(S)-3-bromo-N-(5-(3-fluoro)pyrrolidin-1-yl)pentylbenzenesulfonamide | 1314241-43-4

• 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: (S)-3-bromo-N-(5-(3-fluoro)pyrrolidin-1-yl)pentylbenzenesulfonamide
• 英文别名: 3-bromo-N-[5-[(3S)-3-fluoropyrrolidin-1-yl]pentyl]benzenesulfonamide
• CAS: 1314241-43-4
• 化学式: C₁₅H₂₂BrFN₂O₂S
• 分子量: 393.32
• InChiKey: AWLIDFLGIPHLLW-AWEZNQCLSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  22
• 可旋转键数：
  8
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.6
• 拓扑面积：
  57.8
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  (S)-3-bromo-N-(5-(3-fluoro)pyrrolidin-1-yl)pentylbenzenesulfonamide 、 三氟乙酸 以 二氯甲烷 为溶剂， 以68 mg的产率得到(S)-3-bromo-N-(5-(3-fluoro)pyrrolidin-1-yl)pentylbenzenesulfonamide trifluoroacetic acid
  参考文献：
  名称：

  Small-Molecule Ligands of Methyl-Lysine Binding Proteins

  摘要：

  Proteins which bind methylated lysines ("readers" of the histone code) are important components in the epigenetic regulation of gene expression and can also modulate other proteins that contain methyl-lysine such as p53 and Rb. Recognition of methyl-lysine marks by MBT domains leads to compaction of chromatin and a repressed transcriptional state. Antagonists of MBT domains would serve as probes to interrogate the functional role of these proteins and initiate the chemical biology of methyl-lysine readers as a target class. Small-molecule MBT antagonists were designed based on the structure of histone peptide - MBT complexes and their interaction with MBT domains determined using a chemiluminescent assay and ITC. The ligands discovered antagonize native histone peptide binding, exhibiting 5-fold stronger binding affinity to L3MBTL1 than its preferred histone peptide. The first cocrystal structure of a small molecule bound to L3MBTL1 was determined and provides new insights into binding requirements for further ligand design.

  DOI：

  10.1021/jm200045v
• 作为产物：
  描述：

  3-溴苯磺酰氯 在 三乙胺 作用下， 以 二氯甲烷 、 乙腈 为溶剂， 反应 30.0h， 生成 (S)-3-bromo-N-(5-(3-fluoro)pyrrolidin-1-yl)pentylbenzenesulfonamide
  参考文献：
  名称：

  Small-Molecule Ligands of Methyl-Lysine Binding Proteins

  摘要：

  Proteins which bind methylated lysines ("readers" of the histone code) are important components in the epigenetic regulation of gene expression and can also modulate other proteins that contain methyl-lysine such as p53 and Rb. Recognition of methyl-lysine marks by MBT domains leads to compaction of chromatin and a repressed transcriptional state. Antagonists of MBT domains would serve as probes to interrogate the functional role of these proteins and initiate the chemical biology of methyl-lysine readers as a target class. Small-molecule MBT antagonists were designed based on the structure of histone peptide - MBT complexes and their interaction with MBT domains determined using a chemiluminescent assay and ITC. The ligands discovered antagonize native histone peptide binding, exhibiting 5-fold stronger binding affinity to L3MBTL1 than its preferred histone peptide. The first cocrystal structure of a small molecule bound to L3MBTL1 was determined and provides new insights into binding requirements for further ligand design.

  DOI：

  10.1021/jm200045v

文献信息

• METHODS AND COMPOUNDS FOR THE TREATMENT OF GENETIC DISEASE
  申请人：Design Therapeutics, Inc.

  公开号：US20210284629A1

  公开（公告）日：2021-09-16

  The present disclosure relates to compounds and methods for modulating the expression ofc9orf72 (brain expressed, associated with NEDD4) and treating diseases and conditions in which c9orf72 plays an active role. The compound can be a transcription modulator molecule having a first terminus, a second terminus, and oligomeric backbone, wherein: a) the first terminus comprises a DNA-binding moiety capable of noncovalently binding to a nucleotide repeat sequence GGGGCC; b) the second terminus comprises a protein-binding moiety binding to a regulatory molecule that modulates an expression of a gene comprising the nucleotide repeat sequence GGGGCC; and c) the oligomeric backbone comprising a linker between the first terminus and the second terminus.
• Small-Molecule Ligands of Methyl-Lysine Binding Proteins
  作者：J. Martin Herold、Tim J. Wigle、Jacqueline L. Norris、Robert Lam、Victoria K. Korboukh、Cen Gao、Lindsey A. Ingerman、Dmitri B. Kireev、Guillermo Senisterra、Masoud Vedadi、Ashutosh Tripathy、Peter J. Brown、Cheryl H. Arrowsmith、Jian Jin、William P. Janzen、Stephen V. Frye

  DOI：10.1021/jm200045v

  日期：2011.4.14

  Proteins which bind methylated lysines ("readers" of the histone code) are important components in the epigenetic regulation of gene expression and can also modulate other proteins that contain methyl-lysine such as p53 and Rb. Recognition of methyl-lysine marks by MBT domains leads to compaction of chromatin and a repressed transcriptional state. Antagonists of MBT domains would serve as probes to interrogate the functional role of these proteins and initiate the chemical biology of methyl-lysine readers as a target class. Small-molecule MBT antagonists were designed based on the structure of histone peptide - MBT complexes and their interaction with MBT domains determined using a chemiluminescent assay and ITC. The ligands discovered antagonize native histone peptide binding, exhibiting 5-fold stronger binding affinity to L3MBTL1 than its preferred histone peptide. The first cocrystal structure of a small molecule bound to L3MBTL1 was determined and provides new insights into binding requirements for further ligand design.