2-氨基-6-甲基喹喔啉 | 1687-52-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二氮杂萘
• 中文名称: 2-氨基-6-甲基喹喔啉
• 英文名称: 2-Amino-6-methyl-chinazolin
• 英文别名: 6-Methylquinazolin-2-amine
• CAS: 1687-52-1
• 化学式: C₉H₉N₃
• mdl: MFCD04114088
• 分子量: 159.191
• InChiKey: SNBAZGAHVJGFDT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  12
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.111
• 拓扑面积：
  51.8
• 氢给体数：
  1
• 氢受体数：
  3

安全信息

• 海关编码：
  2933990090

文献信息

• [EN] COMPOUNDS TARGETING PRMT5<br/>[FR] COMPOSÉS CIBLANT PRMT5
  申请人：ALIGOS THERAPEUTICS INC

  公开号：WO2020205867A1

  公开（公告）日：2020-10-08

  Provided herein are compounds of Formula (I), or pharmaceutically acceptable salts thereof, pharmaceutical compositions that include a compound described herein (including pharmaceutically acceptable salts of a compound described herein) and methods of synthesizing the same. Also provided herein are methods of treating diseases and/or conditions with a compound of Formula (I), or a pharmaceutically acceptable salt thereof.

  本文提供了式（I）的化合物或其药用盐，包括含有本文描述的化合物（包括本文描述的化合物的药用盐）的药物组合物以及合成这些化合物的方法。本文还提供了使用式（I）的化合物或其药用盐治疗疾病和/或症状的方法。
• PYRIDOPYRIMIDINE COMPOUNDS ACTING AS MTORC 1/2 DOUBLE-KINASE INHIBITORS
  申请人：MEDSHINE DISCOVERY INC.

  公开号：US20200339568A1

  公开（公告）日：2020-10-29

  Disclosed are a series of pyridopyrimidine compounds and a use of same in the preparation of drugs associated with mTORC 1/2 dual complex inhibitors, and specifically disclosed is a use of the compounds as shown in formula (IV), tautomers thereof or pharmaceutically acceptable salts thereof in the preparation of drugs associated with mTORC 1/2 dual complex inhibitors.

  本文披露了一系列吡啶吡嘧啶化合物及其在制备与mTORC 1/2双复合物抑制剂相关的药物中的用途，具体披露了将所述化合物，其互变异构体或其药学上可接受的盐如公式（IV）所示用于制备与mTORC 1/2双复合物抑制剂相关的药物。
• N-9 SUBSTITUTED PURINE COMPOUNDS, COMPOSITIONS AND METHODS OF USE
  申请人：Pei Zhonghua

  公开号：US20110086841A1

  公开（公告）日：2011-04-14

  The present invention relates to compounds of Formula I: wherein R 1 , R 2 , R 3 , A 1 , A 2 , A 3 , A 4 and D have the meaning described herein. The present invention also relates to pharmaceutical compositions comprising such compounds and therapeutic uses thereof.

  本发明涉及以下化合物的公式I：其中R1、R2、R3、A1、A2、A3、A4和D具有本说明中描述的含义。本发明还涉及包含这些化合物的药物组合物以及其治疗用途。
• Trifluoromethyl substituted benzamides as kinase inhibitors
  申请人：Caravatti Giorgio

  公开号：US20080096883A1

  公开（公告）日：2008-04-24

  The invention relates to trifluoromethyl substituted benzamide compounds of the formula (I), pharmaceuticals comprising these compounds, their use as or for the manufacture of pharmaceuticals, particularly as inhibitors of protein kinases and/or the treatment of a condition, disorder or disease state mediated by a protein kinase activity and/or a proliferative disease, methods of treatment comprising administering the compounds, especially of therapeutic and prophylactic treatment, methods for the manufacture of the compounds and novel intermediates and partial steps for their synthesis.

  本发明涉及式(I)的三氟甲基取代苯甲酰胺化合物，包括这些化合物的药物、它们作为药物或用于制造药物的用途，特别是作为蛋白激酶抑制剂和/或治疗由蛋白激酶活性介导的情况、疾病或疾病状态以及增殖性疾病的方法，包括给予这些化合物的治疗和预防治疗方法，以及制造这些化合物的新中间体和部分合成步骤。
• 1,4-Disubstituted isoquinilone derivatives as raf-kinase inhibitors useful for the treatment of proliferative diseases
  申请人：Fink Anne Cynthia

  公开号：US20070060582A1

  公开（公告）日：2007-03-15

  This invention relates to compounds of the formula (I) wherein the variable substituents are described herein. The compounds are useful for the treatment of conditions and diseases characterized by an aberrant MAP kinase signaling pathway, such as cancer.

  本发明涉及公式（I）中变量取代基的化合物，所述的化合物可用于治疗由异常MAP激酶信号通路引起的疾病和症状，例如癌症。