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Ethyl 2-(4-(1-(tert-butoxycarbonyl)piperidin-4-ylcarbamoyl)-5-methyl-1H-pyrazol-3-yl)-1H-benzo[d]imidazole-5-carboxylate | 1313994-28-3

中文名称
——
中文别名
——
英文名称
Ethyl 2-(4-(1-(tert-butoxycarbonyl)piperidin-4-ylcarbamoyl)-5-methyl-1H-pyrazol-3-yl)-1H-benzo[d]imidazole-5-carboxylate
英文别名
ethyl 2-[5-methyl-4-[[1-[(2-methylpropan-2-yl)oxycarbonyl]piperidin-4-yl]carbamoyl]-1H-pyrazol-3-yl]-3H-benzimidazole-5-carboxylate
Ethyl 2-(4-(1-(tert-butoxycarbonyl)piperidin-4-ylcarbamoyl)-5-methyl-1H-pyrazol-3-yl)-1H-benzo[d]imidazole-5-carboxylate化学式
CAS
1313994-28-3
化学式
C25H32N6O5
mdl
——
分子量
496.566
InChiKey
IDCJZNLNKFEJIK-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):
    2.8
  • 重原子数:
    36
  • 可旋转键数:
    8
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.48
  • 拓扑面积:
    142
  • 氢给体数:
    3
  • 氢受体数:
    7

反应信息

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文献信息

  • Ligand-Directed Covalent Modification of Protein
    申请人:Celgene CAR LLC
    公开号:US20170218353A1
    公开(公告)日:2017-08-03
    The present invention relates to enzyme inhibitors. More specifically, the present invention relates to ligand-directed covalent modification of proteins; method of designing same; pharmaceutical formulation of same; and method of use.
  • [EN] LIGAND-DIRECTED COVALENT MODIFICATION OF PROTEIN<br/>[FR] MODIFICATION COVALENTE DE PROTÉINE, DIRIGÉE SUR UN LIGAND
    申请人:AVILA THERAPEUTICS INC
    公开号:WO2011082285A1
    公开(公告)日:2011-07-07
    The present invention relates to enzyme inhibitors. More specifically, the present invention relates to ligand-directed covalent modification of proteins; method of designing same; pharmaceutical formulation of same; and method of use.
  • LIGAND-DIRECTED COVALENT MODIFICATION OF PROTEIN
    申请人:Petter Russell C.
    公开号:US20110269244A1
    公开(公告)日:2011-11-03
    The present invention relates to enzyme inhibitors. More specifically, the present invention relates to ligand-directed covalent modification of proteins; method of designing same; pharmaceutical formulation of same; and method of use.
    本发明涉及酶抑制剂。更具体地说,本发明涉及配体导向的蛋白共价修饰;相同设计方法;相同的药物配方;以及使用方法。
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