PE20120578A1 - Agonistas y antagonistas del receptor de s1p5, y metodos de uso de los mismos - Google Patents
Agonistas y antagonistas del receptor de s1p5, y metodos de uso de los mismosInfo
- Publication number
- PE20120578A1 PE20120578A1 PE2011001458A PE2011001458A PE20120578A1 PE 20120578 A1 PE20120578 A1 PE 20120578A1 PE 2011001458 A PE2011001458 A PE 2011001458A PE 2011001458 A PE2011001458 A PE 2011001458A PE 20120578 A1 PE20120578 A1 PE 20120578A1
- Authority
- PE
- Peru
- Prior art keywords
- substituted
- antagonists
- methods
- same
- receptor agonists
- Prior art date
Links
- 102000011011 Sphingosine 1-phosphate receptors Human genes 0.000 title 1
- 108050001083 Sphingosine 1-phosphate receptors Proteins 0.000 title 1
- 239000000018 receptor agonist Substances 0.000 title 1
- 229940044601 receptor agonist Drugs 0.000 title 1
- 239000002464 receptor antagonist Substances 0.000 title 1
- 229940044551 receptor antagonist Drugs 0.000 title 1
- -1 BENZIMIDAZOLYL Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 239000000556 agonist Substances 0.000 abstract 1
- 239000005557 antagonist Substances 0.000 abstract 1
- 208000004296 neuralgia Diseases 0.000 abstract 1
- 208000015122 neurodegenerative disease Diseases 0.000 abstract 1
- 208000021722 neuropathic pain Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
Classifications
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- C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D205/04—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/397—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
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- C07C215/04—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated
- C07C215/06—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic
- C07C215/10—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic with one amino group and at least two hydroxy groups bound to the carbon skeleton
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- C07C229/14—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton the nitrogen atom of the amino group being further bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings to carbon atoms of carbon skeletons containing rings
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- C07C229/22—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated the carbon skeleton being further substituted by oxygen atoms
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- C07D207/26—2-Pyrrolidones
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- C07D211/32—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by doubly bound oxygen or sulfur atoms or by two oxygen or sulfur atoms singly bound to the same carbon atom by oxygen atoms
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- C—CHEMISTRY; METALLURGY
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- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- 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
- C07D413/02—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
- C07D413/06—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 linked by a carbon chain containing only aliphatic carbon atoms
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- 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
- C07D417/02—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 two hetero rings
