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(20R)-2-methylene-19,26,27-trinor-1α-hydroxyvitamin D3

中文名称
——
中文别名
——
英文名称
(20R)-2-methylene-19,26,27-trinor-1α-hydroxyvitamin D3
英文别名
(20R)-2α-methyl-19,26,27-trinor-1α,25-dihydroxycalciferol
(20R)-2-methylene-19,26,27-trinor-1α-hydroxyvitamin D<sub>3</sub>化学式
CAS
——
化学式
C25H42O3
mdl
——
分子量
390.607
InChiKey
YZIQNNXLWCGZKG-SSUAOLEZSA-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):
    5.01
  • 重原子数:
    28.0
  • 可旋转键数:
    6.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.84
  • 拓扑面积:
    60.69
  • 氢给体数:
    3.0
  • 氢受体数:
    3.0

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

  • 作为产物:
    描述:
    (S)-2-((3R,3aR,7S,7aR)-octahydro-7-hydroxy-3a-methyl-1H-inden-3-yl)propyl 4-methylbenzenesulfonate吡啶 、 lithium aluminium tetrahydride 、 tris(triphenylphosphine)rhodium(l) chloride 、 pyridinium dichromate 、 nickel(II) chloride hexahydrate 、 氢氟酸氢气4-甲基苯磺酸吡啶苯基锂三乙胺 、 potassium iodide 、 作用下, 以 四氢呋喃乙醚二氯甲烷环己烷丙酮乙腈 为溶剂, 反应 75.0h, 生成 (20R)-2-methylene-19,26,27-trinor-1α-hydroxyvitamin D3 、 (20R)-2β-methyl-19,26,27-trinor-1α-hydroxyvitamin D3
    参考文献:
    名称:
    26- and 27-Methyl groups of 2-substituted, 19-nor-1α,25-dihydroxylated vitamin D compounds are essential for calcium mobilization in vivo
    摘要:
    Twelve new analogs of 19-nor-1 alpha,25-dihydroxyvitamin D-3 6-17, were prepared by a multi-step procedure from known alcohols 18 and 19. We have examined the influence of removing two methyl groups located at C-25, as well as the 25-hydroxy group, on the biological in vitro and in vivo biological activity. Surprisingly, removal of the 26- and 27-methyl groups from either the 2 alpha-methyl or 2-methylene-19-nor-1 alpha,25-dihydroxyvitamin D-3 reduced vitamin D receptor binding, HL-60 differentiation, and 25-hydroxylase transcription in vitro only slightly to moderately (compounds 6-13). However, these compounds were devoid of in vivo bone mobilization activity and had markedly reduced activity on intestinal calcium transport. The analogs 14-17 with a 2 beta-methyl substitution had little or no activity in vitro and in vivo as expected from previous work. (C) 2013 Elsevier Inc. All rights reserved.
    DOI:
    10.1016/j.bioorg.2013.01.001
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文献信息

  • 2-Substituted-1Alpha,25-Dihydroxy-19,26,27-Trinor Vitamin D Analogs and Uses Thereof
    申请人:DeLuca F. Hector
    公开号:US20070238704A1
    公开(公告)日:2007-10-11
    Compounds of formula I, II or III are provided where X 1 , X 2 and X 3 are independently selected from H and hydroxy protecting groups and R 1 and R 2 are independently selected from H or straight or branched chain alkyl groups having from 1 to 8 carbon atoms, straight or branched chain alkenyl groups having from 2 to 8 carbon atoms, straight or branched chain hydroxy-substituted alkyl groups having from 1 to 8 carbon atoms, or straight and branched chain hydroxy-substituted alkenyl groups having from 2 to 8 carbon atoms; and R 3 is independently selected from straight or branched chain alkyl groups having from 1 to 8 carbon atoms, straight or branched chain alkenyl groups having from 2 to 8 carbon atoms, straight or branched chain hydroxy-substituted alkyl groups having from 1 to 8 carbon atoms, or straight and branched chain hydroxy-substituted alkenyl groups having from 2 to 8 carbon atoms. Such compounds are used in preparing pharmaceutical compositions and are useful in treating a variety of biological conditions.
    提供了I、II或III式化合物,其中X1、X2和X3独立地选择自H和羟基保护基团,R1和R2独立地选择自具有1至8个碳原子的直链或支链烷基基团、具有2至8个碳原子的直链或支链烯基基团、具有1至8个碳原子的直链或支链羟基取代烷基基团或具有2至8个碳原子的直链和支链羟基取代烯基基团;而R3独立地选择自具有1至8个碳原子的直链或支链烷基基团、具有2至8个碳原子的直链或支链烯基基团、具有1至8个碳原子的直链或支链羟基取代烷基基团或具有2至8个碳原子的直链和支链羟基取代烯基基团。这些化合物用于制备药物组合物,并且在治疗各种生物状况方面非常有用。
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