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2-(cyclopentylthio)pyrimidine-4,6-diamine | 1099593-11-9

中文名称
——
中文别名
——
英文名称
2-(cyclopentylthio)pyrimidine-4,6-diamine
英文别名
2-cyclopentylsulfanylpyrimidine-4,6-diamine
2-(cyclopentylthio)pyrimidine-4,6-diamine化学式
CAS
1099593-11-9
化学式
C9H14N4S
mdl
——
分子量
210.303
InChiKey
OROVTDMMQRIPBH-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:
    464.5±25.0 °C(Predicted)
  • 密度:
    1.30±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.6
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    103
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    2-(cyclopentylthio)pyrimidine-4,6-diamine 在 sodium nitrite 作用下, 以 为溶剂, 生成
    参考文献:
    名称:
    Exploring 8-benzyl pteridine-6,7-diones as inhibitors of glutamate racemase (MurI) in Gram-positive bacteria
    摘要:
    A successful scaffold-hopping approach gave a novel series of inhibitors of bacterial glutamate racemase (MurI). Early SAR studies of the 8-benzyl pteridine-6,7-diones led to compounds with micromolar enzyme potency and antibacterial activity. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2008.10.022
  • 作为产物:
    描述:
    4,6-二氨基-2-巰基嘧啶 、 alkaline earth salt of/the/ methylsulfuric acid 在 sodium hydroxide 作用下, 以 甲醇N,N-二甲基甲酰胺 为溶剂, 生成 2-(cyclopentylthio)pyrimidine-4,6-diamine
    参考文献:
    名称:
    Exploring 8-benzyl pteridine-6,7-diones as inhibitors of glutamate racemase (MurI) in Gram-positive bacteria
    摘要:
    A successful scaffold-hopping approach gave a novel series of inhibitors of bacterial glutamate racemase (MurI). Early SAR studies of the 8-benzyl pteridine-6,7-diones led to compounds with micromolar enzyme potency and antibacterial activity. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2008.10.022
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文献信息

  • Exploring 8-benzyl pteridine-6,7-diones as inhibitors of glutamate racemase (MurI) in Gram-positive bacteria
    作者:Gloria A. Breault、Janelle Comita-Prevoir、Charles J. Eyermann、Bolin Geng、Randy Petrichko、Peter Doig、Elise Gorseth、Brian Noonan
    DOI:10.1016/j.bmcl.2008.10.022
    日期:2008.12
    A successful scaffold-hopping approach gave a novel series of inhibitors of bacterial glutamate racemase (MurI). Early SAR studies of the 8-benzyl pteridine-6,7-diones led to compounds with micromolar enzyme potency and antibacterial activity. (C) 2008 Elsevier Ltd. All rights reserved.
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