JP2010515750A5 - - Google Patents

Download PDF

Info

Publication number
JP2010515750A5
JP2010515750A5 JP2009545669A JP2009545669A JP2010515750A5 JP 2010515750 A5 JP2010515750 A5 JP 2010515750A5 JP 2009545669 A JP2009545669 A JP 2009545669A JP 2009545669 A JP2009545669 A JP 2009545669A JP 2010515750 A5 JP2010515750 A5 JP 2010515750A5
Authority
JP
Japan
Prior art keywords
group
carbon atoms
groups
nitrogen
ring
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.)
Abandoned
Application number
JP2009545669A
Other languages
English (en)
Japanese (ja)
Other versions
JP2010515750A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2008/050695 external-priority patent/WO2008089015A1/en
Publication of JP2010515750A publication Critical patent/JP2010515750A/ja
Publication of JP2010515750A5 publication Critical patent/JP2010515750A5/ja
Abandoned legal-status Critical Current

Links

JP2009545669A 2007-01-11 2008-01-10 スフィンゴシン−1−ホスフェート(s1p)受容体アンタゴニスト生物活性を有する6−置換インドール−3−カルボン酸アミド化合物 Abandoned JP2010515750A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US88447007P 2007-01-11 2007-01-11
PCT/US2008/050695 WO2008089015A1 (en) 2007-01-11 2008-01-10 6-substituted indole-3-carboxylic acid amide compounds having sphingosine-1-phosphate (s1p) receptor antagonist biological activity

Publications (2)

Publication Number Publication Date
JP2010515750A JP2010515750A (ja) 2010-05-13
JP2010515750A5 true JP2010515750A5 (pl) 2011-03-03

Family

ID=39399972

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2009545669A Abandoned JP2010515750A (ja) 2007-01-11 2008-01-10 スフィンゴシン−1−ホスフェート(s1p)受容体アンタゴニスト生物活性を有する6−置換インドール−3−カルボン酸アミド化合物

Country Status (8)

Country Link
EP (1) EP2125723A1 (pl)
JP (1) JP2010515750A (pl)
KR (1) KR20090101307A (pl)
CN (1) CN101668741A (pl)
AU (1) AU2008206495A1 (pl)
CA (1) CA2674946A1 (pl)
MX (1) MX2009007334A (pl)
WO (1) WO2008089015A1 (pl)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8524917B2 (en) * 2007-01-11 2013-09-03 Allergan, Inc. 6-substituted indole-3-carboxylic acid amide compounds having sphingosine-1-phosphate (S1P) receptor antagonist biological activity
EP2262497A2 (en) * 2008-03-17 2010-12-22 Allergan, Inc. S1p3 receptor inhibitors for treating inflammation
CN104311472B9 (zh) 2008-07-23 2020-03-17 艾尼纳制药公司 经取代的1,2,3,4-四氢环戊并[b]吲哚-3-基乙酸衍生物
MX2011002199A (es) 2008-08-27 2011-05-10 Arena Pharm Inc Derivados de acidos triciclicos substituidos como agonistas del receptor s1p1 utiles en el tratamiento de trastornos autoinmunes e inflamatorios.
CN103221391B (zh) 2010-01-27 2018-07-06 艾尼纳制药公司 (R)-2-(7-(4-环戊基-3-(三氟甲基)苄基氧基)-1,2,3,4-四氢环戊二烯并[b]吲哚-3-基)乙酸及其盐的制备方法
CA2789480A1 (en) 2010-03-03 2011-09-09 Arena Pharmaceuticals, Inc. Processes for the preparation of s1p1 receptor modulators and crystalline forms thereof
TWI522361B (zh) * 2010-07-09 2016-02-21 艾伯維公司 作為s1p調節劑的稠合雜環衍生物
US20160083343A1 (en) 2013-03-15 2016-03-24 Global Blood Therapeutics, Inc Compounds and uses thereof for the modulation of hemoglobin
EA201992707A1 (ru) 2013-11-18 2020-06-30 Глобал Блад Терапьютикс, Инк. Соединения и их применения для модуляции гемоглобина
AU2016205361C1 (en) 2015-01-06 2021-04-08 Arena Pharmaceuticals, Inc. Methods of treating conditions related to the S1P1 receptor
KR102603199B1 (ko) 2015-06-22 2023-11-16 아레나 파마슈티칼스, 인크. S1p1 수용체-관련 장애에서의 사용을 위한 (r)-2-(7-(4-시클로펜틸-3-(트리플루오로메틸)벤질옥시)-1,2,3,4-테트라히드로시클로-펜타[b]인돌-3-일)아세트산 (화합물 1)의 결정성 l-아르기닌 염
CA3010615C (en) 2016-01-14 2024-02-20 Beth Israel Deaconess Medical Center, Inc. Mast-cell modulators and uses thereof
KR20190113955A (ko) 2017-02-16 2019-10-08 아레나 파마슈티칼스, 인크. 장-외 증상을 갖는 염증성 장질환의 치료를 위한 화합물 및 방법
MX2019009841A (es) 2017-02-16 2020-01-30 Arena Pharm Inc Compuestos y metodos para el tratamiento de la colangitis biliar primaria.
CN110483437B (zh) * 2018-05-14 2022-12-06 嘉兴维眸生物科技有限公司 一种含五元环的化合物及其制备和应用
US11555015B2 (en) 2018-09-06 2023-01-17 Arena Pharmaceuticals, Inc. Compounds useful in the treatment of autoimmune and inflammatory disorders

