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| 1251462-68-6

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1251462-68-6
化学式
C35H35FN6O4S
mdl
——
分子量
654.765
InChiKey
STFLQMFLUOPPPC-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

物化性质

  • 沸点:
    752.2±70.0 °C(predicted)
  • 密度:
    1.39±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.61
  • 重原子数:
    47.0
  • 可旋转键数:
    8.0
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    92.51
  • 氢给体数:
    0.0
  • 氢受体数:
    10.0

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Discovery of potent HIV integrase inhibitors active against raltegravir resistant viruses
    摘要:
    A series of novel HIV integrase inhibitors active against rategravir resistant strains are reported. Initial SAR studies revealed that activities against wild-type virus were successfully maintained at single digit nanomolar level with a wide range of substitutions. However, inclusion of nitrogen-based cyclic substitutions was crucial for achieving potency against mutant viruses. Several compounds with excellent activities against wild-type virus as well as against the viruses with the mutations Q148H/G140S or N155H/E92Q were reported. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.07.041
  • 作为产物:
    参考文献:
    名称:
    Discovery of potent HIV integrase inhibitors active against raltegravir resistant viruses
    摘要:
    A series of novel HIV integrase inhibitors active against rategravir resistant strains are reported. Initial SAR studies revealed that activities against wild-type virus were successfully maintained at single digit nanomolar level with a wide range of substitutions. However, inclusion of nitrogen-based cyclic substitutions was crucial for achieving potency against mutant viruses. Several compounds with excellent activities against wild-type virus as well as against the viruses with the mutations Q148H/G140S or N155H/E92Q were reported. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.07.041
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