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Cyclohexanecarboxylic acid, 4-[3-(2-fluoroethyl)-3-nitrosoureido]-, (Z)- | 61137-62-0

中文名称
——
中文别名
——
英文名称
Cyclohexanecarboxylic acid, 4-[3-(2-fluoroethyl)-3-nitrosoureido]-, (Z)-
英文别名
——
Cyclohexanecarboxylic acid, 4-[3-(2-fluoroethyl)-3-nitrosoureido]-, (Z)-化学式
CAS
61137-62-0
化学式
C10H16FN3O4
mdl
——
分子量
261.253
InChiKey
YTWIKXYJTKQLDW-OCAPTIKFSA-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):
    1.29
  • 重原子数:
    18.0
  • 可旋转键数:
    5.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    99.07
  • 氢给体数:
    2.0
  • 氢受体数:
    4.0

安全信息

  • 海关编码:
    2924299090

SDS

SDS:d8749db8d2d2093902ea3600c94a6567
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反应信息

  • 作为产物:
    参考文献:
    名称:
    Synthesis of analogs of N-(2-chloroethyl)-N'-(trans-4-methylcyclohexyl)-N-nitrosourea for evaluation as anticancer agents
    摘要:
    The superior activity of N-(2-chloroethyl)-N'-(trans-4-methylcyclohexyl)-N-nitrosourea (MeCCNU) against advanced murine Lewis lung carcinoma in comparisons with the cis form and other nitrosoureas prompted the synthesis of a number of MeCCNU analogues, including several cis-trans pairs. The methyl group was replaced by a variety of substituents (CO2H, CH2CO2H, CO2Me, CH2OAc, CH2Cl, OMe); the trans-3-methylcyclohexyl, cis-2-methyl-1,3-dithian-5-yl, cis- and trans-2-methyl-1,3-dithian-5-yl-tetraoxide, and 1-methylhexyl (open-chain) analogues were also prepared. Preliminary tests against murine leukemia L1210 revealed therapeutic indices (ED50/LD10) ranging from 0.26 to 0.79; all but three analogues effected 50% cure rates at nontoxic doses, the open-chain analogue being one of the least active. In terms of therapeutic index, diequatorial (trans-4) isomers were, with one exception, as active as or, in four of the eight examples, somewhat more active than the corresponding axial-equatorial (cis-4) isomers. In this series, four of the five 2-fluoroethyl analogues prepared were clearly inferior to the corresponding 2-chloroethyl analogues.
    DOI:
    10.1021/jm00212a019
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