JP2004525873A5 - - Google Patents

Download PDF

Info

Publication number
JP2004525873A5
JP2004525873A5 JP2002551496A JP2002551496A JP2004525873A5 JP 2004525873 A5 JP2004525873 A5 JP 2004525873A5 JP 2002551496 A JP2002551496 A JP 2002551496A JP 2002551496 A JP2002551496 A JP 2002551496A JP 2004525873 A5 JP2004525873 A5 JP 2004525873A5
Authority
JP
Japan
Prior art keywords
alkyl
amino
mono
alkoxy
alkynyl
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.)
Granted
Application number
JP2002551496A
Other languages
English (en)
Japanese (ja)
Other versions
JP5260818B2 (ja
JP2004525873A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2000/026816 external-priority patent/WO2002049993A2/en
Publication of JP2004525873A publication Critical patent/JP2004525873A/ja
Publication of JP2004525873A5 publication Critical patent/JP2004525873A5/ja
Application granted granted Critical
Publication of JP5260818B2 publication Critical patent/JP5260818B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

JP2002551496A 2000-09-29 2000-09-29 高親和性低分子C5a受容体調節物質 Expired - Fee Related JP5260818B2 (ja)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/US2000/026816 WO2002049993A2 (en) 2000-09-29 2000-09-29 High affinity small molecule c5a receptor modulators

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2011092825A Division JP2011219476A (ja) 2011-04-19 2011-04-19 高親和性低分子C5a受容体調節物質

Publications (3)

Publication Number Publication Date
JP2004525873A JP2004525873A (ja) 2004-08-26
JP2004525873A5 true JP2004525873A5 (https=) 2007-11-22
JP5260818B2 JP5260818B2 (ja) 2013-08-14

Family

ID=21741822

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2002551496A Expired - Fee Related JP5260818B2 (ja) 2000-09-29 2000-09-29 高親和性低分子C5a受容体調節物質

Country Status (13)

