MA38425B1 - Composés bicycliques pour une utilisation comme agonistes selectifs pour le recepteur s1p1 - Google Patents
Composés bicycliques pour une utilisation comme agonistes selectifs pour le recepteur s1p1Info
- Publication number
- MA38425B1 MA38425B1 MA38425A MA38425A MA38425B1 MA 38425 B1 MA38425 B1 MA 38425B1 MA 38425 A MA38425 A MA 38425A MA 38425 A MA38425 A MA 38425A MA 38425 B1 MA38425 B1 MA 38425B1
- Authority
- MA
- Morocco
- Prior art keywords
- compounds
- selective agonists
- receptor
- bicyclic compounds
- diseases
- Prior art date
Links
- 239000000556 agonist Substances 0.000 title abstract 2
- 102000011011 Sphingosine 1-phosphate receptors Human genes 0.000 title 1
- 108050001083 Sphingosine 1-phosphate receptors Proteins 0.000 title 1
- 125000002619 bicyclic group Chemical group 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 102000004169 proteins and genes Human genes 0.000 abstract 2
- 108090000623 proteins and genes Proteins 0.000 abstract 2
- 208000023275 Autoimmune disease Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 230000001225 therapeutic effect Effects 0.000 abstract 1
- 208000019553 vascular disease Diseases 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/46—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with hetero atoms directly attached to the ring nitrogen atom
- C07D207/50—Nitrogen atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- 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
-
- 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
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/42—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having amino groups or hydroxy groups bound to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C25/00—Compounds containing at least one halogen atom bound to a six-membered aromatic ring
- C07C25/18—Polycyclic aromatic halogenated hydrocarbons
- C07C25/22—Polycyclic aromatic halogenated hydrocarbons with condensed rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
- C07C49/657—Unsaturated compounds containing a keto groups being part of a ring containing six-membered aromatic rings
- C07C49/665—Unsaturated compounds containing a keto groups being part of a ring containing six-membered aromatic rings a keto group being part of a condensed ring system
- C07C49/67—Unsaturated compounds containing a keto groups being part of a ring containing six-membered aromatic rings a keto group being part of a condensed ring system having two rings, e.g. tetralones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/117—Esters of phosphoric acids with cycloaliphatic alcohols
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
- C07C2601/08—Systems containing only non-condensed rings with a five-membered ring the ring being saturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/10—One of the condensed rings being a six-membered aromatic ring the other ring being six-membered, e.g. tetraline
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Heart & Thoracic Surgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Cardiology (AREA)
- Dermatology (AREA)
- Transplantation (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Epidemiology (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Indole Compounds (AREA)
Abstract
