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3-(1-(5,7-diisopropyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-ylmethyl)-5-(4-methyl-cyclohexyl)-1,2,3,6-tetrahydro-pyridin-4-yl)-5-phenyl-thiophene-2-carboxylic acid | 1383384-58-4

中文名称
——
中文别名
——
英文名称
3-(1-(5,7-diisopropyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-ylmethyl)-5-(4-methyl-cyclohexyl)-1,2,3,6-tetrahydro-pyridin-4-yl)-5-phenyl-thiophene-2-carboxylic acid
英文别名
3-[1-[[5,7-di(propan-2-yl)-[1,2,4]triazolo[1,5-a]pyrimidin-2-yl]methyl]-5-(4-methylcyclohexyl)-3,6-dihydro-2H-pyridin-4-yl]-5-phenylthiophene-2-carboxylic acid
3-(1-(5,7-diisopropyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-ylmethyl)-5-(4-methyl-cyclohexyl)-1,2,3,6-tetrahydro-pyridin-4-yl)-5-phenyl-thiophene-2-carboxylic acid化学式
CAS
1383384-58-4
化学式
C35H43N5O2S
mdl
——
分子量
597.825
InChiKey
BJDRMPRNOCKUOC-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    5.4
  • 重原子数:
    43
  • 可旋转键数:
    8
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.49
  • 拓扑面积:
    112
  • 氢给体数:
    1
  • 氢受体数:
    7

文献信息

  • [EN] INHIBITORS OF HEPATITIS C VIRUS POLYMERASE<br/>[FR] INHIBITEURS DE LA POLYMÉRASE DU VIRUS DE L'HÉPATITE C
    申请人:COCRYSTAL DISCOVERY INC
    公开号:WO2012083105A1
    公开(公告)日:2012-06-21
    The present invention provides, among other things, compounds represented by the general Formula (I) and pharmaceutically acceptable salts thereof, wherein X, Y, R1A, R1B, R2, and R3 are as defined in classes and subclasses herein and compositions (e.g., pharmaceutical compositions) comprising such compounds, which compounds are useful as inhibitors of hepatitis C virus polymerase, and thus are useful, for example, as medicaments for the treatment of HCV infection.
    本发明提供了一种由一般式(I)表示的化合物及其药用盐,其中X、Y、R1A、R1B、R2和R3如本文中的类和子类中所定义,并包括含有这种化合物的组合物(例如,药物组合物),这些化合物可用作丙型肝炎病毒聚合酶的抑制剂,因此可用作治疗HCV感染的药物。
  • Inhibitors of hepatitis C virus polymerase
    申请人:COCRYSTAL DISCOVERY, INC.
    公开号:US10426762B2
    公开(公告)日:2019-10-01
    The present invention provides, among other things, compounds represented by the general Formula I: and pharmaceutically acceptable salts thereof, wherein X, Y, R2, and R3 are as defined in classes and subclasses herein and compositions (e.g., pharmaceutical compositions) comprising such compounds, which compounds are useful as inhibitors of hepatitis C virus polymerase, and thus are useful, for example, as medicaments for the treatment of HCV infection.
    本发明除其他外,提供了通式 I 所代表的化合物:及其药学上可接受的盐,其中 X、Y、R2 和 R3 如本文类和亚类所定义,以及包含此类化合物的组合物(例如药物组合物),这些化合物可用作丙型肝炎病毒聚合酶的抑制剂,因此可用作治疗 HCV 感染的药物等。
  • INHIBITORS OF HEPATITIS C VIRUS POLYMERASE
    申请人:Lee Sam SK
    公开号:US20120183496A1
    公开(公告)日:2012-07-19
    The present invention provides, among other things, compounds represented by the general Formula I: and pharmaceutically acceptable salts thereof, wherein X, Y, R 1A , R 1B , R 2 , and R 3 are as defined in classes and subclasses herein and compositions (e.g., pharmaceutical compositions) comprising such compounds, which compounds are useful as inhibitors of hepatitis C virus polymerase, and thus are useful, for example, as medicaments for the treatment of HCV infection.
  • Inhibitors of Hepatitis C Virus Polymerase
    申请人:COCRYSTAL DISCOVERY, INC.
    公开号:US20170273962A1
    公开(公告)日:2017-09-28
    The present invention provides, among other things, compounds represented by the general Formula I: and pharmaceutically acceptable salts thereof, wherein X, Y, R 2 , and R 3 are as defined in classes and subclasses herein and compositions (e.g., pharmaceutical compositions) comprising such compounds, which compounds are useful as inhibitors of hepatitis C virus polymerase, and thus are useful, for example, as medicaments for the treatment of HCV infection.
  • US8771665B2
    申请人:——
    公开号:US8771665B2
    公开(公告)日:2014-07-08
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同类化合物

