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Isopropyl-carbamic acid 2-isopropylcarbamoyloxymethyl-7-methoxy-1-methyl-1H-benzo[g]indol-3-ylmethyl ester

中文名称
——
中文别名
——
英文名称
Isopropyl-carbamic acid 2-isopropylcarbamoyloxymethyl-7-methoxy-1-methyl-1H-benzo[g]indol-3-ylmethyl ester
英文别名
[2-(isopropylcarbamoyloxymethyl)-7-methoxy-1-methyl-benzo[g]indol-3-yl]methyl N-isopropylcarbamate;[7-methoxy-1-methyl-2-(propan-2-ylcarbamoyloxymethyl)benzo[g]indol-3-yl]methyl N-propan-2-ylcarbamate
Isopropyl-carbamic acid 2-isopropylcarbamoyloxymethyl-7-methoxy-1-methyl-1H-benzo[g]indol-3-ylmethyl ester化学式
CAS
——
化学式
C24H31N3O5
mdl
——
分子量
441.527
InChiKey
WDOHZUOMXMDRRW-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

计算性质

  • 辛醇/水分配系数(LogP):
    3.9
  • 重原子数:
    32
  • 可旋转键数:
    9
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    90.8
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    7-Methoxy-1-methyl-4,5-dihydro-1H-benzo[g]indole-2,3-dicarboxylic acid dimethyl ester 在 lithium aluminium tetrahydride 、 dibutyltin diacetate2,3-二氯-5,6-二氰基-1,4-苯醌 作用下, 以 乙醚二氯甲烷 为溶剂, 反应 2.0h, 生成 Isopropyl-carbamic acid 2-isopropylcarbamoyloxymethyl-7-methoxy-1-methyl-1H-benzo[g]indol-3-ylmethyl ester
    参考文献:
    名称:
    Synthesis and in vitro anticancer activity evaluation of biscarbamic esters of 2,3-bis (hydroxymethyl)-1-methyl-7- and 7,8 -substituted-benzo[g]indoles
    摘要:
    A series of various bis(hydroxymethyl) carbamate derivatives of 7-mono- and 7,8-disubstituted-1-methyl-benzo[g]indoles was prepared in order to evaluate their cytostatic and cytotoxic activities in vitro. Compounds 2a-h showed significant tumor growth inhibition activity and were more potent than the 4,5-dihydrobenzo[g]indole analogues previously described. Compound 2a was the most active in this series, showing high activity and selectivity for some human cancer cell lines in the National Cancer Institute screen. (C) 1998 Elsevier Science S.A. All rights reserved.
    DOI:
    10.1016/s0014-827x(97)00016-5
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文献信息

  • Synthesis and in vitro anticancer activity evaluation of biscarbamic esters of 2,3-bis (hydroxymethyl)-1-methyl-7- and 7,8 -substituted-benzo[g]indoles
    作者:Gérard A. Pinna、Maria A. Pirisi、Mario Sechi、Giuseppe Paglietti
    DOI:10.1016/s0014-827x(97)00016-5
    日期:1998.2
    A series of various bis(hydroxymethyl) carbamate derivatives of 7-mono- and 7,8-disubstituted-1-methyl-benzo[g]indoles was prepared in order to evaluate their cytostatic and cytotoxic activities in vitro. Compounds 2a-h showed significant tumor growth inhibition activity and were more potent than the 4,5-dihydrobenzo[g]indole analogues previously described. Compound 2a was the most active in this series, showing high activity and selectivity for some human cancer cell lines in the National Cancer Institute screen. (C) 1998 Elsevier Science S.A. All rights reserved.
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