2-Methylpyrimido<4,5-d>pyridazin-5-on | 62327-82-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: 2-Methylpyrimido<4,5-d>pyridazin-5-on
• 英文别名: 2-methyl-6H-pyrimido[4,5-d]pyridazin-5-one；2-Methylpyrimido[4,5-d]pyridazin-5(6H)-one；2-methyl-6H-pyrimido[4,5-d]pyridazin-5-one
• CAS: 62327-82-6
• 化学式: C₇H₆N₄O
• 分子量: 162.151
• InChiKey: MRFCOTGJDUNOGR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.3
• 重原子数：
  12
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  67.2
• 氢给体数：
  1
• 氢受体数：
  4

文献信息

• SILICON BASED DRUG CONJUGATES AND METHODS OF USING SAME
  申请人：BlinkBio, Inc.

  公开号：US20170202970A1

  公开（公告）日：2017-07-20

  Described herein are silicon based conjugates capable of delivering one or more payload moieties to a target cell or tissue. Contemplated conjugates may include a silicon-heteroatom core, one or more optional catalytic moieties, a targeting moiety that permits accumulation of the conjugate within a target cell or tissue, one or more payload moieties (e.g., a therapeutic agent or imaging agent), and two or more non-interfering moieties covalently bound to the silicon-heteroatom core.

  本文描述了基于硅的共轭物，能够将一个或多个有效载荷基团传递到靶细胞或组织。考虑到的共轭物可能包括一个硅-杂原子核心，一个或多个可选的催化基团，一个定位基团，允许共轭物在靶细胞或组织内积累，一个或多个有效载荷基团（例如，治疗剂或成像剂），以及与硅-杂原子核心共价结合的两个或更多个不干扰基团。
• [EN] PYRIDAZINO [4, 5 -D] PYRIMIDIN- (6H) -ONE INHIBITORS OF WEE - 1 KINASE<br/>[FR] INHIBITEURS DE KINASE WEE-1 DE TYPE PYRIDAZINO[4,5-D]PYRIMIDIN-(6H)ONE
  申请人：ABBVIE INC

  公开号：WO2013013031A1

  公开（公告）日：2013-01-24

  The present invention relates to compounds of formula (I) or pharmaceutical acceptable salts, Formula (I) wherein B, R1, R2, R4, and m are defined in the description. The present invention relates also to compositions containing said compounds which are useful for inhibiting kinases such as wee-1 and methods of treating diseases such as cancer.

  本发明涉及公式(I)化合物或其药学上可接受的盐，公式(I)中B、R1、R2、R4和m的定义见说明书。本发明还涉及含有上述化合物的组合物，其对抑制wee-1等激酶有用，并且用于治疗癌症等疾病的方法。
• PYRIDAZINO[4,5-D]PYRIMIDIN-5(6H)-ONE INHIBITORS OF KINASES
  申请人：Zhu Gui-Dong

  公开号：US20130023523A1

  公开（公告）日：2013-01-24

  The present invention relates to compounds of formula (I) or pharmaceutical acceptable salts, wherein B, R 1 , R 2 , R 4 , and m are defined in the description. The present invention relates also to compositions containing said compounds which are useful for inhibiting kinases such as wee-1 and methods of treating diseases such as cancer.

  本发明涉及式(I)的化合物或药物可接受的盐，其中B、R1、R2、R4和m在说明书中有定义。本发明还涉及含有所述化合物的组合物，该组合物对于抑制wee-1等激酶以及治疗癌症等疾病的方法是有用的。
• US8796289B2
  申请人：——

  公开号：US8796289B2

  公开（公告）日：2014-08-05
• US9051327B2
  申请人：——

  公开号：US9051327B2

  公开（公告）日：2015-06-09