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4-(tert-butyldimethylsilanyloxy)-3-iodo-5-methoxyphenol | 1470110-74-7

中文名称
——
中文别名
——
英文名称
4-(tert-butyldimethylsilanyloxy)-3-iodo-5-methoxyphenol
英文别名
4-[Tert-butyl(dimethyl)silyl]oxy-3-iodo-5-methoxyphenol
4-(tert-butyldimethylsilanyloxy)-3-iodo-5-methoxyphenol化学式
CAS
1470110-74-7
化学式
C13H21IO3Si
mdl
——
分子量
380.298
InChiKey
PHSOARKQACUBMF-UHFFFAOYSA-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):
    4.39
  • 重原子数:
    18
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.54
  • 拓扑面积:
    38.7
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    4-(tert-butyldimethylsilanyloxy)-3-iodo-5-methoxyphenol4-二甲氨基吡啶 作用下, 以 二氯甲烷 为溶剂, 以93%的产率得到
    参考文献:
    名称:
    The carbonate analogues of 5′-halogenated resiniferatoxin as TRPV1 ligands
    摘要:
    A series of carbonate analogues of 5'-halogenated RTX have been investigated in order to examine the effect of the carbonate group as a linker and the role of halogens in the reversal of activity from agonism to antagonism for rat and human TRPV1 heterologously expressed in Chinese hamster ovary cells. The carbonate analogues showed similar activities to the corresponding RTX derivatives in rat TRPV1 but lower potency in human TRPV1. 5-Halogenation converted the agonists to partial agonists or full antagonists and the extent of antagonism reflected the order of I > Br > Cl > F, with a somewhat greater extent of antagonism for the derivatives of the 4-amino RTX surrogates compared to the corresponding derivatives of RTX itself. The carbonate analogues of I-RTX: (60) and 5-bromo-4-amino-RTX (66) were potent and full antagonists with K-i(ant) = 2.23 and 2.46 nM, respectively, for rat TRPV1, which were ca. 5-fold more potent than I-RTX (2) under our conditions. The conformational analysis of the I-RTX-carbonate (60) indicated that its bent conformation was similar to that of I-RTX, consistent with compound 60 and I-RTX showing comparable potent antagonism. (C) 2013 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2013.07.042
  • 作为产物:
    描述:
    formic acid 4-(tert-butyldimethylsilanyloxy)-3-iodo-5-methoxyphenyl esterpotassium carbonate 作用下, 以 甲醇 为溶剂, 反应 12.0h, 以24%的产率得到4-(tert-butyldimethylsilanyloxy)-3-iodo-5-methoxyphenol
    参考文献:
    名称:
    The carbonate analogues of 5′-halogenated resiniferatoxin as TRPV1 ligands
    摘要:
    A series of carbonate analogues of 5'-halogenated RTX have been investigated in order to examine the effect of the carbonate group as a linker and the role of halogens in the reversal of activity from agonism to antagonism for rat and human TRPV1 heterologously expressed in Chinese hamster ovary cells. The carbonate analogues showed similar activities to the corresponding RTX derivatives in rat TRPV1 but lower potency in human TRPV1. 5-Halogenation converted the agonists to partial agonists or full antagonists and the extent of antagonism reflected the order of I > Br > Cl > F, with a somewhat greater extent of antagonism for the derivatives of the 4-amino RTX surrogates compared to the corresponding derivatives of RTX itself. The carbonate analogues of I-RTX: (60) and 5-bromo-4-amino-RTX (66) were potent and full antagonists with K-i(ant) = 2.23 and 2.46 nM, respectively, for rat TRPV1, which were ca. 5-fold more potent than I-RTX (2) under our conditions. The conformational analysis of the I-RTX-carbonate (60) indicated that its bent conformation was similar to that of I-RTX, consistent with compound 60 and I-RTX showing comparable potent antagonism. (C) 2013 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2013.07.042
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