1-[4-(3,5-Dimethylisoxazole-4-sulfonamido)phenyl]-6-trifluoromethyl-3,4-dihydroisoquinoline | 426838-39-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯氮卓类
• 英文名称: 1-[4-(3,5-Dimethylisoxazole-4-sulfonamido)phenyl]-6-trifluoromethyl-3,4-dihydroisoquinoline
• 英文别名: 3,5-dimethyl-N-[4-[6-(trifluoromethyl)-3,4-dihydroisoquinolin-1-yl]phenyl]-1,2-oxazole-4-sulfonamide
• CAS: 426838-39-3
• 化学式: C₂₁H₁₈F₃N₃O₃S
• 分子量: 449.453
• InChiKey: HLTLFFWXYIAASZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  31
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.24
• 拓扑面积：
  92.9
• 氢给体数：
  1
• 氢受体数：
  9

文献信息

• Bicyclic pyrimidinones as coagulation cascade inhibitors
  申请人：——

  公开号：US20040006065A1

  公开（公告）日：2004-01-08

  The present invention relates generally to compounds that inhibit serine proteases. In particular it is directed to novel amino-bicyclic pyrimidinone compounds of Formula (I): 1 or a stereoisomer or pharmaceutically acceptable salt form thereof, which are useful as selective inhibitors of serine protease enzymes of the coagulation cascade; for example thrombin, factor Xa, factor XIa, factor IXa, and/or factor VIIa. In particular, it relates to compounds that are factor VIIa inhibitors. This invention also relates to pharmaceutical compositions comprising these compounds and methods of using the same.

  本发明一般涉及抑制丝氨酸蛋白酶的化合物。具体而言，本发明涉及式（I）的新型氨基双环嘧啶酮化合物或其立体异构体或药学上可接受的盐形式，这些化合物可用作凝血级联中丝氨酸蛋白酶的选择性抑制剂；例如凝血酶、X因子a、XI因子a、IX因子a和/或VII因子a。特别是，涉及抑制VII因子a的化合物。本发明还涉及包含这些化合物的药物组合物以及使用相同的方法。
• (Dihydro) Isoquinoline derivatives as phosphodiesterase inhibitors
  申请人：——

  公开号：US20040044212A1

  公开（公告）日：2004-03-04

  3,4-Dihydroisoquinoline and isoquinoline compounds of formula I, in which Ar represents a phenyl raidcal of the formulae IIa, IIb or IIc are novel effective PDE7 inhibitors.

  公式I中的3,4-二氢异喹啉和异喹啉化合物中，Ar代表公式IIa、IIb或IIc的苯基团，是新颖的有效PDE7抑制剂。
• (DIHYDRO)ISOQUINOLINE DERIVATIVES AS PHOSPHODIESTERASE INHIBITORS
  申请人：Byk Gulden Lomberg Chemische Fabrik GmbH

  公开号：EP1337515A1

  公开（公告）日：2003-08-27
• US6818651B2
  申请人：——

  公开号：US6818651B2

  公开（公告）日：2004-11-16
• [EN] (DIHYDRO)ISOQUINOLINE DERIVATIVES AS PHOSPHODIESTERASE INHIBITORS<br/>[FR] DERIVES DE (DIHYDRO)ISOQUINOLINE COMME INHIBITEURS DE PHOSPHODIESTERASE
  申请人：BYK GULDEN LOMBERG CHEM FAB

  公开号：WO2002040450A1

  公开（公告）日：2002-05-23

  3,4-Dihydroisoquinoline and isoquinoline compounds of formula I, in which Ar represents a phenyl raidcal of the formulae IIa, IIb or IIc are novel effective PDE7 inhibitors.