(S)-3-amino-1,3,4,5-tetrahydrobenzo[b][1,4]diazepin-2-one hydrochloride | 958488-74-9

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: (S)-3-amino-1,3,4,5-tetrahydrobenzo[b][1,4]diazepin-2-one hydrochloride
• 英文别名: 3-(S)-amino-1,3,4,5-tetrahydro-1,5-benzodiazepin-2-one hydrochloride；(S)-3-amino-1,3,4,5-tetrahydro-benzo[b][1,4]diazepin-2-one hydrochloride；(3S)-3-amino-1,2,3,5-tetrahydro-1,5-benzodiazepin-4-one;hydrochloride
• CAS: 958488-74-9
• 化学式: C₉H₁₁N₃O*ClH
• 分子量: 213.667
• InChiKey: BKDCHDIAIKEAKP-RGMNGODLSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.8
• 重原子数：
  14
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  67.2
• 氢给体数：
  4
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (S)-3-amino-1,3,4,5-tetrahydrobenzo[b][1,4]diazepin-2-one hydrochloride 在 吡啶 、 盐酸 、 1-hydroxy-1H-benzotriazol hydrate 、 caesium carbonate 、 O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate 、 N,N-二异丙基乙胺 作用下， 以 1,4-二氧六环 、 二氯甲烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 5.0h， 生成 (S)-N-((S)-1-((2-methoxynaphthalen-1-yl)methyl)-5-(3-methylbutanoyl)-2-oxo-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-yl)-2-(methylamino)propanamide hydrochloride
  参考文献：
  名称：

  Optimization of Benzodiazepinones as Selective Inhibitors of the X-Linked Inhibitor of Apoptosis Protein (XIAP) Second Baculovirus IAP Repeat (BIR2) Domain

  摘要：

  The IAPs are key regulators of the apoptotic pathways and are commonly overexpressed in many cancer cells. IAPs contain one to three BIR domains that are crucial for their inhibitory function. The pro-survival properties of XIAP come from binding of the BIR domains to the proapoptotic caspases. The BIR3 domain of XIAP binds and inhibits caspase 9, while the BIR2 domain binds and inhibits the terminal caspases 3 and 7. While XIAP BIR3 inhibitors have previously been reported, they also inhibit cIAP1/2 and promote the release of TNF alpha, potentially limiting their therapeutic utility. This paper will focus on the optimization of selective XIAP BIR2 inhibitors leading to the discovery of highly potent benzodiazepinone 36 (IC50 = 45 nM), which has high levels of selectivity over XIAP BIR3 and cIAP1 BIR2/3 and shows efficacy in a xenograft pharmacodynamic model monitoring caspase activity while not promoting the release of TNF alpha in vitro.

  DOI：

  10.1021/jm400732v
• 作为产物：
  描述：

  (S)-tert-butyl (2-oxo-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-yl)carbamate 在 盐酸 作用下， 以 1,4-二氧六环 为溶剂， 反应 6.0h， 生成 (S)-3-amino-1,3,4,5-tetrahydrobenzo[b][1,4]diazepin-2-one hydrochloride
  参考文献：
  名称：

  DERIVATIVES OF 2-ALKOXY-3,4,5-TRIHYDROXY-ALKYL AMIDES, PREPARATION AND USE THEREOF, AND COMPOSITIONS CONTAINING THE SAME

  摘要：

  本发明涉及2-烷氧基-3,4,5-三羟基烷基酰胺衍生物，包括这种化合物的药物组合物，包括这种化合物的治疗方法，制备这种化合物的方法，以及这种化合物的中间体前体。

  公开号：

  US20090075971A1

文献信息

• [EN] TETRAHYDRO-BENZODIAZEPINONES<br/>[FR] TÉTRAHYDRO-BENZODIAZÉPINONES
  申请人：HOFFMANN LA ROCHE

  公开号：WO2015071393A1

  公开（公告）日：2015-05-21

  Disclosed are compounds of Formula I, or pharmaceutically acceptable salts thereof, wherein W, X, Y, Z, R1, R2, R3, R4 and R5 are as described in this application, and methods of using said compounds in the treatment of cancer.

  本申请公开了具有I式化合物或其药用可接受盐的化合物，其中W、X、Y、Z、R1、R2、R3、R4和R5如本申请所述，并且使用所述化合物治疗癌症的方法。
• DERIVATIVES OF 2-ALKOXY-3,4,5-TRIHYDROXY-ALKYL AMIDES, PREPARATION AND USE THEREOF, AND COMPOSITIONS CONTAINING THE SAME
  申请人：Zhang Jidong

  公开号：US20090075971A1

  公开（公告）日：2009-03-19

  The present invention relates to 2-alkoxy-3,4,5-trihydroxyalkylamide derivatives, to pharmaceutical compositions comprising such compounds, to methods of treatment comprising administering such compounds, to processes for the preparation of such compounds, and to intermediate precursors to such compounds.

  本发明涉及2-烷氧基-3,4,5-三羟基烷基酰胺衍生物，包括这种化合物的药物组合物，包括这种化合物的治疗方法，制备这种化合物的方法，以及这种化合物的中间体前体。
• TETRAHYDRO-BENZODIAZEPINONES
  申请人：HOFFMANN-LA ROCHE AG

  公开号：US20160272596A1

  公开（公告）日：2016-09-22

  Disclosed are compounds of Formula I, or pharmaceutically acceptable salts thereof, wherein W, X, Y, Z, R 1 , R 2 , R 3 , R 4 and R 5 are as described in this application, and methods of using said compounds in the treatment of cancer.

  本发明揭示了一种I式化合物或其药学上可接受的盐，其中W、X、Y、Z、R1、R2、R3、R4和R5如本申请所述，并且使用该化合物治疗癌症的方法。
• Tetrahydro-benzodiazepinones
  申请人：Hoffmann-La Roche Inc.

  公开号：US10053431B2

  公开（公告）日：2018-08-21

  Disclosed are compounds of Formula I, or pharmaceutically acceptable salts thereof, wherein W, X, Y, Z, R1, R2, R3, R4 and R5 are as described in this application, and methods of using said compounds in the treatment of cancer.

  公开了式 I 的化合物或其药学上可接受的盐类，其中 W、X、Y、Z、R1、R2、R3、R4 和 R5 如本申请所述，以及使用所述化合物治疗癌症的方法。
• US7994161B2
  申请人：——

  公开号：US7994161B2

  公开（公告）日：2011-08-09