JP2016526571A5 - - Google Patents

Download PDF

Info

Publication number
JP2016526571A5
JP2016526571A5 JP2016525409A JP2016525409A JP2016526571A5 JP 2016526571 A5 JP2016526571 A5 JP 2016526571A5 JP 2016525409 A JP2016525409 A JP 2016525409A JP 2016525409 A JP2016525409 A JP 2016525409A JP 2016526571 A5 JP2016526571 A5 JP 2016526571A5
Authority
JP
Japan
Prior art keywords
och
acceptable salt
pharmaceutically acceptable
pain
compound
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2016525409A
Other languages
English (en)
Japanese (ja)
Other versions
JP6605462B2 (ja
JP2016526571A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2014/045675 external-priority patent/WO2015006280A1/en
Publication of JP2016526571A publication Critical patent/JP2016526571A/ja
Publication of JP2016526571A5 publication Critical patent/JP2016526571A5/ja
Application granted granted Critical
Publication of JP6605462B2 publication Critical patent/JP6605462B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2016525409A 2013-07-10 2014-07-08 イオンチャネルのモジュレーターとしての縮合ピペリジンアミド Active JP6605462B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201361844499P 2013-07-10 2013-07-10
US61/844,499 2013-07-10
PCT/US2014/045675 WO2015006280A1 (en) 2013-07-10 2014-07-08 Fused piperidine amides as modulators of ion channels

Publications (3)

Publication Number Publication Date
JP2016526571A JP2016526571A (ja) 2016-09-05
JP2016526571A5 true JP2016526571A5 (cg-RX-API-DMAC7.html) 2017-08-17
JP6605462B2 JP6605462B2 (ja) 2019-11-13

Family

ID=51230209

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2016525409A Active JP6605462B2 (ja) 2013-07-10 2014-07-08 イオンチャネルのモジュレーターとしての縮合ピペリジンアミド

Country Status (13)