La présente invention concerne des composés de formule (i) et/ou un de leurs sels; dans laquelle r représente -oh ou -op(o)(oh)2. L'invention concerne également des méthodes d'utilisation de tels composés comme agonistes sélectifs pour le récepteur s1p1couplé à la protéine g, et des compositions pharmaceutiques comprenant de tels composés. Ces composés sont utiles dans le traitement, la prévention, ou le ralentissement de la progression de maladies ou de troubles dans des domaines thérapeutiques variés, tels que ceux des maladies auto-immunes et des maladies vasculaires.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201361767531P | 2013-02-21 | 2013-02-21 | |
PCT/US2014/017534 WO2014130752A2 (fr) | 2013-02-21 | 2014-02-21 | Composés bicycliques |
Publications (2)
Publication Number | Publication Date |
---|---|
MA38425A1 MA38425A1 (fr) | 2017-12-29 |
MA38425B1 true MA38425B1 (fr) | 2019-03-29 |
Family
ID=50272738
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MA38425A MA38425B1 (fr) | 2013-02-21 | 2014-02-21 | Composés bicycliques pour une utilisation comme agonistes selectifs pour le recepteur s1p1 |
Country Status (35)
Country | Link |
---|---|
US (3) | US9115054B2 (fr) |
EP (1) | EP2958888B1 (fr) |
JP (1) | JP6277210B2 (fr) |
KR (1) | KR102242265B1 (fr) |
CN (1) | CN105026362B (fr) |
AR (1) | AR094851A1 (fr) |
AU (1) | AU2014218883B2 (fr) |
BR (1) | BR112015019919A2 (fr) |
CA (1) | CA2902168C (fr) |
CL (1) | CL2015002358A1 (fr) |
CY (1) | CY1118641T1 (fr) |
DK (1) | DK2958888T3 (fr) |
EA (1) | EA025294B1 (fr) |
ES (1) | ES2613262T3 (fr) |
HK (1) | HK1218111A1 (fr) |
HR (1) | HRP20170247T1 (fr) |
HU (1) | HUE031626T2 (fr) |
IL (1) | IL240613B (fr) |
LT (1) | LT2958888T (fr) |
MA (1) | MA38425B1 (fr) |
MX (1) | MX2015010347A (fr) |
MY (1) | MY173990A (fr) |
PE (1) | PE20151746A1 (fr) |
PH (1) | PH12015501793A1 (fr) |
PL (1) | PL2958888T3 (fr) |
PT (1) | PT2958888T (fr) |
RS (1) | RS55703B1 (fr) |
SG (1) | SG11201506408TA (fr) |
SI (1) | SI2958888T1 (fr) |
SM (1) | SMT201700115B (fr) |
TN (1) | TN2015000356A1 (fr) |
TW (1) | TWI613182B (fr) |
UY (1) | UY35338A (fr) |
WO (1) | WO2014130752A2 (fr) |
ZA (1) | ZA201506965B (fr) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2015009731A2 (fr) | 2013-07-15 | 2015-01-22 | The Regents Of The University Of California | Analogues azacycliques de fty720 à structure contrainte |
TWI689487B (zh) | 2014-08-20 | 2020-04-01 | 美商必治妥美雅史谷比公司 | 經取代雙環化合物 |
WO2017053990A1 (fr) * | 2015-09-24 | 2017-03-30 | The Regents Of The University Of California | Molécules de type sphingolipide synthétiques, médicaments, procédés pour leur synthèse et procédés de traitement |
US10633354B2 (en) | 2016-09-02 | 2020-04-28 | Bristol-Myers Squibb Company | Substituted tricyclic heterocyclic compounds |
WO2019032631A1 (fr) | 2017-08-09 | 2019-02-14 | Bristol-Myers Squibb Company | Composés d'éther d'oxime |
WO2019032632A1 (fr) | 2017-08-09 | 2019-02-14 | Bristol-Myers Squibb Company | Composés d'alkylphényle |
WO2021062168A1 (fr) * | 2019-09-25 | 2021-04-01 | The Regents Of The University Of California | Molécules inspirees par des sphingolipides synthetiques ayant des groupes pendants heteroaromatiques cytotoxiques, leurs procédés de synthèse et méthodes de traitement |
Family Cites Families (57)
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 |
US6069143A (en) | 1994-12-20 | 2000-05-30 | Smithkline Beecham Corporation | Fibrinogen receptor antagonists |
US20050070506A1 (en) | 2002-01-18 | 2005-03-31 | Doherty George A. | Selective s1p1/edg1 receptor agonists |
EP1470137B1 (fr) | 2002-01-18 | 2009-09-02 | Merck & Co., Inc. | Agonistes du recepteur edg |
