JP5602230B2 - スフィンゴシン−1−リン酸受容体アゴニスト - Google Patents
スフィンゴシン−1−リン酸受容体アゴニスト Download PDFInfo
- Publication number
- JP5602230B2 JP5602230B2 JP2012523967A JP2012523967A JP5602230B2 JP 5602230 B2 JP5602230 B2 JP 5602230B2 JP 2012523967 A JP2012523967 A JP 2012523967A JP 2012523967 A JP2012523967 A JP 2012523967A JP 5602230 B2 JP5602230 B2 JP 5602230B2
- Authority
- JP
- Japan
- Prior art keywords
- phenyl
- oxadiazol
- trifluoromethyl
- ethyl
- hydroxy
- 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.)
- Expired - Fee Related
Links
- 0 *C(*)(C(*)(c1ccc(*)cc1)O)N1CCCC1 Chemical compound *C(*)(C(*)(c1ccc(*)cc1)O)N1CCCC1 0.000 description 7
- FOAQXWYYNWYZNP-UHFFFAOYSA-N CC(C)(C(c(cc1)ccc1C#N)=O)Br Chemical compound CC(C)(C(c(cc1)ccc1C#N)=O)Br FOAQXWYYNWYZNP-UHFFFAOYSA-N 0.000 description 1
- FQTQUXOLYKXIOQ-GFCCVEGCSA-N CC(C)(C)[SH-]O[C@H](CBr)c(cc1)ccc1C#N Chemical compound CC(C)(C)[SH-]O[C@H](CBr)c(cc1)ccc1C#N FQTQUXOLYKXIOQ-GFCCVEGCSA-N 0.000 description 1
- ASFQMTAXEWNEHE-UHFFFAOYSA-N CC(C)Cc1c(C(F)(F)F)c(C(OC)=O)n[o]1 Chemical compound CC(C)Cc1c(C(F)(F)F)c(C(OC)=O)n[o]1 ASFQMTAXEWNEHE-UHFFFAOYSA-N 0.000 description 1
- FTIRVEBTARAWRH-UHFFFAOYSA-N CCCc1c(-c2ccccc2)[o]nc1-c1nc(-c2ccc(C(CN(CC3)CC3C(O)=O)O)cc2)n[o]1 Chemical compound CCCc1c(-c2ccccc2)[o]nc1-c1nc(-c2ccc(C(CN(CC3)CC3C(O)=O)O)cc2)n[o]1 FTIRVEBTARAWRH-UHFFFAOYSA-N 0.000 description 1
- DXZSYFQGYZHPDY-UHFFFAOYSA-N CCCc1c(-c2ccccc2)[o]nc1-c1nc(-c2ccc(C(CN(CC3)CCC3C(O)=O)O)cc2)n[o]1 Chemical compound CCCc1c(-c2ccccc2)[o]nc1-c1nc(-c2ccc(C(CN(CC3)CCC3C(O)=O)O)cc2)n[o]1 DXZSYFQGYZHPDY-UHFFFAOYSA-N 0.000 description 1
- RUWIEFVLBVHOMD-BGERDNNASA-N CCCc1c(-c2ccccc2)[o]nc1-c1nc(-c2ccc(C(CN(CC3)[C@@H]3C(O)=O)O)cc2)n[o]1 Chemical compound CCCc1c(-c2ccccc2)[o]nc1-c1nc(-c2ccc(C(CN(CC3)[C@@H]3C(O)=O)O)cc2)n[o]1 RUWIEFVLBVHOMD-BGERDNNASA-N 0.000 description 1
- FUWAZROVAHRIJA-UHFFFAOYSA-N CCCc1c(-c2ccccc2)[o]nc1-c1nc(-c2ccc(C(CN(CCC3)C3C(O)=O)O)cc2)n[o]1 Chemical compound CCCc1c(-c2ccccc2)[o]nc1-c1nc(-c2ccc(C(CN(CCC3)C3C(O)=O)O)cc2)n[o]1 FUWAZROVAHRIJA-UHFFFAOYSA-N 0.000 description 1
- OYENRGLANAIQRA-PIVQAISJSA-N CCOC([C@@H]1CN(CC(C)(c(cc2)ccc2/C(/N)=N/O)O)CCC1)=O Chemical compound CCOC([C@@H]1CN(CC(C)(c(cc2)ccc2/C(/N)=N/O)O)CCC1)=O OYENRGLANAIQRA-PIVQAISJSA-N 0.000 description 1
- VRVZBXFRIPRDOC-HNNXBMFYSA-N CCOC([C@@H]1CN(CC(c(cc2)ccc2C#N)=O)CCC1)=O Chemical compound CCOC([C@@H]1CN(CC(c(cc2)ccc2C#N)=O)CCC1)=O VRVZBXFRIPRDOC-HNNXBMFYSA-N 0.000 description 1
- LUZZLRLRKJBLSQ-UHFFFAOYSA-N CCOC(c1c(C(F)(F)F)c(-c2ccccc2)n[o]1)=O Chemical compound CCOC(c1c(C(F)(F)F)c(-c2ccccc2)n[o]1)=O LUZZLRLRKJBLSQ-UHFFFAOYSA-N 0.000 description 1
