CAS: 1268140-15-3; 5,7,3'-Trihydroxy-4'-Methoxy-8-Prenylflavanone
该化合物是一种氟芳烃衍生物,其特点是其独特的铬-4-1核心结构,有氢氧,甲氧和乙酰替代成分.该化合物由于其多苯基框架,具有显著的化学特性,有助于其潜在的抗氧化和生物活性特性.多种氢氧基组的存在,增强了其在极溶剂中的溶解性,而前丁基混合物会影响脂性与膜相互作用.其结构特征使它成为研究药用化学和天然产品研究的候选物,特别是在研究结构-活动关系方面.该化合物定义的分子结构允许通过诸如HPLC,NMR和质量光谱测量等技术进行精确的分析识别.
- 英文名称5,7,3'-Trihydroxy-4'-Methoxy-8-Prenylflavanone
- 中文名称5,7,3'-三羟基-4'-甲氧基-8-异戊烯基黄烷酮
- 其它别名5,7,3'-Trihydroxy-4'-Methoxy-8-Prenylflavanone; (2S)-2,3-Dihydro-5,7-Dihydroxy-2-(3-Hydroxy-4-Methoxyphenyl)-8-(3-Methyl-2-Buten-1-yl)-4H-1-Benzopyran-4-One; 5,7-Dihydroxy-2-(3-Hydroxy-4-Methoxyphenyl)-8-(3-Methylbut-2-En-1-yl)Chroman-4-One; 5,7,3'-Trihydroxy-4'-Methoxy-8-P; (2S)-5,7,3'-Trihydroxy-4'-Methoxy-8-(3''-Methylbut-2''-Enyl)-Flavonone; 4H-1-Benzopyran-4-One, 2,3-Dihydro-5,7-Dihydroxy-2-(3-Hydroxy-4-Methoxyphenyl)-8-(3-Methyl-2-Buten-1-yl)-, (2S)-
- CAS编号1268140-15-3
- MFCD编号:MFCD27920545
- 分子式:C21H22O6分子量:370.4
- 产品CID: 424904
- 产品分类天然产物 → 黄酮类化合物
物理性质
上下游产品
S)-5,7-diacetoxy-2-(3-acetoxy-4-methoxy-phenyl)-chroman-4-one(S)-5,7-diacetoxy-2-(3-acetoxy-4-methoxy-phenyl)-chroman-4-one 2-(3-acetoxy-4-methoxyphenyl)-7-hydroxy-4-ox°Chroman-5-yl acetate hesperetin dimethylallyl diphosphate合成工艺路线路线简述
📜橙皮素置于吡啶,咪唑,甲醇,四(三苯基膦)钯,Ammonium Acetate,苯硫酚体系中,用 四氢呋喃,N-甲基吡咯烷酮 用作溶剂,化学反应 29.0H,反应生成5,7,3'-三羟基-4'-甲氧基-8-异戊烯基黄烷酮
参考文献:An Efficient Method For C8-Prenylation Of Flavonols And Flavanones
标题:An Efficient Method For C8-Prenylation Of Flavonols And Flavanones
摘要:Synthesis Of C8-Prenylated Flavonols And Flavanones Via The Palladium-Catalyzed 7-O-1,1-Dimethylprop-2-Enylation,Followed By Claisen Rearrangement Is Described. Two Regioselectivities (Carbon-Carbon Bond Formation At Either The Tail Or Head Of The Prenyl Group And Carbon-Carbon Bond Formation At Either C8 Or C6) Were Efficiently Improved When Acetic Anhydride Was Used As A Solvent Instead Of N,N-Dimethylformamide.
Doi:10.1055/s-0031-1290756
海关参考信息
- 2901210000-乙烯
2901220000-丙烯
2902600000-乙苯
2905121000-正丙醇 - 💡 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
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品牌试剂参考报价(招募中)
📌 第三方产品分析报告
主要参考文献
参考标题:Regio- And Stereospecific Prenylation Of Flavonoids BySophora FlavescensPrenyltransferase作者:Ridao Chen,Xiao Liu,Jianhua Zou,Yunze Yin,Bin Ou,Jianhua Li,Ruishan Wang,Dan Xie,Peicheng Zhang,Jungui Dai |发布日期:2013.6.17
摘要:Activities. The Reaction Catalyzed By Prenyltransferases Represents A Friedel-Crafts Alkylation Of The Flavonoid Skeleton In The Biosynthesis Of Natural Prenylflavonoids And Often Contributes To The Structural Diversity And Biological Activity Of These Compounds. However, Only A Few Plant Flavonoid Prenyltransferases Have Been Identified Thus Far, And These Prenyltransferases Exhibit Strict Substrate
合成参考文献
参考文献:10.1021/np100797y
摘要:Versiani MA, Diyabalanage T, Ratnayake R, Henrich CJ, Bates SE, McMahon JB, Gustafson KR. Flavonoids from eight tropical plant species that inhibit the multidrug resistance transporter ABCG2. J Nat Prod. 2011 Feb 25;74(2):262–6.
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