Country Link
EP (1) EP1322309B1 (https=)
JP (1) JP5260818B2 (https=)
KR (1) KR20030060887A (https=)
CN (1) CN1454086A (https=)
AT (1) ATE404553T1 (https=)
AU (1) AU7622500A (https=)
BR (1) BR0017338A (https=)
DE (1) DE60039921D1 (https=)
IL (1) IL154993A0 (https=)
MX (1) MXPA03002788A (https=)
NO (1) NO20031370L (https=)
WO (1) WO2002049993A2 (https=)
YU (1) YU23503A (https=)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PA8535601A1 (es) 2000-12-21 2002-11-28 Pfizer Derivados benzimidazol y piridilimidazol como ligandos para gabaa
CA2479930A1 (en) * 2002-03-28 2003-10-09 Neurogen Corporation Substituted tetrahydroisoquinolines as c5a receptor modulators
US6858637B2 (en) 2002-03-28 2005-02-22 Neurogen Corporation Substituted biaryl amides as C5a receptor modulators
EP1487796A4 (en) * 2002-03-28 2005-11-16 Neurogen Corp SUBSTITUTED BIARYLAMIDES AS MODULATORS OF THE C5A RECEPTOR
KR20040093487A (ko) * 2002-03-29 2004-11-05 뉴로젠 코포레이션 C5a 수용체 조절자로서의 신규 아릴이미다졸 및 관련화합물
GB0214139D0 (en) * 2002-06-19 2002-07-31 Glaxo Group Ltd Chemical compounds
US7169775B2 (en) 2002-08-21 2007-01-30 Neurogen Corporation Amino methyl imidazoles as C5a receptor modulators
AU2003261974A1 (en) 2002-09-11 2004-04-30 Kureha Chemical Industry Company, Limited Amine compounds and use thereof
AU2003291403A1 (en) 2002-11-08 2004-06-03 Neurogen Corporation 3-substituted-6-aryl pyridined as ligands of c5a receptors
EP2266606B1 (en) 2003-05-15 2014-09-10 Genentech, Inc. Methods and compositions for the prevention and treatment of sepsis
JP3977411B2 (ja) 2004-03-10 2007-09-19 株式会社クレハ アミン系塩基性化合物とその用途
WO2006012373A2 (en) * 2004-07-20 2006-02-02 Critical Therapeutics, Inc. Combination therapies of hmgb and complement inhibitors against inflammation
JP2007284352A (ja) * 2004-08-05 2007-11-01 Dai Ichi Seiyaku Co Ltd ピラゾール誘導体
WO2006060424A2 (en) 2004-12-01 2006-06-08 Kalypsys, Inc. Inducible nitric oxide synthase dimerization inhibitors
JP2008530229A (ja) 2005-02-17 2008-08-07 ワイス シクロアルキル縮合インドール、ベンゾチオフェン、ベンゾフランおよびインデン誘導体
EP1739078A1 (de) 2005-05-30 2007-01-03 Jerini AG C5a-Rezeptor-Antagonisten
RS54998B1 (sr) 2008-12-22 2016-11-30 Chemocentryx Inc Antagonisti c5ar
RS56332B1 (sr) 2010-06-24 2017-12-29 Chemocentryx Inc Antagonisti c5ar
MX2015014688A (es) * 2013-04-22 2016-02-19 Abbvie Inc Tiazoles y usos de los mismos.
DK3200791T3 (da) 2014-09-29 2020-05-25 Chemocentryx Inc Fremgangsmåder og mellemprodukter i fremstilling af C5AR- antagonister
EP3072891A1 (en) * 2015-03-24 2016-09-28 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. New Toll-Like Receptor 9 Antagonists
JP7339733B2 (ja) 2016-01-14 2023-09-06 ケモセントリックス,インコーポレイティド C3腎症を処置する方法
EP3439658B1 (en) 2016-04-04 2021-11-24 ChemoCentryx, Inc. Soluble c5ar antagonists
WO2018222601A1 (en) 2017-05-31 2018-12-06 Chemocentryx, Inc. 5-5 FUSED RINGS AS C5a INHIBITORS
US10562896B2 (en) 2017-05-31 2020-02-18 Chemocentryx, Inc. 6-5 fused rings as C5a inhibitors
CA3077395A1 (en) 2017-10-30 2019-05-09 Chemocentryx, Inc. Deuterated compounds as immunomodulators
WO2019126424A1 (en) 2017-12-22 2019-06-27 Chemocentryx, Inc. DIARYL SUBSTITUTED 6,5-FUSED RING COMPOUNDS AS C5aR INHIBITORS
MX2020006460A (es) 2017-12-22 2020-11-06 Chemocentryx Inc Compuestos de anillo 5,5 fusionado sustituido con diarilo como inhibidores de c5ar.
BR112020019822A2 (pt) 2018-04-02 2021-03-16 Chemocentryx, Inc. Profármacos de antagonistas bicíclicos fundidos de c5ar
CN114957165A (zh) * 2021-02-26 2022-08-30 清华大学 一种抗病毒化合物及其制备方法和应用

