1-[2-(aminomethyl)phenyl]-N-(3-fluoro-2'-sulfamoylbiphenyl-4-yl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide | 228258-45-5

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 1-[2-(aminomethyl)phenyl]-N-(3-fluoro-2'-sulfamoylbiphenyl-4-yl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxamide
• 英文别名: 2-[2-(aminomethyl)phenyl]-N-[2-fluoro-4-(2-sulfamoylphenyl)phenyl]-5-(trifluoromethyl)pyrazole-3-carboxamide
• CAS: 228258-45-5
• 化学式: C₂₄H₁₉F₄N₅O₃S
• 分子量: 533.5
• InChiKey: TYPXEIGMGZWOGB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  37
• 可旋转键数：
  6
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  142
• 氢给体数：
  3
• 氢受体数：
  10

文献信息

• Human plasma kallikrein inhibitors
  申请人：BioCryst Pharmaceuticals, Inc.

  公开号：US10125102B2

  公开（公告）日：2018-11-13

  Disclosed are compounds of formula I as described herein, and pharmaceutically acceptable salts thereof. The compounds are inhibitors of plasma kallikrein. Also disclosed are pharmaceutical compositions comprising at least one such compound, and methods involving use of the compounds and compositions in the treatment and prevention of diseases and conditions characterized by unwanted plasma kallikrein activity.

  公开了式 I 的化合物 及其药学上可接受的盐类。这些化合物是血浆激肽的抑制剂。此外，还公开了包含至少一种此类化合物的药物组合物，以及涉及使用这些化合物和组合物治疗和预防以不需要的血浆激肽活性为特征的疾病和病症的方法。
• TRIFLUOROMETHYL SUBSTITUTED PYRAZOLES AS HUMAN PLASMA KALLIKREIN INHIBITORS
  申请人：Biocryst Pharmaceuticals, Inc.

  公开号：EP3113772B1

  公开（公告）日：2020-09-09
• ASSAY FOR DIFFERENTIATING COMPOUNDS THAT MODULATE THE EXTRINSIC AND/OR INTRINSIC COAGULATION PATHWAYS
  申请人：Wang Xinkang

  公开号：US20080026474A1

  公开（公告）日：2008-01-31

  Methods for differentiating compounds that modulate the extrinsic and/or intrinsic coagulation pathways are provided. Also provided are methods for identifying a compound that modulates the extrinsic coagulation pathway. In addition, methods for determining an effective dosage of an anticoagulant in a patient are provided.
• HUMAN PLASMA KALLIKREIN INHIBITORS
  申请人：BIOCRYST PHARMACEUTICALS, INC.

  公开号：US20170073314A1

  公开（公告）日：2017-03-16

  Disclosed are compounds of formula I as described herein, and pharmaceutically acceptable salts thereof. The compounds are inhibitors of plasma kallikrein. Also disclosed are pharmaceutical compositions comprising at least one such compound, and methods involving use of the compounds and compositions in the treatment and prevention of diseases and conditions characterized by unwanted plasma kallikrein activity.