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2121394A1 (fr) 1971-01-08 1972-08-25 Anvar Procédé d'obtention de dérivés d'acides indole carboxyliques et produits préparables par ce procédé.
EP0146810A3 (de) 1983-12-05 1987-05-13 Solco Basel AG Verfahren zur Herstellung von Sphingosinderivaten
US5110987A (en) 1988-06-17 1992-05-05 Emory University Method of preparing sphingosine derivatives
ZA902794B (en) 1989-04-18 1991-04-24 Duphar Int Res New 3-n substituted carbamoyl-indole derivatives
US5294722A (en) 1992-04-16 1994-03-15 E. R. Squibb & Sons, Inc. Process for the preparation of imidazoles useful in angiotensin II antagonism
US5403851A (en) 1994-04-05 1995-04-04 Interneuron Pharmaceuticals, Inc. Substituted tryptamines, phenalkylamines and related compounds
HUP9900424A2 (hu) * 1996-01-22 1999-05-28 Fujisawa Pharmaceutical Co., Ltd. Tiazolil-benzfurán-származékok és a vegyületeket tartalmazó gyógyászati készítmények
KR100559817B1 (ko) 1997-03-12 2006-03-10 다카라 바이오 가부시키가이샤 스핑고신 유사화합물
US6239297B1 (en) 1997-09-11 2001-05-29 Takara Shuzo Co., Ltd. Sphingosine derivatives and medicinal composition
DE19753522A1 (de) * 1997-12-03 1999-06-10 Boehringer Ingelheim Pharma Substituierte Indole, ihre Herstellung und ihre Verwendung als Arzneimittel
PL349348A1 (en) 1999-01-13 2002-07-15 Millennium Pharmaceuticals Functionalized heterocycles as chemokine receptor modulators
AU2001264313A1 (en) 2000-06-20 2002-01-02 Japan Tobacco Inc. Pyrazolopyridine compounds and use thereof as drugs
ATE367812T1 (de) 2001-06-20 2007-08-15 Wyeth Corp Substituierte indolsäurederivate als inhibitoren von plasminogen-aktivator-inhibitor-1 (pai-1)
JPWO2003070691A1 (ja) * 2002-02-21 2005-06-09 財団法人大阪産業振興機構 N−ヒドロキシカルボキサミド誘導体
AU2007214434B2 (en) 2006-02-15 2012-06-14 Allergan, Inc. Indole-3-carboxylic acid amide, ester, thioamide and thiol ester compounds bearing aryl or heteroaryl groups having sphingosine-1-phosphate (S1P) receptor antagonist biological activity

Similar Documents

Publication Publication Date Title
JP2010515750A5 (pl)
RU2009102535A (ru) Производные карбамидов тропана, их получение и их применение в терапии
JP2018509418A5 (pl)
JP2011513305A5 (pl)
JP2013538801A5 (pl)
CA2565813A1 (en) Substituted methyl aryl or heteroaryl amide compounds
PE20010753A1 (es) DERIVADOS DE PURINA COMO AGONISTAS DEL RECEPTOR DE ADENOSINA A2a
RU2007146798A (ru) ПРОИЗВОДНЫЕ 4-(2-АМИНО-1-ГИДРОКСИЭТИЛ)ФЕНОЛА КАК АГОНИСТЫ β2 АДРЕНЕРГИЧЕСКОГО РЕЦЕПТОРА
JP2018502912A5 (pl)
NO20076418L (no) Heterocyclic compounds as agonists for the thyroid receptor
DE602005014786D1 (de) Oxazolderivate als histamin-h3-rezeptor-wirkstoffe, deren herstellung und therapeutische verwendung
JP2013518129A5 (pl)
RU2008152180A (ru) ПРОИЗВОДНЫЕ ПИРРОЛА, МОДУЛИРУЮЩИЕ АКТИВНОСТЬ CRTh2 РЕЦЕПТОРА
JP2011519374A5 (pl)
RU2009148336A (ru) Гетероциклические соединения в качестве положительных модуляторов метаботропного глутаматного рецептора 2 (рецептора mglu2)
JP2011515398A5 (pl)
RS51016B (sr) Derivati indol-1-il sirćetne kiseline koji imaju aktivnost antagonista pgd2
TW200734322A (en) Indole derivatives exhibiting PGD2 receptor antagonism
TN2009000084A1 (en) Adenosine derivatives as a2a receptor agonists
JP2011515483A5 (pl)
RU2014122035A (ru) Соединения с нематоцидной активностью
NZ588121A (en) Novel estrogen receptor ligands
HK1148740A1 (en) Novel phenylpyrrole derivative
AR062299A1 (es) Derivados de bencimidazol
PE20120655A1 (es) Derivados de triazolopiridina como inhibidores de proteinas cinasas activadas por mitogeno p38 (map)