3-[[[(2-trifluoromethyl)pyrid-6-yl]methyl](3-phenoxycyclohexyl)amino]-1,1,1-trifluoro-2-propanol | 263246-23-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 3-[[[(2-trifluoromethyl)pyrid-6-yl]methyl](3-phenoxycyclohexyl)amino]-1,1,1-trifluoro-2-propanol
• 英文别名: 1,1,1-Trifluoro-3-[(3-phenoxycyclohexyl)-[[6-(trifluoromethyl)pyridin-2-yl]methyl]amino]propan-2-ol
• CAS: 263246-23-7
• 化学式: C₂₂H₂₄F₆N₂O₂
• 分子量: 462.435
• InChiKey: OXKKNXPSMDIOQN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.1
• 重原子数：
  32
• 可旋转键数：
  7
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  45.6
• 氢给体数：
  1
• 氢受体数：
  10

文献信息

• Substituted N-Aliphatic-N-Aromatictertiary-Heteroalkylamines useful for inhibiting cholesteryl ester transfer protein activity
  申请人：G.D. Searle & Co.

  公开号：US20010018446A1

  公开（公告）日：2001-08-30

  The invention relates to substituted N-Aliphatic-N-Aromatic tertiary - Heteroalkylamine compounds useful as inhibitors of cholesteryl ester transfer protein (CETP; plasma lipid transfer protein-I) and compounds, compositions and methods for treating atherosclerosis, dyslipidemia, and other coronary artery disease.

  该发明涉及替代N-脂肪基-N-芳香族三级-杂原子烷胺化合物，可用作胆固醇酯转移蛋白（CETP；血浆脂质转移蛋白-I）的抑制剂，以及治疗动脉粥样硬化、血脂异常和其他冠状动脉疾病的化合物、组合物和方法。
• CETP inhibitors in combination with antihypertensive agents and uses thereof
  申请人：Pfizer Inc.

  公开号：US20040039018A1

  公开（公告）日：2004-02-26

  This invention relates to pharmaceutical combinations of a cholesteryl ester transfer protein (CETP) inhibitor or a pharmaceutically acceptable salt thereof; and an antihypertensive agent or a pharmaceutically acceptable salt thereof, optionally in combination with an HMG CoA reductase inhibitor or a pharmaceutically acceptable salt thereof, kits containing such combinations and methods of using such combinations to treat subjects suffering from atherosclerosis, peripheral vascular disease, dyslipidemia, hyperbetaliproteinemia, hypoalphalipoproteinemia, hypercholesterolemia, hypertriglyceridemia, familial-hypercholesterolemia, cardiovascular disorders, angina, ischemia, cardiac ischemia, stroke, myocardial infarction, reperfusion injury, angioplastic restenosis, hypertension, vascular complications of diabetes, obesity or endotoxemia in a mammal (including a human being either male or female).

  本发明涉及一种胆固醇酯转移蛋白（CETP）抑制剂或其药学上可接受的盐与降压药剂或其药学上可接受的盐的药物组合，可选地与HMG CoA还原酶抑制剂或其药学上可接受的盐的药物组合，包含这种组合的套件以及使用这种组合治疗患有动脉粥样硬化、外周血管疾病、血脂异常、高β脂蛋白血症、低α脂蛋白血症、高胆固醇血症、高三酰甘油血症、家族性高胆固醇血症、心血管疾病、心绞痛、缺血、心肌缺血、中风、心肌梗死、再灌注损伤、血管成形术再狭窄、高血压、糖尿病血管并发症、肥胖或内毒素血症的哺乳动物（包括男性或女性人类）的使用方法。
• Compositions of choleseteryl ester transfer protein inhibitors and HMG-CoA reductase inhibitors
  申请人：Pfizer Inc

  公开号：US20040132771A1

  公开（公告）日：2004-07-08

  A composition comprises (1) a solid amorphous adsorbate comprising a cholesteryl ester transfer protein (CETP) inhibitor and a substrate; and (2) an HMG-CoA reductase inhibitor. The solid amorphous adsorbate provides concentration enhancement of the CETP inhibitor relative to a control composition consisting essentially of the unadsorbed CETP inhibitor alone, resulting in improved bioavailability.

  这篇文章包括(1)一个固态无定形吸附剂，其中包含一个胆固醇酯转移蛋白(CETP)抑制剂和一个底物;和(2)一个HMG-CoA还原酶抑制剂。固态无定形吸附剂相对于仅由未吸附的CETP抑制剂组成的对照组成分提供了CETP抑制剂的浓度增强，从而提高了生物利用度。
• Pharmaceutical compositions of adsorbates of amorphous drug
  申请人：——

  公开号：US20030054037A1

  公开（公告）日：2003-03-20

  Pharmaceutical compositions comprise a low-solubility drug adsorbed onto a high surface area substrate to form an adsorbate. The compositions in some embodiments include a concentration-enhancing polymer.

  药物组合物包括低溶解度药物吸附在高表面积基质上形成吸附剂。在某些实施例中，该组合物包括浓度增强聚合物。
• Pharmaceutical compositions comprising drug and concentration-enhancing polymers
  申请人：Pfizer Products Inc.

  公开号：EP1269994A2

  公开（公告）日：2003-01-02

  A solubility-improved drug form is combined with a concentration-enhancing polymer in a sufficient amount so that the combination provides substantially enhanced drug concentration in a use environment relative to a control comprising the same amount of the same drug form without the concentration-enhancing polymer.

  将溶解度提高的药物形式与足量的浓度增强聚合物结合在一起，使其在使用环境中的药物浓度相对于由相同量的相同药物形式（不含浓度增强聚合物）组成的对照组有大幅提高。