- ZMUBLNWRVTYIDY-UHFFFAOYSA-N OC(CN(CCC1)CC1(C(O)=O)F)c(cc1)ccc1-c1n[o]c(-c2c(C(F)(F)F)c(-c3ccccc3)n[o]2)n1 Chemical compound OC(CN(CCC1)CC1(C(O)=O)F)c(cc1)ccc1-c1n[o]c(-c2c(C(F)(F)F)c(-c3ccccc3)n[o]2)n1 ZMUBLNWRVTYIDY-UHFFFAOYSA-N 0.000 description 1
- VEYWMSKEPZXKDS-MRTLOADZSA-N OC(CN(CCCC1)[C@H]1C(O)=O)c(cc1)ccc1-c1n[o]c(-c2c(C(F)(F)F)c(-c3ccccc3)n[o]2)n1 Chemical compound OC(CN(CCCC1)[C@H]1C(O)=O)c(cc1)ccc1-c1n[o]c(-c2c(C(F)(F)F)c(-c3ccccc3)n[o]2)n1 VEYWMSKEPZXKDS-MRTLOADZSA-N 0.000 description 1
- HHLFDHHZRJJZOP-UHFFFAOYSA-N OC(CN1CC(CC(O)=O)OCC1)c(cc1)ccc1-c1n[o]c(-c2c(C(F)(F)F)c(-c3ccccc3)n[o]2)n1 Chemical compound OC(CN1CC(CC(O)=O)OCC1)c(cc1)ccc1-c1n[o]c(-c2c(C(F)(F)F)c(-c3ccccc3)n[o]2)n1 HHLFDHHZRJJZOP-UHFFFAOYSA-N 0.000 description 1
- ZDBIBQUTMFNXTR-CAWMZFRYSA-N O[C@H](CN1CC(CC(O)=O)CCC1)c(cc1)ccc1-c1n[o]c(-c(nc2)c(C(F)(F)F)[n]2-c(cc2)ccc2Cl)n1 Chemical compound O[C@H](CN1CC(CC(O)=O)CCC1)c(cc1)ccc1-c1n[o]c(-c(nc2)c(C(F)(F)F)[n]2-c(cc2)ccc2Cl)n1 ZDBIBQUTMFNXTR-CAWMZFRYSA-N 0.000 description 1
- YBQLZPRLWZZECJ-OXQOHEQNSA-N O[C@H](CN1C[C@@H](CC(O)=O)CCC1)c(cc1)ccc1-c1n[o]c(-c2c(C(F)(F)F)c(-c3ccccc3)n[o]2)n1 Chemical compound O[C@H](CN1C[C@@H](CC(O)=O)CCC1)c(cc1)ccc1-c1n[o]c(-c2c(C(F)(F)F)c(-c3ccccc3)n[o]2)n1 YBQLZPRLWZZECJ-OXQOHEQNSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Immunology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US23205409P | 2009-08-07 | 2009-08-07 | |
| US61/232,054 | 2009-08-07 | ||
| PCT/US2010/044627 WO2011017578A1 (en) | 2009-08-07 | 2010-08-06 | Sphingosine-1-phosphate receptor agonists |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013501729A JP2013501729A (ja) | 2013-01-17 |
| JP2013501729A5 JP2013501729A5 (cg-RX-API-DMAC7.html) | 2013-08-08 |
| JP5602230B2 true JP5602230B2 (ja) | 2014-10-08 |
Family
ID=43029859
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012523967A Expired - Fee Related JP5602230B2 (ja) | 2009-08-07 | 2010-08-06 | スフィンゴシン−1−リン酸受容体アゴニスト |
Country Status (19)
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2007310897A1 (en) * | 2006-10-25 | 2008-05-02 | Neurosearch A/S | Oxadiazole and thiadiazole compounds and their use as nicotinic acetylcholine receptor modulators |
| EP2560969B1 (en) * | 2010-04-23 | 2015-08-12 | Bristol-Myers Squibb Company | 4-(5-isoxazolyl or 5-pyrrazolyl-1,2,4-oxadiazol-3-yl)-mandelic acid amides as sphingosin-1-phosphate 1 receptor agonists |
| EP2595969B1 (en) | 2010-07-20 | 2015-04-22 | Bristol-Myers Squibb Company | Substituted 3-phenyl-1,2,4-oxadiazole compounds |
| ES2548258T3 (es) | 2010-09-24 | 2015-10-15 | Bristol-Myers Squibb Company | Compuestos de oxadiazol sustituidos y su uso como agonistas de S1P1 |
| US8629282B2 (en) | 2010-11-03 | 2014-01-14 | Bristol-Myers Squibb Company | Heterocyclic compounds as S1P1 agonists for the treatment of autoimmune and vascular diseases |
