(R)-3-Tetradecanoyloxy-tetradecanoic acid (2R,3S,4R,5R)-2-benzyloxycarbonyloxymethyl-3-(diphenoxy-phosphoryloxy)-6-(2,2,2-trichloro-acetimidoyloxy)-5-(2,2,2-trichloro-ethoxycarbonylamino)-tetrahydro-pyran-4-yl ester | 214051-03-3

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (R)-3-Tetradecanoyloxy-tetradecanoic acid (2R,3S,4R,5R)-2-benzyloxycarbonyloxymethyl-3-(diphenoxy-phosphoryloxy)-6-(2,2,2-trichloro-acetimidoyloxy)-5-(2,2,2-trichloro-ethoxycarbonylamino)-tetrahydro-pyran-4-yl ester
• CAS: 214051-03-3
• 化学式: C₅₉H₈₁Cl₆N₂O₁₅P
• 分子量: 1301.99
• InChiKey: GAQOPHXEVPHENY-LKCMGQHCSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  17.38
• 重原子数：
  83.0
• 可旋转键数：
  39.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.61
• 拓扑面积：
  213.53
• 氢给体数：
  2.0
• 氢受体数：
  16.0

反应信息

• 作为反应物：
  描述：

  diphenylmethyl 2,6-anhydro-3-[(R)-3-(benzyloxy)tetradecanamido]-4-O-[(R)-3-(benzyloxy)tetradecanoyl]-3-deoxy-D-glycero-D-ido-heptonate 、 (R)-3-Tetradecanoyloxy-tetradecanoic acid (2R,3S,4R,5R)-2-benzyloxycarbonyloxymethyl-3-(diphenoxy-phosphoryloxy)-6-(2,2,2-trichloro-acetimidoyloxy)-5-(2,2,2-trichloro-ethoxycarbonylamino)-tetrahydro-pyran-4-yl ester 在 三氟甲磺酸三甲基硅酯 、 4 A molecular sieve 作用下， 以 二氯甲烷 为溶剂， 反应 1.0h， 以289 mg的产率得到benzhydryl (2S,3R,4R,5S,6R)-6-[[(2R,3R,4R,5S,6R)-5-diphenoxyphosphoryloxy-6-(phenylmethoxycarbonyloxymethyl)-4-[(3R)-3-tetradecanoyloxytetradecanoyl]oxy-3-(2,2,2-trichloroethoxycarbonylamino)oxan-2-yl]oxymethyl]-5-hydroxy-3-[[(3R)-3-phenylmethoxytetradecanoyl]amino]-4-[(3R)-3-phenylmethoxytetradecanoyl]oxyoxane-2-carboxylate
  参考文献：
  名称：

  Lipid A-Type Pyrancarboxylic Acid Derivatives, their Synthesis and their Biological Activities

  摘要：

  Synthesis of lipid A-type pyrancarboxylic acid derivatives, which have a carboxylic acid group in the anomeric position of the reducing sugar part of the disaccharide instead of the phosphoric acid group in lipid A, is described. We investigated the influence of the substituents in the 2'- and 6'-position of the molecules synthesized on their activities toward human monoblastic U937 cells. It was revealed that a series of compounds, possessing an acetamido group in the 2'-position showed strong LPS-antagonistic activity. (C) 2000 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4020(00)00684-0
• 作为产物：
  描述：

  allyl 2-deoxy-3-O-<(R)-3-tetradecanoyloxytetradecanoyl>-2-(2,2,2-trichloroethoxycarbonylamino)-α-D-glucopyranoside 在 吡啶 、 4-二甲氨基吡啶 、 (1,5-cyclooctadiene)[bis(methyldiphenylphosphine)]iridium(I) hexafluorophosphate 、 氢气 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下， 以 四氢呋喃 、 吡啶 、 二氯甲烷 为溶剂， 反应 6.5h， 生成 (R)-3-Tetradecanoyloxy-tetradecanoic acid (2R,3S,4R,5R)-2-benzyloxycarbonyloxymethyl-3-(diphenoxy-phosphoryloxy)-6-(2,2,2-trichloro-acetimidoyloxy)-5-(2,2,2-trichloro-ethoxycarbonylamino)-tetrahydro-pyran-4-yl ester
  参考文献：
  名称：

  Lipid A-Type Pyrancarboxylic Acid Derivatives, their Synthesis and their Biological Activities

  摘要：

  Synthesis of lipid A-type pyrancarboxylic acid derivatives, which have a carboxylic acid group in the anomeric position of the reducing sugar part of the disaccharide instead of the phosphoric acid group in lipid A, is described. We investigated the influence of the substituents in the 2'- and 6'-position of the molecules synthesized on their activities toward human monoblastic U937 cells. It was revealed that a series of compounds, possessing an acetamido group in the 2'-position showed strong LPS-antagonistic activity. (C) 2000 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4020(00)00684-0