PE20142400A1 - Compuestos novedosos - Google Patents
Compuestos novedososInfo
- Publication number
- PE20142400A1 PE20142400A1 PE2014001780A PE2014001780A PE20142400A1 PE 20142400 A1 PE20142400 A1 PE 20142400A1 PE 2014001780 A PE2014001780 A PE 2014001780A PE 2014001780 A PE2014001780 A PE 2014001780A PE 20142400 A1 PE20142400 A1 PE 20142400A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- chr10
- methylpropyl
- dimethylphenyl
- sulfonamide
- Prior art date
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- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/10—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by doubly bound oxygen or sulphur atoms
- C07D295/112—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by doubly bound oxygen or sulphur atoms with the ring nitrogen atoms and the doubly bound oxygen or sulfur atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
- C07D295/116—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by doubly bound oxygen or sulphur atoms with the ring nitrogen atoms and the doubly bound oxygen or sulfur atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings with the doubly bound oxygen or sulfur atoms directly attached to a carbocyclic ring
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- C07C311/30—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/37—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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- C07C317/22—Sulfones; Sulfoxides having sulfone or sulfoxide groups and singly-bound oxygen atoms bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
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- C07D305/04—Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D305/06—Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring atoms
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- C07D305/04—Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D305/08—Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring atoms
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- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen 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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Abstract
SE REFIERE A UN COMPUESTO DE FORMULA (IA), DONDE R1 SE SELECCIONA DE H, ALQUILO C1-C3, ENTRE OTROS; R2, R3 Y R4 SON H; R5 ES ALQUILO C1-C3; R6 ES ALQUILO C3-C5, -CH2-CICLOALQUILO C3-C4; R7 SE SELCCIONA DE LA FORMULA (II) Y (III); R8 ES HALO, ALQUILO C1-C6, ALCOXI C1-C6, CICLOALQUILO C3-C6, ENTRE OTROS; R9 ES EL GRUPO -(CHR10)S-(X)T-(CHR10)U-R11; R10 ES H, CH3, OH, ENTRE OTROS; X ES CH2, NH, O; R11 ES HETEROCICLOALQUILO; R ES 0-2; S ES 0-2; T ES 0-1; U ES 0-2. SON COMPUESTOS PREFERIDOS N-(2,4-DIMETILFENIL)-N-(2-METILPROPIL)-3-[(OXAN-4-ILMETOXI) METIL] BENCENO-1-SULFONAMIDA; N-(2,4-DIMETILFENIL)-N-(2-METILPROPIL)-4-[2-(MORFOLIN-4-IL) ETOXI] BENCENO-1-SULFONAMIDA; ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA QUE ES UTIL EN EL TRATAMIENTO DE ENFERMEDADES INFLAMATORIAS, METABOLICAS Y AUTOINMUNITARIAS MEDIADAS RECEPTOR HUERFANO RETINOIDEO GAMMA (RORY).
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| EP2928863A1 (en) * | 2012-12-10 | 2015-10-14 | F. Hoffmann-La Roche AG | BENZYL SULFONAMIDE DERIVATIVES AS RORc MODULATORS |
| CA2893638A1 (en) * | 2012-12-10 | 2014-06-19 | F. Hoffmann-La Roche Ag | Benzyl sulfonamide derivatives as rorc modulators |
| ES2845473T3 (es) | 2013-03-14 | 2021-07-26 | Boehringer Ingelheim Int | (Bencil-ciano-metil)-amidas sustituidas de ácido 2-aza-biciclo[2.2.1]heptano-3-carboxílico inhibidores de la catepsina- C |
