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4-[2-butyl-5-((R)-1-hydroxycarbamoylmethyl-2-phenylethylcarbamoyl)imidazol-1-ylmethyl]naphthalene-1-carboxylic acid | 1073548-98-7

中文名称
——
中文别名
——
英文名称
4-[2-butyl-5-((R)-1-hydroxycarbamoylmethyl-2-phenylethylcarbamoyl)imidazol-1-ylmethyl]naphthalene-1-carboxylic acid
英文别名
4-[[2-butyl-5-[[(2R)-4-(hydroxyamino)-4-oxo-1-phenylbutan-2-yl]carbamoyl]imidazol-1-yl]methyl]naphthalene-1-carboxylic acid
4-[2-butyl-5-((R)-1-hydroxycarbamoylmethyl-2-phenylethylcarbamoyl)imidazol-1-ylmethyl]naphthalene-1-carboxylic acid化学式
CAS
1073548-98-7
化学式
C30H32N4O5
mdl
——
分子量
528.608
InChiKey
VLPQCKMSNBAVSP-JOCHJYFZSA-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):
    4.5
  • 重原子数:
    39
  • 可旋转键数:
    12
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    134
  • 氢给体数:
    4
  • 氢受体数:
    6

文献信息

  • Dual-acting antihypertensive agents
    申请人:Allegretti Paul
    公开号:US20080269305A1
    公开(公告)日:2008-10-30
    The invention is directed to compounds having the formula: wherein: Ar, r, Y, Z, Q, W, X, and R 5-7 are as defined in the specification, and pharmaceutically acceptable salts thereof. These compounds have AT 1 receptor antagonist activity and neprilysin inhibition activity. The invention is also directed to pharmaceutical compositions comprising such compounds; methods of using such compounds; and process and intermediates for preparing such compounds.
    该发明涉及具有以下公式的化合物:其中:Ar、r、Y、Z、Q、W、X和R5-7如规范中定义,并且其药学上可接受的盐。这些化合物具有AT1受体拮抗活性和神经肽酶抑制活性。该发明还涉及包含这些化合物的药物组合物;使用这些化合物的方法;以及制备这些化合物的过程和中间体
  • Dual-acting Imidazole antihypertensive agents
    申请人:Allegretti Paul
    公开号:US20090023228A1
    公开(公告)日:2009-01-22
    The invention is directed to compounds having the formula: wherein: Ar, r, R 2-3 , X, and R 5.7 are as defined in the specification, and pharmaceutically acceptable salts thereof. These compounds have AT 1 receptor antagonist activity and neprilysin inhibition activity. The invention is also directed to pharmaceutical compositions comprising such compounds; methods of using such compounds; and process and intermediates for preparing such compounds.
    本发明涉及具有以下结构式的化合物:其中:Ar、r、R2-3、X和R5.7如规范中所定义,并且其药学上可接受的盐。这些化合物具有AT1受体拮抗活性和神经肽酶抑制活性。本发明还涉及包含这些化合物的制药组合物;使用这些化合物的方法;以及制备这些化合物的过程和中间体
  • DUAL-ACTING ANTIHYPERTENSIVE AGENTS
    申请人:Allegretti Paul
    公开号:US20110281925A1
    公开(公告)日:2011-11-17
    The invention is directed to compounds having the formula: wherein: Ar, r, Y, Z, Q, W, X, and R 5-7 are as defined in the specification, and pharmaceutically acceptable salts thereof. These compounds have AT 1 receptor antagonist activity and neprilysin inhibition activity. The invention is also directed to pharmaceutical compositions comprising such compounds; methods of using such compounds; and process and intermediates for preparing such compounds.
    该发明涉及具有以下式子的化合物:其中:Ar、r、Y、Z、Q、W、X和R5-7如规范中所定义,并且其药学上可接受的盐。这些化合物具有AT1受体拮抗活性和酶解酶抑制活性。该发明还涉及包含这些化合物的制药组合物;使用这些化合物的方法;以及制备这些化合物的过程和中间体
  • DUAL-ACTING IMIDAZOLE ANTIHYPERTENSIVE AGENTS
    申请人:ALLEGRETTI Paul
    公开号:US20110092551A1
    公开(公告)日:2011-04-21
    The invention is directed to compounds having the formula: wherein: Ar, r, R 2-3 , X, and R 5-7 are as defined in the specification, and pharmaceutically acceptable salts thereof. These compounds have AT 1 receptor antagonist activity and neprilysin inhibition activity. The invention is also directed to pharmaceutical compositions comprising such compounds; methods of using such compounds; and process and intermediates for preparing such compounds.
    本发明涉及具有下式的化合物:其中:Ar,r,R2-3,X和R5-7如说明书所定义,以及其药学上可接受的盐。这些化合物具有AT1受体拮抗活性和酶解酶抑制活性。本发明还涉及包含这些化合物的制药组合物;使用这些化合物的方法;以及制备这些化合物的过程和中间体
  • US7879896B2
    申请人:——
    公开号:US7879896B2
    公开(公告)日:2011-02-01
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