| UY35338A (es) | 2013-02-21 | 2014-08-29 | Bristol Myers Squibb Company Una Corporación Del Estado De Delaware | Compuestos bicíclicos moduladores de la actividad de s1p1 y composiciones farmacéuticas que los contienen |
| UY36274A (es) | 2014-08-20 | 2016-02-29 | Bristol Myers Squibb Company Una Corporación Del Estado De Delaware | Compuestos bicíclicos sustituidos como agonistas selectivos de la actividad del receptor s1p1 acoplado a la proteína g |
| UY38367A (es) * | 2018-09-13 | 2020-04-30 | Syngenta Participations Ag | Compuestos de azol-amida pesticidamente activos |
| CN114181276A (zh) * | 2021-12-17 | 2022-03-15 | 安徽大学 | 硫酯肽合成方法 |
Family Cites Families (73)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4200750A (en) | 1977-01-07 | 1980-04-29 | Westwood Pharmaceuticals Inc. | 4-Substituted imidazo [1,2-a]quinoxalines |
| JPS6480026A (en) | 1987-09-21 | 1989-03-24 | Mitsubishi Electric Corp | Resist coater |
| DE4102024A1 (de) * | 1991-01-24 | 1992-07-30 | Thomae Gmbh Dr K | Biphenylderivate, diese verbindungen enthaltende arzneimittel und verfahren zu ihrer herstellung |
| TW432061B (en) | 1994-08-09 | 2001-05-01 | Pfizer Res & Dev | Lactams |
| US6069143A (en) * | 1994-12-20 | 2000-05-30 | Smithkline Beecham Corporation | Fibrinogen receptor antagonists |
| AU4064597A (en) | 1996-08-16 | 1998-03-06 | Du Pont Pharmaceuticals Company | Amidinophenyl-pyrrolidines, -pyrrolines, and -isoxazolidines and derivatives thereof |
| AU2003216054B2 (en) * | 2002-01-18 | 2007-01-04 | Merck & Co., Inc. | Selective S1P1/Edg1 receptor agonists |
| DE60329073D1 (de) | 2002-01-18 | 2009-10-15 | Merck & Co Inc | Edg-rezeptoragonisten |
| JP4709488B2 (ja) | 2002-01-18 | 2011-06-22 | メルク・シャープ・エンド・ドーム・コーポレイション | Edg受容体作動薬としてのN−(ベンジル)アミノアルキルカルボン酸化合物、ホスフィン酸化合物、ホスホン酸化合物およびテトラゾール類 |
| US7309721B2 (en) * | 2002-03-01 | 2007-12-18 | Merck + Co., Inc. | Aminoalkylphosphonates and related compounds as Edg receptor agonists |
| CA2483164C (en) * | 2002-04-23 | 2011-06-07 | Bristol-Myers Squibb Company | Pyrrolo-triazine aniline compounds useful as kinase inhibitors |
| JP2005533058A (ja) | 2002-06-17 | 2005-11-04 | メルク エンド カムパニー インコーポレーテッド | Edg受容体アゴニストとしての1−((5−アリール−1,2,4−オキサジアゾール−3−イル)ベンジル)アゼチジン−3−カルボキシラートおよび1−((5−アリール−1,2,4−オキサジアゾール−3−イル)ベンジル)ピロリジン−3−カルボキシラート |
| AU2003279915A1 (en) | 2002-10-15 | 2004-05-04 | Merck And Co., Inc. | Process for making azetidine-3-carboxylic acid |
| WO2004058149A2 (en) | 2002-12-20 | 2004-07-15 | Merck & Co., Inc. | 1-(amino)indanes and (1,2-dihydro-3-amino)-benzofurans, benzothiophenes and indoles |
| EP1594508B1 (en) | 2003-02-11 | 2012-08-08 | Irm Llc | Novel bicyclic compounds and compositions |
