S-(3,5-dideoxy-3-fluoro-1,2-O-isopropylidene-α-D-xylofuranos-5-yl)homocysteine | 1193310-27-8

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: S-(3,5-dideoxy-3-fluoro-1,2-O-isopropylidene-α-D-xylofuranos-5-yl)homocysteine
• CAS: 1193310-27-8
• 化学式: C₁₂H₂₀FNO₅S
• 分子量: 309.359
• InChiKey: XLCKFECENBYVRD-VWVCVJEOSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.74
• 重原子数：
  20.0
• 可旋转键数：
  6.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.92
• 拓扑面积：
  91.01
• 氢给体数：
  2.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  S-(3,5-dideoxy-3-fluoro-1,2-O-isopropylidene-α-D-xylofuranos-5-yl)homocysteine 在 水 、 三氟乙酸 作用下， 反应 0.75h， 生成 S-(3,5-dideoxy-3-fluoro-α-D-xylofuranos-5-yl)-L-homocysteine 、 S-(3,5-dideoxy-3-fluoro-α-D-xylofuranos-5-yl)-D-homocysteine 、 S-(3-deoxy-3-fluoro-β-D-xylosyl)-L-homocysteine 、 S-(3,5-dideoxy-3-fluoro-β-D-xylofuranos-5-yl)-D-homocysteine
  参考文献：
  名称：

  Inhibition of S-ribosylhomocysteinase (LuxS) by substrate analogues modified at the ribosyl C-3 position

  摘要：

  S-Ribosylhomocysteinase (LuxS) catalyzes the cleavage of the thioether bond of S-ribosylhomocysteine (SRH) to produce homocysteine and 4,5-dihydroxy-2,3-pentanedione (DPD), which is the precursor of type 2 autoinducer for bacterial cell-cell communication. In this work, we have synthesized several SRH analogues modi. ed at the ribose C3 position as potential inhibitors of LuxS. While removal or methylation of the C3-OH resulted in simple competitive inhibitors of moderate potency, inversion of the C3 stereochemistry or substitution of. uorine for C3-OH resulted in slow-binding inhibitors of improved potency. The most potent inhibitor showed a K*(I) value of 0.43 mu M. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2009.07.057