(4-(2H-四唑-5-基)苯基)甲胺盐酸盐 | 177595-28-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 中文名称: (4-(2H-四唑-5-基)苯基)甲胺盐酸盐
• 英文名称: [4-(1H-1,2,3,4-tetrazol-5-yl)phenyl]methanamine hydrochloride
• 英文别名: 4-(1H-5-tetrazolyl)benzylamine hydrochloride；4-(1H-tetrazol-5-yl)-benzylamine hydrochloride；(4-(2H-Tetrazol-5-yl)phenyl)methanamine hydrochloride；[4-(2H-tetrazol-5-yl)phenyl]methanamine;hydrochloride
• CAS: 177595-28-7
• 化学式: C₈H₉N₅*ClH
• mdl: MFCD18089384
• 分子量: 211.654
• InChiKey: AYGATWAUTLJNTK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -1.17
• 重原子数：
  14
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.125
• 拓扑面积：
  80.5
• 氢给体数：
  3
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  4-[({[5-fluoro-2-(4-fluorobenzyl)pyridin-3-yl]carbonyl}amino)methyl]benzoic acid 、 (4-(2H-四唑-5-基)苯基)甲胺盐酸盐 生成 5-fluoro-2-(4-fluorobenzyl)-N-[4-(2H-tetrazol-5-yl)benzyl]nicotinamide
  参考文献：
  名称：

  Aryl or heteroaryl amide compounds

  摘要：

  本发明提供了一种式子为（I）的化合物：其中，A代表苯基或类似基团；B代表芳基或类似基团；E代表1,4-苯基基团；R1和R2独立地代表氢原子或类似基团；R3和R4独立地代表氢原子或类似基团；R5代表-CO2H或类似基团；R6代表具有1至6个碳原子的烷基或类似基团；X代表亚甲基或类似基团。这些化合物可用于治疗由前列腺素介导的疾病状态，如哺乳动物中的疼痛或类似症状。本发明还提供了一种包含上述化合物的制药组合物。

  公开号：

  US20050065188A1

文献信息

• 4-ALKYNYL IMIDAZOLE DERIVATIVE AND MEDICINE COMPRISING SAME AS ACTIVE INGREDIENT
  申请人：KAKEN PHARMACEUTICAL CO., LTD.

  公开号：US20160130232A1

  公开（公告）日：2016-05-12

  There are provided 4-alkynylimidazole derivatives represented by the following general formula (I) or phamaceutically acceptable salts thereof; the derivatives have a superior EP4 receptor antagonistic action and are useful as pharmaceuticals for the treatment of diseases associated with the EP4 receptor, for example, as anti-inflammatory and/or analgesic drugs for inflammatory diseases and diseases that involve various kinds of pains, and further as pharmaceuticals for the treatment of immune diseases that result from inflammations as evoked by tissue destruction due to the activation of Th1 cells and/or Th17 cells:

  提供了以下一般式(I)所代表的4-炔基咪唑衍生物或其药用盐；这些衍生物具有优越的EP4受体拮抗作用，可用作治疗与EP4受体相关的疾病的药物，例如，作为抗炎和/或镇痛药物，用于治疗炎症性疾病和涉及各种疼痛的疾病，进一步作为治疗由于Th1细胞和/或Th17细胞激活引起的组织破坏所致的炎症导致的免疫性疾病的药物：
• INDAZOLE DERIVATIVES
  申请人：Ackermann Jean

  公开号：US20080103182A1

  公开（公告）日：2008-05-01

  The invention is concerned with novel indazole derivatives of formula (I) wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , X and Y are as defined in the description and in the claims, as well as physiologically acceptable salts and esters thereof. These compounds inhibit L-CPT1 and can be used in the prevention or treatment of diseases which are modulated by L-CPT1 inhibitors.

  这项发明涉及公式（I）的新型吲唑衍生物，其中R1、R2、R3、R4、R5、R6、X和Y的定义如描述和索赔中所述，以及其生理上可接受的盐和酯。这些化合物抑制L-CPT1，可用于预防或治疗受L-CPT1抑制剂调节的疾病。
• [EN] PHENYL OR PYRIDYL AMIDE COMPOUNDS AS PROSTAGLANDIN E2 ANTAGONISTS<br/>[FR] COMPOSES DE PHENYLE OU DE PYRIDYLE AMIDE UTILES COMME ANTAGONISTES DE LA PROSTAGLANDINE E2
  申请人：PFIZER

  公开号：WO2005021508A1

  公开（公告）日：2005-03-10

  This invention provides a compound of the formula (I): wherein A represents a phenyl group or the like: B represents an aryl or the like: E represents a 1,4-phenylene group; R1 and R2 independently represent a hydrogen atom or the like: R3 and R4 independently represent a hydrogen atom or the like: R5 represents -CO2H or the like:R6 represents an alkyl group having from 1 to 6 carbon atoms or the like: X represents a methylene group or the like. These compounds are useful for the treatment of disease conditions mediated by prostaglandin such as pain, or the like in mammalian. The compounds act as antagonists of the prostaglandin E2 receptor. This invention also provides a pharmaceutical composition comprising the above compound.

  这项发明提供了一个化合物的结构式(I)：其中A代表苯基或类似物：B代表芳基或类似物：E代表1,4-苯基基团；R1和R2独立地代表氢原子或类似物：R3和R4独立地代表氢原子或类似物：R5代表-CO2H或类似物：R6代表具有1至6个碳原子的烷基基团或类似物：X代表亚甲基基团或类似物。这些化合物对于治疗由前列腺素介导的疾病状况，如哺乳动物中的疼痛等，具有用处。这些化合物作为前列腺素E2受体的拮抗剂。这项发明还提供了包含上述化合物的药物组合物。
• Combinations Comprising Alpha-2-Delta Ligands and Ep4 Receptor Antagonists
  申请人：Audoly Laurent Pascal

  公开号：US20090036495A1

  公开（公告）日：2009-02-05

  The instant invention relates to a combination of an EP4-receptor antagonist and an alpha-2-delta ligand, and pharmaceutically acceptable salts thereof, pharmaceutical compositions thereof and their use in the treatment of pain, particularly inflammatory, neuropathic, visceral and nociceptive pain.

  本发明涉及一种EP4受体拮抗剂和α-2-δ配体的组合物，及其药学上可接受的盐、制药组合物及其在治疗疼痛，特别是炎症性、神经病理性、内脏性和伤害性疼痛中的用途。
• [EN] COMBINATIONS COMPRISING ALPHA-2-DELTA LIGANDS AND EP4 RECEPTOR ANTAGONISTS<br/>[FR] COMBINAISONS CONTENANT DES LIGANDS DE ALPHA-2-DELTA
  申请人：PFIZER PROD INC

  公开号：WO2005102389A9

  公开（公告）日：2009-04-30