| CA2524867A1 (en) | 2003-05-15 | 2004-12-02 | Merck & Co., Inc. | 3-(2-amino-1-azacyclyl)-5-aryl-1,2,4-oxadiazoles as s1p receptor agonists |
| BRPI0410746A (pt) | 2003-05-19 | 2006-06-27 | Irm Llc | compostos e composições imunossupressoras |
| AU2004251146A1 (en) | 2003-05-19 | 2005-01-06 | Irm, Llc | Immunosuppressant compounds and compositions |
| MY150088A (en) | 2003-05-19 | 2013-11-29 | Irm Llc | Immunosuppressant compounds and compositions |
| WO2004103309A2 (en) | 2003-05-19 | 2004-12-02 | Irm Llc | Immunosuppressant compounds and compositions |
| JP2007528872A (ja) * | 2003-10-01 | 2007-10-18 | メルク エンド カムパニー インコーポレーテッド | S1p受容体アゴニストとしての3,5−アリール置換、ヘテロアリール置換またはシクロアルキル置換された1,2,4−オキサジアゾール化合物 |
| AU2004299456B2 (en) | 2003-12-17 | 2010-10-07 | Merck Sharp & Dohme Corp. | (3,4-disubstituted)propanoic carboxylates as S1P (Edg) receptor agonists |
| TW200538433A (en) | 2004-02-24 | 2005-12-01 | Irm Llc | Immunosuppressant compounds and compositiions |
| WO2006047195A2 (en) | 2004-10-22 | 2006-05-04 | Merck & Co., Inc. | 2-(aryl)azacyclylmethyl carboxylates, sulfonates, phosphonates, phosphinates and heterocycles as s1p receptor agonists |
| JP2008530135A (ja) | 2005-02-14 | 2008-08-07 | ユニバーシティ オブ バージニア パテント ファンデーション | アミノ基およびフェニル基で置換されたシクロアルカンならびに5員の複素環を含むスフィンゴシン=1−リン酸アゴニスト |
| AU2006226018B2 (en) | 2005-03-23 | 2012-07-12 | Idorsia Pharmaceuticals Ltd | Hydrogenated benzo (C) thiophene derivatives as immunomodulators |
| DK1863474T3 (da) | 2005-03-23 | 2009-02-09 | Actelion Pharmaceuticals Ltd | Hidtil ukendte thiophenderivater som sphingosin-1-phosphat-1-receptoragonister |
| RU2382781C2 (ru) | 2005-04-22 | 2010-02-27 | Дайити Санкио Компани, Лимитед | Гетероциклическое соединение |
| KR20080014009A (ko) | 2005-06-08 | 2008-02-13 | 노파르티스 아게 | 폴리시클릭 옥사디아졸 또는 이속사졸, 및 이들의 s1p수용체 리간드로서의 용도 |
| BRPI0611631A2 (pt) | 2005-06-24 | 2010-09-21 | Actelion Pharmaceuticals Ltd | composto, composição farmacêutica, e, uso de um composto |
| AU2006283175A1 (en) | 2005-08-23 | 2007-03-01 | Irm Llc | Immunosuppressant compounds and compositions |
| TW200800911A (en) | 2005-10-20 | 2008-01-01 | Biolipox Ab | Pyrazoles useful in the treatment of inflammation |
| JP2009520688A (ja) * | 2005-11-23 | 2009-05-28 | エピックス デラウェア, インコーポレイテッド | S1p受容体調節化合物およびそれらの使用 |
| TWI404706B (zh) | 2006-01-11 | 2013-08-11 | Actelion Pharmaceuticals Ltd | 新穎噻吩衍生物 |
| GB0601744D0 (en) | 2006-01-27 | 2006-03-08 | Novartis Ag | Organic compounds |
| TW200806611A (en) | 2006-02-09 | 2008-02-01 | Daiichi Seiyaku Co | Novel amidopropionic acid derivatives and medicine containing the same |
| TW200806633A (en) | 2006-03-21 | 2008-02-01 | Epix Pharm Inc | S1P receptor modulating compounds and use thereof |
