NO20092376L - Sfingosin-1-fosfat-reseptoragonist og -antagonistforbindelser - Google Patents
Sfingosin-1-fosfat-reseptoragonist og -antagonistforbindelserInfo
- Publication number
- NO20092376L NO20092376L NO20092376A NO20092376A NO20092376L NO 20092376 L NO20092376 L NO 20092376L NO 20092376 A NO20092376 A NO 20092376A NO 20092376 A NO20092376 A NO 20092376A NO 20092376 L NO20092376 L NO 20092376L
- Authority
- NO
- Norway
- Prior art keywords
- sphingosine
- receptor agonist
- antagonist compounds
- phosphate receptor
- receptor family
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 2
- 229940121846 Sphingosine 1-phosphate receptor agonist Drugs 0.000 title 1
- 229940122286 Sphingosine 1-phosphate receptor antagonist Drugs 0.000 title 1
- 102000011011 Sphingosine 1-phosphate receptors Human genes 0.000 abstract 2
- 108050001083 Sphingosine 1-phosphate receptors Proteins 0.000 abstract 2
- 102000005962 receptors Human genes 0.000 abstract 2
- 108020003175 receptors Proteins 0.000 abstract 2
- 230000008484 agonism Effects 0.000 abstract 1
- 239000000556 agonist Substances 0.000 abstract 1
- 230000008485 antagonism Effects 0.000 abstract 1
- 239000005557 antagonist Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 230000003389 potentiating effect Effects 0.000 abstract 1
Classifications
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- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/06—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D231/08—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with oxygen or sulfur atoms directly attached to ring carbon atoms
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4006—Esters of acyclic acids which can have further substituents on alkyl
-
- 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
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6527—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having nitrogen and oxygen atoms as the only ring hetero atoms
- C07F9/653—Five-membered rings
-
- 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
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/655—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms
- C07F9/65515—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms the oxygen atom being part of a five-membered ring
-
- 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
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having sulfur atoms, with or without selenium or tellurium atoms, as the only ring hetero atoms
- C07F9/655345—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having sulfur atoms, with or without selenium or tellurium atoms, as the only ring hetero atoms the sulfur atom being part of a five-membered ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
-
- 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
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (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)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Diabetes (AREA)
- Pain & Pain Management (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Rheumatology (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Emergency Medicine (AREA)
- Obesity (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pyridine Compounds (AREA)
- Pyrrole Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US87628806P | 2006-12-21 | 2006-12-21 | |
| US87631806P | 2006-12-21 | 2006-12-21 | |
| PCT/US2007/026263 WO2008079382A1 (fr) | 2006-12-21 | 2007-12-21 | Composés d'agonistes et d'antagonistes des récepteurs de sphingosine-1-phosphate |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO20092376L true NO20092376L (no) | 2009-06-22 |
Family
ID=39562856
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20092376A NO20092376L (no) | 2006-12-21 | 2009-06-22 | Sfingosin-1-fosfat-reseptoragonist og -antagonistforbindelser |
Country Status (19)
| Country | Link |
|---|---|
| EP (1) | EP2120575A4 (fr) |
| JP (1) | JP2010513532A (fr) |
| KR (1) | KR20090095659A (fr) |
| AR (1) | AR064650A1 (fr) |
| AU (1) | AU2007338700A1 (fr) |
| BR (1) | BRPI0720478A2 (fr) |
| CA (1) | CA2672727A1 (fr) |
| CL (1) | CL2007003784A1 (fr) |
| CO (1) | CO6180436A2 (fr) |
| CR (1) | CR10872A (fr) |
| DO (1) | DOP2009000149A (fr) |
| EC (1) | ECSP099435A (fr) |
| MX (1) | MX2009006751A (fr) |