Country Link
US (1) US10233191B2 (cg-RX-API-DMAC7.html)
EP (1) EP3019478B1 (cg-RX-API-DMAC7.html)
JP (1) JP6605462B2 (cg-RX-API-DMAC7.html)
KR (1) KR102306951B1 (cg-RX-API-DMAC7.html)
CN (1) CN105473554B (cg-RX-API-DMAC7.html)
AU (1) AU2014287471C1 (cg-RX-API-DMAC7.html)
CA (1) CA2917198C (cg-RX-API-DMAC7.html)
ES (1) ES2780699T3 (cg-RX-API-DMAC7.html)
IL (1) IL243495B (cg-RX-API-DMAC7.html)
MX (1) MX368728B (cg-RX-API-DMAC7.html)
RU (1) RU2741810C2 (cg-RX-API-DMAC7.html)
SG (1) SG11201600082VA (cg-RX-API-DMAC7.html)
WO (1) WO2015006280A1 (cg-RX-API-DMAC7.html)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EA201891313A1 (ru) 2015-12-18 2018-11-30 Мерк Шарп И Доум Корп. Замещенные гидроксиалкиламинами и гидроксициклоалкиламинами соединения диаминарилсульфонамидов с избирательной активностью в потенциалзависимых натриевых каналах
KR102079844B1 (ko) * 2016-09-20 2020-02-20 가톨릭대학교 산학협력단 담석 용해제를 포함하는 담낭 질환 치료용 약학 조성물
JP6890179B2 (ja) * 2016-12-02 2021-06-18 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft 二環式アミド化合物及びその使用方法
CN110291383B (zh) * 2017-02-23 2021-12-28 株式会社Ihi Oh自由基检测探测器、oh自由基测定装置以及oh自由基测定方法
AU2018300043B2 (en) 2017-07-14 2021-04-01 F. Hoffmann-La Roche Ag Bicyclic ketone compounds and methods of use thereof
CN109574927A (zh) * 2017-09-29 2019-04-05 浙江海正药业股份有限公司 N-(取代磺酰基)苯甲酰胺类衍生物及其制备方法和医药用途
MA50503A (fr) 2017-10-31 2020-09-09 Hoffmann La Roche Sulfones et sulfoxydes bicycliques et procédés d'utilisation associés
KR102812440B1 (ko) * 2018-09-10 2025-05-26 가껭세이야꾸가부시기가이샤 신규한 헤테로방향족 아미드 유도체 및 이를 함유하는 약제
TW202043229A (zh) 2019-01-11 2020-12-01 瑞士商赫孚孟拉羅股份公司 雙環酮化合物及其使用方法
TWI794742B (zh) 2020-02-18 2023-03-01 美商基利科學股份有限公司 抗病毒化合物
TWI775313B (zh) 2020-02-18 2022-08-21 美商基利科學股份有限公司 抗病毒化合物
KR20250133471A (ko) 2020-02-18 2025-09-05 길리애드 사이언시즈, 인코포레이티드 항바이러스 화합물
CA3216162A1 (en) 2021-04-16 2022-10-20 Gilead Sciences, Inc. Methods of preparing carbanucleosides using amides
UY39881A (es) 2021-08-02 2023-06-15 Eurofarma Laboratorios S A “COMPUESTOS N-ACILHIDRAZÓNICOS INHIBIDORES DE Nav 1.7 Y/O Nav 1.8, SUS PROCESOS DE OBTENCIÓN, COMPOSICIONES, USOS, MÉTODOS DE TRATAMIENTO DE ESTOS Y KITS”
UY39882A (es) 2021-08-02 2023-06-15 Eurofarma Laboratorios S A COMPUESTOS NACILHIDRAZÓNICOS INHIBIDORES DE Nav 1.7 Y/O Nav 1.8, SUS PROCESOS DE OBTENCIÓN, COMPOSICIONES, USOS, MÉTODOS DE TRATAMIENTO DE ESTOS Y KITS
WO2023023527A1 (en) 2021-08-18 2023-02-23 Gilead Sciences, Inc. Phospholipid compounds and methods of making and using the same
AR131658A1 (es) 2023-01-30 2025-04-16 Eurofarma Laboratorios S A Hidrazidas bloqueadoras de nav 1.7 y/o nav 1.8, sus procesos de obtención, composiciones, usos, métodos de tratamiento de los mismos y sus kits
EP4660184A1 (en) 2023-01-30 2025-12-10 Eurofarma Laboratórios S.A. Nav1.7- and/or nav1.8-inhibiting hydroxamates, processes for the preparation thereof, compositions, uses, methods for treatment using same, and kits
AR131690A1 (es) 2023-01-30 2025-04-23 Eurofarma Laboratorios S A COMPUESTOS FENÓLICOS BLOQUEADORES DE Nav 1.7 Y/O Nav 1.8, SUS PROCESOS DE OBTENCIÓN, SUS COMPOSICIONES, SUS USOS, LOS MÉTODOS DE TRATAMIENTO DE LOS MISMOS Y LOS KITS
AR131715A1 (es) 2023-01-30 2025-04-23 Eurofarma Laboratorios S A AMIDAS BLOQUEADORAS DE Nav 1.7 Y/O Nav 1.8, SUS PROCESOS DE OBTENCIÓN, COMPOSICIONES, USOS, MÉTODOS DE TRATAMIENTO DE LOS MISMOS Y KITS
WO2024159285A1 (pt) 2023-01-30 2024-08-08 Eurofarma Laboratórios S.A. Compostos aril piridinas bloqueadores de nav 1.7 e/ou nav 1.8, seus processos de obtenção, composições, usos, métodos de tratamento destes e kits
CN119285621B (zh) * 2024-12-13 2025-07-18 嘉兴安帝康生物科技有限公司 作为钠通道调节剂的四氢呋喃甲酰胺类化合物及其在医药上的应用