| WO2007116866A1 (ja) | 2006-04-03 | 2007-10-18 | Astellas Pharma Inc. | ヘテロ化合物 |
| US20100016260A1 (en) | 2006-08-01 | 2010-01-21 | Praecis Pharmaceuticals Incorporated | Agonists of sphingosine-1 phosphate receptor (slp) |
| JP2009269819A (ja) | 2006-08-25 | 2009-11-19 | Asahi Kasei Pharma Kk | アミン化合物 |
| CN101511827B (zh) | 2006-09-07 | 2012-02-01 | 埃科特莱茵药品有限公司 | 作为免疫调制剂的吡啶-4-基衍生物 |
| JP2010504286A (ja) | 2006-09-07 | 2010-02-12 | アラーガン インコーポレイテッド | スフィンゴシン−1−リン酸(s1p)受容体アゴニスト及び/又はアンタゴニスト生物活性を有するヘテロ芳香族化合物 |
| TWI408139B (zh) | 2006-09-07 | 2013-09-11 | Actelion Pharmaceuticals Ltd | 新穎噻吩衍生物 |
| BRPI0716633A2 (pt) * | 2006-09-08 | 2013-09-24 | Actelion Pharmaceuticals Ltd | compostos derivados de piridin-3-ila, composiÇço farmacÊutica e uso de um composto como agente imunomodulador |
| CA2662091A1 (en) | 2006-09-08 | 2008-03-13 | Novartis Ag | N-biaryl (hetero) arylsulphonamide derivatives useful in the treatment of diseases mediated by lymphocytes interactions |
| WO2008035239A1 (en) | 2006-09-21 | 2008-03-27 | Actelion Pharmaceuticals Ltd | Phenyl derivatives and their use as immunomodulators |
| AU2007302262A1 (en) | 2006-09-29 | 2008-04-03 | Novartis Ag | Oxadiazole derivatives with anti-inflammatory and immunosuppressive properties |
| CA2669102A1 (en) | 2006-11-21 | 2008-05-29 | University Of Virginia Patent Foundation | Tetralin analogs having sphingosine 1-phosphate agonist activity |
| JP2010513283A (ja) | 2006-12-15 | 2010-04-30 | アボット・ラボラトリーズ | 新規なオキサジアゾール化合物 |
| JO2701B1 (en) | 2006-12-21 | 2013-03-03 | جلاكسو جروب ليميتد | Vehicles |
| RU2009128062A (ru) | 2006-12-21 | 2011-01-27 | Эбботт Лэборетриз (Us) | Соединения агонисты и антагонисты рецептора сфингозин-1-фосфата |
| GB0625648D0 (en) | 2006-12-21 | 2007-01-31 | Glaxo Group Ltd | Compounds |
| WO2008091967A1 (en) | 2007-01-26 | 2008-07-31 | Smithkline Beecham Corporation | Chemical compounds |
| NZ580454A (en) | 2007-03-16 | 2011-05-27 | Actelion Pharmaceuticals Ltd | Amino- pyridine derivatives as s1p1 /edg1 receptor agonists |
| EP2137181B1 (en) * | 2007-04-19 | 2011-03-02 | Glaxo Group Limited | Oxadiazole substituted indazole derivatives for use as sphingosine 1-phosphate (s1p) agonists |
| US20090069288A1 (en) | 2007-07-16 | 2009-03-12 | Breinlinger Eric C | Novel therapeutic compounds |
| US8202865B2 (en) | 2007-10-04 | 2012-06-19 | Merck Serono Sa | Oxadiazole derivatives |
| BRPI0817597A2 (pt) | 2007-10-04 | 2015-04-07 | Merck Serono Sa | Compostos de diarila de oxadiazol, processo para sua preparação, composições farmacêuticas e kit compreendendo os mesmos, bem como seus usos |
| CN101970430B (zh) | 2007-11-01 | 2013-05-08 | 埃科特莱茵药品有限公司 | 嘧啶衍生物 |
| MX2010007026A (es) | 2007-12-21 | 2010-10-05 | Merck Serono Sa | Derivados de triazoloxadiazoles. |
