JP2016532716A5 - - Google Patents

Download PDF

Info

Publication number
JP2016532716A5
JP2016532716A5 JP2016540921A JP2016540921A JP2016532716A5 JP 2016532716 A5 JP2016532716 A5 JP 2016532716A5 JP 2016540921 A JP2016540921 A JP 2016540921A JP 2016540921 A JP2016540921 A JP 2016540921A JP 2016532716 A5 JP2016532716 A5 JP 2016532716A5
Authority
JP
Japan
Prior art keywords
chloro
propyl
phenoxy
fluoro
phenyl
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
JP2016540921A
Other languages
English (en)
Japanese (ja)
Other versions
JP2016532716A (ja
JP6445565B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2014/054764 external-priority patent/WO2015038533A2/en
Publication of JP2016532716A publication Critical patent/JP2016532716A/ja
Publication of JP2016532716A5 publication Critical patent/JP2016532716A5/ja
Application granted granted Critical
Publication of JP6445565B2 publication Critical patent/JP6445565B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2016540921A 2013-09-10 2014-09-09 とう痛及び糖尿病の治療用ナトリウムチャネル調節物質 Active JP6445565B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201361876046P 2013-09-10 2013-09-10
US61/876,046 2013-09-10
PCT/US2014/054764 WO2015038533A2 (en) 2013-09-10 2014-09-09 Sodium channel modulators for the treatment of pain and diabetes

Publications (3)

Publication Number Publication Date
JP2016532716A JP2016532716A (ja) 2016-10-20
JP2016532716A5 true JP2016532716A5 (en:Method) 2017-10-19
JP6445565B2 JP6445565B2 (ja) 2018-12-26

Family

ID=52666496

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2016540921A Active JP6445565B2 (ja) 2013-09-10 2014-09-09 とう痛及び糖尿病の治療用ナトリウムチャネル調節物質

Country Status (18)

Country Link
US (2) US20160221974A1 (en:Method)
EP (1) EP3043787B1 (en:Method)
JP (1) JP6445565B2 (en:Method)
KR (1) KR20160054570A (en:Method)
CN (1) CN105611923B (en:Method)
AU (1) AU2014318979B2 (en:Method)
BR (1) BR112016005271A2 (en:Method)
CA (1) CA2922851C (en:Method)
ES (1) ES2687598T3 (en:Method)
IL (1) IL244506B (en:Method)
MX (1) MX2016002881A (en:Method)
MY (1) MY181928A (en:Method)
PH (1) PH12016500296A1 (en:Method)
RU (1) RU2016113156A (en:Method)
SG (2) SG11201601367QA (en:Method)
UA (1) UA120353C2 (en:Method)
WO (1) WO2015038533A2 (en:Method)
ZA (1) ZA201702410B (en:Method)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105188694B (zh) * 2013-03-15 2018-07-31 卓莫赛尔公司 用于治疗疼痛的钠通道调节剂
CN105611923B (zh) 2013-09-10 2019-08-23 卓莫赛尔公司 用于治疗疼痛和糖尿病的钠通道调节剂
JP2017527573A (ja) * 2014-09-09 2017-09-21 クロモセル コーポレーション 糖尿病の治療用の選択的NaV1.7阻害剤
AU2016370554B2 (en) 2015-12-18 2018-11-29 Merck Sharp & Dohme Corp. Hydroxyalkylamine- and hydroxycycloalkylamine-substituted diamine-arylsulfonamide compounds with selective activity in voltage-gated sodium channels
ES3022639T3 (en) 2016-05-20 2025-05-28 Xenon Pharmaceuticals Inc Benzenesulfonamide compounds and their use as therapeutic agents
CN105924670A (zh) * 2016-06-02 2016-09-07 扬州兰都塑料科技有限公司 一种电力电缆用耐磨剂
CN105924843A (zh) * 2016-06-02 2016-09-07 扬州兰都塑料科技有限公司 一种耐刮擦的电力电缆
CN106084535A (zh) * 2016-06-02 2016-11-09 扬州兰都塑料科技有限公司 一种耐刮擦的电力电缆的制备方法
SG10201912372XA (en) 2016-12-09 2020-02-27 Xenon Pharmaceuticals Inc Benzenesulfonamide compounds and their use as therapeutic agents
CN106892845B (zh) * 2017-02-28 2018-10-30 四川同晟生物医药有限公司 一种2,4-二氨基丁酸衍生物及其制备方法
WO2019200369A1 (en) * 2018-04-13 2019-10-17 Chromocell Corporation Compounds and methods of using compounds for the prevention or treatment of peripheral nerve damage
WO2019217822A1 (en) * 2018-05-11 2019-11-14 Chromocell Corporation Compounds and methods of using compounds for the prevention or treatment of inflammatory conditions
EP3807281A1 (en) 2018-06-13 2021-04-21 Xenon Pharmaceuticals Inc. Benzenesulfonamide compounds and their use as therapeutic agents
PE20211066A1 (es) 2018-08-31 2021-06-09 Xenon Pharmaceuticals Inc Compuestos de sulfonamida sustituidos con heteroarilo y su uso como agentes terapeuticos
US10752623B2 (en) 2018-08-31 2020-08-25 Xenon Pharmaceuticals Inc. Heteroaryl-substituted sulfonamide compounds and their use as sodium channel inhibitors
CN113527281B (zh) * 2020-04-20 2023-12-22 昆山彭济凯丰生物科技有限公司 杂环化合物及其制备方法和应用

