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4-<4-Ethyl-phenoxy>-pyridin | 33399-14-3

中文名称
——
中文别名
——
英文名称
4-<4-Ethyl-phenoxy>-pyridin
英文别名
4-(4-ethyl-phenoxy)-pyridine;4-(4-Ethylphenoxy)pyridine
4-<4-Ethyl-phenoxy>-pyridin化学式
CAS
33399-14-3
化学式
C13H13NO
mdl
——
分子量
199.252
InChiKey
QQLYUJUBZYTVFD-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):
    3.2
  • 重原子数:
    15
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    22.1
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • [EN] ANTIBACTERIAL AGENTS : ARYLALKYLCARBOXAMIDO PHLOROGLUCINOLS<br/>[FR] AGENTS ANTIBACTÉRIENS : PHLOROGLUCINOLS ARYLALKYLCARBOXAMIDO
    申请人:UNIV RUTGERS
    公开号:WO2019173507A1
    公开(公告)日:2019-09-12
    The invention provides compounds of formula (I) or (II) and tautomers and salts thereof, wherein variables are as described in the specification, as well as compositions comprising a compound of formula (I) or (II) or a tautomer or salt thereof, methods of making a compound of formula (I) or (II) or a tautomer or salt thereof, and methods of using a compound of formula (I) or (II) or a tautomer or salt thereof as, e.g., inhibitors of bacterial RNA polymerase or as antibacterial agents.
    该发明提供了式(I)或(II)的化合物及其互变异构体和盐,其中变量如规范中所述,以及包含式(I)或(II)的化合物或其互变异构体或盐的组合物,制备式(I)或(II)的化合物或其互变异构体或盐的方法,以及使用式(I)或(II)的化合物或其互变异构体或盐的方法,例如,作为细菌RNA聚合酶的抑制剂或抗菌剂。
  • Fungicide N-Cyclopropyl-Sulfonylamide Derivatives
    申请人:Schwarz Hans-Georg
    公开号:US20090137611A1
    公开(公告)日:2009-05-28
    The present invention relates to N-cyclopropyl-sulfonylamide derivatives of formula (I) wherein the substituents are cyclic groups, their process of preparation, their use as fungicide active agents, particularly in the form of fungicide compositions, and methods for the control of phytopathogenic fungi, notably of plants, using these compounds or compositions: (I)
  • SMALL MOLECULE INHIBITORS OF EGFR AND PI3K
    申请人:The Regents of the University of Michigan
    公开号:US20170360788A1
    公开(公告)日:2017-12-21
    This invention is in the field of medicinal chemistry. In particular, the invention relates to a new class of small-molecules having a quinazoline structure or a quinoline structure which function as dual inhibitors of EGFR proteins and PI3K proteins, and their use as therapeutics for the treatment of cancer and other diseases.
  • US7932283B2
    申请人:——
    公开号:US7932283B2
    公开(公告)日:2011-04-26
  • [EN] HETEROARYL COMPOUNDS AND USES THEREOF<br/>[FR] COMPOSÉS HÉTÉROARYLE ET LEURS UTILISATIONS
    申请人:AVILA THERAPEUTICS INC
    公开号:WO2010123870A1
    公开(公告)日:2010-10-28
    The present invention provides compounds, pharmaceutically acceptable compositions thereof, and methods of using the same.
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