trans-2-Hydroxycyclopentancarboxamid | 40481-98-9

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: trans-2-Hydroxycyclopentancarboxamid
• 英文别名: trans-2-Hydroxy-cyclopentancarbonsaeureamid；(1R,2R)-2-Hydroxycyclopentane-1-carboxamide
• CAS: 40481-98-9；40481-99-0；86009-75-8
• 化学式: C₆H₁₁NO₂
• 分子量: 129.159
• InChiKey: XLPNKXDLOYEHIM-RFZPGFLSSA-N

物化性质

• 熔点：
  87-90 °C
• 沸点：
  239.22°C (rough estimate)
• 密度：
  1.1426 (rough estimate)

计算性质

• 辛醇/水分配系数(LogP)：
  -0.1
• 重原子数：
  9
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.83
• 拓扑面积：
  63.3
• 氢给体数：
  2
• 氢受体数：
  2

安全信息

• 安全说明：
  S24/25

反应信息

• 作为反应物：
  描述：

  trans-2-Hydroxycyclopentancarboxamid 、 氢化铝锂 生成 (1S,2R)-trans-2-(aminomethyl)cyclopentanol
  参考文献：
  名称：

  STAJER, G.;SZABO, A. E.;FUELOEP, F.;BERNATH, G.;KALMAN, A.;ARGAY, G.;SOHA+, MAGY. KEM. FOLYOIRAT, 1983, 89, N 10, 460-466

  摘要：

  DOI：

文献信息

• [EN] ISOXAZOLE-THIAZOLE DERIVATIVES AS GABA A RECEPTOR INVERSE AGONISTS FOR USE IN THE TREATMENT OF COGNITIVE DISORDERS<br/>[FR] DÉRIVÉS D'ISOXAZOLE-THIAZOLE COMME AGONISTES INVERSES DU RÉCEPTEUR GABA A, UTILES DANS LE TRAITEMENT DE TROUBLES COGNITIFS
  申请人：HOFFMANN LA ROCHE

  公开号：WO2010127974A1

  公开（公告）日：2010-11-11

  The present invention is concerned with isoxazole-thiazole derivatives of formula I, having affinity and selectivity for GABA A α5 receptor, their manufacture, pharmaceutical compositions containing them and their use as therapeutically active substances. The active compounds of the present invention are useful as cognitive enhancer or for the therapeutic and/or prophylactic treatment of cognitive disorders like Alzheimer's disease.

  本发明涉及式I的异恶唑-噻唑衍生物，具有对GABA A α5受体的亲和力和选择性，其制备、含有它们的药物组合物以及它们作为治疗活性物质的用途。本发明的活性化合物可用作认知增强剂或用于治疗和/或预防认知障碍，如阿尔茨海默病。
• [EN] ISOXAZOLE-PYRAZOLE DERIVATIVES<br/>[FR] DÉRIVÉS D'ISOXAZOLE-PYRAZOLE
  申请人：HOFFMANN LA ROCHE

  公开号：WO2010127975A1

  公开（公告）日：2010-11-11

  The present invention is concerned with isoxazole-pyrazole derivatives of formula I, having affinity and selectivity for GABA A α5 receptor, their manufacture, pharmaceutical compositions containing them and their use as medicaments. The active compounds of the present invention are useful as cognitive enhancer or for the therapeutic and/or prophylactic treatment of cognitive disorders like Alzheimer's disease.

  本发明涉及具有亲和力和选择性对GABA A α5受体的异恶唑-吡唑衍生物，其化学式为I，它们的制备、含有它们的药物组合物以及它们作为药物的用途。本发明的活性化合物可用作认知增强剂，或用于治疗和/或预防认知障碍，如阿尔茨海默病。
• NOVEL COMPOUNDS
  申请人：CHIESI FARMACEUTICI S.p.A.

  公开号：US20160168101A1

  公开（公告）日：2016-06-16

  Compounds of formula (I) described herein are imidazolone derivatives having human neutrophil elastase (HNE) inhibitory properties and are useful for the treatment of diseases and conditions in which HNE is implicated.

  本文描述的化合物的化学式（I）是咪唑酮衍生物，具有对人类中性粒细胞弹性蛋白酶（HNE）具有抑制作用的性质，并且适用于治疗HNE参与的疾病和病状。
• Tetrahydrothiopyrano pyrazole cannabinoid modulators
  申请人：Liotta Fina

  公开号：US20060223798A1

  公开（公告）日：2006-10-05

  The invention relates to a CB modulator compound of Formula (I) or a pharmaceutically acceptable form thereof and a method for use in treating, ameliorating or preventing a CB receptor mediated syndrome, disorder or disease.

  该发明涉及一种化合物，其化学式为（I）或其药用可接受形式，以及用于治疗、改善或预防CB受体介导的综合征、疾病或疾病的方法。
• [EN] ORGANIC COMPOUNDS<br/>[FR] COMPOSÉS ORGANIQUES
  申请人：NOVARTIS AG

  公开号：WO2005051895A1

  公开（公告）日：2005-06-09

  Disclosed are δ-amino-Ϝ-hydroxy-ω-aryl-alkanoic acid amide compounds of formula (I) and the salts thereof, having renin-inhibiting properties. Also disclosed are pharmaceutical compositions comprising these compounds and methods of administering them for the treatment of hypertension, atherosclerosis, unstable coronary syndrome, congestive heart failure, cardiac hypertrophy, cardiac fibrosis, cardiomyopathy postinfarction, unstable coronary syndrome, diastolic dysfunction, chronic kidney disease, hepatic fibrosis, complications resulting from diabetes, such as nephropathy, vasculopathy and neuropathy, diseases of the coronary vessels, restenosis following angioplasty, raised intra-ocular pressure, glaucoma, abnormal vascular growth, hyperaldosteronism, cognitive impairment, alzheimers, dementia, anxiety states and cognitive disorders.

  揭示了具有抑制肾素作用的δ-氨基-Ϝ-羟基-ω-芳基-烷酸酰胺化合物的化学式(I)及其盐。还揭示了包含这些化合物的药物组合物以及用于治疗高血压、动脉粥样硬化、不稳定性冠状动脉综合征、充血性心力衰竭、心肌肥大、心脏纤维化、心肌病后梗死、不稳定性冠状动脉综合征、舒张功能障碍、慢性肾脏疾病、肝纤维化、糖尿病引起的并发症（如肾病、血管病和神经病变）、冠状动脉疾病、血管成形术后再狭窄、眼内压升高、青光眼、异常血管生长、高醛固酮症、认知障碍、阿尔茨海默病、痴呆、焦虑状态和认知障碍的治疗方法。