MX2009006751A - Sphingosine-1 -phosphate receptor agonist and antagonist compounds. - Google Patents
Sphingosine-1 -phosphate receptor agonist and antagonist compounds.Info
- Publication number
- MX2009006751A MX2009006751A MX2009006751A MX2009006751A MX2009006751A MX 2009006751 A MX2009006751 A MX 2009006751A MX 2009006751 A MX2009006751 A MX 2009006751A MX 2009006751 A MX2009006751 A MX 2009006751A MX 2009006751 A MX2009006751 A MX 2009006751A
- Authority
- MX
- Mexico
- 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
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- 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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- 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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- 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
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- 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
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
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- 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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Abstract
The present invention is directed to novel, potent, and selective agents, which are agonists or antagonists of the one or more of the individual receptors of the S1P receptor family. The compounds of the invention are useful as therapeutics for treating medical conditions associated with agonism or antagonism of the individual receptors of the S1P receptor family.
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 (en) | 2006-12-21 | 2007-12-21 | Sphingosine-1 -phosphate receptor agonist and antagonist compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2009006751A true MX2009006751A (en) | 2009-06-30 |
Family
ID=39562856
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2009006751A MX2009006751A (en) | 2006-12-21 | 2007-12-21 | Sphingosine-1 -phosphate receptor agonist and antagonist compounds. |
Country Status (19)
| Country | Link |
|---|---|
| EP (1) | EP2120575A4 (en) |
| JP (1) | JP2010513532A (en) |
| KR (1) | KR20090095659A (en) |
| AR (1) | AR064650A1 (en) |
| AU (1) | AU2007338700A1 (en) |
| BR (1) | BRPI0720478A2 (en) |
| CA (1) | CA2672727A1 (en) |
| CL (1) | CL2007003784A1 (en) |
| CO (1) | CO6180436A2 (en) |
| CR (1) | CR10872A (en) |
| DO (1) | DOP2009000149A (en) |
| EC (1) | ECSP099435A (en) |
| MX (1) | MX2009006751A (en) |
| NO (1) | NO20092376L (en) |
| PE (1) | PE20081561A1 (en) |
| RU (1) | RU2009128062A (en) |
| TW (1) | TW200838497A (en) |
| UY (1) | UY30829A1 (en) |
| WO (1) | WO2008079382A1 (en) |
Families Citing this family (41)
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| EP1986623A2 (en) * | 2006-01-27 | 2008-11-05 | University Of Virginia Patent Foundation | Method for treatment of neuropathic pain |
| JP2009526073A (en) | 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 | Bicyclic sphingosine-1-phosphate receptor analogs |
| EP2097371A2 (en) | 2006-11-21 | 2009-09-09 | University Of Virginia Patent Foundation | Benzocycloheptyl analogs having sphingosine 1-phosphate receptor activity |
| WO2008064320A2 (en) | 2006-11-21 | 2008-05-29 | University Of Virginia Patent Foundation | Hydrindane analogs having sphingosine 1-phosphate receptor agonist activity |
| CA2673076A1 (en) * | 2006-12-21 | 2008-07-03 | Abbott Laboratories | Process for the preparation and isolation of the individual stereoisomers of 1-amino, 3-substituted phenylcyclopentane carboxylates |
| RU2470011C2 (en) | 2007-05-31 | 2012-12-20 | Сепракор Инк. | Cycloalkylamines, containing phenyl as substituent, as inhibitors of monoamine reuptake |
