4-[[6-amino-5-(2-furanylcarbonyl)-2-pyridinyl]amino]-N,N-diethylbenzenesulfonamide

• 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: 4-[[6-amino-5-(2-furanylcarbonyl)-2-pyridinyl]amino]-N,N-diethylbenzenesulfonamide
• 英文别名: 3-Acyl-2,6-diaminopyridine deriv. 2w；4-[[6-amino-5-(furan-2-carbonyl)pyridin-2-yl]amino]-N,N-diethylbenzenesulfonamide
• 化学式: C₂₀H₂₂N₄O₄S
• 分子量: 414.485
• InChiKey: HCINSLFQPLOMBD-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  29
• 可旋转键数：
  8
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  127
• 氢给体数：
  2
• 氢受体数：
  8

反应信息

• 作为产物：
  描述：

  4-碘苯磺酰氯 在 tris(dibenzylideneacetone)dipalladium (0) 、 caesium carbonate 、 R-(+)-1,1'-联萘-2,2'-双二苯膦 作用下， 以 1,4-二氧六环 为溶剂， 生成 4-[[6-amino-5-(2-furanylcarbonyl)-2-pyridinyl]amino]-N,N-diethylbenzenesulfonamide
  参考文献：
  名称：

  3-Acyl-2,6-diaminopyridines as cyclin-dependent kinase inhibitors: synthesis and biological evaluation

  摘要：

  A novel series of 2,6-diamino-3-acylpyridines were designed and synthesized as cyclin-dependent kinase (CDK) inhibitors. The representative compounds 2r and 11 showed potent CDK1 and CDK2 inhibitory activities and inhibited cellular proliferation in HeLa, HCT116, and A375 tumor cells. © 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2005.03.024

文献信息

• 3-Acyl-2,6-diaminopyridines as cyclin-dependent kinase inhibitors: synthesis and biological evaluation
  作者：Ronghui Lin、Yanhua Lu、Steven K. Wetter、Peter J. Connolly、Ignatius J. Turchi、William V. Murray、Stuart L. Emanuel、Robert H. Gruninger、Angel R. Fuentes-Pesquera、Mary Adams、Niranjan Pandey、Sandra Moreno-Mazza、Steven A. Middleton、Linda K. Jolliffe

  DOI：10.1016/j.bmcl.2005.03.024

  日期：2005.5

  A novel series of 2,6-diamino-3-acylpyridines were designed and synthesized as cyclin-dependent kinase (CDK) inhibitors. The representative compounds 2r and 11 showed potent CDK1 and CDK2 inhibitory activities and inhibited cellular proliferation in HeLa, HCT116, and A375 tumor cells. © 2005 Elsevier Ltd. All rights reserved.