US7351725B2 (en) | 2002-01-18 | 2008-04-01 | Merck & Co., Inc. | N-(benzyl)aminoalkylcarboxylates, phosphinates, phosphonates and tetrazoles as Edg receptor agonists |
US7309721B2 (en) | 2002-03-01 | 2007-12-18 | Merck + Co., Inc. | Aminoalkylphosphonates and related compounds as Edg receptor agonists |
US7199142B2 (en) | 2002-06-17 | 2007-04-03 | Merck & Co., Inc. | 1-((5-aryl-1,2,4-oxadiazol-3-yl) benzyl)azetidine-3-carboxylates and 1-((5-aryl-1,2,4-oxadiazol-3-yl)benzyl) pyrrolidine-3-carboxylates as edg receptor agonists |
CL2004001120A1 (es) | 2003-05-19 | 2005-04-15 | Irm Llc | Compuestos derivados de amina sustituidas con heterociclos, inmunosupresores; composicion farmaceutica; y uso para tratar enfermedades mediadas por interacciones de linfocito, tales como enfermedades autoinmunes, inflamatorias, infecciosas, cancer. |
EP1697333A4 (fr) | 2003-12-17 | 2009-07-08 | Merck & Co Inc | Carboxylates propanoiques 3,4-disusbstitues utilises en tant qu'agonistes du recepteur s1p (edg) |
TW200538433A (en) | 2004-02-24 | 2005-12-01 | Irm Llc | Immunosuppressant compounds and compositiions |
WO2006047195A2 (fr) | 2004-10-22 | 2006-05-04 | Merck & Co., Inc. | Carboxylates, sulfonates, phosphonates, phosphinates 2-(aryl)azacyclylmethyle et heterocycles utilises comme agonistes des recepteurs s1p |
MX2007009848A (es) | 2005-02-14 | 2008-03-10 | Univ Virginia | Agonistas de esfingosina 1-fosfato comprendiendo cicloalcanos y heterociclos de 5 miembros substituidos por grupos amino y fenilo. |
BRPI0607156A2 (pt) | 2005-02-18 | 2009-08-11 | Innodia Inc | composto, composição farmacêutica, uso do composto, kit farmacêutico, método para estimular a absorção de glicose por células de músculo e/ou célula de adipócito e método para estimular a secreção pancreática |
US8802840B2 (en) | 2005-03-08 | 2014-08-12 | Biota Scientific Management Pty Ltd. | Bicyclic nucleosides and nucleotides as therapeutic agents |
US7605269B2 (en) | 2005-03-23 | 2009-10-20 | Actelion Pharmaceuticals Ltd. | Thiophene derivatives as Sphingosine-1-phosphate-1 receptor agonists |
JPWO2006115188A1 (ja) | 2005-04-22 | 2008-12-18 | 第一三共株式会社 | ヘテロ環化合物 |
CA2610310A1 (fr) | 2005-06-08 | 2006-12-14 | Novartis Ag | Oxadiazoles polycycliques ou soxazoles i et leur utilisation comme ligands recepteurs de s1p |
CA2619101A1 (fr) | 2005-08-23 | 2007-03-01 | Irm Llc | Composes immunosuppresseurs et compositions associees |
RU2430913C2 (ru) | 2006-01-06 | 2011-10-10 | Сепракор Инк. | Циклоалкиламины в качестве ингибиторов повторного поглощения моноамина |
KR20080086546A (ko) | 2006-01-27 | 2008-09-25 | 유니버시티 오브 버지니아 페이턴트 파운데이션 | 신경병증성 통증의 치료 방법 |
WO2007088450A2 (fr) | 2006-02-01 | 2007-08-09 | Pfizer Products Inc. | Chromane antagoniste du récepteur h-3 |
WO2007109330A2 (fr) | 2006-03-21 | 2007-09-27 | Epix Delaware, Inc. | Composés modulant le récepteur de la sip |
JP2009530381A (ja) | 2006-03-23 | 2009-08-27 | メルク エンド カムパニー インコーポレーテッド | グルカゴン受容体アンタゴニスト化合物、この化合物を含む組成物及び使用方法 |
EP2003132B1 (fr) | 2006-04-03 | 2014-03-05 | Astellas Pharma Inc. | Dérivés d'oxadiazole en tant qu'agonistes du S1P1 |
JP2009269819A (ja) | 2006-08-25 | 2009-11-19 | Asahi Kasei Pharma Kk | アミン化合物 |
EP2069335B1 (fr) | 2006-09-08 | 2012-12-26 | Actelion Pharmaceuticals Ltd. | Dérivés de pyridin-3-yle en tant qu'agents immunomodulateurs |
US8217027B2 (en) | 2006-12-21 | 2012-07-10 | Abbott Laboratories | Sphingosine-1-phosphate receptor agonist and antagonist compounds |
GB0625648D0 (en) | 2006-12-21 | 2007-01-31 | Glaxo Group Ltd | Compounds |