5-(4-甲基苯基)噻唑并[2,3-c]-1,2,4-三唑-3(2H)-硫酮 5-(4-氯苯基)-噻唑并[2,3-c]-1,2,4-三唑-3(2H)-硫酮 1-(6-甲基噻唑并[3,2-B][1,2,4]三唑-5-基)乙酮 1-(6-甲基[1,3]噻唑并[3,2-B] [1,2,4]三唑-5-基)乙醇 (E)-butyl 3-(6-methylthiazolo[3,2-b][1,2,4]triazol-5-yl)acrylate (E)-6-methyl-5-styrylthiazolo[3,2-b][1,2,4]triazole Dimethyl-carbamic acid 6-methyl-thiazolo[3,2-b][1,2,4]triazol-2-yl ester 1-(6-methyl-2-(thiophen-2-yl)thiazolo[3,2-b][1,2,4]triazol-5-yl)ethan-1-one (+/-)-1-[6-methyl-2-(2-thienyl)[1,3]thiazolo[3,2-b][1,2,4]triazol-5-yl]ethanol 6-(4-methoxyphenyl)-5-pyrimidin-5-yl-thiazolo[3,2-b][1,2,4]triazole 6-methyl-5-(pyrimidin-5-yl)thiazolo[3,2-b][1,2,4]triazole 6-(p-tolyl)-5-pyrimidin-5-yl-thiazolo[3,2-b][1,2,4]triazole (+/-)-1-(3-bromo-5-methyl[1,3]thiazolo[2,3-c][1,2,4]triazol-6-yl)ethanol 3-acethoxymethyl-7-acetyl-6-methyl-5-(2-methyl-4-thiazolyl)pyrrolo<2,1-b>thiazole 1-(6-methylthiazolo[3,2-b][1,2,4]triazol-5-yl)-ethan-1-one oxime 6-methyl-5-(pyridin-4-yl)thiazolo[3,2-b][1,2,4]triazole 1-(5-Phenyl-thiazolo[2,3-c][1,2,4]triazol-3-yl)-ethanone; hydrochloride (E)-N-tert-butyl-3-(6-methylthiazolo[3,2-b][1,2,4]triazol-5-yl)acrylamide (+/-)-1-(5-methyl[1,3]thiazolo[2,3-c][1,2,4]triazol-6-yl)ethanol 2-Ethyl-5-p-chlorophenylthiazolo<3,2-b>-s-triazole 4-Imino-6-phenyl-4H-thiazolo[2,3-c][1,2,4]triazine-3-carbonitrile Isopropyl-phosphoramidic acid ethyl ester 6-methyl-thiazolo[3,2-b][1,2,4]triazol-2-yl ester 2-Ethyl-5-phenylthiazolo<3,2-b>-s-triazole 2-(6-methyl[1,3]thiazolo[3,2-b][1,2,4]triazol-5-yl)-2-propanol Dimethyl-phosphinothioic acid O-(6-methyl-thiazolo[3,2-b][1,2,4]triazol-2-yl) ester 2-Hydroxy-6-methyl-thiazolo[3,2-b][1,2,4]triazole-5-carboxylic acid ethyl ester 6-(2-Furanylmethylene)-3-methylthiazolo[2,3-c]-1,2,4-triazol-5(6H)-one 3-Methyl-6-methoxy-1,2,4-triazolo-(2,3-b)-thiazol Thiazolo[2,3-c]-1,2,4-triazole-3-methanamine, 5-(3-fluoro-4-methoxyphenyl)-I+/--methyl- 2-[(4-methoxyphenyl)methyl]-6-methylthiazolo[3,2-b]-1,2,4-triazole-5-carboxylic acid ethyl ester 2-[(4-methoxyphenyl)ethyl]thiazolo[3,2-b]-1,2,4-triazole-6-acetic acid ethyl ester Thiophosphoric acid O-(5-bromo-6-ethyl-thiazolo[3,2-b][1,2,4]triazol-2-yl) ester O',O''-diethyl ester 3-(1-(5,7-diisopropyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-ylmethyl)-5-(4-methyl-cyclohexyl)-1,2,3,6-tetrahydro-pyridin-4-yl)-5-phenyl-thiophene-2-carboxylic acid (E)-6-(4-N,N-dimethylaminobenzylidene)-2-benzylthiazolo[3,2-b][1,2,4]triazol-5(6H)-one 2-[(4-methoxyphenyl)methyl]thiazolo[3,2-b]-1,2,4-triazole-6-acetic acid ethyl ester 5-D-6-phenylthiazolo[3,2-b][1,2,4]triazole 2-[(4-methoxyphenyl)ethyl]-6-methylthiazolo[3,2-b]-1,2,4-triazole-5-carboxylic acid ethyl ester 5,6-diphenylthiazolo[3,2-b]-1,2,4-triazole 1-(4-fluorobenzyl)-4-(4-methyl-5-(5-methyl-1H-1,2,4-triazol-3-yl)thiazol-2-yl)-1H-1,2,4-triazol-5(4H)-one (E)-6-methyl-5-(4-methylstyryl)thiazolo[3,2-b][1,2,4]triazole ethyl 1-(2-fluorobenzyl)-3-(thiazol-2-yl)-1H-1,2,4-triazole-5-carboxylate 6-benzoylamino-2-benzyl-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazolium betaine 2-(1-ethyl-1H-pyrazol-4-yl)-5-iodo-imidazo[2,1-b][1,3,4]thiadiazole 2-Hydroxy-6-methyl-thiazolo[3,2-b][1,2,4]triazole-5-carboxylic acid methyl ester