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1-{[4-(2-methyl-quinolin-4-ylmethoxy)-benzoylamino]-methyl}-cyclopropanecarboxylic acid | 362703-22-8

中文名称
——
中文别名
——
英文名称
1-{[4-(2-methyl-quinolin-4-ylmethoxy)-benzoylamino]-methyl}-cyclopropanecarboxylic acid
英文别名
1-[[[4-[(2-Methylquinolin-4-yl)methoxy]benzoyl]amino]methyl]cyclopropane-1-carboxylic acid
1-{[4-(2-methyl-quinolin-4-ylmethoxy)-benzoylamino]-methyl}-cyclopropanecarboxylic acid化学式
CAS
362703-22-8
化学式
C23H22N2O4
mdl
——
分子量
390.439
InChiKey
XEBRNVWQUYPCHO-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:
    29
  • 可旋转键数:
    7
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    88.5
  • 氢给体数:
    2
  • 氢受体数:
    5

文献信息

  • Triazolone and triazolethione derivatives as inhibitors of matrix metalloproteinases and/or TNF-alpha converting enzyme
    申请人:——
    公开号:US20040116491A1
    公开(公告)日:2004-06-17
    The present application describes novel hydantoin derivatives of formula (I): 1 or pharmaceutically acceptable salt or prodrug forms thereof, wherein A, L, and R 11 are defined in the present specification, which are useful as inhibitors of matrix metalloproteinases (MMP), TNF-&agr; converting enzyme (TACE), aggrecanase, or a combination thereof.
    本申请描述了式 (I) 的新型海因衍生物: 1 或其药学上可接受的盐或原药形式,其中 A、L 和 R 11 可用作基质蛋白酶 (MMP)、TNF-&agr; 转换酶 (TACE)、凝集素酶或其组合的抑制剂
  • EP1558581A4
    申请人:——
    公开号:EP1558581A4
    公开(公告)日:2007-07-25
  • TRIAZOLONE AND TRIAZOLETHIONE DERIVATIVES
    申请人:Bristol-Myers Squibb Company
    公开号:EP1558581A2
    公开(公告)日:2005-08-03
  • US7074810B2
    申请人:——
    公开号:US7074810B2
    公开(公告)日:2006-07-11
  • [EN] TRIAZOLONE AND TRIAZOLETHIONE DERIVATIVES AS INHIBITORS OF MATRIX METALLOPROTEINASES AND/OR TNF-ALPHA CONVERTING ENZYME<br/>[FR] DERIVES DE LA TRIAZOLONE ET DE LA TRIAZOLETHIONE, INHIBITEURS DES METALLOPROTEINASES DE MATRICES ET/OU DE L'ENZYME DE CONVERSION DU TNF DOLLAR G(A)
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2004032846A2
    公开(公告)日:2004-04-22
    The present application describes novel hydantoin derivatives of formula (I): or pharmaceutically acceptable salt or prodrug forms thereof, wherein A, L, and R11 are defined in the present specification, which are useful as inhibitors of matrix metalloproteinases (MMP), TNF-a converting enzyme (TACE), aggrecanase, or a combination thereof.
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