allyl (1S,5R,6S)-2-(4-(3-(hydroxy)-propyl-1,8-naphthosultam)methyl)-6-[1(R)-(allyloxycarbonyl)oxyethyl]-1-methylcarbapen-2-em-3-carboxylate | 198473-47-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: allyl (1S,5R,6S)-2-(4-(3-(hydroxy)-propyl-1,8-naphthosultam)methyl)-6-[1(R)-(allyloxycarbonyl)oxyethyl]-1-methylcarbapen-2-em-3-carboxylate
• CAS: 198473-47-1
• 化学式: C₃₁H₃₄N₂O₉S
• 分子量: 610.685
• InChiKey: GUVCMNPLMFQYSY-BJUWQELWSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.46
• 重原子数：
  43.0
• 可旋转键数：
  12.0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.39
• 拓扑面积：
  139.75
• 氢给体数：
  1.0
• 氢受体数：
  9.0

反应信息

• 作为反应物：
  描述：

  allyl (1S,5R,6S)-2-(4-(3-(hydroxy)-propyl-1,8-naphthosultam)methyl)-6-[1(R)-(allyloxycarbonyl)oxyethyl]-1-methylcarbapen-2-em-3-carboxylate 在 2,6-二甲基吡啶 作用下， 以 二氯甲烷 、 乙腈 为溶剂， 生成
  参考文献：
  名称：

  Synthesis and properties of 2-(naphthosultamyl)methyl-carbapenems with potent anti-MRSA activity: Discovery of L-786,392

  摘要：

  A series of 1 beta-methyl-2-(naphthosultamyl)methyl-carbapenems bearing dicationic groups on the naphthosultamyl moiety was prepared and evaluated for activity against resistant gram-positive bacteria. Based on a combination of excellent in vitro antibacterial activity, acceptable mouse acute toxicity, and a desirable fragmentation pattern on beta-lactam ring opening, the analog 2g (L-786,392) was selected for extended evaluation. (C) 1999 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(99)00071-2