- C07D417/06—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 two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C—CHEMISTRY; METALLURGY
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- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
- C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
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- Hydrogenated Pyridines (AREA)
- Pyrrole Compounds (AREA)
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Abstract
SE REFIERE A UN COMPUESTO DE FORMULA (I) DONDE: EL ANILLO 1 ES SELECCIONADO DE BENZOFURANILO SUSTITUIDO O NO, BENZIMIDAZOLILO SUSTITUIDO O NO, BENZOTIAZOLILO SUSTITUIDO O NO, BENZOTIENILO, SUSTITUIDO O NO, ENTRE OTROS; L SE SELECCIONA ENTRE N(Ra)-, -O- Y C(Ra)2; X SE SELECCIONA ENTRE N SI L ES C(Ra)2, O ES CRa SI L SE SELECCIONA ENTRE N Y O; R2 Y R2a SON H, ALQUILO, ALQUENILO, ALCOXIALQUILO, CICLOALQUILO OPCIONALMENTE SUSTITUIDOS, ENTRE OTROS. REFERIDA TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHO COMPUESTO ES AGONISTA O ANTAGONISTA DE LOS RECEPTORES INDIVIDUALES DE LA FAMILIA DE RECEPTORES DE SIP UTIL EN EL TRATAMIENTO DE TRANSTORNOS NEURODEGENERATIVOS O DOLOR NEUROPATICO
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| US20730109P | 2009-02-10 | 2009-02-10 |
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| JP (1) | JP2012517446A (es) |
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| CN (1) | CN102387704A (es) |
| AU (1) | AU2010213794A1 (es) |
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| CL (1) | CL2011001923A1 (es) |
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| SG (1) | SG172982A1 (es) |
| WO (1) | WO2010093704A1 (es) |
| ZA (1) | ZA201105323B (es) |
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| SG183416A1 (en) | 2010-03-03 | 2012-09-27 | Arena Pharm Inc | Processes for the preparation of s1p1 receptor modulators and crystalline forms thereof |
| EP2646415A1 (en) * | 2010-12-03 | 2013-10-09 | Allergan, Inc. | Novel azetidine derivatives as sphingosine 1-phosphate (s1p) receptor modulators |
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| WO2014018881A1 (en) * | 2012-07-27 | 2014-01-30 | Biogen Idec Ma Inc. | Atx modulating agents |
| US9850206B2 (en) | 2012-11-20 | 2017-12-26 | Biogen Ma Inc. | S1P and/or ATX modulating agents |
| US8871755B2 (en) | 2013-02-12 | 2014-10-28 | Allergan, Inc. | Alkene azetidine derivatives as sphingosine 1-phosphate (S1P) receptor modulators |
| US8957061B2 (en) | 2013-02-13 | 2015-02-17 | Allergan, Inc. | Azetidine derivatives as sphingosine 1-phosphate (S1P) receptor modulators |
| WO2015021109A1 (en) * | 2013-08-08 | 2015-02-12 | Allergan, Inc. | Disubstituted aryl azetidine derivatives as sphingosine-1-phosphate receptors modulators |
| KR20160122260A (ko) * | 2014-02-28 | 2016-10-21 | 깃세이 야쿠힌 고교 가부시키가이샤 | 신규한 아닐린 유도체, 그것을 함유하는 의약 조성물 및 그것들의 용도 |
| PL3242666T3 (pl) | 2015-01-06 | 2025-02-17 | Arena Pharmaceuticals, Inc. | Związek do zastosowania w leczeniu dolegliwości związanych z receptorem s1p1 |
| JP6838744B2 (ja) | 2015-06-22 | 2021-03-03 | 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 | S1P1レセプター関連障害における使用のための(R)−2−(7−(4−シクロペンチル−3−(トリフルオロメチル)ベンジルオキシ)−1,2,3,4−テトラヒドロシクロペンタ[b]インドール−3−イル)酢酸(化合物1)の結晶性L−アルギニン塩 |
| MA42683A (fr) * | 2015-08-27 | 2018-07-04 | Genentech Inc | Composés thérapeutiques et leurs méthodes utilisation |
