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2-(5-amino-4-methyl-2-thiazolyl)-1H-benzimidazole-4-carboxylic acid | 1234834-19-5

中文名称
——
中文别名
——
英文名称
2-(5-amino-4-methyl-2-thiazolyl)-1H-benzimidazole-4-carboxylic acid
英文别名
2-(5-amino-4-methyl-1,3-thiazol-2-yl)-1H-benzimidazole-4-carboxylic acid
2-(5-amino-4-methyl-2-thiazolyl)-1H-benzimidazole-4-carboxylic acid化学式
CAS
1234834-19-5
化学式
C12H10N4O2S
mdl
——
分子量
274.303
InChiKey
DGCMXXNSXFFNFK-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):
    1.8
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    133
  • 氢给体数:
    3
  • 氢受体数:
    6

文献信息

  • Benzimidazole-4-Carboxamide Derivatives, Their Preparation Methods, Pharmaceutical Compositions And Their Uses
    申请人:Luo Xianjin
    公开号:US20110269766A1
    公开(公告)日:2011-11-03
    The present invention relates to the benzimidazole-4-carboxamide derivatives, their preparation methods, pharmaceutical compositions and their uses; wherein X represents monosubstituted or bissubstituted or polysubstitued C 1 -C 14 alkoxy, monosubstituted or bisubstituted or polysubstitued C 1 -C 14 alkyl, monosubstituted or bisubstituted or polysubstitued C 2 -C 14 alkenyl, monosubstituted or bisubstituted or polysubstitued C 6 -C 14 aryl, or monosubstituted or bisubstituted or polysubstitued 5 to 6 membered heterocyclic group, or monosubstituted or bisubstituted or polysubstitued fused ring group containing nitrogen heteroatom; Y represents hydrogen, monosubstituted or bisubstituted or polysubstitued C 1 -C 16 alkyl, monosubstituted or bisubstituted or polysubstitued C 6 -C 12 aryl, or monosubstituted or bisubstituted or polysubstitued 5 to 6 membered heterocyclic group, or monosubstituted or bisubstituted or polysubstitued fused ring group containing nitrogen heteroatom. The derivatives of the present invention have the functions of antiviral medicine.
    本发明涉及苯并咪唑-4-羧酰胺生物,其制备方法,药物组合物及其用途;其中X代表单取代或双取代或多取代的C1-C14烷基,单取代或双取代或多取代的C1-C14烷基,单取代或双取代或多取代的C2-C14基,单取代或双取代或多取代的C6-C14芳基,或单取代或双取代或多取代的含杂原子的5至6成员杂环基,或单取代或双取代或多取代的融合环基团;Y代表,单取代或双取代或多取代的C1-C16烷基,单取代或双取代或多取代的C6-C12芳基,或单取代或双取代或多取代的5至6成员杂环基,或单取代或双取代或多取代的融合环基团含杂原子。本发明的衍生物具有抗病毒药物功能。
  • BENZIMIDAZOLE-4-CARBOXAMIDE DERIVATIVES, THEIR PREPARATION METHODS, PHARMACEUTICAL COMPOSITIONS AND THEIR USES
    申请人:Shanghai Jiao Tong University
    公开号:EP2386553A1
    公开(公告)日:2011-11-16
    The present invention relates to the benzimidazole-4-carboxamide derivatives, their preparation methods, pharmaceutical compositions and their uses; wherein X represents monosubstituted or bissubstituted or polysubstitued C1-C14 alkoxy, monosubstituted or bisubstituted or polysubstitued C1-C14 alkyl, monosubstituted or bisubstituted or polysubstitued C2-C14 alkenyl, monosubstituted or bisubstituted or polysubstitued C6-C14 aryl, or monosubstituted or bisubstituted or polysubstitued 5 to 6 membered heterocyclic group, or monosubstituted or bisubstituted or polysubstitued fused ring group containing nitrogen heteroatom; Y represents hydrogen, monosubstituted or bisubstituted or polysubstitued C1-C16 alkyl, monosubstituted or bisubstituted or polysubstitued C6-C12 aryl, or monosubstituted or bisubstituted or polysubstitued 5 to 6 membered heterocyclic group, or monosubstituted or bisubstituted or polysubstitued fused ring group containing nitrogen heteroatom. The derivatives of the present invention have the functions of antiviral medicine.
    本发明涉及苯并咪唑-4-甲酰胺生物、其制备方法、药物组合物及其用途;其中 X 代表单取代或双取代或多取代的 C1-C14 烷基,单取代或双取代或多取代的 C1-C14 烷基,单取代或双取代或多取代的 C2-C14 基、单取代或双取代或多取代的 C6-C14 芳基,或单取代或双取代或多取代的 5 至 6 位杂环基团,或单取代或双取代或多取代的含杂原子的融合环基团;Y 代表、单取代或双取代或多取代的 C1-C16 烷基、单取代或双取代或多取代的 C6-C12 芳基、或单取代或双取代或多取代的 5 至 6 位杂环基团、或单取代或双取代或多取代的含杂原子的融合环基。本发明的衍生物具有抗病毒药物的功能。
  • US8871946B2
    申请人:——
    公开号:US8871946B2
    公开(公告)日:2014-10-28
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