JP2016532715A5 - - Google Patents

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Publication number
JP2016532715A5
JP2016532715A5 JP2016540455A JP2016540455A JP2016532715A5 JP 2016532715 A5 JP2016532715 A5 JP 2016532715A5 JP 2016540455 A JP2016540455 A JP 2016540455A JP 2016540455 A JP2016540455 A JP 2016540455A JP 2016532715 A5 JP2016532715 A5 JP 2016532715A5
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JP
Japan
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optionally substituted
bicyclic
alkyl
monocyclic
membered
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JP2016540455A
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Japanese (ja)
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JP2016532715A (ja
JP6407285B2 (ja
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Priority claimed from PCT/US2014/054489 external-priority patent/WO2015035278A1/en
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Publication of JP2016532715A5 publication Critical patent/JP2016532715A5/ja
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Expired - Fee Related legal-status Critical Current
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JP2016540455A 2013-09-09 2014-09-08 RORγ調節因子 Expired - Fee Related JP6407285B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201361875220P 2013-09-09 2013-09-09
US61/875,220 2013-09-09
PCT/US2014/054489 WO2015035278A1 (en) 2013-09-09 2014-09-08 RORγ MODULATORS

Publications (3)

Publication Number Publication Date
JP2016532715A JP2016532715A (ja) 2016-10-20
JP2016532715A5 true JP2016532715A5 (enExample) 2017-10-19
JP6407285B2 JP6407285B2 (ja) 2018-10-17

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ID=51541401

Family Applications (1)

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JP2016540455A Expired - Fee Related JP6407285B2 (ja) 2013-09-09 2014-09-08 RORγ調節因子

Country Status (5)

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US (1) US9663469B2 (enExample)
EP (1) EP3044219A1 (enExample)
JP (1) JP6407285B2 (enExample)
CN (1) CN105705501B (enExample)
WO (1) WO2015035278A1 (enExample)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6407285B2 (ja) 2013-09-09 2018-10-17 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company RORγ調節因子
JP6397488B2 (ja) 2013-09-20 2018-09-26 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company RORγ調節因子
WO2015103508A1 (en) 2014-01-06 2015-07-09 Bristol-Myers Squibb Company CARBOCYCLIC SULFONE RORγ MODULATORS
ES2704460T3 (es) 2014-01-06 2019-03-18 Bristol Myers Squibb Co Moduladores de ROR gamma de ciclohexilsulfona
JP6476205B2 (ja) 2014-01-06 2019-02-27 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company RORγ修飾因子としてのヘテロ環式スルホン
HRP20200016T1 (hr) 2014-10-30 2020-03-20 Janssen Pharmaceutica Nv Amidno supstituirani tiazoli kao modulatori rorgamat
TWI705057B (zh) 2014-10-30 2020-09-21 比利時商健生藥品公司 用作RORγt調節劑之三氟甲基醇
EP3212641B1 (en) 2014-10-30 2018-12-05 Janssen Pharmaceutica NV Thiazoles as modulators of roryt
AR104555A1 (es) 2015-05-07 2017-07-26 Bristol Myers Squibb Co SULFONAS TRICÍCLICAS COMO MODULARES DE RORg
AU2016276947A1 (en) * 2015-06-11 2017-12-14 Lycera Corporation Aryl dihydro-2h-benzo[b][1,4]oxazine sulfonamide and related compounds for use as agonists of RORy and the treatment of disease
CN104892546B (zh) * 2015-07-01 2017-03-01 中国科学院南海海洋研究所 一类(2h)1,4‑苯并噻嗪类化合物及其制备方法和应用
JP6812059B2 (ja) * 2015-07-07 2021-01-13 塩野義製薬株式会社 TrkA阻害活性を有する複素環誘導体
TW201803869A (zh) 2016-04-27 2018-02-01 健生藥品公司 作為RORγT調節劑之6-胺基吡啶-3-基噻唑
HRP20250505T1 (hr) 2016-05-20 2025-06-20 Xenon Pharmaceuticals Inc. Spojevi benzensulfonamida i njihova uporaba za terapijska sredstva
WO2017213210A1 (ja) * 2016-06-10 2017-12-14 武田薬品工業株式会社 複素環化合物
ES2967410T3 (es) 2016-12-09 2024-04-30 Xenon Pharmaceuticals Inc Compuestos de bencenosulfonamida y sus usos en forma de agentes terapéuticos
US10822318B2 (en) * 2017-05-24 2020-11-03 Regents Of The University Of Minnesota Lactone-based probes and methods of use thereof
JP2020142989A (ja) * 2017-06-21 2020-09-10 Meiji Seikaファルマ株式会社 イミダゾール誘導体及びそれを含有する医薬
KR20210060367A (ko) * 2018-03-12 2021-05-26 에스칼리에 바이오사이언시스, 비브이 스피로사이클릭 ror-감마 조절제
EP3765009A4 (en) 2018-03-12 2021-11-10 Escalier Biosciences, BV BICYCLIC ROR-GAMMA MODULATORS
CN112262142B (zh) 2018-06-13 2023-11-14 泽农医药公司 苯磺酰胺化合物及其作为治疗剂的用途
JP2021528398A (ja) 2018-06-18 2021-10-21 ヤンセン ファーマシューティカ エヌ.ベー. RORγTのモジュレーターとしての6−アミノピリジン−3−イルピラゾール
ES2929140T3 (es) 2018-06-18 2022-11-25 Janssen Pharmaceutica Nv Imidazoles sustituidos con fenilo y piridinilo como moduladores de RORgammat
JP2021528405A (ja) 2018-06-18 2021-10-21 ヤンセン ファーマシューティカ エヌ.ベー. RORγtのモジュレータとしてのアミド置換チアゾール
EP3807261B1 (en) 2018-06-18 2022-07-13 Janssen Pharmaceutica NV Pyridinyl pyrazoles as modulators of roryt
WO2020011086A1 (zh) * 2018-07-13 2020-01-16 四川科伦博泰生物医药股份有限公司 苯并二氮杂环类化合物、其制备方法及用途
MX2021001380A (es) 2018-08-31 2021-05-27 Xenon Pharmaceuticals Inc Compuestos de sulfonamida sustituidos con heteroarilo y su uso como agentes terapeuticos.
MA53488A (fr) 2018-08-31 2021-12-08 Xenon Pharmaceuticals Inc Composés de sulfonamide substitués par hétéroaryle et leur utilisation en tant qu'inhibiteurs de canaux sodiques