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3549641A (en) * 1966-06-28 1970-12-22 Warner Lambert Pharmaceutical Pyrano pyridines and process for their production
SE7509022L (sv) 1974-09-09 1976-03-10 Du Pont Foreningar med analgetisk verkan
US4301290A (en) * 1975-12-16 1981-11-17 Sandoz Ltd. Organic compounds
DE2655150A1 (de) 1975-12-16 1977-06-23 Sandoz Ag Neue organische verbindungen, ihre herstellung und verwendung
BG30927A3 (bg) * 1977-12-27 1981-09-15 Eli Lilly And Company Метод за получаване на транс-4-алфа-фенил-октахидро-1н-2 пиридини
DE2907461A1 (de) * 1978-03-10 1979-09-20 Sandoz Ag Isochinolinderivate, ihre herstellung und diese enthaltende pharmazeutische zubereitungen
DE4427648A1 (de) 1994-08-04 1996-02-08 Basf Ag N-Stubstituierte 3-Azabicyclo[3,2,0,]heptan-Derivate, ihre Herstellung und Verwendung
DE4341402A1 (de) 1993-12-04 1995-06-08 Basf Ag N-substituierte Azabicycloheptan-Derivate, ihre Herstellung und Verwendung
JP2003327534A (ja) * 1999-11-30 2003-11-19 Toray Ind Inc 頻尿若しくは尿失禁の治療又は予防剤
RU2006106710A (ru) * 2003-08-05 2007-09-20 Вертекс Фармасьютикалз Инкорпорейтед (Us) Конденсированные пиримидиновые соединения в качестве ингибиторов потенциалозависимых ионных каналов
WO2008130319A2 (en) * 2007-04-23 2008-10-30 Astrazeneca Ab Novel n-tetrahydronaphtalene or n-chromane carboxamide derivatives for the treatment of pain
WO2009005459A1 (en) * 2007-06-29 2009-01-08 Astrazeneca Ab Phenyl-1,2, 3,4-tetrahydroisoquinolinone derivatives and their use in the treatment of a pain disorder
WO2010151595A1 (en) * 2009-06-26 2010-12-29 Schering Corporation Pyrrolo-benzo-1,4-diazines useful as sodium channel blockers
WO2011050200A1 (en) * 2009-10-23 2011-04-28 Janssen Pharmaceutica Nv Fused heterocyclic compounds as orexin receptor modulators
PL2670752T3 (pl) * 2011-02-02 2016-09-30 Pirolopirazynowe spirocykliczne piperydynoamidy jako modulatory kanałów jonowych

Similar Documents

Publication Publication Date Title
JP2016526571A5 (cg-RX-API-DMAC7.html)
JP2014508169A5 (cg-RX-API-DMAC7.html)
JP2014508756A5 (cg-RX-API-DMAC7.html)
JP2014504642A5 (cg-RX-API-DMAC7.html)
RU2563030C2 (ru) Сульфонамидные соединения, обладающие антагонистической активностью в отношении trpm8
JP6866967B2 (ja) サイクリン依存性キナーゼcdk9の新規阻害剤
RU2016151727A (ru) Нейроактивные стероиды, композиции и их применения
CA2739739C (en) Sulfoximine-substituted anilino-pyrimidine derivatives as cdk inhibitors, production and use thereof as medicinal products
RU2506261C2 (ru) Производные хиназолина
RU2016104080A (ru) Амиды конденсированного пиперидина в качестве модуляторов ионных каналов
JP2007520504A5 (cg-RX-API-DMAC7.html)
ES2824801T3 (es) Sal de compuesto heterocíclico sustituido con halógeno
KR20100016076A (ko) 신규 피롤리논 유도체 및 그것을 함유하는 의약 조성물
EP4196228A1 (en) N-cyclyl-sulfonamides useful for inhibiting raf
JP7675020B2 (ja) Bax阻害剤およびその使用
CN102134218A (zh) 6-芳氨基吡啶酮磺酰胺和6-芳氨基吡嗪酮磺酰胺mek抑制剂
CA3191829A1 (en) Cd73 inhibitor and application thereof in medicine
JP2020534373A (ja) キナーゼ阻害剤としての環状イミノピリミジン誘導体
CN114349738A (zh) 一类靶向降解cdk2的小分子缀合物及其应用
KR20200073265A (ko) 함질소 6원환 화합물
DE102009015070A1 (de) Aminocabonylamino-substituierte Anilino-Pyrimidinderivate als Tyk-Inhibitoren, deren Herstellung und Verwendung als Arzneimittel
RU2005135850A (ru) Замещенные изохромановые соединения для лечения метаболических расстройств, рака и другие заболеваний
DE102009001438A1 (de) Carbonylamino-substituierte Anilino-Pyrimidinderivate als Tyk-Inhibitoren, deren Herstellung und Verwendung als Arzneimittel
JP6100755B2 (ja) (2−ヘテロアリールアミノ)コハク酸誘導体
CN104119332B (zh) 作为蛋白激酶抑制剂的苯并杂环化合物及其制备方法和用途