| NO (1) | NO20092376L (fr) |
| PE (1) | PE20081561A1 (fr) |
| RU (1) | RU2009128062A (fr) |
| TW (1) | TW200838497A (fr) |
| UY (1) | UY30829A1 (fr) |
| WO (1) | WO2008079382A1 (fr) |
Families Citing this family (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1986623A2 (fr) * | 2006-01-27 | 2008-11-05 | University Of Virginia Patent Foundation | Méthode de traitement pour douleur neuropathique |
| JP2009526073A (ja) | 2006-02-09 | 2009-07-16 | 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 | 二環式スフィンゴシン−1−リン酸受容体アナログ |
| EP2097371A2 (fr) | 2006-11-21 | 2009-09-09 | University Of Virginia Patent Foundation | Analogues benzocycloheptyle ayant une activite de recepteur de sphingosine 1-phosphate |
| WO2008064320A2 (fr) | 2006-11-21 | 2008-05-29 | University Of Virginia Patent Foundation | Analogues d'hydrindane ayant une activité agoniste de récepteur de sphingosine-1-phosphate |
| CA2673076A1 (fr) * | 2006-12-21 | 2008-07-03 | Abbott Laboratories | Procede de preparation et d'isolement des stereoisomeres individuels de carboxylates de phenylcyclopentanes 1-amino, 3-substitutes |
| RU2470011C2 (ru) | 2007-05-31 | 2012-12-20 | Сепракор Инк. | Циклоалкиламины, содержащие в качестве заместителя фенил, как ингибиторы обратного захвата моноаминов |
| US8580841B2 (en) | 2008-07-23 | 2013-11-12 | Arena Pharmaceuticals, Inc. | Substituted 1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetic acid derivatives useful in the treatment of autoimmune and inflammatory disorders |
| CN105816453B (zh) | 2008-08-27 | 2021-03-05 | 艾尼纳制药公司 | 用于治疗自身免疫性病症和炎性病症的作为s1p1受体激动剂的经取代的三环酸衍生物 |
| WO2010043000A1 (fr) | 2008-10-17 | 2010-04-22 | Akaal Pharma Pty Ltd | Modulateurs des récepteurs s1p et leur utilisation |
| WO2010042998A1 (fr) | 2008-10-17 | 2010-04-22 | Akaal Pharma Pty Ltd | Modulateurs des récepteurs s1p |
| PE20100371A1 (es) * | 2008-10-31 | 2010-06-01 | Lexicon Pharmaceuticals Inc | Agonistas del receptor s1p para el tratamiento de malaria cerebral |
| AR074061A1 (es) * | 2008-10-31 | 2010-12-22 | Lexicon Pharmaceuticals Inc | Inhibidores de s1p liasa para el tratamiento de la malaria cerebral y formulacion farmaceutica |
| JP2012515789A (ja) | 2009-01-23 | 2012-07-12 | ブリストル−マイヤーズ スクイブ カンパニー | スフィンゴシン−1−リン酸アゴニストとしてのピラゾール−1,2,4−オキサジアゾール誘導体 |
| CN102361869A (zh) | 2009-01-23 | 2012-02-22 | 百时美施贵宝公司 | 在治疗自身免疫性疾病和炎性疾病中作为s1p激动剂的取代的噁二唑衍生物 |
| EP2382212B1 (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 |
| US8399451B2 (en) | 2009-08-07 | 2013-03-19 | Bristol-Myers Squibb Company | Heterocyclic compounds |
| SG182610A1 (en) | 2010-01-27 | 2012-08-30 | Arena Pharm Inc | Processes for the preparation of (r)-2-(7-(4-cyclopentyl-3-(trifluoromethyl)benzyloxy)-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl)acetic acid and salts thereof |
| CA2789480A1 (fr) | 2010-03-03 | 2011-09-09 | Arena Pharmaceuticals, Inc. | Procedes de synthese de modulateurs des recepteurs s1p1 et leurs formes cristallines |
| 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 |
| 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 |
| TWI543984B (zh) * | 2010-07-09 | 2016-08-01 | 艾伯維公司 | 作為s1p調節劑的螺-哌啶衍生物 |
| TW201206893A (en) | 2010-07-09 | 2012-02-16 | Abbott Healthcare Products Bv | Bisaryl (thio) morpholine derivatives as S1P modulators |
| 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 |
| JO3177B1 (ar) | 2011-04-01 | 2018-03-08 | Novartis Ag | تركيبات تتالف من 2-أمينو-2- [ 2- ( 4- أكتيل فينيل ) إثيل ] بروبان - 3, 1- ديول |
| US9115054B2 (en) * | 2013-02-21 | 2015-08-25 | Bristol-Myers Squibb Company | Tetrahydronaphthalenyl compounds useful as sipi agonists |
| JP6617702B2 (ja) * | 2013-07-15 | 2019-12-11 | ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア | Fty720のアザサイクリック拘束アナログ |
| TW201613864A (en) | 2014-02-20 | 2016-04-16 | Takeda Pharmaceutical | Novel compounds |
| 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 |
| US11007175B2 (en) | 2015-01-06 | 2021-05-18 | Arena Pharmaceuticals, Inc. | Methods of treating conditions related to the S1P1 receptor |
| BR112017027656B1 (pt) | 2015-06-22 | 2023-12-05 | Arena Pharmaceuticals, Inc. | Hábito cristalino de placa livre de sal de l-arginina de ácido (r)-2-(7-(4- ciclopentil-3-(trifluorometil)benzilóxi)- 1,2,3,4-tetra-hidrociclo-penta[b]indol-3- il)acético, composição farmacêutica que o compreende, seus usos e método de preparação do mesmo |
