4-Methyl-pyrido-<3,2-d>-pyrimidin | 51674-88-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶并嘧啶类
• 英文名称: 4-Methyl-pyrido-<3,2-d>-pyrimidin
• 英文别名: 4-methyl-pyrido[3,2-d]pyrimidine；4-Methylpyrido[3,2-d]pyrimidine
• CAS: 51674-88-5
• 化学式: C₈H₇N₃
• 分子量: 145.164
• InChiKey: ZMENDMAMYVBZMD-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1
• 重原子数：
  11
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  38.7
• 氢给体数：
  0
• 氢受体数：
  3

文献信息

• [EN] NOVEL HETEROARYL AND HETEROCYCLE COMPOUNDS, COMPOSITIONS AND METHODS<br/>[FR] NOUVEAUX COMPOSÉS HÉTÉROARYLE ET HÉTÉROCYCLES, COMPOSITIONS ET PROCÉDÉS
  申请人：HUTCHISON MEDIPHARMA LTD

  公开号：WO2014015675A1

  公开（公告）日：2014-01-30

  Provided are novel heteroaryl and heterocycle compounds of formula (I-1), (I-2) or (I-3) and pharmaceutical compositions comprising them, uses and methods thereof for inhibiting the activity of PI3K and for treating inflammatory and autoimmune disorders diseases and cancer.

  提供了化学式(I-1)、(I-2)或(I-3)的新型杂环烷基和杂环化合物，以及包含它们的药物组合物，用途和方法，用于抑制PI3K的活性，并用于治疗炎症性和自身免疫性疾病以及癌症。
• [EN] NOVEL HETEROARYL AND HETEROCYCLE COMPOUNDS, COMPOSITION AND METHODS THEREOF<br/>[FR] NOUVEAUX COMPOSÉS HÉTÉROARYLIQUES ET HÉTÉROCYCLIQUES ET COMPOSITIONS ET PROCÉDÉS S'Y RAPPORTANT
  申请人：HUTCHISON MEDIPHARMA LTD

  公开号：WO2014015830A1

  公开（公告）日：2014-01-30

  Disclosed are novel heteroaryl and heterocycle compounds of formula I-1, I-2 or I-3 and pharmaceutical compositions comprising them, uses and methods thereof for inhibiting the activity of PI3K and for treating inflammatory and autoimmune diseases and cancer.

  揭示了一种新颖的杂环芳基和杂环化合物，其化学式为I-1、I-2或I-3，以及包含它们的药物组合物，用途和方法，用于抑制PI3K的活性，治疗炎症性和自身免疫性疾病以及癌症。
• PHOSPHATIDYLINOSITOL 3-KINASE INHIBITORS
  申请人：Gilead Sciences, Inc.

  公开号：US20150361068A1

  公开（公告）日：2015-12-17

  The present application provides the compounds of formula (J), or pharmaceutically acceptable salts, isomers, tautomer, or a mixture thereof, wherein n, W, A′, B′, R 1 , R 2 , and R 3 are described herein. The compounds are inhibitors to the activities of phosphatidylinositol 3-kinase (PI3K) and are useful for treating conditions mediated by one or more PI3K isoforms. The present application further provides pharmaceutical compositions that include a compound of formula (I), or pharmaceutically acceptable salts, isomers, tautomer, or mixture thereof, and methods of using these compounds and compositions for treating conditions mediated by one or more PI3K isoforms.

  本申请提供了式（J）的化合物，或其药学上可接受的盐、异构体、互变异构体或其混合物，其中n、W、A′、B′、R1、R2和R3如本文所述。这些化合物是磷脂酰肌醇3-激酶（PI3K）活性的抑制剂，可用于治疗由一个或多个PI3K同工型介导的疾病。本申请还提供了包括式（I）的化合物、或其药学上可接受的盐、异构体、互变异构体或其混合物的药物组合物，以及使用这些化合物和组合物治疗由一个或多个PI3K同工型介导的疾病的方法。
• BICYCLIC HETEROARYLAMINOALKYL PHENYL DERIVATIVES AS PI3K INHIBITORS
  申请人：Incyte Corporation

  公开号：US20150361094A1

  公开（公告）日：2015-12-17

  This application relates to derivatives of Formula I: and pharmaceutically acceptable salts thereof, which are inhibitors of PI3K, and compositions and methods of treatment related thereto.

  该申请涉及 Formula I 衍生物及其药用可接受的盐，这些化合物是 PI3K 的抑制剂，并涉及与之相关的治疗组合物和方法。
• BICYCLIC AZAHETEROCYCLOBENZYLAMINES AS PI3K INHIBITORS
  申请人：INCYTE CORPORATION

  公开号：US20130261101A1

  公开（公告）日：2013-10-03

  The present invention provides bicyclic azaheterocyclobenzylamines of Formula I: wherein the variables are defined herein, that modulate the activity of phosphoinositide 3-kinases (PI3Ks) and are useful in the treatment of diseases related to the activity of PI3Ks including, for example, inflammatory disorders, immune-based disorders, cancer, and other diseases.

  本发明提供了公式I的双环氮杂杂环苄胺化合物，其中变量在此处定义，可调节磷脂酰肌醇3-激酶（PI3Ks）的活性，并且在治疗与PI3Ks活性相关的疾病方面具有用途，包括但不限于炎症性疾病、免疫性疾病、癌症和其他疾病。