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(20S)-2α-methyl-19,26,27-trinor-1α,25-dihydroxyvitamin D3

中文名称
——
中文别名
——
英文名称
(20S)-2α-methyl-19,26,27-trinor-1α,25-dihydroxyvitamin D3
英文别名
(20S)-2α-methyl-19,26,27-trinor-1α-hydroxyvitamiin D3;2α-methyl-19,26,27-trinor-(20S)-1α hydroxyvitamin D3
(20S)-2α-methyl-19,26,27-trinor-1α,25-dihydroxyvitamin D<sub>3</sub>化学式
CAS
——
化学式
C25H42O2
mdl
——
分子量
374.607
InChiKey
MGADROAPTBMHLU-XOIYRWTMSA-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):
    6.03
  • 重原子数:
    27.0
  • 可旋转键数:
    5.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.84
  • 拓扑面积:
    40.46
  • 氢给体数:
    2.0
  • 氢受体数:
    2.0

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

点击查看最新优质反应信息

文献信息

  • 2alpha-Methyl and 2beta-methyl analogs of 19,26,27-trinor-(20S)-1alpha-hydroxyvitamin D3 and their uses
    申请人:DeLuca F. Hector
    公开号:US20060116352A1
    公开(公告)日:2006-06-01
    This invention discloses 2α-methyl and 2β-methyl analogs of 19,26,27-trinor-(20S) -1α-hydroxyvitamin D 3 and pharmaceutical uses therefor. These compounds exhibit pronounced activity in arresting the proliferation of undifferentiated cells and inducing their differentiation to the monocyte thus evidencing use as an anti-cancer agent and for the treatment of skin diseases such as psoriasis as well as skin conditions such as wrinkles, slack skin, dry skin and insufficient sebum secretion. These compounds also have little, if any, calcemic activity and therefore may be used to treat autoimmune disorders or inflammatory diseases in humans as well as renal osteodystrophy. These compounds may also be used for the treatment or prevention of obesity.
    本发明揭示了19,26,27-三去(20S)-1α-羟基维生素D3的2α-甲基和2β-甲基类似物及其药用。这些化合物在抑制未分化细胞的增殖和诱导它们分化为单核细胞方面表现出显著活性,因此可作为抗癌剂以及用于治疗银屑病等皮肤疾病以及皱纹、松弛皮肤、干燥皮肤和皮脂分泌不足等皮肤状况。这些化合物也几乎没有钙代谢活性,因此可用于治疗人类的自身免疫性疾病或炎症性疾病以及肾性骨病。这些化合物还可用于肥胖的治疗或预防。
  • 26- and 27-Methyl groups of 2-substituted, 19-nor-1α,25-dihydroxylated vitamin D compounds are essential for calcium mobilization in vivo
    作者:Pawel Grzywacz、Lori A. Plum、Margaret Clagett-Dame、Hector F. DeLuca
    DOI:10.1016/j.bioorg.2013.01.001
    日期:2013.4
    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.
  • Vitamin D analogs for obesity prevention and treatment
    申请人:DeLuca F. Hector
    公开号:US20050119242A1
    公开(公告)日:2005-06-02
    Methods for treating and preventing obesity, inhibiting adipocyte differentiation, inhibiting increased SCD-1 gene transcription, and/or reducing body fat in a subject include administering at least one analog of 1α,25-dihydroxyvitamin D 3 or 1α,25-dihydroxyvitamin D 2 or a pharmaceutical composition that includes such an analog to a subject in need thereof. The analog may be a 19-nor vitamin D analog such as a compound of formula IA, a compound of formula IB, or a mixture thereof where the variables R 1 , R 2 , and R 3 have the values described herein.
    治疗和预防肥胖的方法,抑制脂肪细胞分化,抑制增加的SCD-1基因转录,和/或减少受试者体脂肪的方法包括向需要的受试者施用至少一种1α,25-二羟基维生素D3或1α,25-二羟基维生素D2的类似物或包含这种类似物的药物组合物。该类似物可以是19-去甲基维生素D类似物,如式IA的化合物,式IB的化合物,或其中的混合物,其中变量R1、R2和R3具有此处描述的值。
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