CAS: 41514-64-1; Koaburaside Monomethyl Ether
- 英文名称Koaburaside Monomethyl Ether
- 中文名称3,4,5-三甲氧基苯基 β-D-吡喃葡萄糖苷
- IUPAC名称(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(3,4,5-trimethoxyphenoxy)tetrahydro-2H-pyran-3,4,5-triol
- 其它别名3,4,5-Trimethoxy-Phenol 1-O-Beta-Glucopyranoside; 3,4,5-Trimethoxyphenyl B-D-Glucopyranoside; Koaburaside Momethyl Ether; Koaburaside Monomethyl Ether; 3,4,5-Trimethoxyphenyl Beta-D-Glucopyranoside; β-D-Glucopyranoside, 3,4,5-Trimethoxyphenyl; 3,4,5-Trimethoxyphenylβ-D-Glucopyranoside; 3,4,5-Trimethoxyphenyl-O-β-D-Glucopyranoside
- CAS编号41514-64-1
- MFCD编号:MFCD11975488
- 分子式:C15H22O9分子量:346.33
- 产品CID: 1429342
- 产品分类天然产物 → 酚类
物理性质
MSDS等安全信息
上下游产品
2,3,4,6-tetraacetyl-3,4,5-trimethoxyphenyl-β-D-glucoside 3,4,5-trimethoxyphenol-1-O-β-D-(6′-O-galloyl)glucopyranoside 3,4,5-trimethoxyphenol 3,4,5-Trimethoxyaniline合成工艺路线路线简述
- 合成目标产物 3,4,5-Trimethoxyphenyl B-D-Glucopyranoside 主要起始原料 β-D-Glucopyranoside, 3,4,5-Trimethoxyphenyl, Tetraacetate (9CI)
- (文献来源)合成步骤主要原料 β-D-Glucopyranoside, 3,4,5-Trimethoxyphenyl, Tetraacetate (9Ci)
📜3,4,5-三甲氧基苯酚置于sodium Hydroxide,苄基三乙基氯化铵,Sodium Methylate体系中,用 甲醇,氯仿 作为反应溶剂,化学反应 23.0H,反应生成 3,4,5-三甲氧基苯基 Beta-D-吡喃葡萄糖苷
参考文献:In Vitro Antiplasmodial Activity Of Extracts Of Tristaniopsis Species And Identification Of The Active Constituents: Ellagic Acid And 3,4,5-Trimethoxyphenyl-(6'-O-Galloyl)-O-β-D-Glucopyranoside
标题:In Vitro Antiplasmodial Activity Of Extracts Of Tristaniopsis Species And Identification Of The Active Constituents: Ellagic Acid And 3,4,5-Trimethoxyphenyl-(6'-O-Galloyl)-O-β-D-Glucopyranoside
摘要:Screening Of Plants From New Caledonia For Antiplasmodial Activity Against Plasmodium Falciparum Revealed That Methanolic Extracts Of The Leaves And Bark Of Tristaniopsis Calobuxus,T. Yateensis,And T. Glauca Inhibited The Growth Of Chloroquine-Sensitive And-Resistant Clones. Ellagic Acid And The New Compound 3,4,5-Trimethoxyphenyl-(6 '-O-Galloyl)-O-Beta-D-Glucopyranoside Were Identified As The Active Constituents (Ic50 0.5 And 3.2 Mum,Respectively). The Growth Inhibition Of Both Clones Was Comparable. The Compounds Showed Negligible Or Very Low Cytotoxicity To Human Skin Fibroblasts And Hep G2 Cells When Tested At Concentrations Ranging From 0.5 To 100 Mum.
DOI:10.1021/np000306J
海关参考信息
- 2905122000-异丙醇
2905310000-1,2-乙二醇
2905320000-1,2-丙二醇
2905399001-1,3-丙二醇 - 💡 提示：海关信息按照顺序优先匹配，如需确认的海关信息，请参考相关资料。
- 详情请参考：📖 海关编码查询和海关进出口税则
供应商参考报价(招募中)
品牌试剂参考报价(招募中)
📌 第三方产品分析报告
合成参考文献
参考文献:10.1016/s0031-9422(96)00777-7
摘要:Achenbach H, Benirschke G. Joannesialactone and other compounds from Joannesia princeps. Phytochemistry. 1997 May;45(1):149–57. doi: 10.1016/s0031-9422(96)00777-7.
参考文献:10.1021/np3007638
摘要:Yang Kuo LM, Zhang LJ, Huang HT, Lin ZH, Liaw CC, Cheng HL, Lee KH, Morris-Natschke SL, Kuo YH, Ho HO. Antioxidant lignans and chromone glycosides from Eurya japonica. J Nat Prod. 2013 Apr 26;76(4):580–7. doi: 10.1021/np3007638.
参考文献:10.1016/0031-9422(88)83166-2
摘要:Shimomura H, Sashida Y, Oohara M, Tenma H. Phenolic glucosides from Parabenzoin praecox. Phytochemistry. 1988 Jan;27(2):644–6. doi: 10.1016/0031-9422(88)83166-2.
参考文献:10.1007/s11101-024-09990-4
摘要:Linh NTT, Van Tuyen N, Pham TV, Awale S, Son NT. The genus Pittosporum: current knowledge on traditional use, phytochemistry, and pharmacological activity. Phytochem Rev. 2024 Jun 27;24(2):2015–58. doi: 10.1007/s11101-024-09990-4.
参考文献:10.1007/s43450-025-00686-0
摘要:de Oliveira KA, Caldas CP, da Silva WAV, dos Santos Dantas T, Machado JCB, Ferreira MRA, Soares LAL. Spondias tuberosa: A Promising Food Species from the Caatinga Biome—A Comprehensive Review of Its Chemistry, Biological and Nutritional Potential, and Applications. Rev. Bras. Farmacogn. 2025 Aug 01;35(5):922–34. doi: 10.1007/s43450-025-00686-0.
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