SG11201401032YA - (4-phenylimidazol-2-yl) ethylamine derivatives useful as sodium channel modulators - Google Patents

(4-phenylimidazol-2-yl) ethylamine derivatives useful as sodium channel modulators

Info

Publication number
SG11201401032YA
SG11201401032YA SG11201401032YA SG11201401032YA SG11201401032YA SG 11201401032Y A SG11201401032Y A SG 11201401032YA SG 11201401032Y A SG11201401032Y A SG 11201401032YA SG 11201401032Y A SG11201401032Y A SG 11201401032YA SG 11201401032Y A SG11201401032Y A SG 11201401032YA
Authority
SG
Singapore
Prior art keywords
phenylimidazol
sodium channel
derivatives useful
channel modulators
ethylamine derivatives
Prior art date
Application number
SG11201401032YA
Other languages
English (en)
Inventor
Sharanjeet Kaur Bagal
Mark Ian Kemp
Duncan Charles Miller
Yoshihisa Murata
Original Assignee
Pfizer Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=47278356&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SG11201401032Y(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Pfizer Ltd filed Critical Pfizer Ltd
Publication of SG11201401032YA publication Critical patent/SG11201401032YA/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/06Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
    • A61K31/41781,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Pain & Pain Management (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Rheumatology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
SG11201401032YA 2011-10-26 2012-10-15 (4-phenylimidazol-2-yl) ethylamine derivatives useful as sodium channel modulators SG11201401032YA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201161551628P 2011-10-26 2011-10-26
PCT/IB2012/055610 WO2013061205A2 (fr) 2011-10-26 2012-10-15 Composés chimiques

Publications (1)

Publication Number Publication Date
SG11201401032YA true SG11201401032YA (en) 2014-07-30

Family

ID=47278356

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11201401032YA SG11201401032YA (en) 2011-10-26 2012-10-15 (4-phenylimidazol-2-yl) ethylamine derivatives useful as sodium channel modulators

Country Status (28)

Country Link
US (1) US9079878B2 (fr)
EP (1) EP2771335A2 (fr)
JP (1) JP5946538B2 (fr)
KR (1) KR101586966B1 (fr)
CN (1) CN103906746B (fr)
AP (1) AP2014007579A0 (fr)
AU (1) AU2012328034B2 (fr)
BR (1) BR112014009102A2 (fr)
CA (1) CA2850925C (fr)
CL (1) CL2014000956A1 (fr)
CO (1) CO6940427A2 (fr)
CR (1) CR20140185A (fr)
CU (1) CU20140046A7 (fr)
DO (1) DOP2014000085A (fr)
EA (1) EA023375B1 (fr)
EC (1) ECSP14013324A (fr)
GT (1) GT201400079A (fr)
HK (1) HK1198650A1 (fr)
IL (1) IL232267A (fr)
MD (1) MD20140037A2 (fr)
MX (1) MX337469B (fr)
NI (1) NI201400031A (fr)
PE (1) PE20141682A1 (fr)
SG (1) SG11201401032YA (fr)
TN (1) TN2014000147A1 (fr)
UA (1) UA109220C2 (fr)
WO (1) WO2013061205A2 (fr)
ZA (1) ZA201402281B (fr)

