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胆甾烷-3,7,12,26,27-五醇 | 2952-70-7

中文名称
胆甾烷-3,7,12,26,27-五醇
中文别名
——
英文名称
5alpha-Cyprinol
英文别名
(3R,5R,7R,8R,9S,10S,12S,13R,14S,17R)-17-[(2R)-7-hydroxy-6-(hydroxymethyl)heptan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,7,12-triol
胆甾烷-3,7,12,26,27-五醇化学式
CAS
2952-70-7
化学式
C27H48O5
mdl
——
分子量
452.7
InChiKey
JNMALBXXJSWZQY-BBBUMGABSA-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):
    4
  • 重原子数:
    32
  • 可旋转键数:
    7
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    101
  • 氢给体数:
    5
  • 氢受体数:
    5

文献信息

  • BILE ALCOHOL AND DRUG CONTAINING THE SAME AS ACTIVE INGREDIENT
    申请人:TSUMURA CO., LTD.
    公开号:EP0489933A1
    公开(公告)日:1992-06-17
    A novel bile alcohol of general formula (I), having an efficacious physiological activity and being specified in the configurations of particularly the 20-, 24- and 25-positions; formula (I) wherein one of the groups R₁ and R₂ represents a group of formula (A) or (B) while the other represents -OH or -H; R₃ and R₄ represent each -CH₂OH, -CH₃ or -CH₂OSO₃Na; or alternatively R₂ and R₃ are combined together to represent -OCH₂-, R₂ and R₄ are combined together to represent -OCH₂-, or R₃ and R₄ are combined together to represent -CH₂OCH₂-; provided that R₃ and R₄ do not represent -CH₃ at the same time and that R₁ represents -OH or -H and R₂ represents the group of formula (A) or (B) when R₃ and R₄ represent -CH₂OH at the same time. A drug containing the bile alcohol, including those wherein R₃ and R₄ in the above formula (I) represent each -H, -CH₂OH, -CH₃ or -CH₂OSO₃Na (except for the case where both R₃ and R₄ represent -H at the same time), and 3α 7α, 12α, 24-tetrahydroxy-5α- or -5β-cholane is efficacious as a cerebral function protective agent, cholagogue, cell activator, microcirculation improver, antiarteriosclerotic agent, antihyperlipemia drug, hepatic function improver, anti-inflammatory drug, antithrombotic drug and hypertensive.
    通式(I)的新胆醇具有有效的生理活性,特别是在20、24和25位的构型中进行了指定。其中,R₁和R₂中的一个代表公式(A)或(B)的基团,而另一个代表-OH或-H;R₃和R₄分别代表-CH₂OH、-CH₃或-CH₂OSO₃Na;或者R₂和R₃结合在一起代表-OCH₂-,R₂和R₄结合在一起代表-OCH₂-,或者R₃和R₄结合在一起代表-CH₂OCH₂-;前提是R₃和R₄不能同时表示-CH₃,而且当R₃和R₄同时表示-CH₂OH时,R₁表示-OH或-H,R₂表示公式(A)或(B)的基团。含有胆醇的药物,包括上述公式(I)中R₃和R₄分别表示-H、-CH₂OH、-CH₃或-CH₂OSO₃Na的药物(除了R₃和R₄同时表示-H的情况),以及3α 7α,12α,24-四羟基-5α-或-5β-胆烷作为脑功能保护剂、胆汁促进剂、细胞活化剂、微循环改善剂、抗动脉硬化药、降脂药、肝功能改善剂、抗炎药、抗血栓药和降压药具有有效性。
  • METHODS, COMPOSITIONS, AND KITS FOR THE TREATMENT OF CANCER
    申请人:Haggerty Timothy J.
    公开号:US20140335050A1
    公开(公告)日:2014-11-13
    The invention features methods, compositions, and kits for the administration of an HSP90 inhibitor, OBAA, flunarizine, aphidicolin, damnacanthal, dantrolene, or an analog thereof, alone, or in combination with, e.g., a TAA, an antigen-binding scaffold (e.g., an antibody, a soluble T cell receptor, or a chimeric receptor) specific for a TAA, a cell (e.g., a white blood cell that targets a cancer cell), and/or an IFN-β receptor agonist or an IFN-γ receptor agonist, for the treatment of cancer.
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