carbonic acid 2-(14-allyloxyimino-4-ethyl-11-methoxy-2,2,3a,7,9,11,13,15-octamethyl-6,8-dioxo-dodecahydro-1,3,5-trioxa-cyclopentacyclotetradecen-10-yloxy)-4-(benzyloxycarbonyl-methyl-amino)-6-methyl-tetrahydro-pyran-3-yl ester benzyl ester | 869317-78-2

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: carbonic acid 2-(14-allyloxyimino-4-ethyl-11-methoxy-2,2,3a,7,9,11,13,15-octamethyl-6,8-dioxo-dodecahydro-1,3,5-trioxa-cyclopentacyclotetradecen-10-yloxy)-4-(benzyloxycarbonyl-methyl-amino)-6-methyl-tetrahydro-pyran-3-yl ester benzyl ester
• CAS: 869317-78-2
• 化学式: C₅₁H₇₂N₂O₁₄
• 分子量: 937.138
• InChiKey: YSRJAWGGMPSGIY-PQNMOIGBSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  8.58
• 重原子数：
  67.0
• 可旋转键数：
  13.0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.63
• 拓扑面积：
  176.18
• 氢给体数：
  0.0
• 氢受体数：
  15.0

反应信息

• 作为反应物：
  描述：

  carbonic acid 2-(14-allyloxyimino-4-ethyl-11-methoxy-2,2,3a,7,9,11,13,15-octamethyl-6,8-dioxo-dodecahydro-1,3,5-trioxa-cyclopentacyclotetradecen-10-yloxy)-4-(benzyloxycarbonyl-methyl-amino)-6-methyl-tetrahydro-pyran-3-yl ester benzyl ester 在 palladium diacetate 、 palladium dihydroxide 甲酸 、 acetate buffer 、 氢气 、 三乙胺 、 三苯基膦 作用下， 以 四氢呋喃 、 乙醇 、 水 为溶剂， 反应 7.5h， 生成
  参考文献：
  名称：

  9-Oxime-3-ketolides: Modification at the C-11,12-diol moiety and antibacterial activities against key respiratory pathogens

  摘要：

  In the search for new types of ketolide antibiotics active against key respiratory pathogens including erythromycin-resistant strains, we conducted an extensive study on the modification at the C-11,12-diol moiety of 9-oxime-3-ketolide derivatives. Among the derivatives prepared, compound 6 with carbonate at the C-11, 12 position was found to have potent antibacterial activities against erythromycin-resistant Staphylococcus aureus as well as other erythromycin-susceptible strains. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2005.06.003
• 作为产物：
  描述：

  carbonic acid 2-(10-allyloxyimino-14-ethyl-4,12,13-trihydroxy-7-methoxy-3,5,7,9,11,13-hexamethyl-2-oxo-oxacyclotetradec-6-yloxy)-4-(benzyloxycarbonyl-methyl-amino)-6-methyl-tetrahydro-pyran-3-yl ester benzyl ester 在 对甲苯磺酸 、 二甲基亚砜 、 三乙胺 、 三氟乙酸酐 作用下， 以 二氯甲烷 、 甲苯 为溶剂， 反应 73.0h， 生成 carbonic acid 2-(14-allyloxyimino-4-ethyl-11-methoxy-2,2,3a,7,9,11,13,15-octamethyl-6,8-dioxo-dodecahydro-1,3,5-trioxa-cyclopentacyclotetradecen-10-yloxy)-4-(benzyloxycarbonyl-methyl-amino)-6-methyl-tetrahydro-pyran-3-yl ester benzyl ester
  参考文献：
  名称：

  9-Oxime-3-ketolides: Modification at the C-11,12-diol moiety and antibacterial activities against key respiratory pathogens

  摘要：

  In the search for new types of ketolide antibiotics active against key respiratory pathogens including erythromycin-resistant strains, we conducted an extensive study on the modification at the C-11,12-diol moiety of 9-oxime-3-ketolide derivatives. Among the derivatives prepared, compound 6 with carbonate at the C-11, 12 position was found to have potent antibacterial activities against erythromycin-resistant Staphylococcus aureus as well as other erythromycin-susceptible strains. (c) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2005.06.003