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AP2016009287A0 (en) 2013-12-13 2016-06-30 Vertex Pharma Prodrugs of pyridone amides useful as modulators of sodium channels
KR102192572B1 (ko) 2014-06-09 2020-12-18 삼성전자주식회사 광원 모듈의 불량 검사방법, 광원 모듈의 제조 방법 및 광원 모듈 검사장치
EP3209303A1 (fr) * 2014-10-24 2017-08-30 Avectas Limited Administration à travers des membranes plasmiques de cellules
EP3258925B1 (fr) 2015-02-19 2023-03-29 Purdue Pharma LP Méthodes et compositions pour réduire la vidange gastrique
IS2977B (is) 2015-02-23 2017-07-15 Actavis Group Ptc Ehf. Aðferð til framleiðslu á milliefnum sem eru nytsamleg við nýsmíði á elúxadólíni
CN116676292A (zh) 2015-12-30 2023-09-01 阿维塔斯有限公司 基因编辑蛋白和组合物向细胞和组织的无载体递送
EP3481856A1 (fr) * 2016-07-06 2019-05-15 Crispr Therapeutics AG Matériaux et procédés de traitement de troubles liés à la douleur
CN109843914B (zh) 2016-07-06 2024-03-15 沃泰克斯药物股份有限公司 用于治疗疼痛相关病症的材料和方法
EP3625214B1 (fr) 2017-05-16 2022-07-06 Vertex Pharmaceuticals Incorporated Amides de pyridone deutérés et leurs promédicaments utilisés en tant que modulateurs de canaux sodiques
TW201920081A (zh) 2017-07-11 2019-06-01 美商維泰克斯製藥公司 作為鈉通道調節劑的羧醯胺
CA3091012A1 (fr) 2018-02-12 2019-08-15 Vertex Pharmaceuticals Incorporated Methode de traitement de la douleur
US20220110923A1 (en) 2019-01-10 2022-04-14 Vertex Pharmaceuticals Incorporated Esters and carbamates as modulators of sodium channels
US20230062053A1 (en) 2019-01-10 2023-03-02 Vertex Pharmaceuticals Incorporated Carboxamides as modulators of sodium channels
WO2020176763A1 (fr) 2019-02-27 2020-09-03 Vertex Pharmaceuticals Incorporated Forme posologique comprenant un promédicament inhibiteur de canal sodique na 1,8
WO2020219867A1 (fr) 2019-04-25 2020-10-29 Vertex Pharmaceuticals Incorporated Compositions de co-cristaux d'amide de pyridone pour le traitement de la douleur
CA3164134A1 (fr) 2019-12-06 2021-06-10 Vertex Pharmaceuticals Incorporated Tetrahydrofuranes substitues en tant que modulateurs de canaux sodiques
CA3222197A1 (fr) 2021-06-04 2022-12-08 Vertex Pharmaceuticals Incorporated Formes galeniques solides et schemas posologiques comprenant du (2r,3s,4s,5r)-4-[[3-(3,4-difluoro-2-methoxy-phenyl)-4,5-dimethyl-5-(trifluoromethyl)tetrahydrofuran-2-carbonyl]amino]pyridine-2-carboxamide
EP4347033A1 (fr) 2021-06-04 2024-04-10 Vertex Pharmaceuticals Incorporated Tétrahydrofuranes à substitution hydroxy et (halo)alkoxy utiles en tant que modulateurs de canaux sodiques
EP4347032A1 (fr) 2021-06-04 2024-04-10 Vertex Pharmaceuticals Incorporated Tétrahydrofuran-2-carboxamides substitués utiles en tant que modulateurs de canaux sodiques
JP2024520646A (ja) 2021-06-04 2024-05-24 バーテックス ファーマシューティカルズ インコーポレイテッド ナトリウムチャネルのモジュレーターとしてのn-(ヒドロキシアルキル(ヘテロ)アリール)テトラヒドロフランカルボキサミド類似体
UY39800A (es) 2021-06-04 2023-01-31 Vertex Pharma N–(hidroxialquil (hetero)aril) tetrahidrofuran carboxamidas como moduladores de canales de sodio
WO2022256676A1 (fr) 2021-06-04 2022-12-08 Vertex Pharmaceuticals Incorporated Analogues de tétrahydrofurane substitués utiles en tant que modulateurs de canaux sodiques
WO2023205468A1 (fr) 2022-04-22 2023-10-26 Vertex Pharmaceuticals Incorporated Composés hétéroaryle pour le traitement de la douleur
US20230382910A1 (en) 2022-04-22 2023-11-30 Vertex Pharmaceuticals Incorporated Heteroaryl compounds for the treatment of pain
WO2023205463A1 (fr) 2022-04-22 2023-10-26 Vertex Pharmaceuticals Incorporated Composés hétéroaryles pour le traitement de la douleur
WO2023205465A1 (fr) 2022-04-22 2023-10-26 Vertex Pharmaceuticals Incorporated Composés hétéroaryles pour le traitement de la douleur
WO2023211990A1 (fr) 2022-04-25 2023-11-02 Siteone Therapeutics, Inc. Inhibiteurs d'amides hétérocycliques bicycliques de na v1.8 pour le traitement de la douleur
WO2024123815A1 (fr) 2022-12-06 2024-06-13 Vertex Pharmaceuticals Incorporated Procédé de synthèse de modulateurs de tétrahydrofurane substitués de canaux sodiques