RU2009128062A (ru) * | 2006-12-21 | 2011-01-27 | Эбботт Лэборетриз (Us) | Соединения агонисты и антагонисты рецептора сфингозин-1-фосфата |
CN101610674A (zh) * | 2006-12-21 | 2009-12-23 | 艾博特公司 | 鞘氨醇-1-磷酸酯受体激动剂和拮抗剂化合物 |
JP5248528B2 (ja) | 2007-02-02 | 2013-07-31 | エフ.ホフマン−ラ ロシュ アーゲー | Cns疾患用のtaar1リガンドとしての新規2−アミノオキサゾリン |
JP2010521450A (ja) | 2007-03-16 | 2010-06-24 | アクテリオン ファーマシューティカルズ リミテッド | S1p1/edg1受容体アゴニストとしてのアミノ−ピリジン誘導体 |
ES2622423T3 (es) | 2007-10-04 | 2017-07-06 | Merck Serono S.A. | Derivados de oxadiazol |
WO2009057079A2 (fr) | 2007-11-01 | 2009-05-07 | Actelion Pharmaceuticals Ltd | Nouveaux dérivés de pyrimidine |
GB0725105D0 (en) | 2007-12-21 | 2008-01-30 | Glaxo Group Ltd | Compounds |
ES2431354T3 (es) | 2008-04-01 | 2013-11-26 | Theravance, Inc. | Derivados de 2-aminotetralina como antagonistas del receptor de opioide mu |
WO2010042998A1 (fr) | 2008-10-17 | 2010-04-22 | Akaal Pharma Pty Ltd | Modulateurs des récepteurs s1p |
KR20110100624A (ko) | 2008-12-18 | 2011-09-14 | 메르크 세로노 에스. 에이. | 다발성 경화증의 치료에 유용한 옥사디아졸 융합된 헤테로사이클릭 유도체 |
EP2202232A1 (fr) | 2008-12-26 | 2010-06-30 | Laboratorios Almirall, S.A. | Dérivés du 1,2,4-oxadiazole et leur application thérapeutique |
EP2210890A1 (fr) | 2009-01-19 | 2010-07-28 | Almirall, S.A. | Dérivés d'oxadiazoles en tant qu'agonistes du récepteur S1P1 |
EP2389377B1 (fr) | 2009-01-23 | 2014-07-16 | Bristol-Myers Squibb Company | Dérivés d'oxadiazole substitués comme agonistes de s1p dans le traitement de maladies auto-immunes et inflammatoires |
WO2010085581A1 (fr) | 2009-01-23 | 2010-07-29 | Bristol-Myers Squibb Company | Dérivés d'oxadiazole substitués comme agonistes de s1p dans le traitement de maladies auto-immunes et inflammatoires |
EP2382211B1 (fr) | 2009-01-23 | 2012-12-19 | Bristol-Myers Squibb Company | Dérivés de pyrazole-1,2,4-oxadiazole en tant qu'agonistes de sphingosine-1-phosphate |
JP2012517445A (ja) | 2009-02-10 | 2012-08-02 | アボット・ラボラトリーズ | S1p受容体アゴニストおよびアンタゴニストを調製するための方法 |
US8399451B2 (en) | 2009-08-07 | 2013-03-19 | Bristol-Myers Squibb Company | Heterocyclic compounds |
JP5728487B2 (ja) | 2009-10-29 | 2015-06-03 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | 三環式ヘテロ環化合物 |
WO2011133734A1 (fr) | 2010-04-23 | 2011-10-27 | Bristol-Myers Squibb Company | Amides d'acide 4-(5-isoxazolyl ou 5-pyrazolyl-1,2,4-oxadiazol-3-yl)-mandélique comme agonistes du récepteur de la sphingosine-1-phosphate de type 1 |
CN102260177A (zh) | 2010-05-25 | 2011-11-30 | 中国医学科学院药物研究所 | 丙二醇类衍生物、其制备方法和其药物组合物与用途 |
CN102260178A (zh) | 2010-05-25 | 2011-11-30 | 中国医学科学院药物研究所 | 羟基丙二醇类衍生物、其制备方法和其药物组合物与用途 |
WO2012012477A1 (fr) | 2010-07-20 | 2012-01-26 | Bristol-Myers Squibb Company | Composés 3-phényl-1,2,4-oxadiazole substitués |
CN103237795B (zh) | 2010-09-24 | 2015-10-21 | 百时美施贵宝公司 | 经取代的噁二唑化合物及其作为s1p1激动剂的用途 |
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 |
US9682078B2 (en) | 2011-03-18 | 2017-06-20 | University Of Virginia Patent Foundation | Compositions and methods for tissue engineering and cell based therapies |
EP2541155B1 (fr) | 2011-04-26 | 2016-02-24 | Panasonic Intellectual Property Management Co., Ltd. | Système de chauffage, et procédé de commande de système de chauffage |
GB201107325D0 (en) * | 2011-05-04 | 2011-06-15 | Glaxosmithkline Llc | Novel compounds |
ES2758841T3 (es) | 2011-05-13 | 2020-05-06 | Celgene Int Ii Sarl | Moduladores heterocíclicos selectivos del receptor de la esfingosina-1-fosfato |
CN104684560B (zh) | 2012-07-27 | 2018-08-17 | 比奥根艾迪克Ma公司 | 作为s1p调节剂和/或atx调节剂的化合物 |
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