ATE402926T1 - Substituierte pyrazole als ppar-agonisten - Google Patents

Substituierte pyrazole als ppar-agonisten

Info

Publication number
ATE402926T1
ATE402926T1 AT04818779T AT04818779T ATE402926T1 AT E402926 T1 ATE402926 T1 AT E402926T1 AT 04818779 T AT04818779 T AT 04818779T AT 04818779 T AT04818779 T AT 04818779T AT E402926 T1 ATE402926 T1 AT E402926T1
Authority
AT
Austria
Prior art keywords
ppar agonists
substituted pyrazoles
pyrazoles
substituted
ppar
Prior art date
Application number
AT04818779T
Other languages
English (en)
Inventor
N E Faucher
Paul Martres
Original Assignee
Smithkline Beecham Corp
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
Priority claimed from GB0326747A external-priority patent/GB0326747D0/en
Priority claimed from GB0329462A external-priority patent/GB0329462D0/en
Application filed by Smithkline Beecham Corp filed Critical Smithkline Beecham Corp
Application granted granted Critical
Publication of ATE402926T1 publication Critical patent/ATE402926T1/de

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/14Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/06Antihyperlipidemics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • 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
    • A61P9/04Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • 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
    • C07D401/02Heterocyclic 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
    • C07D401/10Heterocyclic 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 aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic 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
    • C07D405/02Heterocyclic 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
    • C07D405/10Heterocyclic 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 carbon chain containing aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/10Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
AT04818779T 2003-11-17 2004-11-15 Substituierte pyrazole als ppar-agonisten ATE402926T1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB0326747A GB0326747D0 (en) 2003-11-17 2003-11-17 Chemical compounds
GB0329462A GB0329462D0 (en) 2003-12-19 2003-12-19 Chemical compounds

Publications (1)

Publication Number Publication Date
ATE402926T1 true ATE402926T1 (de) 2008-08-15

Family

ID=34621661

Family Applications (1)

Application Number Title Priority Date Filing Date
AT04818779T ATE402926T1 (de) 2003-11-17 2004-11-15 Substituierte pyrazole als ppar-agonisten

Country Status (9)

Country Link
US (1) US20080021030A1 (de)
EP (1) EP1685113B1 (de)
JP (1) JP2007511485A (de)
AR (1) AR046625A1 (de)
AT (1) ATE402926T1 (de)
DE (1) DE602004015498D1 (de)
ES (1) ES2311179T3 (de)
TW (1) TW200526588A (de)
WO (1) WO2005049578A1 (de)

