2,4,7-trimethyl-7H-pyrrolo[2,3-d]pyrimidine | 14988-10-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯并嘧啶类
• 英文名称: 2,4,7-trimethyl-7H-pyrrolo[2,3-d]pyrimidine
• 英文别名: 2,4,7-Trimethylpyrrolo[2,3-d]pyrimidine
• CAS: 14988-10-4
• 化学式: C₉H₁₁N₃
• 分子量: 161.206
• InChiKey: NVHSPXWGDPWHFV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  12
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  30.7
• 氢给体数：
  0
• 氢受体数：
  2

文献信息

• SUBSTITUTED NUCLEOTIDE ANALOGS
  申请人：ALIOS BIOPHARMA, INC.

  公开号：US20130164261A1

  公开（公告）日：2013-06-27

  Disclosed herein are phosphorothioate nucleotide analogs, methods of synthesizing phosphorothioate nucleotide analogs and methods of treating diseases and/or conditions such as viral infections, cancer, and/or parasitic diseases with the phosphorothioate nucleotide analogs.

  本文披露了磷硫酸酯核苷类似物，合成磷硫酸酯核苷类似物的方法，以及利用磷硫酸酯核苷类似物治疗病毒感染、癌症和/或寄生虫病等疾病和/或症状的方法。
• CYCLIC NUCLEOTIDE ANALOGS
  申请人：Beigelman Leonid

  公开号：US20120165286A1

  公开（公告）日：2012-06-28

  Disclosed herein are cyclic nucleotide analogs, methods of synthesizing cyclic nucleotide analogs and methods of treating diseases and/or conditions such as viral infections, cancer, and/or parasitic diseases with cyclic nucleotide analogs.

  本文揭示了环核苷酸类似物，合成环核苷酸类似物的方法，以及使用环核苷酸类似物治疗疾病和/或状况，如病毒感染、癌症和/或寄生虫病的方法。
• 2-[2--1H-Pyrrolo[2,3-D]Pyrimidin-4-YL)Amino] Benzamide Derivatives As IGF-1R Inhibitors For The Treatment Of Cancer
  申请人：Chamberlain Stanley Dawes

  公开号：US20100204196A1

  公开（公告）日：2010-08-12

  Novel pyrrolopyrimidines as shown in formula (I): and pharmaceutically acceptable derivatives thereof. The compounds are useful in the inhibition of IGF-1R.

  式(I)所示的新型吡咯吡咪啉及其药学上可接受的衍生物。这些化合物在抑制IGF-1R方面是有用的。
• THIENOPYRIMIDIONES FOR TREATMENT OF INFLAMMATORY DISORDERS AND CANCERS
  申请人：White Stephen L.

  公开号：US20100216820A1

  公开（公告）日：2010-08-26

  The current invention provides compounds of formula (1): wherein: one of Q 1 , Q 2 and Q 3 is S, and the other of two of Q 1 , Q 2 and Q 3 are —CR 1 —, which are inhibitors of PI3K-delta. These compounds are useful for treatment of conditions mediated by PI3K-delta, such as hematopoietic cancers, immune disorders, and bone resorption disorders. The invention further provides pharmaceutical compositions comprising a compound of formula (1) and methods of using these compounds and compositions to treat conditions mediated by PI3K-delta.

  当前的发明提供了式（1）的化合物：其中：Q1、Q2和Q3中的一个是S，而Q1、Q2和Q3中的另外两个是—CR1—，这些化合物是PI3K-delta的抑制剂。这些化合物对于治疗由PI3K-delta介导的疾病，如造血系统癌症、免疫系统疾病和骨吸收障碍等，是有用的。该发明还提供了包含式（1）化合物的制药组合物以及使用这些化合物和组合物治疗由PI3K-delta介导的疾病的方法。
• TREATMENT OF LIVER DISORDERS WITH P13K INHIBITORS
  申请人：Ulrich Roger G.

  公开号：US20120178767A1

  公开（公告）日：2012-07-12

  The invention provides methods to treat certain liver disorders by administering a compound that inhibits PD K isoforms, particularly the delta isoform. It further provides specific compounds useful for these methods and ways to identify subjects who are particularly suitable for receiving these treatments.

  本发明提供了通过给予抑制PD K同工酶特别是δ同工酶的化合物来治疗某些肝脏疾病的方法。它还提供了用于这些方法的特定化合物和识别适合接受这些治疗的受试者的方法。