| 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 (en) | 2008-08-27 | 2021-03-05 | 艾尼纳制药公司 | Substituted tricyclic acid derivatives as S1P1 receptor agonists for the treatment of autoimmune and inflammatory disorders |
| WO2010043000A1 (en) | 2008-10-17 | 2010-04-22 | Akaal Pharma Pty Ltd | S1p receptors modulators and their use thereof |
| WO2010042998A1 (en) | 2008-10-17 | 2010-04-22 | Akaal Pharma Pty Ltd | S1p receptors modulators |
| PE20100371A1 (en) * | 2008-10-31 | 2010-06-01 | Lexicon Pharmaceuticals Inc | S1P RECEPTOR AGONISTS FOR THE TREATMENT OF CEREBRAL MALARIA |
| AR074061A1 (en) * | 2008-10-31 | 2010-12-22 | Lexicon Pharmaceuticals Inc | S1P LIASA INHIBITORS FOR THE TREATMENT OF CEREBRAL MALARIA AND PHARMACEUTICAL FORMULATION |
| JP2012515789A (en) | 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 | Pyrazole-1,2,4-oxadiazole derivatives as sphingosine-1-phosphate agonists |
| CN102361869A (en) | 2009-01-23 | 2012-02-22 | 百时美施贵宝公司 | Substituted oxadiazole derivatives as s1p agonists in the treatment of autoimmune and inflammatory diseases |
| 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 |
| 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 (en) | 2010-03-03 | 2011-09-09 | Arena Pharmaceuticals, Inc. | Processes for the preparation of s1p1 receptor modulators and crystalline forms thereof |
| WO2011133734A1 (en) | 2010-04-23 | 2011-10-27 | Bristol-Myers Squibb Company | 4 - (5 - isoxazolyl or 5 - pyrrazolyl -1,2,4- oxadiazol - 3 - yl) -mandelic acid amides as sphingosin- 1 - phosphate 1 rreceptor agonists |
| TWI522361B (en) | 2010-07-09 | 2016-02-21 | 艾伯維公司 | Fused heterocyclic derivative as S1P regulator |
| TWI543984B (en) * | 2010-07-09 | 2016-08-01 | 艾伯維公司 | Spiro-piperidine derivatives as S1P regulators |
| TW201206893A (en) | 2010-07-09 | 2012-02-16 | Abbott Healthcare Products Bv | Bisaryl (thio) morpholine derivatives as S1P modulators |
| CN103237795B (en) | 2010-09-24 | 2015-10-21 | 百时美施贵宝公司 | Substituted oxadiazole compounds and their use as S1P1 agonists |
| JO3177B1 (en) | 2011-04-01 | 2018-03-08 | Novartis Ag | Formulations comprising 2-amino-2-[2-(4-octylphenyl)ethyl]propane-1,3-diol |
| US9115054B2 (en) * | 2013-02-21 | 2015-08-25 | Bristol-Myers Squibb Company | Tetrahydronaphthalenyl compounds useful as sipi agonists |
| JP6617702B2 (en) * | 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 azacyclic constraint analog |
| TW201613864A (en) | 2014-02-20 | 2016-04-16 | Takeda Pharmaceutical | Novel compounds |
| TWI689487B (en) | 2014-08-20 | 2020-04-01 | 美商必治妥美雅史谷比公司 | Substituted bicyclic compounds |
| US11007175B2 (en) | 2015-01-06 | 2021-05-18 | Arena Pharmaceuticals, Inc. | Methods of treating conditions related to the S1P1 receptor |
| BR112017027656B1 (en) | 2015-06-22 | 2023-12-05 | Arena Pharmaceuticals, Inc. | CRYSTALLINE HABIT OF SALT-FREE PLATE OF ACID L-ARGININE (R)-2-(7-(4- CYCLOPENTYL-3-(TRIFLUOROMETHYL)BENZYLOXY)- 1,2,3,4-TETRA-HYDROCYCLO-PENTA[B ]INDOL-3- IL)ACETIC, PHARMACEUTICAL COMPOSITION THAT COMPRISES IT, ITS USES AND METHOD OF PREPARATION THEREOF |
| EP3352753A4 (en) | 2015-09-24 | 2019-03-13 | The Regents of The University of California | SYNTHETIC SPHINGOLIPID MOLECULES, MEDICAMENTS, METHODS FOR THEIR SYNTHESIS, AND METHODS OF TREATMENT |
| WO2018045149A1 (en) * | 2016-09-02 | 2018-03-08 | Bristol-Myers Squibb Company | Substituted tricyclic heterocyclic compounds |
| JP2020507610A (en) | 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 | Compounds and methods for the treatment of inflammatory bowel disease with parenteral symptoms |
| CA3053418A1 (en) | 2017-02-16 | 2018-08-23 | Arena Pharmaceuticals, Inc. | Compounds and methods for treatment of primary biliary cholangitis |