| PT2291080E (pt) | 2008-05-14 | 2015-10-30 | Scripps Research Inst | Novos modelamodeladores dos recetores da esfingosina fosfato |
| WO2010041655A1 (ja) | 2008-10-06 | 2010-04-15 | 昭和電工株式会社 | 触媒およびその製造方法ならびにその用途 |
| US20100160369A1 (en) * | 2008-12-04 | 2010-06-24 | Exelixis, Inc. | S1P1 Agonists and Methods of Making And Using |
| EP2354134B1 (en) | 2008-12-05 | 2016-02-24 | Astellas Pharma Inc. | 2h-chromene derivatives as stimulators of sphingosine 1-phosphate receptor |
| JP5855942B2 (ja) | 2008-12-18 | 2016-02-09 | メルク セローノ ソシエテ アノニム | 多発性硬化症の治療に有用なオキサジアゾール縮合複素環式誘導体 |
| WO2010072712A1 (en) | 2008-12-23 | 2010-07-01 | Novartis Ag | Biaryl benzylamine derivatives |
| EP2202232A1 (en) | 2008-12-26 | 2010-06-30 | Laboratorios Almirall, S.A. | 1,2,4-oxadiazole derivatives and their therapeutic use |
| EP2210890A1 (en) | 2009-01-19 | 2010-07-28 | Almirall, S.A. | Oxadiazole derivatives as S1P1 receptor agonists |
| CN102361868A (zh) | 2009-01-23 | 2012-02-22 | 百时美施贵宝公司 | 作为1-磷酸-鞘氨醇激动剂的吡唑-1,2,4-噁二唑衍生物 |
| EP2382212B1 (en) | 2009-01-23 | 2014-07-16 | Bristol-Myers Squibb Company | Substituted oxadiazole derivatives as s1p agonists in the treatment of autoimmune and inflammatory diseases |
| WO2010085582A1 (en) | 2009-01-23 | 2010-07-29 | Bristol-Myers Squibb Company | Substituted oxadiazole derivatives as s1p agonists in the treatment of autoimmune and inflammatory diseases |
| JP5669363B2 (ja) | 2009-03-31 | 2015-02-12 | 昭和電工株式会社 | 樹脂組成物及びこれで処理された紙又は繊維加工品 |
| WO2010113528A1 (en) | 2009-04-03 | 2010-10-07 | Panasonic Corporation | Mobile communication method, mobile communication system, and corresponding apparatus |
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- 2010-08-06 CN CN2010800453726A patent/CN102548989A/zh active Pending
- 2010-08-06 SG SG2012003430A patent/SG177691A1/en unknown
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|---|---|
| ES2533095T3 (es) | 2015-04-07 |
| PE20120732A1 (es) | 2012-06-20 |
| KR20120108963A (ko) | 2012-10-05 |
| CA2770194A1 (en) | 2011-02-10 |
| EP2462139B1 (en) | 2015-01-14 |
| JP2013501729A (ja) | 2013-01-17 |
| WO2011017578A1 (en) | 2011-02-10 |
| EP2462139A1 (en) | 2012-06-13 |
| AR077819A1 (es) | 2011-09-28 |
| US20110190255A1 (en) | 2011-08-04 |
| ZA201200641B (en) | 2013-06-26 |
| AU2010279354A1 (en) | 2012-02-09 |
| MX2012001160A (es) | 2012-02-13 |
| US8399451B2 (en) | 2013-03-19 |
| CO6430439A2 (es) | 2012-04-30 |
| CL2012000326A1 (es) | 2012-10-19 |
| SG177691A1 (en) | 2012-02-28 |
| CN102548989A (zh) | 2012-07-04 |
| EA201270266A1 (ru) | 2012-07-30 |
| TW201109323A (en) | 2011-03-16 |
| BR112012002824A2 (pt) | 2019-09-24 |
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