| AU2014340107B2 (en) * | 2013-10-25 | 2017-08-31 | Glaxosmithkline Llc | Novel compounds |
| CN104530014B (zh) * | 2013-12-25 | 2018-03-20 | 中国科学院广州生物医药与健康研究院 | 2‑氧代‑1,2‑二氢苯并[cd]吲哚‑6‑磺酰胺类化合物及其组合物和应用 |
| JP6466461B2 (ja) | 2014-02-03 | 2019-02-06 | ヴァイティー ファーマシューティカルズ,インコーポレイテッド | Rorガンマのジヒドロピロロピリジン阻害剤 |
| CA2949229A1 (en) * | 2014-05-23 | 2015-11-26 | F. Hoffmann-La Roche Ag | Benzene sulfonamide derivatives and their use as rorc modulators |
| CA2950220A1 (en) | 2014-05-28 | 2015-12-03 | Glaxosmithkline Intellectual Property Development Limited | Novel compounds |
| KR20170012389A (ko) | 2014-05-28 | 2017-02-02 | 글락소스미스클라인 인털렉츄얼 프로퍼티 디벨로프먼트 리미티드 | 신규 화합물 |
| CN107001342B (zh) | 2014-05-28 | 2020-02-07 | 葛兰素史密斯克莱知识产权发展有限公司 | 新化合物 |
| US10105373B2 (en) | 2014-06-25 | 2018-10-23 | Piramal Enterprises Limited | Fused triterpene compounds and uses thereof |
| MX367316B (es) | 2014-09-12 | 2019-08-15 | Boehringer Ingelheim Int | Inhibidores espirociclicos de catepsina c. |
| DK3207043T6 (da) | 2014-10-14 | 2020-01-20 | Vitae Pharmaceuticals Llc | Dihydropyrrolopyridin-inhibitorer af ror-gamma |
| US9663515B2 (en) | 2014-11-05 | 2017-05-30 | Vitae Pharmaceuticals, Inc. | Dihydropyrrolopyridine inhibitors of ROR-gamma |
| US9845308B2 (en) | 2014-11-05 | 2017-12-19 | Vitae Pharmaceuticals, Inc. | Isoindoline inhibitors of ROR-gamma |
| FR3030516B1 (fr) | 2014-12-19 | 2019-12-27 | Galderma Research & Development | Derives sulfonamides bicycles en tant qu'agonistes inverses du recepteur gamma orphelin associe aux retinoides ror gamma (t) |
| FR3030518B1 (fr) * | 2014-12-19 | 2018-03-23 | Galderma Research & Development | Derives sulfonamides en tant qu'agonistes inverses du recepteur gamma orphelin associe aux retinoides ror gamma (t) |
| EP3268087A4 (en) | 2015-03-12 | 2018-08-29 | The Regents of the University of California | METHODS FOR TREATING CANCER WITH RORgamma INHIBITORS |
| EP3331876B1 (en) | 2015-08-05 | 2020-10-07 | Vitae Pharmaceuticals, LLC | Modulators of ror-gamma |
| MX385332B (es) | 2015-11-20 | 2025-03-18 | Vitae Pharmaceuticals Llc | Moduladores de ror-gamma. |
| TW202220968A (zh) | 2016-01-29 | 2022-06-01 | 美商維它藥物有限責任公司 | ROR-γ調節劑 |
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| FR3063079B1 (fr) | 2017-02-17 | 2019-03-22 | Galderma Research & Development | Derives sulfonamides hydroxyles en tant qu'agonistes inverses du recepteur gamma orphelin associe aux retinoides ror gamma (t) |
| FR3065000A1 (fr) | 2017-04-06 | 2018-10-12 | Galderma Research & Development | Derives pyrazoles en tant qu'agonistes inverses du recepteur gamma orphelin associe aux retinoides ror gamma (t) |
| CN109111418B (zh) * | 2017-06-23 | 2022-10-11 | 江苏柯菲平医药股份有限公司 | 一类2,3-二氢-1H-茚-4-磺酰胺RORγ调节剂及其用途 |
| UA126583C2 (uk) | 2017-07-24 | 2022-11-02 | Вітае Фармасьютікалс, Ллс | ІНГІБІТОРИ ROR<font face="Symbol">g</font> |
| WO2019018975A1 (en) | 2017-07-24 | 2019-01-31 | Vitae Pharmaceuticals, Inc. | INHIBITORS OF ROR GAMMA |
| CN110945002B (zh) | 2017-08-01 | 2021-12-24 | 正大天晴药业集团股份有限公司 | 作为RORγ抑制剂的双环化合物 |
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| CN109896998B (zh) * | 2017-12-10 | 2022-06-07 | 复旦大学 | 一种3,4-二氢异喹啉磺酰胺类化合物及其应用 |
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| US20250248980A1 (en) * | 2022-04-01 | 2025-08-07 | President And Fellows Of Harvard College | Immune modulatory agents |
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| JP6182594B2 (ja) | 2017-08-16 |
| AU2013254657B2 (en) | 2015-12-24 |
| TWI593678B (zh) | 2017-08-01 |
| MX2014012989A (es) | 2015-01-22 |
| EA201491973A1 (ru) | 2015-02-27 |
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