| KR101891051B1 (en) * | 2018-01-29 | 2018-08-31 | 주식회사 세종바이오메드 | Sphingosine-1-Phosphate analogue and synthetic method thereof |
| BR112020024762A2 (en) | 2018-06-06 | 2021-03-23 | Arena Pharmaceuticals, Inc. | methods of treating conditions related to the s1p1 receptor |
| CN119751336A (en) | 2018-09-06 | 2025-04-04 | 艾尼纳制药公司 | Compounds useful for treating autoimmune and inflammatory disorders |
| US11034669B2 (en) | 2018-11-30 | 2021-06-15 | Nuvation Bio Inc. | Pyrrole and pyrazole compounds and methods of use thereof |
| CN110808093A (en) * | 2019-09-16 | 2020-02-18 | 中山大学孙逸仙纪念医院 | A predictive model for clinical prognosis of radiation encephalopathy and its construction method |
| BR112022008113A2 (en) | 2019-10-31 | 2022-07-19 | Escape Bio Inc | SOLID FORMS OF A S1P RECEIVER MODULATOR |
| CN117007818B (en) * | 2023-08-04 | 2024-04-09 | 徐州医科大学科技园发展有限公司 | Application of S1PR1 as a target in developing or preparing drugs for preventing chronic pain-related memory impairment diseases |
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| 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 (en) * | 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 | Sphingosine = 1-phosphate agonist containing a cycloalkane substituted with an amino group and a phenyl group and a 5-membered heterocyclic ring |
| JP2009527501A (en) * | 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 | Phenyl-cycloalkyl derivatives and phenyl-heterocyclic derivatives as S1P receptor agonists |
-
2007
- 2007-12-21 AU AU2007338700A patent/AU2007338700A1/en not_active Abandoned
- 2007-12-21 UY UY30829A patent/UY30829A1/en not_active Application Discontinuation
- 2007-12-21 JP JP2009542960A patent/JP2010513532A/en not_active Withdrawn
- 2007-12-21 CL CL200703784A patent/CL2007003784A1/en unknown
- 2007-12-21 RU RU2009128062/04A patent/RU2009128062A/en not_active Application Discontinuation
- 2007-12-21 WO PCT/US2007/026263 patent/WO2008079382A1/en not_active Ceased
- 2007-12-21 CA CA002672727A patent/CA2672727A1/en not_active Abandoned
- 2007-12-21 BR BRPI0720478-7A patent/BRPI0720478A2/en not_active Application Discontinuation
- 2007-12-21 AR ARP070105818A patent/AR064650A1/en not_active Application Discontinuation
- 2007-12-21 TW TW096149594A patent/TW200838497A/en unknown
- 2007-12-21 KR KR1020097015385A patent/KR20090095659A/en not_active Withdrawn
- 2007-12-21 EP EP07863237A patent/EP2120575A4/en not_active Withdrawn
- 2007-12-21 MX MX2009006751A patent/MX2009006751A/en not_active Application Discontinuation
-
2008
- 2008-01-02 PE PE2008000051A patent/PE20081561A1/en not_active Application Discontinuation
-
2009
- 2009-06-02 CO CO09056803A patent/CO6180436A2/en not_active Application Discontinuation
- 2009-06-15 EC EC2009009435A patent/ECSP099435A/en unknown
- 2009-06-19 CR CR10872A patent/CR10872A/en not_active Application Discontinuation
- 2009-06-19 DO DO2009000149A patent/DOP2009000149A/en unknown
- 2009-06-22 NO NO20092376A patent/NO20092376L/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| NO20092376L (en) | 2009-06-22 |
| RU2009128062A (en) | 2011-01-27 |
| KR20090095659A (en) | 2009-09-09 |
| DOP2009000149A (en) | 2010-05-15 |
| CR10872A (en) | 2009-07-23 |
| AR064650A1 (en) | 2009-04-15 |
| JP2010513532A (en) | 2010-04-30 |
| WO2008079382A1 (en) | 2008-07-03 |
| EP2120575A1 (en) | 2009-11-25 |
| UY30829A1 (en) | 2008-07-31 |
| PE20081561A1 (en) | 2008-10-30 |
| CL2007003784A1 (en) | 2008-06-27 |
| TW200838497A (en) | 2008-10-01 |
| BRPI0720478A2 (en) | 2014-01-14 |
| EP2120575A4 (en) | 2011-04-27 |
| AU2007338700A1 (en) | 2008-07-03 |
| CO6180436A2 (en) | 2010-07-19 |
| ECSP099435A (en) | 2009-07-31 |
| CA2672727A1 (en) | 2008-07-03 |
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