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chloromethyl 11β,17α-dihydroxy-3-oxo-androst-4-ene-17β-carboxylate | 82034-75-1

中文名称
——
中文别名
——
英文名称
chloromethyl 11β,17α-dihydroxy-3-oxo-androst-4-ene-17β-carboxylate
英文别名
11β,17α-dihydroxy-3-oxoandrost-4-ene 17β-carboxylic acid, chloromethyl ester;chloromethyl 11β,17α-dihydroxyandrost-4-en-3-one-17β-carboxylate;chloromethyl (8S,9S,10R,11S,13S,14S,17R)-11,17-dihydroxy-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthrene-17-carboxylate
chloromethyl 11β,17α-dihydroxy-3-oxo-androst-4-ene-17β-carboxylate化学式
CAS
82034-75-1
化学式
C21H29ClO5
mdl
——
分子量
396.911
InChiKey
GYZBEEMAEDGMPO-MXRBDKCISA-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

物化性质

  • 沸点:
    528.3±50.0 °C(Predicted)
  • 密度:
    1.31±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.6
  • 重原子数:
    27
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.81
  • 拓扑面积:
    83.8
  • 氢给体数:
    2
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Soft steroids having anti-inflammatory activity
    申请人:Otsuka Pharmaceutical Co., Ltd.
    公开号:US04710495A1
    公开(公告)日:1987-12-01
    Novel soft steroid anti-inflammatory agents, said agents being esters or thioesters of 17.alpha.-alkoxy-11.beta.-hydroxyandrost-4-en-3-one-17.beta.-carboxylic acids, pharmaceutical compositions containing said agents, novel chemical intermediates useful in the preparation of said agents and methods of administering same to mammals in the treatment of inflammation. Preferred compounds are the haloalkyl esters of 17.alpha.-alkoxy-11.beta.-hydroxyandrost-4-en-3-one-17.beta.-carboxylic acids.
    一种新型软性类固醇抗炎剂,该剂为17α-烷氧基-11β-羟基雄甾-4-烯-3-酮-17β-羧酸酯或硫酯,含有该剂的制药组合物,用于制备该剂的新型化学中间体以及在治疗炎症中向哺乳动物施用该剂的方法。优选的化合物是17α-烷氧基-11β-羟基雄甾-4-烯-3-酮-17β-羧酸的卤代烷基酯。
  • ——
    作者:Roy J. Little、Nicholas Bodor、Thorsteinn Loftsson
    DOI:10.1023/a:1018907026460
    日期:——
    Purpose. The soft drug approach was applied to the design of analogs of highly potent synthetic steroids but with a metabolically labile ester group which at the same time served as an activating group.Methods. Several structural modifications of soft antiinflammatory steroids were synthesized and tested in several assays of biological activity. The hydrolytic stability of the compounds was also determined.Results. One of the compounds synthesized was determined to be a very potent steroid and had a highly significant separation of topical from systemic activity. However, the compound demonstrated greater than expected stability in the hydrolysis studies.Conclusions. The goal of the soft drug approach has been achieved with the development of a highly potent drug which displays little or no systemic activity as measured in the tests presented here. The anticipated hydrolytic instability of the compounds was not corroborated, however, in view of other results, the interpretation is allowed that the rapid hydrolysis of the unbound fraction of the drug is an important factor in its lack of systemic effects.
  • Regioselective O-alkylation of cortienic acid and synthesis of a new class of glucocorticoids containing a 17α-alkoxy, a 17α-(1′-alkoxyethyloxy), a 17α-alkoxymethyloxy, or a 17α-methylthiomethyloxy function
    作者:Pascal Druzgala、Nicholas Bodor
    DOI:10.1016/0039-128x(91)90008-j
    日期:1991.9
    The synthesis of a new class of glucocorticoids, to be evaluated as anti-inflammatory agents with expected low systemic toxicity, is described. The new steroids possess a 17-beta-chloromethyl carboxylate function and a 17-alpha-alkoxy, a 17-alpha-(1'-alkoxyethyloxy), a 17-alpha-alkoxymethyloxy, or a 17-alpha-methylthiomethyloxy function. A 17-alpha-alkoxy function is a new feature in cortisol analogs.
  • EP0334853A4
    申请人:——
    公开号:EP0334853A4
    公开(公告)日:1990-02-26
  • US4710495A
    申请人:——
    公开号:US4710495A
    公开(公告)日:1987-12-01
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