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1762568A1 (de) * 2004-07-01 2007-03-14 Daiichi Pharmaceutical Co., Ltd. Pyrazolderivate
US20090240058A1 (en) * 2005-02-28 2009-09-24 Shogo Sakuma Activator for Peroxisome Proliferator-Activating Receptor Delta
CA2613517A1 (en) 2005-06-27 2007-01-04 Exelixis, Inc. Pyrazole based lxr modulators
SI2014652T1 (sl) 2006-04-18 2014-12-31 Nippon Chemiphar Co., Ltd. Aktivacijsko sredstvo za peroksisomski proliferatorski aktivirani receptor
WO2008073825A1 (en) 2006-12-08 2008-06-19 Exelixis, Inc. Lxr and fxr modulators
WO2008125600A2 (en) * 2007-04-11 2008-10-23 Glaxo Group Limited Pyrazole derivatives as p2x7 modulators
CN102083810B (zh) 2008-04-15 2014-10-29 日本化学医药株式会社 过氧化物酶体增殖剂活化受体的活化剂
CN102224142B (zh) * 2008-11-21 2015-07-22 拉夸里亚创药株式会社 具有5-ht2b受体拮抗活性的新型吡唑-3-羧酰胺衍生物
WO2011016576A1 (en) 2009-08-04 2011-02-10 Takeda Pharmaceutical Company Limited Alanine derivatives as inhibitors of apoptosis proteins
JP5753856B2 (ja) * 2009-12-15 2015-07-22 バイエル・クロップサイエンス・アーゲーBayer Cropscience Ag 1−アルキル−/1−アリール−5−ピラゾールカルボン酸誘導体を調製する方法
TWI508968B (zh) * 2010-02-08 2015-11-21 Biota Scient Management 用於治療呼吸道融合性病毒感染的化合物
SG10201502484SA (en) 2010-03-30 2015-05-28 Verseon Corp Multisubstituted aromatic compounds as inhibitors of thrombin
CN101870676B (zh) * 2010-06-24 2011-09-07 山东大学 1-(2-肟基-2-苯基乙基)-3-苯基-1h-吡唑-5-甲酸乙酯衍生物及其制备与应用
CN105209440B (zh) 2013-03-15 2019-07-23 维颂公司 作为凝血酶抑制剂的卤代吡唑
LT2968297T (lt) 2013-03-15 2019-01-10 Verseon Corporation Multipakeistieji aromatiniai junginiai kaip serino proteazės inhibitoriai
TWI636047B (zh) 2013-08-14 2018-09-21 英商卡爾維斯塔製藥有限公司 雜環衍生物
CN106687445A (zh) 2014-09-17 2017-05-17 维颂公司 作为丝氨酸蛋白酶抑制剂的吡唑基取代的吡啶酮化合物
GB201421083D0 (en) * 2014-11-27 2015-01-14 Kalvista Pharmaceuticals Ltd Enzyme inhibitors
GB201421085D0 (en) 2014-11-27 2015-01-14 Kalvista Pharmaceuticals Ltd New enzyme inhibitors
CA2977993A1 (en) 2015-02-27 2016-09-01 Verseon Corporation Substituted pyrazole compounds as serine protease inhibitors
RU2020140891A (ru) 2016-05-31 2021-02-10 Калвиста Фармасьютикалз Лимитед Производные пиразола в качестве ингибиторов калликреина
GB201609607D0 (en) 2016-06-01 2016-07-13 Kalvista Pharmaceuticals Ltd Polymorphs of N-(3-Fluoro-4-methoxypyridin-2-yl)methyl)-3-(methoxymethyl)-1-({4-((2-oxopy ridin-1-yl)methyl)phenyl}methyl)pyrazole-4-carboxamide and salts
GB201609603D0 (en) 2016-06-01 2016-07-13 Kalvista Pharmaceuticals Ltd Polymorphs of N-[(6-cyano-2-fluoro-3-methoxyphenyl)Methyl]-3-(methoxymethyl)-1-({4-[(2-ox opyridin-1-YL)Methyl]phenyl}methyl)pyrazole-4-carboxamide
WO2018034901A1 (en) 2016-08-16 2018-02-22 Stealth Biotherapeutics N-carboxyanhydride-based-scale synthesis of elamipretide
WO2018224455A1 (en) 2017-06-07 2018-12-13 Basf Se Substituted cyclopropyl derivatives
SI3716952T1 (sl) 2017-11-29 2022-04-29 Kalvista Pharmaceuticals Limited Farmacevtske oblike, ki obsegajo zaviralec plazemskega kalikreina
GB201719881D0 (en) 2017-11-29 2018-01-10 Kalvista Pharmaceuticals Ltd Solid forms of plasma kallikrein inhibitor and salts thereof
TWI805699B (zh) 2018-03-01 2023-06-21 日商日本煙草產業股份有限公司 甲基內醯胺環化合物及其用途
BR112020019939A2 (pt) 2018-04-04 2021-01-05 Japan Tobacco, Inc. Compostos de pirazol substituídos com heteroarila e seu uso farmacêutico
WO2019243999A1 (en) * 2018-06-18 2019-12-26 Janssen Pharmaceutica Nv Phenyl substituted pyrazoles as modulators of roryt
CN114206852A (zh) 2019-08-09 2022-03-18 卡尔维斯塔制药有限公司 血浆激肽释放酶抑制剂