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US5376645A (en) 1990-01-23 1994-12-27 University Of Kansas Derivatives of cyclodextrins exhibiting enhanced aqueous solubility and the use thereof
KR0166088B1 (ko) 1990-01-23 1999-01-15 . 수용해도가 증가된 시클로덱스트린 유도체 및 이의 용도
GB9518953D0 (en) 1995-09-15 1995-11-15 Pfizer Ltd Pharmaceutical formulations
WO2000035296A1 (fr) 1996-11-27 2000-06-22 Wm. Wrigley Jr. Company Liberation amelioree d'agents medicamenteux actifs par un enrobage de chewing-gum
GB9711643D0 (en) 1997-06-05 1997-07-30 Janssen Pharmaceutica Nv Glass thermoplastic systems
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US7291641B2 (en) * 1999-10-11 2007-11-06 Societe De Conseils De Recherches Et D'applications Scientifiques (S.C.R.A.S.) Derivatives of heterocycles with 5 members, their preparation and their use as medicaments
US7112366B2 (en) 2001-01-05 2006-09-26 The Ohio State University Chemical monolayer and micro-electronic junctions and devices containing same
TWI248438B (en) * 2001-04-10 2006-02-01 Sod Conseils Rech Applic Derivatives of heterocycles with 5 members, their preparation and their use as medicaments
FR2842808B1 (fr) * 2002-07-25 2004-09-10 Sod Conseils Rech Applic Nouveaux derives d'arylimidazoles, leur preparation et leurs applications therapeutiques
US7456164B2 (en) * 2004-05-07 2008-11-25 Pfizer, Inc 3- or 4-monosubtituted phenol and thiophenol derivatives useful as H3 ligands
GEP20094826B (en) * 2004-05-07 2009-11-10 Warner Lambert Co 3- or 4-monosubstituted phenol and thiophenol derivatives useful as h3 ligands
EP2371954A1 (fr) 2004-10-27 2011-10-05 Schering Corporation Compositions et procédés d'inhibition par des petits acides nucléiques interférents dirigés contre NAv1.8
US7855227B2 (en) 2005-12-22 2010-12-21 Newron Pharmaceuticals S.P.A. 2-phenylethylamino derivatives as calcium and/or sodium channel modulators
EP2076508B1 (fr) 2006-10-18 2011-01-05 Pfizer Products Inc. Composés d'urée de bisaryle éther
ES2340640T3 (es) 2007-03-23 2010-06-07 Icagen, Inc. Inhibidores de canales de iones.
WO2008135826A2 (fr) 2007-05-03 2008-11-13 Pfizer Limited Dérivés de la pyridine
JP2010526051A (ja) * 2007-05-03 2010-07-29 ファイザー・リミテッド 疼痛を治療するためのnav1.8チャネルモジュレーターとしてのn−[6−アミノ−5−(フェニル)ピラジン−2−イル]−イソオキサゾール−4−カルボキサミド誘導体および関連化合物
CA2693588C (fr) 2007-07-13 2015-11-17 Icagen, Inc. Inhibiteurs des canaux sodiques

Also Published As

Publication number Publication date
NI201400031A (es) 2014-10-01
US20140296313A1 (en) 2014-10-02
EP2771335A2 (fr) 2014-09-03
AU2012328034B2 (en) 2015-04-23
CN103906746B (zh) 2015-12-09
MD20140037A2 (ro) 2014-08-31
IL232267A0 (en) 2014-06-30
KR101586966B1 (ko) 2016-01-19
CU20140046A7 (es) 2014-10-02
JP2014530900A (ja) 2014-11-20
AU2012328034A1 (en) 2014-05-15
CA2850925C (fr) 2017-01-10
TN2014000147A1 (fr) 2015-09-30
EA201490864A1 (ru) 2014-08-29
KR20140069234A (ko) 2014-06-09
WO2013061205A3 (fr) 2013-06-27
CL2014000956A1 (es) 2014-07-18
ECSP14013324A (es) 2014-05-31
CO6940427A2 (es) 2014-05-09
CR20140185A (es) 2014-06-03
DOP2014000085A (es) 2014-08-31
US9079878B2 (en) 2015-07-14
IL232267A (en) 2016-10-31
BR112014009102A2 (pt) 2017-04-18
CA2850925A1 (fr) 2013-05-02
ZA201402281B (en) 2015-11-25
CN103906746A (zh) 2014-07-02
JP5946538B2 (ja) 2016-07-06
WO2013061205A8 (fr) 2014-03-27
UA109220C2 (uk) 2015-07-27
EA023375B1 (ru) 2016-05-31
WO2013061205A2 (fr) 2013-05-02
MX337469B (es) 2016-03-02
MX2014004738A (es) 2014-08-01
GT201400079A (es) 2015-06-02
HK1198650A1 (en) 2015-05-22
NZ623090A (en) 2015-10-30
AP2014007579A0 (en) 2014-04-30
PE20141682A1 (es) 2014-11-14

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