2-(Aminomethoxy)benzoic acid | 63351-74-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 2-(Aminomethoxy)benzoic acid
• CAS: 63351-74-6
• 化学式: C₈H₉NO₃
• 分子量: 167.16
• InChiKey: VAMUGOMJRVPWSV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -1.5
• 重原子数：
  12
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  72.6
• 氢给体数：
  2
• 氢受体数：
  4

文献信息

• [EN] PIPERAZINE-SUBSTITUTED 7-METHOXY-[1,2,4]TRIAZOLO[1,5-C]QUINAZOLIN-5-AMINE COMPOUNDS WITH A2A ANTAGONIST PROPERTIES<br/>[FR] COMPOSÉS DE 7-MÉTHOXY-[1,2,4]TRIAZOLO[1,5-C]QUINAZOLINE-5-AMINE À SUBSTITUTION PIPÉRAZINE PRÉSENTANT DES PROPRIÉTÉS D'ANTAGONISTE D'A2A
  申请人：MERCK SHARP & DOHME

  公开号：WO2014101113A1

  公开（公告）日：2014-07-03

  Disclosed are compounds of Formula (A), as defined herein, which have binding activity for an A2A-receptor and are believed to be useful for treatment or management of CNS diseases or conditions which can be treated or managed using compounds which have A2A receptor antagonist activity.

  本公开的是本文所定义的Formula (A)的化合物，它们具有与A2A受体的结合活性，并被认为对于治疗或管理可以使用具有A2A受体拮抗活性的化合物来治疗或管理的中枢神经系统疾病或疾况是有用的。
• PIPERAZINE-SUBSTITUTED [1,2,4]TRIAZOLO[1,5-C]QUINAZOLIN-5-AMINE COMPOUNDS WITH A2A ANTAGONIST PROPERTIES
  申请人：ALI Amjad

  公开号：US20160194330A1

  公开（公告）日：2016-07-07

  Disclosed are compounds of Formula A: (structurally represented) where “RG1”, “RG2a”, “RG4”, “RG5”, “MG1”, “n” and “m” are defined herein which compounds are antagonists of A2A receptor. Disclosed herein also are uses of the compounds described herein as antagonists of the A2a receptor in the potential treatment or prevention of neurological disorders and diseases in which A2A receptors are involved. Disclosed herein also are pharmaceutical compositions comprising these compounds and uses of these pharmaceutical compositions.

  本发明公开了A式化合物，其中“RG1”、“RG2a”、“RG4”、“RG5”、“MG1”、“n”和“m”在此被定义，这些化合物是A2A受体拮抗剂。本发明还公开了上述化合物作为A2A受体拮抗剂在潜在的涉及A2A受体的神经系统疾病的治疗或预防中的用途。本发明还公开了包含这些化合物的制药组合物以及这些制药组合物的用途。
• Time-resolved fluorimetric detection of lanthanide labeled nucleotides
  申请人：THE PERKIN-ELMER CORPORATION

  公开号：EP0340675A2

  公开（公告）日：1989-11-08

  Nucleotides conjugated with a chelating agent and labeled with a lanthanide, especially terbium, are readily detected by time-resolved fluorimetry during and following gel electrophoresis. The labeled nucleotide conjugates are very stable, highly fluorescent with a long radiative lifetime and remain fluorescent during dilution and during gel electrophoresis and since an enhancement solution is not required for detection, the labeled nucleotide conjugates can be detectd on-line, if desired.

  核苷酸与螯合剂共轭并用镧系元素（尤其是铽元素）标记后，在凝胶电泳过程中和电泳后很容易通过时间分辨荧光测定法进行检测。标记的核苷酸共轭物非常稳定，荧光强度高，辐射寿命长，在稀释过程中和凝胶电泳过程中都能保持荧光，而且由于检测不需要增强溶液，如果需要，标记的核苷酸共轭物可以在线检测。
• 4-AMINO-N --(4-METHYL-4-PIPERIDINYL)-2-METHOXYBENZAMIDES
  申请人：JANSSEN PHARMACEUTICA N.V.

  公开号：EP0650475A1

  公开（公告）日：1995-05-03
• 4-AMINO-N-(4-METHYL-4-PIPERIDINYL)-2-METHOXYBENZAMIDES, THEIR PREPARATION AND THEIR USE AS 5-HT2 ANTAGONISTS
  申请人：JANSSEN PHARMACEUTICA N.V.

  公开号：EP0650475B1

  公开（公告）日：1999-09-01