1-(1-(4-fluorophenyl)cyclopropyl)-2-hydroxyethanone | 1067187-76-1

• 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-(1-(4-fluorophenyl)cyclopropyl)-2-hydroxyethanone
• 英文别名: 1-[1-(4-Fluorophenyl)cyclopropyl]-2-hydroxyethanone
• CAS: 1067187-76-1
• 化学式: C₁₁H₁₁FO₂
• 分子量: 194.206
• InChiKey: XUAIEJINIIPHFQ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.3
• 重原子数：
  14
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  37.3
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  7-异丙基靛红 、 1-(1-(4-fluorophenyl)cyclopropyl)-2-hydroxyethanone 在 sodium hydroxide 作用下， 以 乙醇 、 水 为溶剂， 以39%的产率得到2-(1-(4-fluorophenyl)cyclopropyl)-3-hydroxy-8-isopropylquinoline-4-carboxylic acid
  参考文献：
  名称：

  Discovery of 2-[1-(4-Chlorophenyl)cyclopropyl]-3-hydroxy-8-(trifluoromethyl)quinoline-4-carboxylic Acid (PSI-421), a P-Selectin Inhibitor with Improved Pharmacokinetic Properties and Oral Efficacy in Models of Vascular Injury

  摘要：

  Previously, we reported the discovery of PSI-697 (1a), a C-2 benzyl substituted quinoline salicylic acid-based P-selectin inhibitor. It is active in a variety of animal models of cardiovascular disease. Compound 1a has also been shown to be well tolerated and safe in healthy volunteers at doses of up to 1200 mg in a phase 1 single ascending dose study. However, its oral bioavailability was low. Our goal was to identify a back up compound with equal potency, increased solubility, and increased exposure. We expanded our structure activity-studies in this series by branching at the alpha position of the C-2 benzyl side chain and through modification of substituents on the carboxylic A-ring of the quinoline. This resulted in discovery of PSI-421 with marked improvement in aqueous solubility and pharmacokinetic properties. This compound has shown oral efficacy in animal models of arterial and venous injury and was selected as a preclinical development compound for potential treatment of such diseases as atherosclerosis and deep vein thrombosis.

  DOI：

  10.1021/jm9013696
• 作为产物：
  描述：

  三(三甲基硅氧基)乙烯 、 1-(4-Fluorophenyl)cyclopropane-1-carbonyl chloride 在 盐酸 作用下， 以 1,4-二氧六环 、 水 为溶剂， 生成 1-(1-(4-fluorophenyl)cyclopropyl)-2-hydroxyethanone
  参考文献：
  名称：

  Discovery of 2-[1-(4-Chlorophenyl)cyclopropyl]-3-hydroxy-8-(trifluoromethyl)quinoline-4-carboxylic Acid (PSI-421), a P-Selectin Inhibitor with Improved Pharmacokinetic Properties and Oral Efficacy in Models of Vascular Injury

  摘要：

  Previously, we reported the discovery of PSI-697 (1a), a C-2 benzyl substituted quinoline salicylic acid-based P-selectin inhibitor. It is active in a variety of animal models of cardiovascular disease. Compound 1a has also been shown to be well tolerated and safe in healthy volunteers at doses of up to 1200 mg in a phase 1 single ascending dose study. However, its oral bioavailability was low. Our goal was to identify a back up compound with equal potency, increased solubility, and increased exposure. We expanded our structure activity-studies in this series by branching at the alpha position of the C-2 benzyl side chain and through modification of substituents on the carboxylic A-ring of the quinoline. This resulted in discovery of PSI-421 with marked improvement in aqueous solubility and pharmacokinetic properties. This compound has shown oral efficacy in animal models of arterial and venous injury and was selected as a preclinical development compound for potential treatment of such diseases as atherosclerosis and deep vein thrombosis.

  DOI：

  10.1021/jm9013696

文献信息

• Methods and Compositions for Selectin Inhibition
  申请人：Kaila Neelu

  公开号：US20080255192A1

  公开（公告）日：2008-10-16

  The present teachings relate to novel compounds of formula I: wherein the constituent variables are as defined herein. Compounds of the present teachings can act as antagonists of the mammalian adhesion proteins known as selecting. Methods for treating or preventing selectin-mediated disorders are provided, which include administration of these compounds in a therapeutically effective amount.

  本教学涉及到式I的新化合物： 其中组成变量如本文所定义。本教学的化合物可以作为被称为选择素的哺乳动物粘附蛋白的拮抗剂。提供了治疗或预防选择素介导的疾病的方法，包括以治疗有效剂量给予这些化合物。
• Vanilloid receptor ligands, pharmaceutical compositions containing them, process for making them and use thereof for treating pain and other conditions
  申请人：Frank Robert

  公开号：US20080275044A1

  公开（公告）日：2008-11-06

  Compounds corresponding to formula I: which act as vanilloid receptor ligands, pharmaceutical compositions containing such compounds, a process for the producing such compounds, and the use thereof to treat or inhibit pain and/or various other disorders or conditions.

  与公式I对应的化合物：作为辣椒素受体配体的化合物，含有这种化合物的药物组合物，生产这种化合物的过程，以及利用它们治疗或抑制疼痛和/或其他多种疾病或症状的用途。
• QUINOLINE DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS COMPRISING THEM FOR SELECTIN INHIBITION
  申请人：Wyeth

  公开号：EP2134692A2

  公开（公告）日：2009-12-23
• US8735426B2
  申请人：——

  公开号：US8735426B2

  公开（公告）日：2014-05-27
• [EN] METHODS AND COMPOSITIONS FOR SELECTIN INHIBITION<br/>[FR] PROCÉDÉS ET COMPOSITIONS POUR L'INHIBITION DE LA SÉLECTINE
  申请人：WYETH CORP

  公开号：WO2008121817A2

  公开（公告）日：2008-10-09

  [EN] The present teachings relate to novel compounds of formula I: wherein the constituent variables are as defined herein. Compounds of the present teachings can act as antagonists of the mammalian adhesion proteins known as selectins. Methods for treating or preventing selectin-mediated disorders are provided, which include administration of these compounds in a therapeutically effective amount.
  [FR] La présente invention concerne de nouveaux composés de la formule I: LA FORMULE CHIMIQUE DOIT ETRE INSEREE ICI TELLE QU'ELLE APPARAiT SUR LE RESUME DU FORMAT PAPIER, où les variables sont telles que définies ici. Les composés de la présente invention peuvent agir comme antagonistes des protéines mammaliennes d'adhésion connus comme sélectines. Des procédés de traitement ou de prévention de désordres à médiation par les sélectines sont décrits, lesquels comprennent l'administration de ces composés en une quantité thérapeutiquement efficace.