1-(8-amino-1,3,4,5-tetrahydro-2H-pyrido[4,3-b]indol-2-yl)ethan-1-one | 1512863-36-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: 1-(8-amino-1,3,4,5-tetrahydro-2H-pyrido[4,3-b]indol-2-yl)ethan-1-one
• 英文别名: 1-(8-Amino-1,3,4,5-tetrahydropyrido[4,3-b]indol-2-yl)ethanone；1-(8-amino-1,3,4,5-tetrahydropyrido[4,3-b]indol-2-yl)ethanone
• CAS: 1512863-36-3
• 化学式: C₁₃H₁₅N₃O
• 分子量: 229.282
• InChiKey: YNMVCBQLNXOWSI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.7
• 重原子数：
  17
• 可旋转键数：
  0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  62.1
• 氢给体数：
  2
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  2,3,4,5-四氢-1H-吡啶并[4,3-b]吲哚-8-羧酸 在 叠氮磷酸二苯酯 、 三乙胺 、 三氟乙酸 作用下， 以 二氯甲烷 、 水 、 甲苯 为溶剂， 反应 32.0h， 生成 1-(8-amino-1,3,4,5-tetrahydro-2H-pyrido[4,3-b]indol-2-yl)ethan-1-one
  参考文献：
  名称：

  Targeting Low-Druggability Bromodomains: Fragment Based Screening and Inhibitor Design against the BAZ2B Bromodomain

  摘要：

  Bromodomains are epigenetic reader domains that have recently become popular targets. In contrast to BET bromodomains, which have proven druggable, bromodomains from other regions of the phylogenetic tree have shallower pockets. We describe successful targeting of the challenging BAZ2B bromodomain using biophysical fragment screening and structure-based optimization of high ligand-efficiency fragments into a novel series of low-micromolar inhibitors. Our results provide attractive leads for development of BAZ2B chemical probes and indicate the whole family may be tractable.

  DOI：

  10.1021/jm401582c

文献信息

• Targeting Low-Druggability Bromodomains: Fragment Based Screening and Inhibitor Design against the BAZ2B Bromodomain
  作者：Fleur M. Ferguson、Oleg Fedorov、Apirat Chaikuad、Martin Philpott、Joao R. C. Muniz、Ildiko Felletar、Frank von Delft、Tom Heightman、Stefan Knapp、Chris Abell、Alessio Ciulli

  DOI：10.1021/jm401582c

  日期：2013.12.27

  Bromodomains are epigenetic reader domains that have recently become popular targets. In contrast to BET bromodomains, which have proven druggable, bromodomains from other regions of the phylogenetic tree have shallower pockets. We describe successful targeting of the challenging BAZ2B bromodomain using biophysical fragment screening and structure-based optimization of high ligand-efficiency fragments into a novel series of low-micromolar inhibitors. Our results provide attractive leads for development of BAZ2B chemical probes and indicate the whole family may be tractable.