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)
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Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US87631806P | 2006-12-21 | 2006-12-21 | |
US87628806P | 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 |
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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 (ja) |
JP (1) | JP2010513532A (ja) |
KR (1) | KR20090095659A (ja) |
AR (1) | AR064650A1 (ja) |
AU (1) | AU2007338700A1 (ja) |
BR (1) | BRPI0720478A2 (ja) |
CA (1) | CA2672727A1 (ja) |
CL (1) | CL2007003784A1 (ja) |
CO (1) | CO6180436A2 (ja) |
CR (1) | CR10872A (ja) |
DO (1) | DOP2009000149A (ja) |
EC (1) | ECSP099435A (ja) |
MX (1) | MX2009006751A (ja) |
NO (1) | NO20092376L (ja) |
PE (1) | PE20081561A1 (ja) |
RU (1) | RU2009128062A (ja) |
TW (1) | TW200838497A (ja) |
UY (1) | UY30829A1 (ja) |
WO (1) | WO2008079382A1 (ja) |
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JP2009528274A (ja) * | 2006-01-27 | 2009-08-06 | 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 | 神経因性疼痛の治療法 |
WO2007092638A1 (en) | 2006-02-09 | 2007-08-16 | University Of Virginia Patent Foundation | Bicyclic sphingosine 1-phosphate analogs |
JP2010510250A (ja) | 2006-11-21 | 2010-04-02 | 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 | スフィンゴシン=1−燐酸受容体アゴニスト活性を有するヒドリンダンアナログ |
JP2010510251A (ja) | 2006-11-21 | 2010-04-02 | 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 | スフィンゴシン=1−燐酸受容体活性を有するベンゾシクロヘプチルアナログ |
EP2102145A4 (en) * | 2006-12-21 | 2014-06-18 | Abbott Lab | PROCESS FOR THE PREPARATION AND ISOLATION OF INDIVIDUAL STEREOISOMERS OF 1-AMINO, 3-SUBSTITUTED PHENYLCYCLOPENTAN CARBOXYLATES |
EP3296289A3 (en) | 2007-05-31 | 2018-06-20 | Sunovion Pharmaceuticals Inc. | Phenyl substituted cycloalkylamines as monoamine reuptake inhibitors |
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. |
JP2012505836A (ja) | 2008-10-17 | 2012-03-08 | アカール ファーマ ピーティーワイ リミテッド | S1p受容体モジュレーターおよびそれらの使用 |
WO2010042998A1 (en) | 2008-10-17 | 2010-04-22 | Akaal Pharma Pty Ltd | S1p receptors modulators |
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 |
US8354398B2 (en) | 2009-01-23 | 2013-01-15 | Bristol-Myers Squibb Company | Substituted isoxazole compounds |
US8389509B2 (en) | 2009-01-23 | 2013-03-05 | Bristol-Myers Squibb Company | Substituted pyrazole compounds |
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 |
US8399451B2 (en) | 2009-08-07 | 2013-03-19 | Bristol-Myers Squibb Company | Heterocyclic compounds |
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 |
US8835470B2 (en) | 2010-04-23 | 2014-09-16 | Bristol-Myers Squibb Company | Mandelamide heterocyclic compounds |
TW201643169A (zh) * | 2010-07-09 | 2016-12-16 | 艾伯維股份有限公司 | 作為s1p調節劑的螺-哌啶衍生物 |
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 |
TW201206893A (en) | 2010-07-09 | 2012-02-16 | Abbott Healthcare Products Bv | Bisaryl (thio) morpholine derivatives as S1P modulators |
EP2619190B1 (en) | 2010-09-24 | 2015-08-12 | Bristol-Myers Squibb Company | Substituted oxadiazole compounds and their use as s1p1 agonists |
AR085749A1 (es) | 2011-04-01 | 2013-10-23 | Novartis Ag | Formulaciones |
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 |
US10077236B2 (en) | 2013-07-15 | 2018-09-18 | The Regents Of The University Of California | Azacyclic constrained analogs of FTY720 |
TW201613864A (en) | 2014-02-20 | 2016-04-16 | Takeda Pharmaceutical | Novel compounds |
