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2-<(2,2-dimethyl-2H-1-benzopyran-6-yl)methylene>hydrazinecarboximidamide

中文名称
——
中文别名
——
英文名称
2-<(2,2-dimethyl-2H-1-benzopyran-6-yl)methylene>hydrazinecarboximidamide
英文别名
2-[(2,2-dimethyl-2H-1-benzopyran-6-yl)methylene]hydrazinecarboximidamide;2-[(E)-(2,2-dimethylchromen-6-yl)methylideneamino]guanidine
2-<(2,2-dimethyl-2H-1-benzopyran-6-yl)methylene>hydrazinecarboximidamide化学式
CAS
——
化学式
C13H16N4O
mdl
——
分子量
244.296
InChiKey
SUWHSMVLNNYPQE-LZYBPNLTSA-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):
    1.4
  • 重原子数:
    18
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    86
  • 氢给体数:
    2
  • 氢受体数:
    3

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:
    6-formyl-2,2-dimethyl-2H-chromene氨基胍硝酸盐乙醇 为溶剂, 反应 1.0h, 以81%的产率得到2-<(2,2-dimethyl-2H-1-benzopyran-6-yl)methylene>hydrazinecarboximidamide
    参考文献:
    名称:
    Guanabenz-related amidinohydrazones: potent non-azole inhibitors of aldosterone biosynthesis
    摘要:
    A new series of potent, guanabenz-derived, non-steroidal aldosterone biosynthesis inhibitors are presented. Salient features of the structure-activity relationship indicate the requirement of a hydrophobic core, presence of a hydrophilic (or basic) peripheral appendage, and, in some cases, profound dependence on hydrazone stereochemistry. The most potent compound of the series, 29, was 2 orders of magnitude more potent than guanabenz as an aldosterone biosynthesis inhibitor.
    DOI:
    10.1016/0223-5234(94)90040-x
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文献信息

  • Guanabenz-related amidinohydrazones: potent non-azole inhibitors of aldosterone biosynthesis
    作者:RM Soll、PJ Dollings、RD Mitchell、DA Hafner
    DOI:10.1016/0223-5234(94)90040-x
    日期:1994.1
    A new series of potent, guanabenz-derived, non-steroidal aldosterone biosynthesis inhibitors are presented. Salient features of the structure-activity relationship indicate the requirement of a hydrophobic core, presence of a hydrophilic (or basic) peripheral appendage, and, in some cases, profound dependence on hydrazone stereochemistry. The most potent compound of the series, 29, was 2 orders of magnitude more potent than guanabenz as an aldosterone biosynthesis inhibitor.
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