Vincetoxicoside A (BioDeep_00000872723)
Main id: BioDeep_00000398375
PANOMIX_OTCML-2023
代谢物信息卡片
化学式: C27H30O16 (610.1534)
中文名称: 槲皮素-3-O-葡萄糖-7-O-鼠李糖苷
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O
InChI: InChI=1S/C27H30O16/c1-8-17(32)20(35)22(37)26(39-8)40-10-5-13(31)16-14(6-10)41-24(9-2-3-11(29)12(30)4-9)25(19(16)34)43-27-23(38)21(36)18(33)15(7-28)42-27/h2-6,8,15,17-18,20-23,26-33,35-38H,7H2,1H3/t8-,15+,17-,18+,20+,21-,22+,23+,26-,27-/m0/s1
描述信息
Quercetin 3-galactoside 7-rhamnoside is a member of the class of compounds known as flavonoid-7-o-glycosides. Flavonoid-7-o-glycosides are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C7-position. Quercetin 3-galactoside 7-rhamnoside is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Quercetin 3-galactoside 7-rhamnoside can be found in broad bean, fruits, and root vegetables, which makes quercetin 3-galactoside 7-rhamnoside a potential biomarker for the consumption of these food products.
同义名列表
相关代谢途径
Reactome(0)
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代谢反应
0 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
0 个相关的物种来源信息
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：
- PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。
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文献列表
- Jonathon Roepke, Gale G Bozzo. Arabidopsis thaliana β-glucosidase BGLU15 attacks flavonol 3-O-β-glucoside-7-O-α-rhamnosides.
Phytochemistry.
2015 Jan; 109(?):14-24. doi:
10.1016/j.phytochem.2014.10.028. [PMID: 25468534] - Jonathon Roepke, Gale G Bozzo. Biocatalytic synthesis of quercetin 3-O-glucoside-7-O-rhamnoside by metabolic engineering of Escherichia coli.
Chembiochem : a European journal of chemical biology.
2013 Dec; 14(18):2418-22. doi:
10.1002/cbic.201300474. [PMID: 24203527] - Yuni Wahyuni, Ana-Rosa Ballester, Enny Sudarmonowati, Raoul J Bino, Arnaud G Bovy. Metabolite biodiversity in pepper (Capsicum) fruits of thirty-two diverse accessions: variation in health-related compounds and implications for breeding.
Phytochemistry.
2011 Aug; 72(11-12):1358-70. doi:
10.1016/j.phytochem.2011.03.016. [PMID: 21514607] - Leonardo M Loscalzo, Cristina Wasowski, Mariel Marder. Neuroactive flavonoid glycosides from Tilia petiolaris DC. extracts.
Phytotherapy research : PTR.
2009 Oct; 23(10):1453-7. doi:
10.1002/ptr.2800. [PMID: 19288528]
