1999-12-20 Inhibitoren der alpha-4 beta-1 vermittelten zelladhäsion Expired - Fee Related DE69915692T2 (de)

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US11350198P 1998-12-22 1998-12-22
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PCT/US1999/030665 WO2000037429A2 (en) 1998-12-22 1999-12-20 INHIBITORS OF α4β1 MEDIATED CELL ADHESION

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MY153569A (en) 1998-01-20 2015-02-27 Mitsubishi Tanabe Pharma Corp Inhibitors of ?4 mediated cell adhesion
JP2003506491A (ja) * 1999-08-13 2003-02-18 バイオジェン インコーポレイテッド 細胞接着インヒビター
US6388084B1 (en) 1999-12-06 2002-05-14 Hoffmann-La Roche Inc. 4-pyridinyl-n-acyl-l-phenylalanines
YU40502A (sh) * 1999-12-06 2005-03-15 F.Hoffmann-La Roche Ag. 4-piridinil-n-acil-l-fenilalanini
WO2001047868A1 (fr) 1999-12-28 2001-07-05 Ajinomoto Co., Inc. Nouveaux derives de phenylalanine
EP1270547A4 (de) 2000-03-23 2005-07-13 Ajinomoto Kk Neue phenylalaninderivate
MY129000A (en) 2000-08-31 2007-03-30 Tanabe Seiyaku Co INHIBITORS OF a4 MEDIATED CELL ADHESION
KR20030036724A (ko) * 2000-09-14 2003-05-09 도레이 가부시끼가이샤 우레아 유도체 및 그것을 유효성분으로 하는 접착분자저해제
DE10124041A1 (de) * 2001-05-16 2002-11-21 Graffinity Pharm Design Gmbh Protease Inhibitoren
MY140707A (en) 2002-02-28 2010-01-15 Mitsubishi Tanabe Pharma Corp Process for preparing a phenylalanine derivative and intermediates thereof
US7122580B2 (en) 2002-08-09 2006-10-17 Transtech Pharma, Inc. Aryl and heteroaryl compounds and methods to modulate coagulation
WO2005014533A2 (en) 2003-08-08 2005-02-17 Transtech Pharma, Inc. Aryl and heteroaryl compounds, compositions, and methods of use
US7208601B2 (en) 2003-08-08 2007-04-24 Mjalli Adnan M M Aryl and heteroaryl compounds, compositions, and methods of use
WO2005014534A1 (en) 2003-08-08 2005-02-17 Transtech Pharma, Inc. Aryl and heteroaryl compounds, compositions, and methods of use
AU2007205578B2 (en) 2006-01-11 2012-06-28 Seikagaku Corporation Cycloalkylcarbonylamino acid ester derivative and process for producing the same
JP3975226B2 (ja) 2006-01-11 2007-09-12 生化学工業株式会社 シクロアルキルカルボニルアミノ酸誘導体及びその製造方法
JP4047365B2 (ja) 2006-01-11 2008-02-13 生化学工業株式会社 シクロアルカンカルボキサミド誘導体及びその製造方法
AU2008219115A1 (en) 2007-02-16 2008-08-28 Synta Pharmaceuticals Corp. Substituted fused-ring compounds for inflammation and immune-related uses
WO2011094890A1 (en) * 2010-02-02 2011-08-11 Argusina Inc. Phenylalanine derivatives and their use as non-peptide glp-1 receptor modulators
CN106588690B (zh) * 2016-12-19 2019-06-04 广西中医药大学 毛鸡骨草甲素Abrusamide的制备方法

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US6306840B1 (en) * 1995-01-23 2001-10-23 Biogen, Inc. Cell adhesion inhibitors
DK0991619T3 (da) * 1997-06-23 2003-12-29 Tanabe Seiyaku Co Inhibitorer af alfa 4-beta 1-medieret celleadhæsion

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AU2209500A (en) 2000-07-12
DK1144365T3 (da) 2004-06-28
PT1144365E (pt) 2004-06-30
ATE261932T1 (de) 2004-04-15
EP1144365A3 (de) 2003-07-09
ES2220140T3 (es) 2004-12-01
JP2003524614A (ja) 2003-08-19
EP1144365B1 (de) 2004-03-17
WO2000037429A2 (en) 2000-06-29
WO2000037429A3 (en) 2003-05-22
EP1144365A2 (de) 2001-10-17

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