摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

2-(4-Chlorphenoxy)-3-methylpyridin | 28355-55-7

中文名称
——
中文别名
——
英文名称
2-(4-Chlorphenoxy)-3-methylpyridin
英文别名
2-(4-chloro-phenoxy)-3-methyl-pyridine;2-(4-Chlorophenoxy)-3-methylpyridine
2-(4-Chlorphenoxy)-3-methylpyridin化学式
CAS
28355-55-7
化学式
C12H10ClNO
mdl
——
分子量
219.671
InChiKey
NFDYYJVGDFJKPA-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):
    3.7
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    22.1
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • SUBSTITUTED HETEROARYL PYRIDOPYRIMIDONE DERIVATIVES
    申请人:FAYOL Aude
    公开号:US20090306088A1
    公开(公告)日:2009-12-10
    A pyrimidone derivative represented by formula (I) or a salt thereof, or a solvate thereof or a hydrate thereof are disclosed and claimed. Wherein m, n, o, Y, Z, R1, R2, R3, R4, R5 R6 and R7 are as described herein. Also disclosed are the salts of compounds of formula (I). The invention relates also to a medicament comprising the said derivative or a salt thereof as an active ingredient which is used for preventive and/or therapeutic treatment of a neurodegenerative disease caused by abnormal activity of GSK3β, such as Alzheimer disease.
    本发明揭示和声明了由式(I)表示的吡啶酮衍生物,或其盐、溶剂或合物。其中m、n、o、Y、Z、R1、R2、R3、R4、R5、R6和R7如本文所述。本发明还揭示了式(I)化合物的盐。本发明涉及一种药物,其包括所述衍生物或其盐作为活性成分,用于预防和/或治疗由GSK3β异常活性引起的神经退行性疾病,如阿尔茨海默病。
  • Imine Compound
    申请人:Saito Shiuji
    公开号:US20080312435A1
    公开(公告)日:2008-12-18
    An imine compound represented by the formula: wherein A represents a heterocyclic group; R 1 , R 2 , an R 3 each represent a hydrogen atom, a halogen atom, a C 1-10 alkyl group optionally substituted with an aryl group(s) substituted with a halogen atom(s), a C 3-10 cycloalkyl group, a C 1-6 haloalkyl group, a C 1-10 alkoxy group, etc.; R 4 represents an optionally substituted C 1-10 alkyl, C 2-6 alkenyl, or aryl group; R 5 represents a hydrogen atom, a C 1-10 alkoxy group, a C 1-6 haloalkyl group, an optionally substituted C 1-10 alkyl or C 2-6 alkenyl group, an optionally substituted aryl or heterocyclic group, etc.; W represents —CO—, —CO—CO—, —CO—NH—, —CS—NH—, or —SO 2 —, or a cannabinoid-receptor agonist comprising said imine compound as an active ingredient. The imine compound of the present invention has a cannabinoid-receptor agonist effect, and is useful as a therapeutic or prophylactic drug for pains and autoimmune diseases.
    一种以以下式表示的亚胺化合物:其中A代表杂环基团;R1、R2和R3分别表示氢原子、卤素原子、C1-10烷基,该烷基可选地取代有芳基,所述芳基取代有卤素原子,C3-10环烷基,C1-6卤代烷基,C1-10烷氧基等;R4表示可选地取代的C1-10烷基,C2-6烯基或芳基;R5表示氢原子,C1-10烷氧基,C1-6卤代烷基,可选地取代的C1-10烷基或C2-6烯基,可选地取代的芳基或杂环基团等;W表示—CO—,—CO—CO—,—CO—NH—,—CS—NH—或—SO2—,或以该亚胺化合物为活性成分的大麻素受体激动剂。本发明的亚胺化合物具有大麻素受体激动剂作用,可用作治疗或预防疼痛和自身免疫性疾病的药物。
  • US8198287B2
    申请人:——
    公开号:US8198287B2
    公开(公告)日:2012-06-12
查看更多