摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

11α,15α-dihydroxypregn-4-ene-3,20-dione | 640-33-5

中文名称
——
中文别名
——
英文名称
11α,15α-dihydroxypregn-4-ene-3,20-dione
英文别名
11α,15α-dihydroxy-pregn-4-ene-3,20-dione;11α,15α-Dihydroxy-pregn-4-en-3,20-dion;11alpha,15alpha-Dihydroxypregn-4-ene-3,20-dione;(8S,9S,10R,11R,13S,14S,15S,17S)-17-acetyl-11,15-dihydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
11α,15α-dihydroxypregn-4-ene-3,20-dione化学式
CAS
640-33-5
化学式
C21H30O4
mdl
——
分子量
346.467
InChiKey
BXGCPPYCSCLHER-LBZTYHDASA-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):
    1.2
  • 重原子数:
    25
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.81
  • 拓扑面积:
    74.6
  • 氢给体数:
    2
  • 氢受体数:
    4

SDS

SDS:4b260e284aaa109f0f7e6ad0502ac74f
查看

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

反应信息

点击查看最新优质反应信息

文献信息

  • Microbial Hydroxylation of Hydroxyprogesterones and α-Glucosidase Inhibition Activity of Their Metabolites
    作者:Muhammad Iqbal Choudhary、Muhammad Nasir、Shamsun N. Khan、Muhammad Atif、Rahat A. Ali、Syed M. Khalil、Atta-ur Rahman
    DOI:10.1515/znb-2007-0419
    日期:2007.4.1
    elegans and Fusarium lini yielded 11α,17α- dihydroxypregn-4-ene-3,20-dione (9), and 17α-hydroxypregna-1,4-diene-3,20-dione (10). The structures of the metabolites 3 - 10 were deduced on the basis of spectroscopic methods. Compound 3 was identified as a new metabolite, which exhibited a promising inhibitory activity against the α-glucosidase enzyme.
    11α-羟基孕酮 (1) 与 Cunninghamella elegans、Gibberella fujikuroi、Fusarium lini 和白色念珠菌的微生物转化产生 11α,15α,16α-trihydroxypregn-4-ene-3,20-dione (3), 11α-hydroxy pregnane-3,20-dione (4), 6β,11α-dihydroxypregn-4-ene-3,20-dione (5), 11α-hydroxypregna-1,4-diene-3,20-dione (6), 11α ,17β-dihydroxyandrost-4-en-3-one (7) 和 11α,15α-dihydroxypregn-4-ene-3,20-dione (8)。另一方面,17α-羟基孕酮 (2) 与 Cunninghamella elegans 和 Fusarium
  • Studies on Digitalis Glycosides. XII. Structures of Digipronin and Digiprogenin.
    作者:Daisuke Satoh
    DOI:10.1248/cpb.10.43
    日期:——
    Digipronin, a digitanol glycoside, and its aglycone, γ-digiprogenin, were respectively converted to isodigipronin and its aglycone, α-digiprogenin, by treatment with dilute alkali or acid. On refluxing with acid, α-digiprogenin lost an element of water and formed β-digiprogenin. The structure of the ⊿4-3-oxo compound, obtained from β-digiprogenin by reduction with acetic acid and zinc dust followed by Oppenauer oxidation, was established as 14β, 17α-pregn-4-ene-3, 11, 15, 20-tetrone by comparison with the product of isomerization of pregn-4-ene-3, 11, 15, 20-tetrone with alkali or acid. Consequently, the structure of β-digiprogenin was presumed as 3β-hydroxy-14β-pregna-5, 16-diene-11, 15, 20-trione and the tertiary hydroxyl group in α-and γ-digiprogenin would be located at 17-position. In view of the stability of α-digiprogenin to dilute alkali or acid and its negative contribution to optical rotation compared to γ-digiprogenin, it would be appropriate to give the structure of 3β, 17α-dihydroxy-14β-pregn-5-ene-11, 15, 20-trione and 3β, 17α-dihydroxypregn-5-ene-11, 15, 20-trione to α-and γ-digiprogenin, respectively. Digipronin is a monodigitaloside of γ-digiprogenin.
    通过稀碱或稀酸的处理,地吉孕宁(地吉孕酚苷)及其苷元--γ-地吉孕宁分别转化为异地吉孕宁及其苷元--α-地吉孕宁。用酸回流时,α-二脂原素失去了水元素,形成了 β-二脂原素。通过与孕-4-烯-3,11,15,20-四酮与碱或酸异构化的产物进行比较,从 β-二脂原素中用乙酸和锌粉还原,再用奥普瑙尔氧化法得到的⊿4-3-氧代化合物的结构被确定为 14β,17α-孕-4-烯-3,11,15,20-四酮。因此,β-二脂原蛋白的结构被推测为 3β-hydroxy-14β-pregna-5, 16-diene-11, 15, 20-triione,而 α 和 γ-二脂原蛋白中的叔羟基将位于 17 位。鉴于α-二降头素对稀碱或稀酸的稳定性,以及与γ-二降头素相比它对光学旋转的负作用,将 3β,17α-二羟基-14β-孕甾-5-烯-11,15,20-三酮和 3β,17α-二羟基孕甾-5-烯-11,15,20-三酮的结构分别赋予α-和γ-二降头素是合适的。地吉孕宁是γ-地吉孕宁的单二萜苷。
  • Satoh,D., Chemical and pharmaceutical bulletin, 1960, vol. 8, p. 270 - 272
    作者:Satoh,D.
    DOI:——
    日期:——
  • Schubert; Siebert, Chemische Berichte, 1958, vol. 91, p. 1856,1859
    作者:Schubert、Siebert
    DOI:——
    日期:——
  • Schubert et al., Chemische Berichte, 1957, vol. 90, p. 2576,2579
    作者:Schubert et al.
    DOI:——
    日期:——
查看更多