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3621775A1 (de) * 1986-03-13 1988-01-07 Thomae Gmbh Dr K Neue substituierte thiazole und oxazole, diese verbindungen enthaltende arzneimittel und verfahren zu ihrer herstellung
GB9604242D0 (en) * 1996-02-28 1996-05-01 Glaxo Wellcome Inc Chemical compounds
IL135177A0 (en) * 1997-10-02 2001-05-20 Sankyo Co Amidocarboxylic acid derivatives and pharmaceutical compositions containing the same
DE60012213T2 (de) * 1999-11-10 2005-07-21 Takeda Chemical Industries, Ltd. Fünfgliedrige n-heterocyclen mit hypoglykämischer und hypolipidemischer wirkung
PE20011010A1 (es) * 1999-12-02 2001-10-18 Glaxo Group Ltd Oxazoles y tiazoles sustituidos como agonista del receptor activado por el proliferador de peroxisomas humano
JP3372923B2 (ja) * 2000-02-25 2003-02-04 エヌイーシーマイクロシステム株式会社 半導体集積回路
JP4383177B2 (ja) * 2002-03-01 2009-12-16 スミスクライン ビーチャム コーポレーション hPPAR活性化剤

Also Published As

Publication number Publication date
AR046625A1 (es) 2005-12-14
WO2005049578A1 (en) 2005-06-02
DE602004015498D1 (de) 2008-09-11
EP1685113A1 (de) 2006-08-02
JP2007511485A (ja) 2007-05-10
TW200526588A (en) 2005-08-16
US20080021030A1 (en) 2008-01-24
ES2311179T3 (es) 2009-02-01
EP1685113B1 (de) 2008-07-30

Similar Documents

Publication Publication Date Title
ATE402926T1 (de) Substituierte pyrazole als ppar-agonisten
ATE517886T1 (de) Pyrazolderivate
ATE435207T1 (de) Pyridin-3-carbonsäureamidderivate als cb1-inverse agonisten
ATE352552T1 (de) Substituierte pyrazole
ATE504559T1 (de) Arylanilinderivate als agonisten des beta2- adrenergen rezeptors
DE602004015724D1 (de) Diazepinoindolderivate als kinaseinhibitoren
DE602005015204D1 (de) Oxadiazolonderivate als ppar-delta-agonisten
DE60317365D1 (de) Substituierte 4-alkoxyoxazol derivate als ppar agonisten
DE602004022159D1 (de) Koaxiale schnellkupplung
DE602004024420D1 (de) Chinazolinderivate als antitumormittel
DE60308670D1 (de) Substituierte indole als alpha-1 agonisten
PL377844A1 (pl) Podstawione pirazole
ATE388937T1 (de) Agonisten des cannabinoidrezeptors
ATE421506T1 (de) Neue benzimidazolderivate
DE602004017782D1 (de) Substituierte arylpyrazole als parasitizide
ATE393159T1 (de) Heterobicyclische pyrazolderivate als kinaseinhibitoren
ATE369358T1 (de) Substituierte benzoylderivate als herbizide
ATE459618T1 (de) 3-piperidinylisochroman-5-ole als dopaminagonisten
NL1027084A1 (nl) Gesubstitueerde triazoolderivaten als oxytocine-antagonisten.
ATE248164T1 (de) Substituierte benzoylpyrazole als herbizide
ATE365161T1 (de) Pyrazolverbindungen
DE602004004295D1 (de) 6-ä(substituiertes)phenylütriazolopyrimidine als antikrebsmittel
DE602005004515D1 (de) (indol-3-yl)-heterozyklus-derivate als agonisten des cannabinoid-cb1-rezeptors
ATE394372T1 (de) G-lactamderivate als prostaglandinagonisten
ATE364601T1 (de) Substituierte pyrazolverbindungen

Legal Events

Date Code Title Description
RER Ceased as to paragraph 5 lit. 3 law introducing patent treaties