O-2,6-dideoxy-β-D-ribo-hexopyranosyl-(1->4)-2,6-dideoxy-D-ribo-hexose | 90762-99-5

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: O-2,6-dideoxy-β-D-ribo-hexopyranosyl-(1->4)-2,6-dideoxy-D-ribo-hexose
• 英文别名: (4S,5S,6R)-5-[(2S,4S,5S,6R)-4,5-dihydroxy-6-methyloxan-2-yl]oxy-6-methyloxane-2,4-diol
• CAS: 90762-99-5；90763-00-1；90763-10-3；90790-04-8
• 化学式: C₁₂H₂₂O₇
• 分子量: 278.302
• InChiKey: JZAXAWSTQDKQAL-FZMYCWRESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -1.2
• 重原子数：
  19
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  109
• 氢给体数：
  4
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  3-[(3S,5R,8R,9S,10S,13R,14S,17R)-14-hydroxy-3-(methoxyamino)-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 、 O-2,6-dideoxy-β-D-ribo-hexopyranosyl-(1->4)-2,6-dideoxy-D-ribo-hexose 在 溶剂黄146 作用下， 以 甲醇 、 氯仿 为溶剂， 以72%的产率得到
  参考文献：
  名称：

  A Direct Comparison of the Anticancer Activities of Digitoxin MeON-Neoglycosides and O-Glycosides

  摘要：

  Digitoxin is a cardiac glycoside currently being investigated for potential use in oncology; however, an investigation of anticancer activity as a function, of oligosaccharide chain length has not yet been performed. We generated mono-, di-, and tri-O-digitoxoside derivatives, of digitoxin and compared their activities to the corresponding MeON-neoglycosides. Both classes of cardenolide derivatives display comparable oligosaccharide chain length-dependent cytotoxicity toward human cancer cell lines. Further investigation revealed that both classes of compounds induce caspase-9-mediated apoptosis in non-small cell lung cancer cells (NCI-H460). Because O-glycosides and MeON-neoglycosides share a similar mode of action, the convenience of MeON-neoglycosylation could be exploited in future SAR work to rapidly survey large numbers of carbohydrates to prioritize selected O-glycoside candidates for traditional synthesis.

  DOI：

  10.1021/ml1000933
• 作为产物：
  描述：

  penta-O-acetyldigoxose 在 盐酸 、 氢氧化钾 作用下， 以 甲醇 、 水 为溶剂， 反应 129.0h， 生成 O-2,6-dideoxy-β-D-ribo-hexopyranosyl-(1->4)-2,6-dideoxy-D-ribo-hexose
  参考文献：
  名称：

  地高糖的结构

  摘要：

  摘要从虎眼兰（Orthenthera viminea）（家庭：Asclepiadaceae）的干燥树枝中分离出了一种新的三糖，称为地高糖。根据化学和光谱学证据，该新三糖的结构已确定为O-β-d -digitoxopyranosyl-（1→4）-O-β-d -digitoxopyranosyl-（1→4）-α-d -digitoxopyranose。

  DOI：

  10.1016/0008-6215(84)85310-0

文献信息

• De Novo Approach to 2-Deoxy-β-glycosides:  Asymmetric Syntheses of Digoxose and Digitoxin¹
  作者：Maoquan Zhou、George A. O'Doherty

  DOI：10.1021/jo062534+

  日期：2007.3.1

  straightforward route to trisaccharide natural products digoxose and digitoxin has been developed. Key to this approach is the iterative application of the palladium-catalyzed glycosylation reaction, reductive 1,3-transposition, diastereoselective dihydroxylation, and regioselective protection. The first total synthesis of natural product digoxose was accomplished in 19 total steps from achiral 2-acylfuran

  已经开发出了高度对映选择性和直接的途径来制备三糖天然产物地高糖和洋地黄毒苷。该方法的关键是钯催化糖基化反应，还原性1,3-移位，非对映选择性二羟基化和区域选择性保护的迭代应用。天然产物digoxose的第一全合成是在非手性从2- acylfuran 19个总步骤完成，和洋地黄毒苷在15个步骤塑成从洋地黄毒苷开始2和吡喃酮8 β。这种灵活的合成策略还允许制备地高糖和洋地黄毒苷的单糖和二糖类似物。
• A Direct Comparison of the Anticancer Activities of Digitoxin MeON-Neoglycosides and <i>O</i>-Glycosides
  作者：Anand Krishnan V. Iyer、Maoquan Zhou、Neelam Azad、Hosam Elbaz、Leo Wang、Derek K. Rogalsky、Yon Rojanasakul、George A. O'Doherty、Joseph M. Langenhan

  DOI：10.1021/ml1000933

  日期：2010.10.14

  Digitoxin is a cardiac glycoside currently being investigated for potential use in oncology; however, an investigation of anticancer activity as a function, of oligosaccharide chain length has not yet been performed. We generated mono-, di-, and tri-O-digitoxoside derivatives, of digitoxin and compared their activities to the corresponding MeON-neoglycosides. Both classes of cardenolide derivatives display comparable oligosaccharide chain length-dependent cytotoxicity toward human cancer cell lines. Further investigation revealed that both classes of compounds induce caspase-9-mediated apoptosis in non-small cell lung cancer cells (NCI-H460). Because O-glycosides and MeON-neoglycosides share a similar mode of action, the convenience of MeON-neoglycosylation could be exploited in future SAR work to rapidly survey large numbers of carbohydrates to prioritize selected O-glycoside candidates for traditional synthesis.
• Structure of digoxose
  作者：Kamal N. Tiwari、Naveen K. Khare、Anakshi Khare、Maheshwari P. Khare

  DOI：10.1016/0008-6215(84)85310-0

  日期：1984.7

  Abstract A new trisaccharide, named digoxose, has been isolated from the dried twigs of Orthenthera viminea (Family: Asclepiadaceae). On the basis of chemical and spectroscopic evidence, the structure of this new trisaccharide has been established as O -β- d -digitoxopyranosyl-(1→4)- O -β- d -digitoxopyranosyl-(1→4)-α- d -digitoxopyranose.

  摘要从虎眼兰（Orthenthera viminea）（家庭：Asclepiadaceae）的干燥树枝中分离出了一种新的三糖，称为地高糖。根据化学和光谱学证据，该新三糖的结构已确定为O-β-d -digitoxopyranosyl-（1→4）-O-β-d -digitoxopyranosyl-（1→4）-α-d -digitoxopyranose。