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Methanamine, 1-(6,12-diphenyl-9H-bis[1,2,4]triazolo[3,4-d:4',3'-a][1,5]benzodiazepin-9-ylidene)-N,N-dimethyl-

中文名称
——
中文别名
——
英文名称
Methanamine, 1-(6,12-diphenyl-9H-bis[1,2,4]triazolo[3,4-d:4',3'-a][1,5]benzodiazepin-9-ylidene)-N,N-dimethyl-
英文别名
1-(3,11-diphenyl-2,4,5,9,10,12-hexazatetracyclo[11.4.0.02,6.08,12]heptadeca-1(17),3,5,8,10,13,15-heptaen-7-ylidene)-N,N-dimethylmethanamine
Methanamine, 1-(6,12-diphenyl-9H-bis[1,2,4]triazolo[3,4-d:4',3'-a][1,5]benzodiazepin-9-ylidene)-N,N-dimethyl-化学式
CAS
——
化学式
C26H21N7
mdl
——
分子量
431.5
InChiKey
IVDOVSVVGGCAGC-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):
    3.5
  • 重原子数:
    33
  • 可旋转键数:
    3
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    64.7
  • 氢给体数:
    0
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    Diphenyl-1,7 ditriazolo<4,3-a;3,4-d>benzodiazeoine-1,5N,N-二甲基甲酰胺二甲基缩醛吡啶 作用下, 反应 24.0h, 以62%的产率得到Methanamine, 1-(6,12-diphenyl-9H-bis[1,2,4]triazolo[3,4-d:4',3'-a][1,5]benzodiazepin-9-ylidene)-N,N-dimethyl-
    参考文献:
    名称:
    1,5-Benzodiazepines XIV. Synthesis of new substituted 9H-bis-[1,2,4]triazolo[4,3-a:3′,4′-d] [1,5]benzodiazepines and relate compounds endowed with in vitro cytotoxic properties
    摘要:
    A series of 11 new 9H-bis-[1,2,4]triazolo[4,3-a:3',4'-d] [1,5]benzodiazepine derivatives 8e-o was synthesized. Ten of these compounds (8e-m,o), along with four analogues (8a-d) (previously synthesized by us) were tested in vitro in order to evaluate their cytotoxic and anti-HIV-1 properties. In this connection other six original compounds, i.e., five 9-substituted compounds prepared starting from the 6,12-diphenylderivative 8c (compounds 10, 11, 12, 13a,b) and the bis-triazolone derivative 14, were synthesized and tested for the same purpose. While none of the 20 compounds tested exhibited any appreciable anti-HIV-1 activity, some of them exhibited interesting cytotoxic properties, the best results being shown by compounds 8c,d,k and 11 (CC(50) range=3-12 microM). Therefore, these four compounds were further evaluated for their antiproliferative activity against a panel of human tumor cell lines; actually, compounds 8d, 8k and 11 showed antiproliferative properties against either or both leukemia- and lymphoma-derived cell lines in the low micromolar range.
    DOI:
    10.1016/j.farmac.2004.12.005
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