6-tert-Butyl-2-ethyl-1H-benzimidazole | 5805-63-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并咪唑类
• 英文名称: 6-tert-Butyl-2-ethyl-1H-benzimidazole
• CAS: 5805-63-0
• 化学式: C₁₃H₁₈N₂
• 分子量: 202.3
• InChiKey: CLKWONXWXDWMSJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  15
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.46
• 拓扑面积：
  28.7
• 氢给体数：
  1
• 氢受体数：
  1

文献信息

• Anti-Viral Compounds
  申请人：Donner Pamela L.

  公开号：US20100267634A1

  公开（公告）日：2010-10-21

  Compounds effective in inhibiting replication of Hepatitis C virus (“HCV”) are described. This invention also relates to processes of making such compounds, compositions comprising such compounds, and methods of using such compounds to treat HCV infection.

  本发明描述了在抑制丙型肝炎病毒("HCV")复制方面有效的化合物。这项发明还涉及到制造这类化合物的过程、包含这类化合物的组合物，以及使用这类化合物治疗HCV感染的方法。
• ANTIVIRAL COMPOUNDS
  申请人：Alam Muzaffar

  公开号：US20120230951A1

  公开（公告）日：2012-09-13

  The present invention provides compounds, compositions and methods for the treatment of hepatitis C virus (HCV) infection. Also disclosed are pharmaceutical compositions containing such compounds and methods for using these compounds in the treatment of HCV infection.

  本发明提供了用于治疗丙型肝炎病毒（HCV）感染的化合物、组合物和方法。还公开了含有这些化合物的药物组合物以及使用这些化合物治疗HCV感染的方法。
• Amines as Small Molecule Inhibitors
  申请人：Wahhab Amal

  公开号：US20080280925A1

  公开（公告）日：2008-11-13

  The present invention relates to compounds that are useful as inhibitors of protein arginine methyltransferase that have a formula selected from Formula (I), Formula (II) and Formula (III), as well as racemic mixtures, diastereomers, enantiomers and tautomers thereof and N-oxides, hydrates, solvates, pharmaceutically acceptable salts, prodrugs and complexes thereof as defined herein. Said compound are useful as inhibitors of PRMTs and/or CARM-I. The invention further relates to compositions comprising such compounds and methods for their use.

  本发明涉及一种具有以下公式（I）、公式（II）和公式（III）之一的化合物，以及它们的外消旋混合物、对映异构体、恒定异构体和互变异构体以及N-氧化物、水合物、溶剂物、药学上可接受的盐、前药和复合物，其作为蛋白质精氨酸甲基转移酶抑制剂。所述化合物作为PRMTs和/或CARM-I的抑制剂具有用途。本发明还涉及包含这些化合物的组合物和它们的使用方法。
• ANTIBACTERIAL AGENTS
  申请人：BROWN David Ryall

  公开号：US20120122918A1

  公开（公告）日：2012-05-17

  Compounds of formula (1) have antibacterial activity: wherein R represents hydrogen or 1, 2 or 3 optional substituents; W is ═C(R 1 )—; R 1 is hydrogen and R 2 is hydrogen, methyl, or fluorine; or R 1 and R 2 taken together are —CH 2 —, —CH 2 CH 2 , —O—, or, in either orientation, —O—CH 2 — or —OCH 2 CH 2 —; and R 3 is a radical of formula -(Alk 1 ) m -(Z) p -(Alk 2 )-Q.

  式（1）的化合物具有抗菌活性：其中R代表氢或1、2或3个可选取代基；W为═C（R1）—；R1为氢，R2为氢、甲基或氟；或R1和R2组合为—CH2—、—CH2CH2—、—O—，或者以任何方向为—O—CH2—或—OCH2CH2—；R3是式-(Alk1)m-(Z)p-(Alk2)-Q的基团。
• QUINOLINE AND QUINAZOLINE AMIDES AS MODULATORS OF SODIUM CHANNELS
  申请人：VERTEX PHARMACEUTICLAS INCORPORATED

  公开号：US20140228371A1

  公开（公告）日：2014-08-14

  The invention relates to compounds of formula I or pharmaceutically acceptable salts thereof, useful as inhibitors of sodium channels: The invention also provides pharmaceutically acceptable compositions comprising the compounds of the invention and methods of using the compositions in the treatment of various disorders, including pain.

  本发明涉及公式I的化合物或其药学上可接受的盐，其作为钠通道抑制剂有用：本发明还提供了包含本发明化合物的药学上可接受的组合物以及使用这些组合物治疗各种疾病，包括疼痛的方法。