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(2,2-dimethyl-[1,3]-dioxolan-4-yl)-methylamine

中文名称
——
中文别名
——
英文名称
(2,2-dimethyl-[1,3]-dioxolan-4-yl)-methylamine
英文别名
(2,2-dimethyl-1,3-dioxolan-4-yl)methanamine;(2,2-Dimethyl-[1,3]dioxolan-4-yl)-methylamine;N,2,2-trimethyl-1,3-dioxolan-4-amine
(2,2-dimethyl-[1,3]-dioxolan-4-yl)-methylamine化学式
CAS
——
化学式
C6H13NO2
mdl
——
分子量
131.175
InChiKey
KSUOODHGNBDGGQ-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):
    0.2
  • 重原子数:
    9
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    30.5
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

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文献信息

  • 12-EPI PLEUROMUTILINS
    申请人:NABRIVA THERAPEUTICS AG
    公开号:US20160332963A1
    公开(公告)日:2016-11-17
    A compound selected from 14-O-[((Alkyl-, cycloalkyl-, heterocycloalkyl-, heteoroaryl-, or aryl)-sulfanyl)-acetyl]-12-epi-mutilins, or 14-O-[((Alkyl-, cycloalkyl-, heterocycloalkyl-, heteoroaryl-, or aryl)-oxy)-acetyl]-12-epi-mutilins, wherein 12-epi-mutilin is characterized in that the mutilin ring at position 12 is substituted by two substituents, the first substituent at position 12 of the mutilin ring is a methyl group which methyl group has the inverse stereochemistry compared with the stereochemistry of the methyl group at position 12 of the naturally occurring pleuromutilin ring, the second substituent at position 12 of the mutilin ring is a hydrocarbon group comprising at least one nitrogen atom and all other substituents of the mutilin ring having the same stereochemistry compared with the stereochemistry of the substituents at the corresponding positions in the naturally occurring pleuromutilin ring; optionally in the form of a salt and/or solvate, wherein the naturally occurring pleuromutilin is of formula processes for the preparation of such compounds and their use as pharmaceuticals.
    从14-O-[((烷基、环烷基、杂环烷基、杂环芳基或芳基)-硫基)-乙酰基]-12-epi-木替林,或14-O-[((烷基、环烷基、杂环烷基、杂环芳基或芳基)-氧基)-乙酰基]-12-epi-木替林中选择的一种化合物,其中12-epi-木替林的特征在于木替林环在位置12被两个取代基取代,木替林环在位置12的第一个取代基是一个甲基基团,该甲基基团的立体化学与天然存在的普鲁木替林环在位置12的甲基基团的立体化学相反,木替林环在位置12的第二个取代基是一个含有至少一个氮原子的碳氢基团,木替林环的所有其他取代基与天然存在的普鲁木替林环中相应位置的取代基的立体化学相同;可选地以盐和/或溶剂的形式存在,其中天然存在的普鲁木替林的化学式为 制备这类化合物的方法以及它们作为药物的用途。
  • Kinase Inhibitors
    申请人:Wurster A. Julie
    公开号:US20070032478A1
    公开(公告)日:2007-02-08
    The present invention relates to organic molecules capable of modulating tyrosine kinase signal transduction in order to regulate, modulate and/or inhibit abnormal cell proliferation.
    本发明涉及有机分子,能够调节酪氨酸激酶信号传导,以调节、调控和/或抑制异常细胞增殖。
  • Heterocyclic cannabinoid receptor antagonists
    申请人:Mayweg Alexander
    公开号:US20050250769A1
    公开(公告)日:2005-11-10
    The present invention relates to compounds of formula I and pharmaceutically acceptable salts thereof. The compounds are useful for the treatment and/or prophylaxis of diseases which are associated with the modulation of CB1 receptors.
    本发明涉及公式I的化合物及其药用盐。这些化合物可用于治疗和/或预防与CB1受体调节相关的疾病。
  • KINASE INHIBITORS FOR THE TREATMENT OF DISEASE
    申请人:Allergan, Inc.
    公开号:US20040102509A1
    公开(公告)日:2004-05-27
    The present invention relates to organic molecules capable of modulating tyrosine kinase signal transduction in order to regulate, modulate and/or inhibit abnormal cell proliferation.
    本发明涉及有机分子,能够调节酪氨酸激酶信号传导,以调控、调节和/或抑制异常细胞增殖。
  • 1,6- AND 1,8-NAPHTHYRIDINES
    申请人:Luk Kin-Chun
    公开号:US20120184562A1
    公开(公告)日:2012-07-19
    Compounds of formula and pharmaceutically acceptable salts thereof are described, as well as the pharmaceutical compositions containing said compounds and their pharmaceutically acceptable salts, and the use of said compounds and pharmaceutical compositions for the treatment, control or amelioration of proliferative diseases, including cancer, Down syndrome or early onset Alzheimer's disease.
    描述了具有以下结构的化合物及其药用盐,以及含有这些化合物和它们的药用盐的药物组合物,以及这些化合物和药物组合物用于治疗、控制或改善增殖性疾病(包括癌症、唐氏综合征或早发性阿尔茨海默病)的用途。
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