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5-[(8R,9S,10S,13S,14S,17S)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pyran-2-one

中文名称
——
中文别名
——
英文名称
5-[(8R,9S,10S,13S,14S,17S)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pyran-2-one
英文别名
——
5-[(8R,9S,10S,13S,14S,17S)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pyran-2-one化学式
CAS
——
化学式
C24H34O2
mdl
——
分子量
354.5
InChiKey
YBPMPRDOWHIVNA-JKBCNOLGSA-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):
    7.2
  • 重原子数:
    26
  • 可旋转键数:
    1
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.79
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • [EN] HELLEBRIN AND HELLEBRIGENIN DERIVATIVES<br/>[FR] HELLÉBRINE ET DÉRIVÉS D'HELLÉBRIGÉNINE
    申请人:UNIBIOSCREEN SA
    公开号:WO2010102673A1
    公开(公告)日:2010-09-16
    The present invention relates to new cardiotonic Steroid Compounds of Formula (I) or (II) wherein X1, X2, X3, L, R1, R2, R3, R4, and R5 have the same meaning as that defined in the Claims. The invention also relates to the use of said Compounds as medicaments, in particular in the treatment of Cancer.
    本发明涉及具有以下式(I)或(II)的新心力素类化合物,其中X1、X2、X3、L、R1、R2、R3、R4和R5的含义与权利要求中定义的含义相同。该发明还涉及将所述化合物用作药物,特别是用于癌症治疗。
  • AhR mediators
    申请人:Krutmann Jean
    公开号:US20090028804A1
    公开(公告)日:2009-01-29
    The invention relates to a method for finding and assessing agonists [and] antagonists of the aryl hydrocarbon receptor (Ah receptor; AhR), to the agonists and antagonists themselves and to uses thereof.
    这项发明涉及一种用于寻找和评估芳香族羟基化合物受体(Ah受体;AhR)的激动剂和拮抗剂的方法,以及这些激动剂和拮抗剂本身及其用途。
  • Modulators of Hypoxia Inducible Factor-1 and Related Uses
    申请人:Gardiner Gregory
    公开号:US20090023666A1
    公开(公告)日:2009-01-22
    The invention features compounds of formulas I or II: and pharmaceutically acceptable salts and prodrugs thereof, as well methods for modulating the effects of local and systemic hypoxic events using the compounds.
    这项发明涉及公式I或II的化合物:以及这些化合物的药用盐和前药,以及使用这些化合物调节局部和全身缺氧事件效应的方法。
  • Topical and oral formulations of cardiac glycosides for treating skin diseases
    申请人:Streeper Robert
    公开号:US20060205679A1
    公开(公告)日:2006-09-14
    The present invention provides method, preparation and use of a variety of pharmaceutical compositions containing at least one digitalis glycoside such as oleandrin, odoroside-A, neriifolin, proscillaridin-A, methyl-proscillaridin-A, digitoxin, digoxin alone or at least one digitalis glycoside complexed with cyclodextrins. In another aspect, the present invention provides an effective method to treat diseases in mammals. In yet another aspect, the present invention provides an effective method for treating skin diseases in a human or non-human animal.
    本发明提供了一种方法、制备和使用多种含有至少一种毛地黄苷类药物成分的药物组合物,例如奥利安定、奥多罗苷A、内里福林、普罗斯西拉里丁A、甲基普罗斯西拉里丁A、地高辛、地高辛或至少一种毛地黄苷类与环糊精络合的药物。另一方面,本发明提供了一种有效的方法来治疗哺乳动物的疾病。另一方面,本发明提供了一种有效的方法来治疗人类或非人类动物的皮肤疾病。
  • [EN] A METHOD FOR LABELING OF ALDEHYDE CONTAINING TARGET MOLECULES<br/>[FR] PROCÉDÉ DE MARQUAGE DE MOLÉCULES CIBLES CONTENANT UN ALDÉHYDE
    申请人:HOFFMANN LA ROCHE
    公开号:WO2018189214A1
    公开(公告)日:2018-10-18
    The present invention relates to a method for binding to a target molecule comprising an aldehyde a compound derived from N- (2-aminoethyl)pyrrole, which compound also comprises a moiety of interest, to compounds (conjugates) obtained by this method, comprising both the target molecule and the moiety of interest and to novel substances derived from N-(2-aminoethyl)pyrrole.
    本发明涉及一种与目标分子结合的方法,包括一种由N-(2-氨基乙基)吡咯烷衍生的醛化合物,该化合物还包括一个感兴趣的基团,以及通过该方法获得的化合物(结合物),包括既含有目标分子又含有感兴趣基团的物质,以及由N-(2-氨基乙基)吡咯烷衍生的新物质。
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