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| 1333340-91-2

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1333340-91-2
化学式
C25H24F3N5O2
mdl
——
分子量
483.493
InChiKey
HKXBVZBXXUGMFT-MRXNPFEDSA-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):
    4.68
  • 重原子数:
    35.0
  • 可旋转键数:
    7.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    101.88
  • 氢给体数:
    2.0
  • 氢受体数:
    4.0

反应信息

  • 作为反应物:
    描述:
    在 sodium tetrahydroborate 作用下, 以 甲醇 为溶剂, 生成 N-((R)-cyano-methyl-methyl)-3-{5-[4-(isopropylaminomethyl)phenyl]-1H-pyrazol-3-yl}benzamide
    参考文献:
    名称:
    3,5-Diarylazoles as novel and selective inhibitors of protein kinase D
    摘要:
    The synthesis and preliminary studies of the SAR of novel 3,5-diarylazole inhibitors of Protein Kinase D (PKD) are reported. Notably, optimized compounds in this class have been found to be active in cellular assays of phosphorylation-dependant HDAC5 nuclear export, orally bioavailable, and highly selective versus a panel of additional putative histone deacetylase (HDAC) kinases. Therefore these compounds could provide attractive tools for the further study of PKD / HDAC5 signaling. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2011.01.014
  • 作为产物:
    参考文献:
    名称:
    3,5-Diarylazoles as novel and selective inhibitors of protein kinase D
    摘要:
    The synthesis and preliminary studies of the SAR of novel 3,5-diarylazole inhibitors of Protein Kinase D (PKD) are reported. Notably, optimized compounds in this class have been found to be active in cellular assays of phosphorylation-dependant HDAC5 nuclear export, orally bioavailable, and highly selective versus a panel of additional putative histone deacetylase (HDAC) kinases. Therefore these compounds could provide attractive tools for the further study of PKD / HDAC5 signaling. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2011.01.014
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