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(E)-3-Ethyl-hex-2-enoic acid | 63718-58-1

中文名称
——
中文别名
——
英文名称
(E)-3-Ethyl-hex-2-enoic acid
英文别名
3-Ethylhex-2-enoic acid
(E)-3-Ethyl-hex-2-enoic acid化学式
CAS
63718-58-1
化学式
C8H14O2
mdl
——
分子量
142.198
InChiKey
WRPMHFHMXOUTTI-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

物化性质

  • 熔点:
    1.7°C (estimate)
  • 沸点:
    256.29°C (estimate)
  • 密度:
    0.9565 (rough estimate)

计算性质

  • 辛醇/水分配系数(LogP):
    2.6
  • 重原子数:
    10
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.62
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2916190090

反应信息

  • 作为反应物:
    描述:
    (E)-3-Ethyl-hex-2-enoic acid氯化亚砜 作用下, 生成 N-<3-Ethyl-hexen-(2)-oyl>-4-nitro-3-trifluormethyl-anilin
    参考文献:
    名称:
    一些硝基三氟甲基苯胺的合成和抑菌活性。
    摘要:
    DOI:
    10.1021/jm00313a020
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文献信息

  • Derivatives of Natural Product Agrimophol as Disruptors of Intrabacterial pH Homeostasis in <i>Mycobacterium tuberculosis</i>
    作者:Jie Wu、Ran Mu、Mingna Sun、Nan Zhao、Miaomiao Pan、Hongshuang Li、Yi Dong、Zhaogang Sun、Jie Bai、Minwan Hu、Carl F. Nathan、Babak Javid、Gang Liu
    DOI:10.1021/acsinfecdis.8b00325
    日期:2019.7.12
    This article reports the rational medicinal chemistry of a natural product, agrimophol (1), as a new disruptor of intrabacterial pH (pH(IB)) homeostasis in Mycobacterium tuberculosis (Mtb). Through the systematic investigation of the structure-activity relationship of 1, scaffold-hopping of the diphenylmethane scaffold, pharmacophore displacement strategies, and studies of the structure-metabolism relationship, a new derivative 5a was achieved. Compound 5a showed 100-fold increased potency in the ability to reduce pH(IB) to pH 6.0 and similarly improved mycobactericidal activity compared with 1 against both Mycobacterium bovis-BCG and Mtb. Compound 5a possessed improved metabolic stability in human liver microsomes and hepatocytes, lower cytotoxicity, higher selectivity index, and similar pK(a) value to natural 1. This study introduces a novel scaffold to an old drug, resulting in improved mycobactericidal activity through decreasing pH(IB), and may contribute to the critical search for new agents to overcome drug resistance and persistence in the treatment of tuberculosis.
  • Synthesis and Bacteriostatic Activity of Some Nitrotrifluoro methylanilides
    作者:Joseph W. Baker、Gerald L. Bachman、Ignatius. Schumacher、Daniel P. Roman、Alan L. Tharp
    DOI:10.1021/jm00313a020
    日期:1967.1.1
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