Vicenin (BioDeep_00000227146)

human metabolite natural product

代谢物信息卡片

5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-bis({[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})-4H-chromen-4-one

化学式: C27H30O17 (626.148293)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O
InChI: InChI=1S/C27H30O17/c28-6-12-15(32)18(35)20(37)26(41-12)43-24-17(34)14-10(31)5-11(8-1-3-9(30)4-2-8)40-23(14)25(22(24)39)44-27-21(38)19(36)16(33)13(7-29)42-27/h1-5,12-13,15-16,18-21,26-30,32-39H,6-7H2/t12-,13-,15-,16-,18+,19+,20-,21-,26+,27+/m1/s1

描述信息

Vicenin is a member of the class of compounds known as flavonoid-8-o-glycosides. Flavonoid-8-o-glycosides are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C8-position. Vicenin is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Vicenin can be found in dill and prairie turnip, which makes vicenin a potential biomarker for the consumption of these food products.

同义名列表

4 个代谢物同义名

5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-bis({[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})-4H-chromen-4-one; 5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-bis({[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})chromen-4-one; Vicinin 2; Vicenin

数据库引用编号

6 个数据库交叉引用编号

PubChem: 5315206
HMDB: HMDB0302244
ChEMBL: CHEMBL538921
foodb: FDB003879
CAS: 90456-53-4
LOTUS: LTS0203509

分类词条

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)

23 个相关的物种来源信息

4219 - Artemisia: LTS0203509
265783 - Artemisia capillaris: 10.1016/S0968-0896(00)00225-X
265783 - Artemisia capillaris: LTS0203509
4210 - Asteraceae: LTS0203509
41503 - Centaurea: LTS0203509
1436092 - Centaurea hierapolitana: 10.1016/J.PHYTOCHEM.2006.10.013
1436092 - Centaurea hierapolitana: LTS0203509
41549 - Cirsium: LTS0203509
39165 - Collinsonia: LTS0203509
2759 - Eukaryota: LTS0203509
3803 - Fabaceae: LTS0203509
46347 - Glycyrrhiza: LTS0203509
49827 - Glycyrrhiza glabra: 10.1016/S0031-9422(00)00337-X
49827 - Glycyrrhiza glabra: LTS0203509
9606 - Homo sapiens: -
1874236 - Keiskea: LTS0203509
1874237 - Keiskea japonica: 10.1248/CPB.60.121
1874237 - Keiskea japonica: LTS0203509
4136 - Lamiaceae: LTS0203509
3398 - Magnoliopsida: LTS0203509
35493 - Streptophyta: LTS0203509
58023 - Tracheophyta: LTS0203509
33090 - Viridiplantae: LTS0203509

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。

文献列表

Anna Lisa Piccinelli, Milagros García Mesa, Dulce María Armenteros, María Antonia Alfonso, Ana Carolina Arevalo, Luca Campone, Luca Rastrelli. HPLC-PDA-MS and NMR characterization of C-glycosyl flavones in a hydroalcoholic extract of Citrus aurantifolia leaves with antiplatelet activity. Journal of agricultural and food chemistry. 2008 Mar; 56(5):1574-81. doi: 10.1021/jf073485k. [PMID: 18278866]