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3β-(12-amino-4,9-diaza-dodecyl)amino-cholestane | 177745-14-1

中文名称
——
中文别名
——
英文名称
3β-(12-amino-4,9-diaza-dodecyl)amino-cholestane
英文别名
N-(3-aminopropyl)-N'-[3-[[(3S,5S,8R,9S,10S,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl]amino]propyl]butane-1,4-diamine
3β-(12-amino-4,9-diaza-dodecyl)amino-cholestane化学式
CAS
177745-14-1
化学式
C37H72N4
mdl
——
分子量
573.005
InChiKey
ZVJHDZDKTAFFTJ-OVUDSTMFSA-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):
    9.8
  • 重原子数:
    41
  • 可旋转键数:
    18
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    62.1
  • 氢给体数:
    4
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    精胺5-Alpha-胆甾烷-3-酮titanium(IV) isopropylate 、 sodium tetrahydroborate 作用下, 以 甲醇 为溶剂, 反应 14.0h, 以95%的产率得到3β-(12-amino-4,9-diaza-dodecyl)amino-cholestane
    参考文献:
    名称:
    New stereoselective titanium reductive amination synthesis of 3-amino and polyaminosterol derivatives possessing antimicrobial activities
    摘要:
    A series of 3-amino and polyaminosterol analogues of squalamine and trodusquemine were synthesized involving a new stereoselective titanium reductive amination reaction in high chemical yields of up to 95% in numerous cases. These derivatives were evaluated for their in vitro antimicrobial properties against human pathogens. Activity was highly dependent on the different compounds' structures involved and best results have been obtained with aminosterol derivatives 4b, 4e and 6i exhibiting activities against yeasts, Gram positive and Gram negative bacteria at average concentrations of 6.25-12.5 mu g/mL. (c) 2007 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2007.04.006
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文献信息

  • New stereoselective titanium reductive amination synthesis of 3-amino and polyaminosterol derivatives possessing antimicrobial activities
    作者:Chanaz Salmi、Celine Loncle、Nicolas Vidal、Yves Letourneux、Jean Michel Brunel
    DOI:10.1016/j.ejmech.2007.04.006
    日期:2008.3
    A series of 3-amino and polyaminosterol analogues of squalamine and trodusquemine were synthesized involving a new stereoselective titanium reductive amination reaction in high chemical yields of up to 95% in numerous cases. These derivatives were evaluated for their in vitro antimicrobial properties against human pathogens. Activity was highly dependent on the different compounds' structures involved and best results have been obtained with aminosterol derivatives 4b, 4e and 6i exhibiting activities against yeasts, Gram positive and Gram negative bacteria at average concentrations of 6.25-12.5 mu g/mL. (c) 2007 Elsevier Masson SAS. All rights reserved.
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