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5-(4-hydroxybutyl)-2-thiouracil | 53438-94-1

中文名称
——
中文别名
——
英文名称
5-(4-hydroxybutyl)-2-thiouracil
英文别名
5-(4-hydroxy-butyl)-2-thioxo-2,3-dihydro-1H-pyrimidin-4-one;5-(4-hydroxybutyl)-2-sulfanylidene-1H-pyrimidin-4-one
5-(4-hydroxybutyl)-2-thiouracil化学式
CAS
53438-94-1
化学式
C8H12N2O2S
mdl
——
分子量
200.261
InChiKey
GPRVYPHJBFLMRG-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

  • 密度:
    1.32±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.1
  • 重原子数:
    13
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    93.4
  • 氢给体数:
    3
  • 氢受体数:
    3

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    5-(4-hydroxybutyl)-2-thiouracil四溴化碳三苯基膦 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 1.0h, 以84%的产率得到5-(4-bromobutyl)-2-thiouracil
    参考文献:
    名称:
    Affinity therapeutics. 1. Selective incorporation of 2-thiouracil derivatives in murine melanomas. Cytostatic activity of 2-thiouracil arotinoids, 2-thiouracil retinoids, arotinoids, and retinoids
    摘要:
    The incorporation of 2-[35S]thiouracil and two of its derivatives into murine melanomas, in vivo, was studied. It was confirmed [J. R. Whittaker, J. Biol. Chem., 246, 6217--6226 (1971)] that 2-thiouracil has a marked affinity for melanin-producing tissue and that an affinity for such tissue could be sustained by 5-substituted 2-thiouracils. A series of derivatives of arotinoids and retinoids, with or without a 2-thiouracil group as a potential carrier to obtain affinity for melanomas, was examined for cytostatic activity, in vitro. None of these showed significant activity against murine melanomas.
    DOI:
    10.1021/jm00350a014
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文献信息

  • Affinity therapeutics. 1. Selective incorporation of 2-thiouracil derivatives in murine melanomas. Cytostatic activity of 2-thiouracil arotinoids, 2-thiouracil retinoids, arotinoids, and retinoids
    作者:Frank Waetjen、Ole Buchardt、Eyvind Langvad
    DOI:10.1021/jm00350a014
    日期:1982.8
    The incorporation of 2-[35S]thiouracil and two of its derivatives into murine melanomas, in vivo, was studied. It was confirmed [J. R. Whittaker, J. Biol. Chem., 246, 6217--6226 (1971)] that 2-thiouracil has a marked affinity for melanin-producing tissue and that an affinity for such tissue could be sustained by 5-substituted 2-thiouracils. A series of derivatives of arotinoids and retinoids, with or without a 2-thiouracil group as a potential carrier to obtain affinity for melanomas, was examined for cytostatic activity, in vitro. None of these showed significant activity against murine melanomas.
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