| EP3500308A4 (en) * | 2016-08-18 | 2020-04-22 | Memorial Sloan Kettering Cancer Center | INHIBITION OF THE SPHINGOSIN-1-PHOSPHATE RECEPTOR FOR TREATING AND PREVENTING LYMPHEDEMES |
| AU2018220521A1 (en) | 2017-02-16 | 2019-09-05 | Arena Pharmaceuticals, Inc. | Compounds and methods for treatment of primary biliary cholangitis |
| CA3053416A1 (en) | 2017-02-16 | 2018-08-23 | Arena Pharmaceuticals, Inc. | Compounds and methods for treatment of inflammatory bowel disease with extra-intestinal manifestations |
| CN110869011B (zh) | 2017-05-15 | 2024-01-05 | 考格尼申治疗股份有限公司 | 用于治疗神经退行性疾病的组合物 |
| EP3655392A1 (en) * | 2017-07-17 | 2020-05-27 | Abbvie Deutschland GmbH & Co. KG | 1,2,3,4-substituted quinoline compounds as s1p modulators |
| WO2019032631A1 (en) | 2017-08-09 | 2019-02-14 | Bristol-Myers Squibb Company | Oxime ether compounds |
| WO2019032632A1 (en) | 2017-08-09 | 2019-02-14 | Bristol-Myers Squibb Company | ALKYLPHENYL COMPOUNDS |
| KR102859841B1 (ko) | 2018-06-06 | 2025-09-12 | 아레나 파마슈티칼스, 인크. | S1p1 수용체와 관련된 병태의 치료 방법 |
| 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 |
| CN111630029B (zh) * | 2018-12-06 | 2021-04-30 | 上海济煜医药科技有限公司 | 作为免疫调节剂的化合物及其制备方法和应用 |
| TW202100526A (zh) | 2019-03-06 | 2021-01-01 | 日商第一三共股份有限公司 | 吡咯并吡唑衍生物 |
| CN114460217B (zh) * | 2022-01-29 | 2023-06-30 | 杭州沐源生物医药科技有限公司 | 一种分离检测硫酸特布他林注射液及其杂质的方法 |
| TW202515535A (zh) * | 2023-08-31 | 2025-04-16 | 美商速通醫療公司 | 醯胺前藥及其用途 |
| CN119638588A (zh) * | 2023-09-15 | 2025-03-18 | 中国医学科学院药物研究所 | 一种三氟甲基苄醚取代的氨基酸类衍生物、其制法和用途 |
| CN119638586A (zh) * | 2023-09-15 | 2025-03-18 | 中国医学科学院药物研究所 | 一种三氟甲基环己基苄醚取代的含氮有机酸类衍生物、其制法和用途 |
| CN119874633B (zh) * | 2023-10-25 | 2025-10-21 | 中国石油化工股份有限公司 | 一种油田水处理缓蚀剂及其合成方法 |
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| US4529544A (en) * | 1982-03-15 | 1985-07-16 | The Dow Chemical Company | Formation of azetidines by decarboxylation of tetrahydro-1,3-oxazin-2-ones |
| US4571393A (en) * | 1982-08-19 | 1986-02-18 | A. H. Robins Company, Incorporated | 3-Phenoxy-1-azetidinecarboxamides |
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| US6221865B1 (en) * | 1995-11-06 | 2001-04-24 | University Of Pittsburgh | Inhibitors of protein isoprenyl transferases |
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| TW200906396A (en) * | 2007-02-14 | 2009-02-16 | Janssen Pharmaceutica Nv | LTA4H modulators and uses thereof |
| US20090069288A1 (en) * | 2007-07-16 | 2009-03-12 | Breinlinger Eric C | Novel therapeutic compounds |
| WO2009073056A1 (en) * | 2007-09-07 | 2009-06-11 | Dr. Reddy's Laboratories Ltd. | Novel tetracycline derivatives as antibacterial agents |
| CA2740484C (en) * | 2008-10-17 | 2021-09-21 | Akaal Pharma Pty Ltd | S1p receptors modulators and their use thereof |
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| EP2395835A1 (en) | 2011-12-21 |
| EP2395835A4 (en) | 2013-04-17 |
| IL214049A0 (en) | 2011-08-31 |
| CN102387704A (zh) | 2012-03-21 |
| CL2011001923A1 (es) | 2011-11-11 |
| JP2012517446A (ja) | 2012-08-02 |
| CR20110421A (es) | 2011-12-08 |
| KR20110117706A (ko) | 2011-10-27 |
| SG172982A1 (en) | 2011-08-29 |
| MX2011008450A (es) | 2011-09-01 |
| AU2010213794A1 (en) | 2011-09-01 |
| ZA201105323B (en) | 2012-03-28 |
| CA2749960A1 (en) | 2010-08-19 |
| BRPI1008060A2 (pt) | 2015-08-25 |
| CO6400170A2 (es) | 2012-03-15 |
| RU2011137454A (ru) | 2013-03-20 |
| US20100216762A1 (en) | 2010-08-26 |
| ECSP11011243A (es) | 2011-09-30 |
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