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

[4-(2-amino-5-phenylpyrimidin-4-yl)-1H-pyrrol-2-yl]-(3-hydroxypiperidin-1-yl)methanone

中文名称
——
中文别名
——
英文名称
[4-(2-amino-5-phenylpyrimidin-4-yl)-1H-pyrrol-2-yl]-(3-hydroxypiperidin-1-yl)methanone
英文别名
——
[4-(2-amino-5-phenylpyrimidin-4-yl)-1H-pyrrol-2-yl]-(3-hydroxypiperidin-1-yl)methanone化学式
CAS
——
化学式
C20H21N5O2
mdl
——
分子量
363.4
InChiKey
ROZHBVGIRRXHEV-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):
    1.6
  • 重原子数:
    27
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    108
  • 氢给体数:
    3
  • 氢受体数:
    5

文献信息

  • Heterocyclic inhibitors of ERK2 and uses thereof
    申请人:——
    公开号:US20030092714A1
    公开(公告)日:2003-05-15
    Described herein are compounds that are useful as protein kinase inhibitors having the formula: 1 wherein Z 1 and Z 2 are each independently nitrogen or CH and Ring A, T m R 1 , QR 2 , U n R 3 , and Sp are as described in the specification. The compounds are especially useful as inhibitors of ERK2 and for treating diseases in mammals that are alleviated by a protein kinase inhibitor, particularly diseases such as cancer, inflammatory disorders, restenosis, diabetes, and cardiovascular disease.
    本文描述了一些化合物,这些化合物可用作蛋白激酶抑制剂,其化学式如下: 1 其中Z 1 和Z 2 分别独立地为氮或CH,环A,T m R 1 ,QR 2 ,U n R 3 和Sp如规范中所述。这些化合物特别适用于ERK2的抑制剂,并用于治疗通过蛋白激酶抑制剂缓解的哺乳动物疾病,特别是癌症、炎症性疾病、再狭窄、糖尿病和心血管疾病等疾病。
  • HETEROCYCLIC INHIBITORS OF ERK2 AND USES THEREOF
    申请人:VERTEX PHARMACEUTICALS INCORPORATED
    公开号:EP1363906A2
    公开(公告)日:2003-11-26
  • US6743791B2
    申请人:——
    公开号:US6743791B2
    公开(公告)日:2004-06-01
  • US7253187B2
    申请人:——
    公开号:US7253187B2
    公开(公告)日:2007-08-07
  • [EN] HETEROCYCLIC INHIBITORS OF ERK2 AND USES THEREOF<br/>[FR] INHIBITEURS HETEROCYCLIQUES DE ERK2 ET LEURS UTILISATIONS
    申请人:VERTEX PHARMA
    公开号:WO2002064586A2
    公开(公告)日:2002-08-22
    Described herein are compounds that are useful as protein kinase inhibitors having the formula (I) wherein Z?1 and Z2¿ are each independently nitrogen or CH and Ring A, T¿m?R?1, QR2, U¿nR3, and Sp are as described in the specification. The compounds are especially useful as inhibitors of ERK2 and for treating diseases in mammals that are alleviated by a protein kinase inhibitor, particularly diseases such as cancer, inflammatory disorders, restenosis, diabetes, and cardiovascular disease.
查看更多