AR101591A1 (es) | 2014-08-20 | 2016-12-28 | Bristol Myers Squibb Co | Compuestos bicíclicos sustituidos |
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 |
WO2017053990A1 (en) | 2015-09-24 | 2017-03-30 | The Regents Of The University Of California | Synthetic sphingolipid-like molecules, drugs, methods of their synthesis and methods of treatment |
EP3507278B1 (en) * | 2016-09-02 | 2021-01-27 | Bristol-Myers Squibb Company | Substituted tricyclic heterocyclic compounds |
MX2019009841A (es) | 2017-02-16 | 2020-01-30 | Arena Pharm Inc | Compuestos y metodos para el tratamiento de la colangitis biliar primaria. |
KR20190113955A (ko) | 2017-02-16 | 2019-10-08 | 아레나 파마슈티칼스, 인크. | 장-외 증상을 갖는 염증성 장질환의 치료를 위한 화합물 및 방법 |
KR101891051B1 (ko) * | 2018-01-29 | 2018-08-31 | 주식회사 세종바이오메드 | 스핑고신-1-포스페이트 유사체 및 이의 합성 방법 |
US11555015B2 (en) | 2018-09-06 | 2023-01-17 | Arena Pharmaceuticals, Inc. | Compounds useful in the treatment of 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 (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 |
TW202132311A (zh) | 2019-10-31 | 2021-09-01 | 美商E 斯蓋普生物股份有限公司 | S1p受體調節劑之固體形式 |
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)
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JP3333510B2 (ja) * | 1991-10-02 | 2002-10-15 | スミスクライン・ビーチャム・コーポレイション | 抗アレルギー、抗炎症および腫瘍壊死因子抑制活性を有するシクロペンタンおよびシクロペンテン誘導体 |
US5314896A (en) * | 1991-11-20 | 1994-05-24 | Warner-Lambert Company | 1,3-substituted cycloalkenes and cycloalkanes as central nervous system agents |
AU2006214314B2 (en) * | 2005-02-14 | 2012-02-09 | University Of Virginia Patent Foundation | Sphingosine 1- phos phate agonists comprising cycloalkanes and 5 -membered heterocycles substituted by amino and phenyl groups |
RU2008137553A (ru) * | 2006-02-21 | 2010-03-27 | Юниверсити Оф Вирджиния Пэтент Фаундейшн (Us) | Фенил-циклоалкильные соединения, содержащие гетероциклические структуры |
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2007
- 2007-12-21 WO PCT/US2007/026263 patent/WO2008079382A1/en active Search and Examination
- 2007-12-21 MX MX2009006751A patent/MX2009006751A/es not_active Application Discontinuation
- 2007-12-21 CA CA002672727A patent/CA2672727A1/en not_active Abandoned
- 2007-12-21 TW TW096149594A patent/TW200838497A/zh unknown
- 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 EP EP07863237A patent/EP2120575A4/en not_active Withdrawn
- 2007-12-21 AR ARP070105818A patent/AR064650A1/es not_active Application Discontinuation
- 2007-12-21 AU AU2007338700A patent/AU2007338700A1/en not_active Abandoned
- 2007-12-21 KR KR1020097015385A patent/KR20090095659A/ko not_active Application Discontinuation
- 2007-12-21 RU RU2009128062/04A patent/RU2009128062A/ru not_active Application Discontinuation
- 2007-12-21 BR BRPI0720478-7A patent/BRPI0720478A2/pt 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 |
---|---|
TW200838497A (en) | 2008-10-01 |
CO6180436A2 (es) | 2010-07-19 |
WO2008079382A1 (en) | 2008-07-03 |
ECSP099435A (es) | 2009-07-31 |
CR10872A (es) | 2009-07-23 |
AU2007338700A1 (en) | 2008-07-03 |
EP2120575A1 (en) | 2009-11-25 |
MX2009006751A (es) | 2009-06-30 |
UY30829A1 (es) | 2008-07-31 |
RU2009128062A (ru) | 2011-01-27 |
CL2007003784A1 (es) | 2008-06-27 |
KR20090095659A (ko) | 2009-09-09 |
CA2672727A1 (en) | 2008-07-03 |
AR064650A1 (es) | 2009-04-15 |
JP2010513532A (ja) | 2010-04-30 |
EP2120575A4 (en) | 2011-04-27 |
DOP2009000149A (es) | 2010-05-15 |
PE20081561A1 (es) | 2008-10-30 |
BRPI0720478A2 (pt) | 2014-01-14 |
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