1H-Pyrrolo[3,2-b]pyridine-2-carboxylic acid, 5-chloro-1-(phenylsulfonyl)- | 1266114-76-4

• 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: 1H-Pyrrolo[3,2-b]pyridine-2-carboxylic acid, 5-chloro-1-(phenylsulfonyl)-
• 英文别名: 1-(benzenesulfonyl)-5-chloropyrrolo[3,2-b]pyridine-2-carboxylic acid
• CAS: 1266114-76-4
• 化学式: C₁₄H₉ClN₂O₄S
• 分子量: 336.8
• InChiKey: DYWALYMCHXHTSN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  22
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  97.6
• 氢给体数：
  1
• 氢受体数：
  5

文献信息

• TRICYCLIC HETEROCYCLES AS BET PROTEIN INHIBITORS
  申请人：Incyte Corporation

  公开号：US20150175604A1

  公开（公告）日：2015-06-25

  The present invention relates to tricyclic heterocycles which are inhibitors of BET proteins such as BRD2, BRD3, BRD4, and BRD-t and are useful in the treatment of diseases such as cancer.

  本发明涉及三环杂环化合物，它们是BET蛋白的抑制剂，如BRD2、BRD3、BRD4和BRD-t，并且在治疗癌症等疾病中具有用处。
• NOVEL AZA-OXO-INDOLES FOR THE TREATMENT AND PROPHYLAXIS OF RESPIRATORY SYNCYTIAL VIRUS INFECTION
  申请人：Hoffmann-La Roche Inc.

  公开号：US20160068531A1

  公开（公告）日：2016-03-10

  The invention provides novel compounds having the general formula: wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , W 1 , W 2 , W 3 , A and X are as described herein, compositions including the compounds and methods of using the compounds.

  本发明提供了一种具有一般式的新化合物：其中R1、R2、R3、R4、R5、R6、W1、W2、W3、A和X如本文所述，包括该化合物的组合物和使用该化合物的方法。
• Aza-oxo-indoles for the treatment and prophylaxis of respiratory syncytial virus infection
  申请人：Hoffmann-La Roche Inc.

  公开号：US10189838B2

  公开（公告）日：2019-01-29

  The invention provides novel compounds having the general formula: wherein R1, R2, R3, R4, R5, R6, W1, W2, W3, A and X are as described herein, compositions including the compounds and methods of using the compounds for the treatment and prophylaxis of respiratory syncytial virus infection.

  本发明提供了具有通式的新型化合物： 其中 R1、R2、R3、R4、R5、R6、W1、W2、W3、A 和 X 如本文所述；包括这些化合物的组合物；以及使用这些化合物治疗和预防呼吸道合胞病毒感染的方法。
• Tricyclic heterocycles as bet protein inhibitors
  申请人：Incyte Corporation

  公开号：US10442803B2

  公开（公告）日：2019-10-15

  The present invention relates to tricyclic heterocycles which are inhibitors of BET proteins such as BRD2, BRD3, BRD4, and BRD-t and are useful in the treatment of diseases such as cancer.

  本发明涉及三环杂环化合物，它们是 BET 蛋白（如 BRD2、BRD3、BRD4 和 BRD-t）的抑制剂，可用于治疗癌症等疾病。
• Tricyclic heterocycles as BET protein inhibitors
  申请人：Incyte Corporation

  公开号：US11091484B2

  公开（公告）日：2021-08-17

  The present invention relates to tricyclic heterocycles which are inhibitors of BET proteins such as BRD2, BRD3, BRD4, and BRD-t and are useful in the treatment of diseases such as cancer.

  本发明涉及三环杂环化合物，它们是 BET 蛋白（如 BRD2、BRD3、BRD4 和 BRD-t）的抑制剂，可用于治疗癌症等疾病。