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ITMI20012060A1 (it) * 2001-10-05 2003-04-05 Recordati Chem Pharm Nuovi eterocilcli n-acilati
US7741317B2 (en) * 2005-10-21 2010-06-22 Bristol-Myers Squibb Company LXR modulators
EP2368886A1 (en) * 2010-03-01 2011-09-28 Phenex Pharmaceuticals AG Novel compounds for modulation of orphan nuclear receptor RAR-related orphan receptor-gamma (ROR gamma, NR1F3) activity and for the treatment of chronic inflammatory and autoimmune desease
WO2012064744A2 (en) 2010-11-08 2012-05-18 Lycera Corporation Tetrahydroquinoline and related bicyclic compounds for inhibition of rorϒ activity and the treatment of disease
WO2013064231A1 (en) * 2011-10-31 2013-05-10 Phenex Pharmaceuticals Ag SEVEN-MEMBERED SULFONAMIDES AS MODULATORS OF RAR-RELATED ORPHAN RECEPTOR-GAMMA (RORγ, NR1F3)
US9290476B2 (en) * 2012-10-16 2016-03-22 Janssen Pharmaceutica Nv Methylene linked quinolinyl modulators of RORγt
WO2014062938A1 (en) 2012-10-19 2014-04-24 Bristol-Myers Squibb Company Rory modulators
JP6407285B2 (ja) 2013-09-09 2018-10-17 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company RORγ調節因子
JP6397488B2 (ja) 2013-09-20 2018-09-26 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company RORγ調節因子
JP6476205B2 (ja) 2014-01-06 2019-02-27 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company RORγ修飾因子としてのヘテロ環式スルホン
EA030849B1 (ru) 2014-01-06 2018-10-31 Бристол-Маерс Сквибб Компани ПИРРОЛИДИНИЛСУЛЬФОНОВЫЕ МОДУЛЯТОРЫ RORγ
WO2015103508A1 (en) 2014-01-06 2015-07-09 Bristol-Myers Squibb Company CARBOCYCLIC SULFONE RORγ MODULATORS
ES2704460T3 (es) 2014-01-06 2019-03-18 Bristol Myers Squibb Co Moduladores de ROR gamma de ciclohexilsulfona

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