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25,27-Dihydroxycholestan-26-oic acid | 70021-49-7

中文名称
——
中文别名
——
英文名称
25,27-Dihydroxycholestan-26-oic acid
英文别名
(6R)-6-[(8R,9S,10S,13R,14S,17R)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-hydroxy-2-(hydroxymethyl)heptanoic acid
25,27-Dihydroxycholestan-26-oic acid化学式
CAS
70021-49-7
化学式
C27H46O4
mdl
——
分子量
434.7
InChiKey
LIBMVGAVFUIWNV-CZAZNYCHSA-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):
    7.5
  • 重原子数:
    31
  • 可旋转键数:
    7
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.96
  • 拓扑面积:
    77.8
  • 氢给体数:
    3
  • 氢受体数:
    4

文献信息

  • METHODS FOR THE DETECTION OF PREECLAMPSIA
    申请人:The University Of Western Ontario
    公开号:EP2147309A1
    公开(公告)日:2010-01-27
  • METHODS AND COMPOSITIONS FOR DIAGNOSING, PROGNOSING, AND CONFIRMING PREECLAMPSIA
    申请人:Cooper, Matthew
    公开号:EP3175239A1
    公开(公告)日:2017-06-07
  • COMPOSITIONS AND METHODS FOR TREATMENT OF PEROXISOMAL DISORDERS AND LEUKODYSTROPHIES
    申请人:The Johns Hopkins University
    公开号:EP3368088A1
    公开(公告)日:2018-09-05
  • METHODS FOR DETECTION OF PREECLAMPSIA
    申请人:Lajoie Gilles Andre
    公开号:US20100113286A1
    公开(公告)日:2010-05-06
    Biomarkers associated with preeclampsia were identified. Nine proteins were identified as being differentially regulated between the control and the under 28-weeks preeclamptic samples. Similarly three proteins were identified as being differentially regulated between the control and the over 28-weeks preeclamptic samples. These 12 proteins can be used as potential biomarkers in the diagnosing and prognosing of preeclampsia.
  • A SCREENING METHOD FOR CEREBROTENDINOUS XANTHOMATOSIS USING BILE ALCOHOL GLUCURONIDES AND METABOLITE RATIOS
    申请人:Academisch Medisch Centrum
    公开号:US20210033626A1
    公开(公告)日:2021-02-04
    The invention relates to a method of diagnosing or screening for 27-hydroxylase (CYP27A1) deficiency in an animal comprising: determining in a biological sample the intensity signal by mass analysis of at least a bile alcohol glucuronide and a C24- or C27-bile acid or a conjugate thereof, comparing the intensity signals to a control sample or control value, and determining 27-hydroxylase (CYP27A1) deficiency based on said comparison.
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