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6-bromo-5-[4-(methylsulfonyl)phenoxy]-2-(2-pyridinyl)-1H-benzimidazole | 886976-46-1

中文名称
——
中文别名
——
英文名称
6-bromo-5-[4-(methylsulfonyl)phenoxy]-2-(2-pyridinyl)-1H-benzimidazole
英文别名
6-bromo-5-(4-methylsulfonylphenoxy)-2-pyridin-2-yl-1H-benzimidazole
6-bromo-5-[4-(methylsulfonyl)phenoxy]-2-(2-pyridinyl)-1H-benzimidazole化学式
CAS
886976-46-1
化学式
C19H14BrN3O3S
mdl
——
分子量
444.308
InChiKey
CHRAPAUTIBSDIU-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):
    3.6
  • 重原子数:
    27
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    93.3
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

点击查看最新优质反应信息

文献信息

  • Aryloxy-Substituted Benzimidazole Derivatives
    申请人:Hashimoto Noriaki
    公开号:US20080125429A1
    公开(公告)日:2008-05-29
    A glucokinase activator is provided; and a treatment and/or a preventive for diabetes, or a treatment and/or a preventive for diabetes such as retinopathy, nephropathy, neurosis, ischemic cardiopathy, arteriosclerosis, and further a treatment and/or a preventive for obesity are provided. The invention relates to a compound of a formula (I): [wherein R 1 and R 2 represent a hydrogen, etc.; R 3 represents a hydrogen atom, a halogen atom, etc.; R 4 each independently represents a hydrogen atom, a lower alkyl group, etc.; Q represents a carbon atom, a nitrogen atom or a sulfur atom (the sulfur atom may be mono- or di-substituted with an oxo group); R 5 and R 6 each represent a hydrogen atom, a lower alkyl group, etc.; X 1 , X 2 , X 3 and X 4 each independently represent a carbon atom or a nitrogen atom; Z represents an oxygen atom, a sulfur atom or a nitrogen atom; Ar represents an aryl or heteroaryl group optionally mono to tri-substituted with a group selected from the substituent group β; ring A represents a 5- or 6-membered nitrogen-containing heteroaromatic group; m indicates an integer of from 1 to 6; n indicates an integer of from 0 to 3; p indicates an integer of from 0 to 2 (provided that at least two of X 1 to X 4 are carbon atoms); q indicates 0 or 1] or its pharmaceutically-acceptable salt, which has an effect of glucokinase activation and is useful as a treatment for diabetes.
    本发明提供了一种葡萄糖激酶激活剂;以及用于糖尿病的治疗和/或预防,或用于糖尿病如视网膜病变、肾病、神经病、缺血性心脏病、动脉硬化等的治疗和/或预防,以及用于肥胖症的治疗和/或预防。本发明涉及一种化合物的公式(I):[其中R1和R2分别表示氢等;R3表示氢原子、卤原子等;R4各自独立地表示氢原子、低级烷基等;Q表示碳原子、氮原子或硫原子(硫原子可以是单取代或双取代的氧基);R5和R6各自表示氢原子、低级烷基等;X1、X2、X3和X4各自独立地表示碳原子或氮原子;Z表示氧原子、硫原子或氮原子;Ar表示芳基或杂环芳基,可选择性地单取代至三取代于β取代基;环A表示一个含氮的5-或6成员杂芳基;m表示1至6的整数;n表示0至3的整数;p表示0至2的整数(前提是X1至X4中至少有两个是碳原子);q表示0或1]或其药学上可接受的盐,具有葡萄糖激酶激活的作用,并且可用作糖尿病的治疗。
  • Aryloxy-substituted benzimidazole derivatives
    申请人:MSD K.K.
    公开号:US07932394B2
    公开(公告)日:2011-04-26
    A glucokinase activator is provided; and a treatment and/or a preventive for diabetes, or a treatment and/or a preventive for diabetes such as retinopathy, nephropathy, neurosis, ischemic cardiopathy, arteriosclerosis, and further a treatment and/or a preventive for obesity are provided. The invention relates to a compound of a formula (I): [wherein R1 and R2 represent a hydrogen, etc.; R3 represents a hydrogen atom, a halogen atom, etc.; R4 each independently represents a hydrogen atom, a lower alkyl group, etc.; Q represents a carbon atom, a nitrogen atom or a sulfur atom (the sulfur atom may be mono- or di-substituted with an oxo group); R5 and R6 each represent a hydrogen atom, a lower alkyl group, etc.; X1, X2, X3 and X4 each independently represent a carbon atom or a nitrogen atom; Z represents an oxygen atom, a sulfur atom or a nitrogen atom; Ar represents an aryl or heteroaryl group optionally mono to tri-substituted with a group selected from the substituent group β; ring A represents a 5- or 6-membered nitrogen-containing heteroaromatic group; m indicates an integer of from 1 to 6; n indicates an integer of from 0 to 3; p indicates an integer of from 0 to 2 (provided that at least two of X1 to X4 are carbon atoms); q indicates 0 or 1] or its pharmaceutically-acceptable salt, which has an effect of glucokinase activation and is useful as a treatment for diabetes.
    本发明提供了一种葡萄糖激酶激活剂;以及一种治疗和/或预防糖尿病,或一种治疗和/或预防糖尿病如视网膜病变、肾病、神经病、缺血性心脏病、动脉硬化,以及进一步治疗和/或预防肥胖症的药物。本发明涉及公式(I)的化合物:[其中R1和R2代表氢等;R3代表氢原子、卤原子等;R4各自独立地代表氢原子、较低的烷基等;Q代表碳原子、氮原子或硫原子(硫原子可以是单取代或双取代的氧基);R5和R6各自代表氢原子、较低的烷基等;X1、X2、X3和X4各自独立地代表碳原子或氮原子;Z代表氧原子、硫原子或氮原子;Ar代表芳基或杂环芳基,可选择性地单取代至三取代于从取代基β选择的基团;环A代表一含有5-或6-成员的含氮杂环芳基;m表示1至6的整数;n表示0至3的整数;p表示0至2的整数(但至少X1至X4中的两个为碳原子);q表示0或1]或其药学上可接受的盐,具有葡萄糖激酶激活的作用,可用于治疗糖尿病。
  • US7932394B2
    申请人:——
    公开号:US7932394B2
    公开(公告)日:2011-04-26
  • ARYLOXY-SUBSTITUTED BENZIMIDAZOLE DERIVATIVES
    申请人:MSD K.K.
    公开号:EP1810969B1
    公开(公告)日:2013-08-07
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