EP1189612A4 - VLA-4 INHIBITORY COMPOUNDS - Google Patents

VLA-4 INHIBITORY COMPOUNDS

Info

Publication number
EP1189612A4
EP1189612A4 EP00945035A EP00945035A EP1189612A4 EP 1189612 A4 EP1189612 A4 EP 1189612A4 EP 00945035 A EP00945035 A EP 00945035A EP 00945035 A EP00945035 A EP 00945035A EP 1189612 A4 EP1189612 A4 EP 1189612A4
Authority
EP
European Patent Office
Prior art keywords
vla
inhibitory compounds
inhibitory
compounds
Prior art date
Legal status (The legal status 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 status listed.)
Withdrawn
Application number
EP00945035A
Other languages
German (de)
French (fr)
Other versions
EP1189612A1 (en
Inventor
John J Baldwin
Edward Mcdonald
Kevin Joseph Moriarty
Christopher Ronald Sarko
Nobuo Machinaga
Atsushi Nakayama
Jun Chiba
Shin Iimura
Yoshiyuki Yoneda
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.)
Daiichi Pharmaceutical Co Ltd
Pharmacopeia Drug Discovery Inc
Original Assignee
Daiichi Pharmaceutical Co Ltd
Pharmacopeia 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 Daiichi Pharmaceutical Co Ltd, Pharmacopeia Inc filed Critical Daiichi Pharmaceutical Co Ltd
Publication of EP1189612A1 publication Critical patent/EP1189612A1/en
Publication of EP1189612A4 publication Critical patent/EP1189612A4/en
Withdrawn legal-status Critical Current

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    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/08Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • C07D207/18Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
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    • C07D207/22Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member 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
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    • C07D401/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
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    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/06Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
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    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
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EP00945035A 1999-06-30 2000-06-30 VLA-4 INHIBITORY COMPOUNDS Withdrawn EP1189612A4 (en)

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US14160199P 1999-06-30 1999-06-30
US14160299P 1999-06-30 1999-06-30
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PCT/US2000/018079 WO2001000206A1 (en) 1999-06-30 2000-06-30 Vla-4 inhibitor compounds

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WO2001098268A2 (en) 2000-06-21 2001-12-27 Bristol-Myers Squibb Pharma Company Piperidine amides as modulators of chemokine receptor activity
US7157487B2 (en) 2000-12-28 2007-01-02 Daiichi Pharmaceutical Co., Ltd. Vla-4 inhibitors
ES2296979T3 (en) 2001-06-27 2008-05-01 Smithkline Beecham Corporation FLUOROPIRROLIDINS AS INHIBITORS OF DIPEPTIDIL PEPTIDASA.
GB0123765D0 (en) * 2001-10-03 2001-11-21 Bayer Ag Para-amino benzoic acids
JP2005530772A (en) * 2002-05-09 2005-10-13 ミモトープス・プロプライエタリー・リミテッド Amino acid analogs
BR0312023A (en) 2002-06-27 2005-03-22 Novo Nordisk As Compound, glucose kinase activating compound, method for preventing hypoglycemia, use of a compound, and pharmaceutical composition
RU2340605C2 (en) * 2002-06-27 2008-12-10 Ново Нордиск А/С Arylcarbonyl derivatives as therapeutic agents
JP4691988B2 (en) * 2002-10-03 2011-06-01 小野薬品工業株式会社 LPA receptor antagonist
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JP4834840B2 (en) 2004-01-06 2011-12-14 ノヴォ ノルディスク アー/エス Heteroaryl ureas and their use as glucokinase activators
JP2005350417A (en) * 2004-06-11 2005-12-22 Dai Ichi Seiyaku Co Ltd Method for producing pyrrolidine derivatives using reductive etherification
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CN112040945A (en) 2018-06-12 2020-12-04 Vtv治疗有限责任公司 Therapeutic use of a glucokinase activator in combination with insulin or insulin analogs
AU2019373242B2 (en) 2018-10-30 2023-07-13 Gilead Sciences, Inc. Compounds for inhibition of alpha 4 beta 7 integrin
EP4541422A3 (en) 2018-10-30 2025-06-25 Gilead Sciences, Inc. Quinoline derivatives as alpha4beta7 integrin inhibitors
KR102659859B1 (en) 2018-10-30 2024-04-25 길리애드 사이언시즈, 인코포레이티드 Compounds for inhibition of alpha4β7 integrin
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AU781438B2 (en) 2005-05-26
HK1043318A1 (en) 2002-09-13
MXPA01013406A (en) 2003-09-04
EP1189612A1 (en) 2002-03-27
IL146288A0 (en) 2002-07-25
NO324892B1 (en) 2007-12-27
WO2001000206A1 (en) 2001-01-04
CA2369308A1 (en) 2001-01-04
JP2003503350A (en) 2003-01-28
TWI283240B (en) 2007-07-01
AR035011A1 (en) 2004-04-14

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