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25-Hydroxy-26,26,26,27,27,27-hexafluorovitamin D3 | 75303-43-4

中文名称
——
中文别名
——
英文名称
25-Hydroxy-26,26,26,27,27,27-hexafluorovitamin D3
英文别名
26,26,26,27,27,27-hexafluoro-25-hydroxyvitamin D3/26,26,26,27,27,27-hexafluoro-25-hydroxycholecalciferol;(1S,3Z)-3-[(2E)-2-[(1R,3aS,7aR)-7a-methyl-1-[(2R)-7,7,7-trifluoro-6-hydroxy-6-(trifluoromethyl)heptan-2-yl]-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-4-methylidenecyclohexan-1-ol
25-Hydroxy-26,26,26,27,27,27-hexafluorovitamin D3化学式
CAS
75303-43-4
化学式
C27H38F6O2
mdl
——
分子量
508.588
InChiKey
UYSBDEYGNDFSLX-CSWVGKENSA-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):
    7.7
  • 重原子数:
    35
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.78
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    8

SDS

SDS:efb0b6afac4686347f5b8dd6bd0c2603
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上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    25-Hydroxy-26,26,26,27,27,27-hexafluorovitamin D3氧气 、 rose bengal 作用下, 以 乙醇 为溶剂, 反应 0.25h, 以40%的产率得到26,26,26,27,27,27-hexafluoro-25-hydroxy-6,19-dihydro-6,19-epidioxyvitamin D3
    参考文献:
    名称:
    Syntheses and differentiating action of vitamin D endoperoxides. Singlet oxygen adducts of vitamin D derivatives in human myeloid leukemia cells (HL-60)
    摘要:
    Singlet oxygen adducts of various vitamin D derivatives, 6,19-dihydro-6,19-epidioxyvitamin D (vitamin D endoperoxides, 2 and 2'), were chemically synthesized, and their biological activity in inducing differentiation of a human myeloid leukemia cell line (HL-60 cells) was examined. The potency of the endoperoxides derived from vitamin D derivatives possessing the 1 alpha-hydroxyl group such as 1 alpha, 25-dihydroxyvitamin D3 endoperoxides (2b and 2b') was markedly (10(-2)) diminished relative to the respective parent vitamin D compounds. In contrast, 25-hydroxyvitamin D3 endoperoxides [25-(OH)D3 endoperoxides, 2a and 2a'] and their analogues fluorinated at the 24- or 26- and 27-positions were 2.5-10 times more potent than 25-hydroxyvitamin D3 (1a) in spite of the absence of the conjugated triene structure typical of vitamin D compounds. The potency of these vitamin D endoperoxides (2 and 2'), especially those lacking the 1 alpha-hydroxyl group, in inducing differentiation of HL-60 cells was not correlated with their activity in binding to the cytosol receptor for 1 alpha, 25-dihydroxyvitamin D3 (1b). The binding efficiency to the receptor was relatively lower than the differentiating activity. To examine the action of vitamin D endoperoxides, carbon analogues of 25-(OH)D3 endoperoxides, two C-6 epimers of 25-hydroxy-6,19-dihydro-6,19-ethanovitamin D3 (6 and 6'), were synthesized. The carbon analogues (6 and 6') had no potential to induce differentiation of HL-60 cells. These results suggest that vitamin D endoperoxides (2 and 2') express their biological activity probably after being converted to some other compounds.
    DOI:
    10.1021/jm00147a005
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文献信息

  • Composition for solid pharmaceutical preparations of active vitamins D3 and process for preparation thereof
    申请人:TEIJIN LIMITED
    公开号:EP0116755B1
    公开(公告)日:1987-08-05
  • US4248791A
    申请人:——
    公开号:US4248791A
    公开(公告)日:1981-02-03
  • US4594192A
    申请人:——
    公开号:US4594192A
    公开(公告)日:1986-06-10
  • US4613594A
    申请人:——
    公开号:US4613594A
    公开(公告)日:1986-09-23
  • US4729895A
    申请人:——
    公开号:US4729895A
    公开(公告)日:1988-03-08
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