Family Cites Families (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5356897A (en) 1991-09-09 1994-10-18 Fujisawa Pharmaceutical Co., Ltd. 3-(heteroaryl)-pyrazololi[1,5-a]pyrimidines
HUP0401211A3 (en) * 2001-03-14 2008-03-28 Gruenenthal Gmbh Substituted pyrazoles pyrazolopyrimidines and thiazolopyrimidines, process for their preparation, their use and pharmaceutical compositions containg them
US7659082B2 (en) 2002-02-19 2010-02-09 Xenon Pharmaceuticals Inc. Methods for identifying analgesic agents
BR0312023A (pt) 2002-06-27 2005-03-22 Novo Nordisk As Composto, composto ativador da glicose cinase, método para evitar a hipoglicemia, uso de um composto, e, composição farmacêutica
GB0324792D0 (en) 2003-10-23 2003-11-26 Sterix Ltd Compound
EP1689719A1 (en) 2003-11-25 2006-08-16 Eli Lilly And Company 7-phenyl-isoquinoline-5-sulfonylamino derivatives as inhibitors of akt (proteinkinase b)
CA2564355C (en) 2004-05-07 2012-07-03 Amgen Inc. Protein kinase modulators and method of use
CA2574600C (en) * 2004-07-23 2010-08-31 Pfizer Inc. Pyridine derivatives
US20090093485A1 (en) 2004-10-29 2009-04-09 Astrazeneca Ab Novel Sulphonamide Derivatives as Glucocorticoid Receptor Modulators for the Treatment of Inflammatory Diseases
SG170767A1 (en) * 2005-12-23 2011-05-30 Zealand Pharma As Modified lysine-mimetic compounds
TW200838539A (en) * 2007-02-05 2008-10-01 Xenon Pharmaceuticals Inc Pyridopyrimidinone compounds useful in treating sodium channel-mediated diseases or conditions
EP2173743A2 (en) 2007-07-13 2010-04-14 Icagen, Inc. Sodium channel inhibitors
CA2694748A1 (en) 2007-07-13 2009-01-22 Icagen, Inc. Sodium channel inhibitors
CN102348697B (zh) 2009-01-12 2014-12-10 辉瑞股份有限公司 磺酰胺衍生物
JP5685203B2 (ja) 2009-05-29 2015-03-18 ラクオリア創薬株式会社 カルシウムチャネル遮断薬またはナトリウムチャネル遮断薬としてのアリール置換カルボキサミド誘導体
US8895608B2 (en) 2010-04-23 2014-11-25 Kineta, Inc. Sulfonamide anti-viral compounds
ES2533065T3 (es) * 2010-07-09 2015-04-07 Pfizer Limited Bencenosulfonamidas útiles como inhibidores de los canales de sodio
WO2012004706A2 (en) 2010-07-09 2012-01-12 Pfizer Limited Chemical compounds
JP5860045B2 (ja) 2010-07-09 2016-02-16 ファイザー・リミテッドPfizer Limited 化合物
ES2532357T3 (es) 2010-07-12 2015-03-26 Pfizer Limited Derivados de sulfonamida como inhibidores de Nav1.7 para el tratamiento del dolor
EP2665822A1 (en) 2011-01-18 2013-11-27 Amgen Inc. Nav1.7 knockout mice and uses thereof
TWI549944B (zh) * 2011-07-01 2016-09-21 吉李德科學股份有限公司 作為離子通道調節劑之稠合雜環化合物
EP2744805A1 (en) 2011-08-17 2014-06-25 Amgen Inc. Heteroaryl sodium channel inhibitors
JP2014531454A (ja) * 2011-09-21 2014-11-27 ギリアード サイエンシーズ, インコーポレイテッド グルカゴン分泌を減少させるナトリウムチャネルブロッカー
MX2014005304A (es) 2011-10-31 2015-03-20 Xenon Pharmaceuticals Inc Biaril eter sulfonamidas y su uso como agentes terapeuticos.
CA2890897A1 (en) 2012-11-14 2014-05-22 The Board Of Regents Of The University Of Texas System Inhibition of hif-2.alpha. heterodimerization with hif 1.beta. (arnt)
CN105188694B (zh) * 2013-03-15 2018-07-31 卓莫赛尔公司 用于治疗疼痛的钠通道调节剂
ES2784454T3 (es) 2013-09-09 2020-09-25 Peloton Therapeutics Inc Aril éteres y usos de los mismos
CN105611923B (zh) 2013-09-10 2019-08-23 卓莫赛尔公司 用于治疗疼痛和糖尿病的钠通道调节剂
JP2017527573A (ja) * 2014-09-09 2017-09-21 クロモセル コーポレーション 糖尿病の治療用の選択的NaV1.7阻害剤

