albinoside II | 1400878-59-2

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: albinoside II
• 英文别名: Albinoside Ii；[(1R,3S,5R,6R,7S,9S,11S,12S,13R,25S,27R,29R,30S,31S,32R,34S,36S,37R,38R,39R,40R)-12,30,31,37,39-pentahydroxy-5,11,29,36-tetramethyl-38-[(E)-2-methylbut-2-enoyl]oxy-15-oxo-25-propyl-40-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,4,8,10,14,26,28,33,35-nonaoxapentacyclo[32.2.2.13,7.19,13.027,32]tetracontan-6-yl] (E)-2-methylbut-2-enoate
• CAS: 1400878-59-2
• 化学式: C₅₄H₈₈O₂₄
• 分子量: 1121.28
• InChiKey: ABOXHMBRQLJXDS-QFONWEIGSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  78
• 可旋转键数：
  10
• 环数：
  7.0
• sp3杂化的碳原子比例：
  0.87
• 拓扑面积：
  333
• 氢给体数：
  8
• 氢受体数：
  24

反应信息

• 作为反应物：
  描述：

  albinoside II 在 盐酸 、 水 作用下， 反应 2.08h， 生成
  参考文献：
  名称：

  Mammalian Multidrug Resistance Lipopentasaccharide Inhibitors fromIpomoea albaSeeds

  摘要：

  As part of an ongoing project to identify inhibitors of multidrug efflux pumps, three new resin glycosides, albinosides I-III (1-3), were isolated from a CHCl3-soluble extract from the seeds of moon vine (Ipomoea alba). Their structures were established through NMR spectroscopy and mass spectrometry as partially acylated branched pentasaccharides derived from three new glycosidic acids, named albinosinic acids A-C (4-6). The same oligosaccharide core formed by two D-quinovose, one D-glucose, and two L-rhamnose units was linked to either convolvulinolic or jalapinolic acid for 1 and 3, respectively. They were partially esterified with (2R,3R)-3-hydroxy-2-methylbutanoic, acetic, or 2-methyl-2-butenoic acid. Compound 2 has two D-quinovose and three L-rhamnose units, linked to convolvulinolic acid, and its esterifying residues were characterized as two units of 2-methyl-2-butenoic acid. The aglycone lactonization site was located at C-2 of the terminal rhamnose unit (Rha) for 1, at C-3 of the terminal rhamnose unit (Rha') for 2, and at C-3 of the second saccharide unit (Glc) for 3. Reversal of multidrug resistance by this class of plant metabolites was also evaluated in vinblastine-resistant human breast carcinoma cells (MCF-7/Vin). The noncytotoxic compound 3 exerted the strongest potentiation effect of vinblastine susceptibility to over 2140-fold, while a moderate activity was observed for 1 (3.1-fold) and 2 (2.6-fold) at a concentration of 25 mu g/mL.

  DOI：

  10.1021/np300414d

文献信息

• Mammalian Multidrug Resistance Lipopentasaccharide Inhibitors from<i>Ipomoea alba</i>Seeds
  作者：Sara Cruz-Morales、Jhon Castañeda-Gómez、Gabriela Figueroa-González、Alma Delia Mendoza-García、Argelia Lorence、Rogelio Pereda-Miranda

  DOI：10.1021/np300414d

  日期：2012.9.28

  As part of an ongoing project to identify inhibitors of multidrug efflux pumps, three new resin glycosides, albinosides I-III (1-3), were isolated from a CHCl3-soluble extract from the seeds of moon vine (Ipomoea alba). Their structures were established through NMR spectroscopy and mass spectrometry as partially acylated branched pentasaccharides derived from three new glycosidic acids, named albinosinic acids A-C (4-6). The same oligosaccharide core formed by two D-quinovose, one D-glucose, and two L-rhamnose units was linked to either convolvulinolic or jalapinolic acid for 1 and 3, respectively. They were partially esterified with (2R,3R)-3-hydroxy-2-methylbutanoic, acetic, or 2-methyl-2-butenoic acid. Compound 2 has two D-quinovose and three L-rhamnose units, linked to convolvulinolic acid, and its esterifying residues were characterized as two units of 2-methyl-2-butenoic acid. The aglycone lactonization site was located at C-2 of the terminal rhamnose unit (Rha) for 1, at C-3 of the terminal rhamnose unit (Rha') for 2, and at C-3 of the second saccharide unit (Glc) for 3. Reversal of multidrug resistance by this class of plant metabolites was also evaluated in vinblastine-resistant human breast carcinoma cells (MCF-7/Vin). The noncytotoxic compound 3 exerted the strongest potentiation effect of vinblastine susceptibility to over 2140-fold, while a moderate activity was observed for 1 (3.1-fold) and 2 (2.6-fold) at a concentration of 25 mu g/mL.