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1H-Pyrrole-3-carboxylic acid, 2-(2-methoxyphenyl)-4-methyl-, methyl ester | 1370419-17-2

中文名称
——
中文别名
——
英文名称
1H-Pyrrole-3-carboxylic acid, 2-(2-methoxyphenyl)-4-methyl-, methyl ester
英文别名
methyl 2-(2-methoxyphenyl)-4-methyl-1H-pyrrole-3-carboxylate
1H-Pyrrole-3-carboxylic acid, 2-(2-methoxyphenyl)-4-methyl-, methyl ester化学式
CAS
1370419-17-2
化学式
C14H15NO3
mdl
——
分子量
245.27
InChiKey
HSXYKQHZGHTXCL-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):
    2.6
  • 重原子数:
    18
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.21
  • 拓扑面积:
    51.3
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • NOVEL PIPERAZINE ANALOGS WITH SUBSTITUTED HETEROARYL GROUPS AS BROAD-SPECTRUM INFLUENZA ANTIVIRALS
    申请人:Cianci Christopher W.
    公开号:US20120245176A1
    公开(公告)日:2012-09-27
    A compound of Formula I is set forth, including pharmaceutically acceptable salts thereof: wherein Het is a 5 or 6-membered heterocycle with —N, —O, or —S adjacent to the —Ar substituent or adjacent to the point of attachment for the —Ar substituent; Ar is aryl or heteroaryl; R is —CH 3 , —CH 2 F, —CHF 2 or —CH═CH 2 ; V is —H, —CH 3 or ═O; W is —NO 2 , —Cl, —Br, —CH 2 OH, or —CN; X is —Cl, —Br, —F, —CH 3 , —OCH 3 , or —CN; Y is —CH or —N; and Z is —CH or —N. This compound is useful in compositions for the prevention and treatment of influenza virus.
    本发明涉及一种I式化合物,包括其药学上可接受的盐:其中,Het是一种5或6元杂环,其中- N,-O或-S与-Ar取代基相邻或与-Ar取代基的连接点相邻;Ar是芳基或杂芳基;R是-CH3,-CH2F,-CHF2或-CH═CH2;V是-H,-CH3或═O;W是-NO2,-Cl,-Br,-CH2OH或-CN;X是-Cl,-Br,-F,-CH3,-OCH3或-CN;Y是-CH或-N;以及Z是-CH或-N。该化合物在预防和治疗流感病毒的组合物中有用。
  • [EN] NOVEL PIPERAZINE ANALOGS WITH SUBSTITUTED HETEROARYL GROUPS AS BROAD-SPECTRUM INFLUENZA ANTIVIRALS<br/>[FR] NOUVEAUX ANALOGUES DE LA PIPÉRAZINE COMPORTANT DES GROUPES HÉTÉROARYLE SUBSTITUÉS UTILISÉS COMME ANTIVIRAUX À LARGE SPECTRE PROTÉGEANT DE LA GRIPPE
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2012044531A1
    公开(公告)日:2012-04-05
    A compound of the following Formula (I) is set forth, including pharmaceutically acceptable salts thereof: wherein Het is a 5 or 6-membered heterocycle with -N, -O, or -S adjacent to the -Ar substituent or adjacent to the point of attachment for the -Ar substituent; Ar is aryl or heteroaryl; R is -CH3, -CH2F, -CHF2 or -CH=CH2; V is -H, -CH3 or =0; W is -NO2, -CI, -Br, -CH2OH, or -CN; X is -CI, -Br, -F, -CH3, -OCH3, or -CN; Y is -CH or -N; and Z is -CH or -N. This compound is useful in compositions for the prevention and treatment of influenza virus.
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