4-(1-Phenylcyclopentyl)-1,3-thiazol-2-amine

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 4-(1-Phenylcyclopentyl)-1,3-thiazol-2-amine
• 化学式: C₁₄H₁₆N₂S
• 分子量: 244.36
• InChiKey: OGEZYPPIKAJNGR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  17
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  67.2
• 氢给体数：
  1
• 氢受体数：
  3

文献信息

• N-(5-MEMBERED AROMATIC RING)-AMIDO ANTI-VIRAL COMPOUNDS
  申请人：Schmitz Ulrich Franz

  公开号：US20070265265A1

  公开（公告）日：2007-11-15

  Disclosed are compounds having Formula (I) and the compositions and methods thereof for treating or preventing a viral infection mediated at least in part by a virus in the Flaviviridae family of viruses, wherein A, R 2 , m, R, V, W, T, Z, R 1 , Y, and p are disclosed herein.

  揭示了具有Formula (I)的化合物，以及用于治疗或预防由Flaviviridae病毒家族中的病毒至少部分介导的病毒感染的组合物和方法，其中A、R2、m、R、V、W、T、Z、R1、Y和p在此处被揭示。
• [EN] 2-AMINOTHIAZOLE COMPOUNDS USEFUL AS ASPARTYL PROTEASE INHIBITORS<br/>[FR] COMPOSES DE 2-AMINOTHIAZOLE UTILES EN TANT QU'INHIBITEURS DE L'ASPARTYLE-PROTEASE
  申请人：MERCK & CO INC

  公开号：WO2005097767A1

  公开（公告）日：2005-10-20

  The present invention is directed to 2-aminothiazole compounds which are aspartyl protease inhibitors, and are inhibitors of both the beta-secretase enzyme and HIV protease, and that are useful in the treatment of diseases in which the beta-secretase enzyme and HIV are involved, such as Alzheimer's disease, HIV Infection and AIDS. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the treatment of such diseases in which the beta-secretase enzyme and HIV protease are involved.

  本发明涉及2-氨基噻唑化合物，它们是天冬氨酸蛋白酶抑制剂，同时也是β-分泌酶和HIV蛋白酶的抑制剂，可用于治疗涉及β-分泌酶和HIV的疾病，如阿尔茨海默病、HIV感染和艾滋病。该发明还涉及包含这些化合物的药物组合物，以及在治疗涉及β-分泌酶和HIV蛋白酶的疾病中使用这些化合物和组合物。
• N-(5-Membered Aromatic Ring)-Amido Anti-Viral Compounds
  申请人：Schmitz Franz Ulrich

  公开号：US20100004441A1

  公开（公告）日：2010-01-07

  Disclosed are compounds having Formula (I) and the compositions and methods thereof for treating or preventing a viral infection mediated at least in part by a virus in the Flaviviridae family of viruses, wherein A, R 2 , m, R, V, W, T, Z, R 1 , Y, and p are disclosed herein.

  本发明涉及具有式（I）的化合物及其组合物和方法，用于治疗或预防由Flaviviridae病毒家族中的病毒至少部分介导的病毒感染。其中，本文披露了A、R2、m、R、V、W、T、Z、R1、Y和p。
• 2-Aminothiazole Compounds Useful As Aspartyl Protease Inhibitors
  申请人：Coburn A. Craig

  公开号：US20070203147A1

  公开（公告）日：2007-08-30

  The present invention is directed to 2-aminothiazole compounds which are aspartyl protease inhibitors, and are inhibitors of both the beta-secretase enzyme and HIV protease, and that are useful in the treatment of diseases in which the beta-secretase enzyme and HIV are involved, such as Alzheimer's disease, HIV Infection and AIDS. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the treatment of such diseases in which the beta-secretase enzyme and HIV protease are involved.

  本发明涉及2-氨基噻唑化合物，它们是天冬氨酸蛋白酶抑制剂，同时也是β-秘密酶酶和HIV蛋白酶的抑制剂，可用于治疗涉及β-秘密酶酶和HIV的疾病，如阿尔茨海默病、HIV感染和艾滋病。本发明还涉及包含这些化合物的制药组合物以及使用这些化合物和组合物治疗涉及β-秘密酶酶和HIV蛋白酶的疾病。
• N-(5-MEMBERED HETEROAROMATIC RING)-AMIDO ANTI-VIRAL COMPOUNDS
  申请人：GENELABS TECHNOLOGIES, INC.

  公开号：EP1971597A2

  公开（公告）日：2008-09-24