CAS: 87585-32-8; (2R,3R,4S,5S,6R)-2-(((1S,2R,3R)-7-Hydroxy-1-(4-Hydroxy-3,5-Dimethoxyphenyl)-3-(Hydroxymethyl)-6,8-Dimethoxy-1,2,3,4-Tetrahydronaphthalen-2-yl)Methoxy)-6-(Hydroxymethyl)Tetrahydro-2H-Pyran-3,4,5-Triol
该化合物是一种自然产生的液态胶质,主要见于某些植物物种,该化合物具有潜在生物活性特性,包括抗氧化剂和抗炎效应,因此引起兴趣.其结构由9' 位置的葡萄糖溶剂相关联的流质素组成,与甘油形式相比,它提高了溶性性和生物利用率.研究人员认为该化合物在植物化学研究中的作用,特别是在植物衍生治疗方法的探索方面.其高纯度和精密结构使其适合分析标准,代谢研究和药理研究.在受控制条件下的稳定性进一步证明了其在实验室和工业应用中的实用性.
- 英文名称(2R,3R,4S,5S,6R)-2-(((1S,2R,3R)-7-Hydroxy-1-(4-Hydroxy-3,5-Dimethoxyphenyl)-3-(Hydroxymethyl)-6,8-Dimethoxy-1,2,3,4-Tetrahydronaphthalen-2-yl)Methoxy)-6-(Hydroxymethyl)Tetrahydro-2H-Pyran-3,4,5-Triol
- 中文名称(+)-南烛木树脂酚 9'-O-葡萄糖甙
- IUPAC名称(2R,3R,4S,5S,6R)-2-(((1S,2R,3R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl)methoxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
- 其它别名(+)-Lyoniresinol 9'-O-Glucoside; 3Alpha-O-(Beta-D-Glucopyranosyl)-Lyoniresinol; Lyoniresinol 9'-Beta-D-Glucopyranoside; (+)-Lyoniresinol9'-O-β-Glucoside; β-D-Glucopyranoside, [(1S,2R,3R)-1,2,3,4-Tetrahydro-7-Hydroxy-1-(4-Hydroxy-3,5-Dimethoxyphenyl)-3-(Hydroxymethyl)-6,8-Dimethoxy-2-Naphthalenyl]Methyl; (+)-Lyoniresinol 3α-O-β-D-Glucopyranoside; (+)-Lyoniresinol 9'-O-Glucoside
- CAS编号87585-32-8
- MFCD编号:MFCD26406079
- 分子式:C28H38O13分子量:582.6
- 产品CID: 1883822
- 产品分类天然产物 → 木脂素
物理性质
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合成参考文献
参考文献:10.1590/s0103-50532007000700017
摘要:Silva VCD, Bolzani VDS, Young MCM, Lopes MN. A new antifungal phenolic glycoside derivative, iridoids and lignans from Alibertia sessilis (vell.) k. schum. (Rubiaceae). J. Braz. Chem. Soc. 2007;18(7):1405–9. doi: 10.1590/s0103-50532007000700017.
参考文献:10.1016/s0031-9422(00)89656-9
摘要:Arruda MSP, Fernandes JB, Vieira PC, Fatima Das G.F. Da Silva M, Pirani JR. Protolimonoid and lignans from Zanthoxylum petiolare. Phytochemistry. 1994 Aug;36(5):1303–6. doi: 10.1016/s0031-9422(00)89656-9.
参考文献:10.1002/hlca.200890234
摘要:Zou Y, Tan C, Wang B, Zhu D, Kim S. Chemical Constituents from Myrsine africana L. Helvetica Chimica Acta. 2008 Nov;91(11):2168–73. doi: 10.1002/hlca.200890234.
参考文献:10.1016/s0031-9422(98)00409-9
摘要:Yoshikawa K, Kondo Y, Kimura E, Arihara S. A lupane-triterpene and a 3(2→1)abeolupane glucoside from Hovenia trichocarea. Phytochemistry. 1998 Dec;49(7):2057–60. doi: 10.1016/s0031-9422(98)00409-9.
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