CAS: 55033-90-4; Isorhamnetin-3-O-Neohespeidoside
该化合物是一个来自异丙烯酸混合物混合物的裂变胶合体,一种甲基甲酸氟氯酚,含有新希斯帕里剂量.该化合物显示出显著的生物活动,包括抗氧化剂,抗炎和潜在的心血管保护效应,其原因是它有能力蒸发自由基和调制细胞信号路径.其晶体结构与丙酮形式相比,提高了溶解性和生物利用率,使其有利于在营养和药物应用方面的研究.Isorhamnetin-3-O-neohespeidoside的分析标准在HPLC和LC-MS中用于植物提取物和草药配方的定量和质量控制.其稳定性和特性精密特性支持了可再生实验结果.
- 英文名称Isorhamnetin-3-O-Neohespeidoside
- 中文名称异鼠李素-3-O-新橙皮苷
- IUPAC名称3-(((2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-(((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)oxy)-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4H-chromen-4-one
- 其它别名ISORHAMNETIN 3-O-NEOHESPEROSIDE; Calendoflavoside; Isorhamnetin 3-O-neohesperidin
- CAS编号55033-90-4
- MFCD编号:MFCD11042252
- 分子式:C28H32O16分子量:624.55
- 产品CID: 2498558
- 产品分类生物化工 → 提取物
- 相似结构搜索
- 产品信息参考
;;;; - InChIKey: QHLKSZBFIJJREC-SPSUIZEHSA-N
- QHLKSZBFIJJREC-PSKHSWTNNA-N
- 计算化学: 氢键受体数16.0氢键供体数9.0可旋转键数7.0
物理性质
MSDS等安全信息
合成工艺路线路线简述
📜4',7-Di-O-Benzyl-3'-O-Methylquercetin-3-Yl 2,3,4-Tri-O-Benzoyl-α-L-Rhamnopyranosyl-(1->2)-4,6-Di-O-Acetyl-3-O-Benzoyl-β-D-Glucopyranoside置于palladium On Activated Charcoal 氢气,Sodium Methylate体系中,用 乙醇,乙酸乙酯,甲醇,二氯甲烷 作为反应溶剂,20.0~40.0 °C,101.32 Kpa 条件下,反应 11.0H,以86%的收率获得产物异鼠李素-3-O-新橙皮苷
参考文献:Synthesis Of Tamarixetin And Isorhamnetin 3-O-Neohesperidoside
标题:Synthesis Of Tamarixetin And Isorhamnetin 3-O-Neohesperidoside
摘要:Two Isomeric Flavonol 3-O-Glycosides,Tamarixetin And Isorhamnetin 3-O-Neohesperido Side (1 And 2),Were Synthesized. The Natural Product From Costus Spicatus Assigned As The Former Compound Is Revised To The Latter Structure. (C) 2005 Elsevier Ltd. All Rights Reserved.
DOI:10.1016/j.Carres.2005.04.021
专利信息
专利号:CN-110408649-A
优先权日:2019-07-25
标题:Application of the protein of NOR gene and its coding in regulation tamato fruit in flavonoids synthesis
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
主要参考文献
1: Das P, Majumder R, Mandal M, Basak P. In-Silico approach for identification of effective and stable inhibitors for COVID-19 main protease (Mpro) from flavonoid based phytochemical constituents of Calendula officinalis. J Biomol Struct Dyn. 2020 Jul
24:1-16. doi: 10.1080/07391102.2020.1796799. Epub ahead of print.
合成参考文献
参考文献:10.1016/j.phytochem.2006.04.009
摘要:Saleem M, Kim HJ, Han CK, Jin C, Lee YS. Secondary metabolites from Opuntia ficus-indica var. saboten. Phytochemistry. 2006 Jul;67(13):1390–4. doi: 10.1016/j.phytochem.2006.04.009.
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