| EP3352753A4 (fr) | 2015-09-24 | 2019-03-13 | The Regents of The University of California | Molécules de type sphingolipide synthétiques, médicaments, procédés pour leur synthèse et procédés de traitement |
| WO2018045149A1 (fr) * | 2016-09-02 | 2018-03-08 | Bristol-Myers Squibb Company | Composés hétérocycliques tricycliques substitués |
| JP2020507610A (ja) | 2017-02-16 | 2020-03-12 | アリーナ ファーマシューティカルズ, インコーポレイテッド | 腸管外症状を伴う炎症性腸疾患の治療のための化合物および方法 |
| CA3053418A1 (fr) | 2017-02-16 | 2018-08-23 | Arena Pharmaceuticals, Inc. | Composes et methodes de traitement de l'angiocholite biliaire primitive |
| KR101891051B1 (ko) * | 2018-01-29 | 2018-08-31 | 주식회사 세종바이오메드 | 스핑고신-1-포스페이트 유사체 및 이의 합성 방법 |
| BR112020024762A2 (pt) | 2018-06-06 | 2021-03-23 | Arena Pharmaceuticals, Inc. | métodos de tratamento de condições relacionadas ao receptor s1p1 |
| CN119751336A (zh) | 2018-09-06 | 2025-04-04 | 艾尼纳制药公司 | 可用于治疗自身免疫性病症和炎性病症的化合物 |
| US11034669B2 (en) | 2018-11-30 | 2021-06-15 | Nuvation Bio Inc. | Pyrrole and pyrazole compounds and methods of use thereof |
| CN110808093A (zh) * | 2019-09-16 | 2020-02-18 | 中山大学孙逸仙纪念医院 | 一种放射性脑病临床预后的预测模型及其构建方法 |
| BR112022008113A2 (pt) | 2019-10-31 | 2022-07-19 | Escape Bio Inc | Formas sólidas de um modulador de receptor s1p |
| CN117007818B (zh) * | 2023-08-04 | 2024-04-09 | 徐州医科大学科技园发展有限公司 | S1pr1作为靶点在开发或制备用于预防慢性疼痛相关记忆损伤疾病的药物中的应用 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2807192A (en) * | 1991-10-02 | 1993-05-03 | Smithkline Beecham Corporation | Cyclopentane and cyclopentene derivatives with antiallergic antiinflammatory and tumor necrosis factor inhibiting activity |
| US5314896A (en) * | 1991-11-20 | 1994-05-24 | Warner-Lambert Company | 1,3-substituted cycloalkenes and cycloalkanes as central nervous system agents |
| 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 |
| JP2009527501A (ja) * | 2006-02-21 | 2009-07-30 | 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 | S1p受容体アゴニストとしてのフェニル−シクロアルキル誘導体およびフェニル−複素環誘導体 |
-
2007
- 2007-12-21 AU AU2007338700A patent/AU2007338700A1/en not_active Abandoned
- 2007-12-21 UY UY30829A patent/UY30829A1/es not_active Application Discontinuation
- 2007-12-21 JP JP2009542960A patent/JP2010513532A/ja not_active Withdrawn
- 2007-12-21 CL CL200703784A patent/CL2007003784A1/es unknown
- 2007-12-21 RU RU2009128062/04A patent/RU2009128062A/ru not_active Application Discontinuation
- 2007-12-21 WO PCT/US2007/026263 patent/WO2008079382A1/fr not_active Ceased
- 2007-12-21 CA CA002672727A patent/CA2672727A1/fr not_active Abandoned
- 2007-12-21 BR BRPI0720478-7A patent/BRPI0720478A2/pt not_active Application Discontinuation
- 2007-12-21 AR ARP070105818A patent/AR064650A1/es not_active Application Discontinuation
- 2007-12-21 TW TW096149594A patent/TW200838497A/zh unknown
- 2007-12-21 KR KR1020097015385A patent/KR20090095659A/ko not_active Withdrawn
- 2007-12-21 EP EP07863237A patent/EP2120575A4/fr not_active Withdrawn
- 2007-12-21 MX MX2009006751A patent/MX2009006751A/es not_active Application Discontinuation
-
2008
- 2008-01-02 PE PE2008000051A patent/PE20081561A1/es not_active Application Discontinuation
-
2009
- 2009-06-02 CO CO09056803A patent/CO6180436A2/es not_active Application Discontinuation
- 2009-06-15 EC EC2009009435A patent/ECSP099435A/es unknown
- 2009-06-19 CR CR10872A patent/CR10872A/es not_active Application Discontinuation
- 2009-06-19 DO DO2009000149A patent/DOP2009000149A/es unknown
- 2009-06-22 NO NO20092376A patent/NO20092376L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| RU2009128062A (ru) | 2011-01-27 |
| KR20090095659A (ko) | 2009-09-09 |
| DOP2009000149A (es) | 2010-05-15 |
| MX2009006751A (es) | 2009-06-30 |
| CR10872A (es) | 2009-07-23 |
| AR064650A1 (es) | 2009-04-15 |
| JP2010513532A (ja) | 2010-04-30 |
| WO2008079382A1 (fr) | 2008-07-03 |
| EP2120575A1 (fr) | 2009-11-25 |
| UY30829A1 (es) | 2008-07-31 |
| PE20081561A1 (es) | 2008-10-30 |
| CL2007003784A1 (es) | 2008-06-27 |
| TW200838497A (en) | 2008-10-01 |
| BRPI0720478A2 (pt) | 2014-01-14 |
| EP2120575A4 (fr) | 2011-04-27 |
| AU2007338700A1 (en) | 2008-07-03 |
| CO6180436A2 (es) | 2010-07-19 |
| ECSP099435A (es) | 2009-07-31 |
| CA2672727A1 (fr) | 2008-07-03 |
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