Similar Documents

Publication Publication Date Title
JP2016532716A5 (en:Method)
RU2016113156A (ru) Модуляторы натриевого канала для лечения боли и диабета
Pea et al. Pharmacokinetic considerations for antimicrobial therapy in patients receiving renal replacement therapy
JP2016512844A5 (en:Method)
JP2010534647A5 (en:Method)
JP2018518537A5 (en:Method)
EP2433650A3 (en) Administration of anti-CD3 antibodies in the treatment of autoimmune diseases
FI3597646T3 (fi) Hi-virusinfektion profylaktiseen tai terapeuttiseen hoitoon käyttökelpoisia terapeuttisia yhdisteitä
JP2016525122A5 (en:Method)
JP2013500977A5 (en:Method)
JP2015513544A5 (en:Method)
EP2141155A4 (en) PROPHYLACTIC AND / OR THERAPEUTIC AGENT AGAINST HYPERLIPEMY
JP2019529541A5 (en:Method)
FI3681857T3 (fi) Fluorifenyyli-beeta-hydroksietyyliamiineja ja niiden käyttö hyperglykaemian hoidossa
JP2008532974A5 (en:Method)
JP2013530974A5 (en:Method)
NO20076425L (no) Fremgangsmater for behandling av drug-resistent cancer
BRPI0911197A2 (pt) composto, ativador de receptor ativado pelo proliferador de peroxissoma, e, medicamento para o tratamento e /ou profilaxia de uma doença.
FI3229828T3 (fi) Glargiini-insuliinin/liksisenatidin vakiosuhteinen formulaatio
HRP20150049T1 (hr) Derivati oksazolil-metiletera kao agonisti alx-receptora
RU2016114098A (ru) Новое производное аналога инсулина
WO2018005801A3 (en) Novel non-systemic tgr5 agonists
WO2010044581A2 (ko) N1-벤조[1,3]다이옥솔-5-일메틸-n2-치환된 바이구아나이드 유도체, 이의 제조방법 및 이를 함유하는 약학 조성물
EP4545142A3 (en) 5-[[4-[2-[5-(1-hydroxyethyl)pyridin-2-yl]ethoxy]phenyl]methyl]-1,3-thiazolidine-2,4-dione and its salts for use in the treatment of mitochondrial diseases
JP2018513193A5 (en:Method)