4-((2-fluoro-4-methylphenyl)amino)-1,3,8-trimethylpyrido[2,3-d]pyridazine-2,5(1H,6H)-dione | 853109-68-9

• 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: 4-((2-fluoro-4-methylphenyl)amino)-1,3,8-trimethylpyrido[2,3-d]pyridazine-2,5(1H,6H)-dione
• 英文别名: 4-(2-fluoro-4-methylphenylamino)-1,3,8-trimethyl-1H,6H-pyrido[2,3-d]pyridazine-2,5-dione；4-(2-fluoro-4-methylanilino)-1,3,8-trimethyl-6H-pyrido[2,3-d]pyridazine-2,5-dione
• CAS: 853109-68-9
• 化学式: C₁₇H₁₇FN₄O₂
• 分子量: 328.346
• InChiKey: BDCNZJFEXWRTQE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.1
• 重原子数：
  24
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.24
• 拓扑面积：
  73.8
• 氢给体数：
  2
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  4-chloro-2-(1-ethoxyvinyl)-1,5-dimethyl-6-oxo-1,6-dihydropyridine-3-carbonitrile 在 盐酸 、 一水合肼 、 溶剂黄146 、 lithium hexamethyldisilazane 作用下， 以 四氢呋喃 、 1,4-二氧六环 、 乙腈 为溶剂， 反应 49.0h， 生成 4-((2-fluoro-4-methylphenyl)amino)-1,3,8-trimethylpyrido[2,3-d]pyridazine-2,5(1H,6H)-dione
  参考文献：
  名称：

  [EN] CERTAIN PROTEIN KINASE INHIBITORS
  [FR] CERTAINS INHIBITEURS DE PROTÉINE KINASE

  摘要：

  本文披露了蛋白激酶抑制剂，更具体地是吡啶并衍生物以及其药物组合物，以及使用方法。

  公开号：

  WO2014169843A1

文献信息

• [EN] CERTAIN PROTEIN KINASE INHIBITORS<br/>[FR] CERTAINS INHIBITEURS DE PROTÉINE KINASE
  申请人：SHANGHAI FOCHON PHARMACEUTICAL CO LTD

  公开号：WO2014169843A1

  公开（公告）日：2014-10-23

  Disclosed herein are protein kinase inhibitors,more particularly pyridazine derivatives and pharmaceutical compositions thereof,and method of use thereof.

  本文披露了蛋白激酶抑制剂，更具体地是吡啶并衍生物以及其药物组合物，以及使用方法。
• Heterocyclic inhibitors of MEK and methods of use thereof
  申请人：Marlow L. Allison

  公开号：US20050256123A1

  公开（公告）日：2005-11-17

  Disclosed are compounds of the Formula I and pharmaceutically acceptable salts and prodrugs thereof, wherein R 1 , R 2 , R 7 , R 8 and R 9 , W, X and Y are as defined in the specification. Such compounds are MEK inhibitors and useful in the treatment of hyperproliferative diseases, such as cancer and inflammation, in mammals, and inflammatory conditions. Also disclosed are methods of using such compounds in the treatment of hyperproliferative diseases in mammals and pharmaceutical compositions containing such compounds.

  本文披露了式I的化合物及其药用盐和前药，其中R1、R2、R7、R8和R9、W、X和Y的定义如规范中所述。这些化合物是MEK抑制剂，在哺乳动物中用于治疗高增殖性疾病，如癌症和炎症，以及炎症病症。还披露了在哺乳动物中治疗高增殖性疾病的方法以及含有这些化合物的药物组合物。
• HETEROCYCLIC INHIBITORS OF MEK AND METHODS OF USE THEREOF
  申请人：Marlow Allison L.

  公开号：US20090215834A1

  公开（公告）日：2009-08-27

  Disclosed are compounds of the Formula V and pharmaceutically acceptable salts and prodrugs thereof, wherein R 1 , R 2 , R 7 , R 8 and R 9 , and W are as defined in the specification. Such compounds are MEK inhibitors and useful in the treatment of hyperproliferative diseases, such as cancer and inflammation, and inflammatory conditions in mammals. Also disclosed are methods of using such compounds in the treatment of hyperproliferative diseases and inflammatory conditions in mammals and pharmaceutical compositions containing such compounds.

  本发明涉及公式V的化合物，以及其药学上可接受的盐和前药，其中R1、R2、R7、R8和R9以及W在说明书中定义。这些化合物是MEK抑制剂，可用于治疗哺乳动物的高增殖性疾病，如癌症和炎症，以及炎症状况。本发明还涉及使用这些化合物治疗哺乳动物的高增殖性疾病和炎症状况的方法，以及含有这些化合物的制药组合物。
• Novel 4-Arylamino Pyridone Derivatives as Mek Inhibitors for the Treatment of Hyper-Proliferative Disorders
  申请人：Abel Ulrich

  公开号：US20070293544A1

  公开（公告）日：2007-12-20

  The invention provides novel, substituted 4-arylamino pyridone compounds (formula (I)), pharmaceutically acceptable salts, solvates and prodrug compounds thereof, wherein W, R 1, R2, R9, R 10, R 11, R 12, R 13, R 14 and L are as defined in the specification. Such compounds are MEK inhibitors and useful in the treatment of hyperproliferative diseases, such as cancer, restenosis and inflammation. Also disclosed is the use of such compounds in the treatment of hyperproliferative diseases in mammals, especially humans, and pharmaceutical compositions containing such compounds.

  本发明提供了一种新型的取代的4-芳基氨基吡啶酮化合物（式（I）），其药学上可接受的盐、溶剂化物和前药化合物，其中W、R1、R2、R9、R10、R11、R12、R13、R14和L如规范中所定义。这些化合物是MEK抑制剂，可用于治疗过度增殖性疾病，如癌症、再狭窄和炎症。还揭示了在哺乳动物，特别是人类中使用这些化合物治疗过度增殖性疾病以及含有这些化合物的制药组合物的用途。
• Dihydropyridine and dihydropyridazine derivatives as inhibitors of MEK and methods of use thereof
  申请人：Array BioPharma Inc.

  公开号：US07732616B2

  公开（公告）日：2010-06-08

  Disclosed are compounds of the Formulas I and V and pharmaceutically acceptable salts and prodrugs thereof, wherein R1, R2, R7, R8 and R9, W, X and Y are as defined in the specification. Such compounds are MEK inhibitors and useful in the treatment of hyperproliferative diseases, such as cancer and inflammation, in mammals, and inflammatory conditions. Also disclosed are methods of using such compounds in the treatment of hyperproliferative diseases in mammals and pharmaceutical compositions containing such compounds.

  本发明揭示了I和V式化合物及其药学上可接受的盐和前药，其中R1、R2、R7、R8和R9、W、X和Y的定义如规范中所述。这些化合物是MEK抑制剂，可用于治疗哺乳动物的高增殖性疾病，如癌症和炎症，以及炎症情况。还揭示了使用这些化合物治疗哺乳动物的高增殖性疾病的方法和包含这些化合物的药物组合物。