Family Cites Families (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6157590A (ja) * 1984-08-29 1986-03-24 Asahi Shiyueebell Kk シラン化合物およびその製造法
US5159083A (en) * 1990-12-28 1992-10-27 Neurogen Corporation Certain aminomethyl phenylimidazole derivatives; a class of dopamine receptor subtype specific ligands
US5681956A (en) * 1990-12-28 1997-10-28 Neurogen Corporation 4-aryl substituted piperazinylmethyl phenylimidazole derivatives; a new class of dopamine receptor subtype specific ligands
MX9308025A (es) * 1992-12-22 1994-08-31 Lilly Co Eli Compuestos inhibidores de la proteasa del virus dela inmunodeficiencia humana, procedimiento para supreparacion y formulacion farmaceutica que los contiene.
US5652237A (en) * 1994-09-09 1997-07-29 Warner-Lambert Company 2-substituted-4H-3, 1-benzoxazin-4-ones and benzthiazin-4-ones as inhibitors of complement C1r protease for the treatment of inflammatory processes
EP0793653A1 (en) * 1994-11-23 1997-09-10 Neurogen Corporation Certain 4-aminomethyl-2-substituted imidazole derivatives and 2-aminomethyl-4-substituted imidazole derivatives; new classes of dopamine receptor subtype specific ligands
GB9426103D0 (en) * 1994-12-23 1995-02-22 Merck Sharp & Dohme Therapeutic agents
AR007857A1 (es) * 1996-07-13 1999-11-24 Glaxo Group Ltd Compuestos heterociclicos fusionados como inhibidores de proteina tirosina quinasa, sus metodos de preparacion, intermediarios uso en medicina ycomposiciones farmaceuticas que los contienen.
JP2001517245A (ja) * 1997-05-29 2001-10-02 メルク エンド カンパニー インコーポレーテッド 細胞接着阻害薬としてのビアリールアルカン酸類
MY153569A (en) * 1998-01-20 2015-02-27 Mitsubishi Tanabe Pharma Corp Inhibitors of ?4 mediated cell adhesion
CN1181817C (zh) * 1998-03-20 2004-12-29 第一三得利制药株式会社 以苯基甲苯醌为有效成分的NF-kB抑制剂
KR100605140B1 (ko) * 1998-05-22 2006-07-28 싸이오스 인크 심장병 및 다른 질병을 치료하기 위한 헤테로 고리 화합물및 그 치료 방법
US6365602B1 (en) * 1998-07-10 2002-04-02 Astra Zeneca Ab N-substituted naphthalene carboxamides as neurokinin-receptor antagonists
US6423519B1 (en) * 1998-07-15 2002-07-23 Gpc Biotech Inc. Compositions and methods for inhibiting fungal growth
WO2000010573A1 (en) * 1998-08-21 2000-03-02 Viropharma Incorporated Compounds, compositions and methods for treating or preventing viral infections and associated diseases
US6437146B1 (en) * 1998-09-25 2002-08-20 Fujisawa Pharmaceutical Co., Ltd. Oxazole compounds as prostaglandin e2 agonists or antagonists
WO2000025780A1 (en) * 1998-10-29 2000-05-11 Bristol-Myers Squibb Company Compounds derived from an amine nucleus that are inhibitors of impdh enzyme
US6503905B1 (en) * 1998-12-29 2003-01-07 Pfizer Inc 3,3-biarylpiperidine and 2,2-biarylmorpholine derivatives
AP1654A (en) * 1999-03-24 2006-09-01 Anormed Inc Chemokine receptor binding heterocyclic compounds.
US6369226B1 (en) * 1999-06-21 2002-04-09 Agouron Pharmaceuticals, Inc. Substituted benzamide inhibitors of rhinovirus 3C protease
AU7031500A (en) * 1999-09-23 2001-04-24 Astrazeneca Ab Therapeutic quinazoline compounds
US6734191B2 (en) * 2000-09-15 2004-05-11 Anormed, Inc. Chemokine receptor binding heterocyclic compounds

Similar Documents

Publication Publication Date Title
JP2004525873A5 (https=)
US10653674B2 (en) Multisubstituted aromatic compounds as inhibitors of thrombin
EP1322309B1 (en) High affinity small molecule c5a receptor modulators
KR101214665B1 (ko) 트리아졸 유도체 또는 그의 염
KR101589332B1 (ko) 2h-크로멘 화합물 및 그의 유도체
JP2002511463A (ja) インテグリンのそれの受容体への結合を阻害するn,n−ジ置換アミド
TW415940B (en) Condensed cyclic carboxylic acid compound or salt thereof, and medical composition containing which
JPWO2000039116A1 (ja) アミノピラゾール誘導体
HUP0104364A2 (hu) Pirrolidinszármazékok, CCR-3 receptor antagonisták és ezeket tartalmazó gyógyszerkészítmények
WO2008023720A1 (en) Urea compound or salt thereof
JPH09501404A (ja) 新規化合物
JP2007507529A (ja) 複素環式アミドおよびスルホンアミド
KR20060095865A (ko) 글리신 수송 억제제로서의 비시클릭 [3.1.0] 유도체
CN103228643B (zh) 作为组胺h4受体配体的苯并唑衍生物
EP2379533A1 (en) N-substituted saturated heterocyclic sulfone compounds with cb2 receptor agonistic activity
CA2569654A1 (en) Benzimidazolone carboxylic acid derivatives
RU2453540C2 (ru) 2,3-замещенные пиразинсульфонамиды в качестве ингибиторов crth2
JP2007518816A (ja) バニロイド受容体リガンド及び炎症性及び神経因性疼痛の治療におけるこれらの使用
US20040010147A1 (en) Cyclic amine compounds and pharmaceutical composition containing the same
AU2003228419A1 (en) New aryl imidazoles and related compounds as c5a receptor modulators
WO2006106812A1 (ja) プロパン-1,3-ジオン誘導体又はその塩
JP2007186422A (ja) アリールスルフィド誘導体
RU2003105218A (ru) Малые молекулы модуляторов рецепторов с5а высокой аффинности
JP2015506967A (ja) イミダゾリルケトン誘導体asdアルドステロン合成酵素阻害剤
JP2011219476A (ja) 高親和性低分子C5a受容体調節物質