2-amino-cyclohexanecarboxylic acid ; hydrochloride | 24716-92-5

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: 2-amino-cyclohexanecarboxylic acid ; hydrochloride
• 英文别名: 2-Amino-cyclohexancarbonsaeure; Hydrochlorid；(2-carboxycyclohexyl)azanium;chloride
• CAS: 24716-92-5；57266-55-4；57266-57-6；107313-10-0；107313-16-6
• 化学式: C₇H₁₃NO₂*ClH
• mdl: MFCD22196561
• 分子量: 179.647
• InChiKey: QNIOBHOEZYKCJV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -1.71
• 重原子数：
  11
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.857
• 拓扑面积：
  63.3
• 氢给体数：
  3
• 氢受体数：
  3

安全信息

• 危险性防范说明：
  P261,P280,P301+P312,P302+P352,P305+P351+P338
• 危险性描述：
  H302,H315,H319,H335

文献信息

• Composition for the treatment of damaged tissue
  申请人：Pfizer Inc.

  公开号：US20030199440A1

  公开（公告）日：2003-10-23

  A pharmaceutical for use in damaged tissue, such as wound, treatment (e.g. healing) is described. The pharmaceutical comprising a composition which comprises: (a) a growth factor; and (b) an inhibitor agent; and optionally (c) a pharmaceutically acceptable carrier, diluent or excipient; wherein the inhibitor agent can inhibit the action of at least one specific adverse protein (e.g. a specific protease) that is upregulated in a damaged tissue, such as a wound, environment.

  描述了一种用于受损组织，如伤口治疗（例如愈合）的药物。该药物包括包含以下成分的组合物：（a）生长因子；和（b）抑制剂；以及可选的（c）药用载体、稀释剂或赋形剂；其中抑制剂可以抑制至少一种在受损组织，如伤口环境中上调的特定不良蛋白质（例如特定蛋白酶）的作用。
• [EN] BIPHENYL-ETHYL-PYRROLIDINE DERIVATIVES AS HISTAMINE H3 RECEPTOR MODULATORS FOR THE TREATMENT OF COGNITIVE DISORDERS<br/>[FR] DÉRIVÉS DE BIPHÉNYL-ÉTHYL-PYRROLIDINE EN TANT QUE MODULATEURS DES RÉCEPTEURS H3 DE L'HISTAMINE POUR LE TRAITEMENT DE TROUBLES COGNITIFS
  申请人：ARENA PHARM INC

  公开号：WO2014110103A1

  公开（公告）日：2014-07-17

  The present invention relates to compounds of Formula (Ia) and pharmaceutically acceptable salts, solvates, and hydrates thereof, that modulate the activity of the histamine H3 receptor (Ia). Compounds of the present invention and pharmaceutical compositions thereof are directed to methods useful in the treatment of histamine H3-associated disorders.

  本发明涉及式(Ia)的化合物及其药用可接受的盐、溶剂合物和水合物，其调节组胺H3受体(Ia)的活性。本发明的化合物和药物组合物用于治疗组胺H3相关疾病的方法。
• [EN] PIPERAZINE DERIVATIVES AS HIV PROTEASE INHIBITORS<br/>[FR] DÉRIVÉS DE PIPÉRAZINE UTILISÉS EN TANT QU'INHIBITEURS DE LA PROTÉASE DU VIH
  申请人：MERCK SHARP & DOHME

  公开号：WO2015138220A1

  公开（公告）日：2015-09-17

  The present invention is directed to compounds of Formula I pharmaceutical compositions comprising the same, and their use in the inhibition of HIV protease, the inhibition of HIV replication, the prophylaxis of infection by HIV, the treatment of infection by HIV, and the prophylaxis, treatment, and delay in the onset or progression of AIDS.

  本发明涉及公式I化合物、包含这些化合物的药物组合物，以及它们在抑制HIV蛋白酶、抑制HIV复制、预防HIV感染、治疗HIV感染，以及预防、治疗和延缓艾滋病发作或进展中的用途。
• SULFONAMIDE DERIVATIVE AND USE THEREOF
  申请人：Fukumoto Shoji

  公开号：US20140024650A1

  公开（公告）日：2014-01-23

  Provided is a compound having an AMPA receptor function enhancing action, and useful as a prophylactic or therapeutic drug for depression, Alzheimer's disease, schizophrenia, attention deficit hyperactivity disorder (ADHD) and the like. A compound represented by the formula (I): wherein each symbol is as defined in the present specification, or a salt thereof.

  提供了一种具有AMPA受体功能增强作用的化合物，可用作预防或治疗抑郁症、阿尔茨海默病、精神分裂症、注意力缺陷多动障碍（ADHD）等药物。该化合物由式（I）表示：其中每个符号如本说明书所定义，或其盐。
• AZAINDOLES AS JANUS KINASE INHIBITORS
  申请人：MERCK SHARP & DOHME CORP

  公开号：US20140303142A1

  公开（公告）日：2014-10-09

  The instant invention provides compounds of formula I which are JAK inhibitors, and as such are useful for the treatment of JAK-mediated diseases such as rheumatoid arthritis, asthma, COPD and cancer.

  本发明提供了式I的化合物，它们是JAK抑制剂，因此可用于治疗JAK介导的疾病，如类风湿性关节炎、哮喘、慢性阻塞性肺疾病和癌症。