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17β-(N-diphenylmethylcarbamoyl)androsta-4-ene-3-one

中文名称
——
中文别名
——
英文名称
17β-(N-diphenylmethylcarbamoyl)androsta-4-ene-3-one
英文别名
17beta-(N-Diphenylmethylcarbamoyl)androsta-4-ene-3-one;(8S,9S,10R,13S,14S,17S)-N-benzhydryl-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthrene-17-carboxamide
17β-(N-diphenylmethylcarbamoyl)androsta-4-ene-3-one化学式
CAS
——
化学式
C33H39NO2
mdl
——
分子量
481.678
InChiKey
ZZYNAUKSQXRBQG-IJSUORRQSA-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):
    6.7
  • 重原子数:
    36
  • 可旋转键数:
    4
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.52
  • 拓扑面积:
    46.2
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    pyridin-2-yl 3-oxo-androst-4-ene-17β-carbothioate二苯甲胺 以the title compound was obtained in a yield of 85%的产率得到17β-(N-diphenylmethylcarbamoyl)androsta-4-ene-3-one
    参考文献:
    名称:
    Steroid derivatives
    摘要:
    发明的化合物##STR1##可用于生产具有5α-还原酶抑制活性的类固醇-17酰胺。
    公开号:
    US05698720A1
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文献信息

  • Steroid derivatives for the treatment of prostatic hypertrophy their
    申请人:Sankyo Company, Limited
    公开号:US05536714A1
    公开(公告)日:1996-07-16
    The invention includes compounds of formula (I): ##STR1## in which R.sup.1 is hydrogen, alkyl, aryl-substituted alkyl or aromatic heterocyclic-substituted alkyl; R.sup.2 is aryl-substituted alkyl, aromatic heterocyclic-substituted alkyl or diarylamino; and R.sup.3 is carboxy or a group of formula --CONHSO.sub.2 R.sup.4 wherein R.sup.4 is alkyl; and pharmaceutically acceptable salts and esters of the compounds. The compounds have valuable 5.alpha.-reductase inhibitory activity and can thus be used for the treatment and prophylaxis of, inter alia, prostatic hypertrophy as well as other disorders arising from excess levels of 5.alpha.-dihydro-testosterone.
    该发明包括式(I)的化合物:##STR1##其中R.sup.1是氢,烷基,芳基取代的烷基或芳香杂环基取代的烷基;R.sup.2是芳基取代的烷基,芳香杂环基取代的烷基或二芳基胺基;R.sup.3是羧基或具有式--CONHSO.sub.2 R.sup.4的基团,其中R.sup.4是烷基;以及该化合物的药用可接受盐和酯。这些化合物具有有价值的5α-还原酶抑制活性,因此可用于治疗和预防前列腺肥大等疾病,以及由于5α-二氢睾酮水平过高而引起的其他疾病。
  • Steroid derivatives
    申请人:Sankyo Company, Limited
    公开号:US05698720A1
    公开(公告)日:1997-12-16
    The invented compound ##STR1## is useful for the production of steroidal-17-amides that have 5.alpha.-reductase inhibitory activity.
    发明的化合物##STR1##可用于生产具有5α-还原酶抑制活性的类固醇-17酰胺。
  • Steroid derivatives for the treatment of prostatic hypertrophy, their
    申请人:Sankyo Company, Limited
    公开号:US05760025A1
    公开(公告)日:1998-06-02
    Compounds of formula (I): ##STR1## \x9bwherein: R.sup.1 is hydrogen, alkyl, aryl-substituted alkyl or aromatic heterocyclic-substituted alkyl; R.sup.2 is: aryl-substituted alkyl, aromatic heterocyclic-substituted alkyl or diarylamino; and R.sup.3 is carboxy or a group of formula --CONHSO.sub.2 R.sup.4 wherein R.sup.4 is alkyl!; and pharmaceutically acceptable salts and esters thereof have valuable 5.alpha.-reductase inhibitory activity and can thus be used for the treatment and prophylaxis of, inter alia, prostatic hypertrophy as well as other disorders arising from excess levels of 5.alpha.-dihydrotestosterone.
    式(I)的化合物:##STR1## 其中:R.sup.1是氢、烷基、芳基取代的烷基或芳香族杂环取代的烷基;R.sup.2是芳基取代的烷基、芳香族杂环取代的烷基或二芳基氨基;R.sup.3是羧基或式--CONHSO.sub.2 R.sup.4中的基团,其中R.sup.4是烷基!;以及其药学上可接受的盐和酯具有有价值的5α-还原酶抑制活性,因此可用于治疗和预防前列腺肥大等由过量5α-二氢睾酮水平引起的其他疾病。
  • Steroid derivatives for the treatment of prostatic hypertrophy, their preparation and uses
    申请人:SANKYO COMPANY LIMITED
    公开号:EP0567271A2
    公开(公告)日:1993-10-27
    Compounds of formula (I): [wherein : R1 is hydrogen, alkyl, aryl-substituted alkyl or aromatic heterocyclic-substituted alkyl ; R2 is: aryl-substituted alkyl, aromatic heterocyclic-substituted alkyl or diarylamino; and R3 is carboxy or a group of formula -CONHS02 R4 wherein R4 is alkyl] ; and pharmaceutically acceptable salts and esters thereof have valuable 5α-reductase inhibitory activity and can thus be used for the treatment and prophylaxis of, inter alia, prostatic hypertrophy as well as other disorders arising from excess levels of 5α-dihydro-testosterone.
    式(I)化合物: [其中 :R1 是氢、烷基、芳基取代的烷基或芳香杂环取代的烷基;R2 是:芳基取代的烷基、芳香杂环取代的烷基或二芳基氨基;以及 R3 是羧基或式 -CONHS02 R4 的基团,其中 R4 是烷基];及其药学上可接受的盐类和酯类具有重要的 5α 还原酶抑制活性,因此可用于治疗和预防前列腺肥大以及因 5α 二氢睾酮水平过高而引起的其他疾病。
  • Compounds suitable for use as intermediates in the preparation of Androst-3,5-dien-3-carboxy derivatives
    申请人:SANKYO COMPANY LIMITED
    公开号:EP0725074A2
    公开(公告)日:1996-08-07
    A compound of formula (IV) and a process for the preparation of a compound of the following formula: in which R10 is a hydroxy group, a group -OR5, in which R5 is a carboxy protecting group, a group -NR1R2, in which R1 is hydrogen, alkyl, aryl-substituted alkyl or aromatic heterocyclic-substituted alkyl and R2 is aryl-substituted alkyl, aromatic heterocyclic-substituted alkyl or diarylamino, or a group -NRR', in which R and R' are hydrogen or alkyl.
    式(IV)化合物 以及制备下式化合物的工艺: 其中 R10 是羟基、基团-OR5(其中 R5 是羧基保护基)、基团-NR1R2(其中 R1 是氢、烷基、芳基取代的烷基或芳香杂环取代的烷基,R2 是芳基取代的烷基、芳香杂环取代的烷基或二芳基氨基)或基团-NRR'(其中 R 和 R' 是氢或烷基)。
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