Quercetin 3-O-diglucoside (BioDeep_00000017389)
Secondary id: BioDeep_00000602950
human metabolite PANOMIX_OTCML-2023 Volatile Flavor Compounds
代谢物信息卡片
化学式: C27H30O17 (626.148293)
中文名称: 槲皮素-3-龙胆二糖甙, 槲皮素-3-龙胆二糖苷
谱图信息:
最多检出来源 Chinese Herbal Medicine(otcml) 75%
分子结构信息
SMILES: c1(cc(c2c(c1)oc(c(c2=O)O[C@H]1[C@H]([C@@H]([C@@H]([C@H](O1)CO[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O)O)O)O)c1ccc(c(c1)O)O)O)O
InChI: InChI=1S/C27H30O17/c28-6-14-17(33)20(36)22(38)26(42-14)40-7-15-18(34)21(37)23(39)27(43-15)44-25-19(35)16-12(32)4-9(29)5-13(16)41-24(25)8-1-2-10(30)11(31)3-8/h1-5,14-15,17-18,20-23,26-34,36-39H,6-7H2/t14-,15-,17-,18-,20+,21+,22-,23-,26-,27+/m1/s1
描述信息
Quercetin 3-gentiobioside is a member of the class of compounds known as flavonoid-3-o-glycosides. Flavonoid-3-o-glycosides are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C3-position. Quercetin 3-gentiobioside is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). Quercetin 3-gentiobioside can be found in guava, opium poppy, and soy bean, which makes quercetin 3-gentiobioside a potential biomarker for the consumption of these food products.
Quercetin 3-beta-gentiobioside is a quercetin O-glycoside in which the hydroxy hydrogen at position 3 of quercetin has been replaced by a gentiobiosyl group. It has a role as a Brassica napus metabolite. It is a quercetin O-glycoside, a disaccharide derivative and a tetrahydroxyflavone. It is functionally related to a gentiobiose.
Quercetin 3-gentiobioside is a natural product found in Senegalia pennata, Vachellia tortilis, and other organisms with data available.
A quercetin O-glycoside in which the hydroxy hydrogen at position 3 of quercetin has been replaced by a gentiobiosyl group.
Quercetin 3-gentiobioside is isolated from A. iwayomogi, AR and AGE formation inhibitor, demonstrates biological activities against Aldose reductase (AR) and the formation of advanced glycation endproducts (AGEs)[1].
Quercetin 3-gentiobioside is isolated from A. iwayomogi, AR and AGE formation inhibitor, demonstrates biological activities against Aldose reductase (AR) and the formation of advanced glycation endproducts (AGEs)[1].
同义名列表
26 个代谢物同义名
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-((((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-4H-chromen-4-one; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-({[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}chromen-4-one; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl beta-D-glucopyranosyl-(1->6)-beta-D-glucopyranoside; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl 6-O-beta-D-glucopyranosyl-beta-D-glucopyranoside; 2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl β-D-glucopyranosyl-(1->6)-β-D-glucopyranoside; 2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl b-D-glucopyranosyl-(1->6)-b-D-glucopyranoside; 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl beta-D-glucosyl-(1->6)-beta-D-glucoside; 2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl b-D-glucosyl-(1->6)-b-D-glucoside; 2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl β-D-glucosyl-(1->6)-β-D-glucoside; quercetin beta-D-glucopyranosyl-(1->6)-beta-D-glucopyranoside; Quercetin β-D-glucopyranosyl-(1->6)-β-D-glucopyranoside; Quercetin b-D-glucopyranosyl-(1->6)-b-D-glucopyranoside; beta-D-glucosyl-(1->6)-beta-D-glucoside; Β-D-glucosyl-(1->6)-β-D-glucoside; b-D-Glucosyl-(1->6)-b-D-glucoside; quercetin 3-beta-gentiobioside; Quercetin 3-β-gentiobioside; Quercetin 3-O-gentiobioside; Quercetin 3-b-gentiobioside; quercetin 3-O-gentobioside; Quercetin 3-O-diglucoside; Quercetin 3-gentiobioside; quercetin-3-gentiobioside; Quercetin
数据库引用编号
19 个数据库交叉引用编号
- ChEBI: CHEBI:136778
- PubChem: 5320834
- HMDB: HMDB0301692
- ChEMBL: CHEMBL1097317
- LipidMAPS: LMPK12112096
- MeSH: quercetin 3-O-gentobioside
- MetaCyc: CPD-14820
- KNApSAcK: C00005411
- foodb: FDB000178
- chemspider: 4478805
- CAS: 7431-83-6
- CAS: 117-39-5
- medchemexpress: HY-N4089
- MetaboLights: MTBLC136778
- KEGG: C00389
- PubChem: 3679
- KNApSAcK: 16243
- LOTUS: LTS0183115
- wikidata: Q104993730
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
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
- 3559 - Chenopodium album: 10.1021/JF800421J
- 240045 - Dysphania botrys: 10.1007/BF00563912
- 291461 - Fagonia glutinosa: 10.1016/0305-1978(92)90060-Q
- 291466 - Fagonia latifolia: 10.1016/0305-1978(92)90060-Q
- 245579 - Fagonia scabra: 10.1016/0305-1978(92)90060-Q
- 3635 - Gossypium hirsutum: 10.1021/JF60229A021
- 9606 - Homo sapiens: -
- 254779 - Lathyrus pratensis: 10.1016/0031-9422(81)84073-3
- 264972 - Ochradenus baccatus: 10.1016/0031-9422(91)80109-E
- 296033 - Phyllanthus virgatus: 10.1021/NP970336V
- 33090 - Plants: -
- 159015 - Primula spectabilis: 10.1016/J.PHYTOCHEM.2011.04.010
- 3755 - Prunus dulcis: 10.1016/S0031-9422(00)97883-X
- 3760 - Prunus persica: 10.1007/BF00567046
- 286862 - Ranunculus biternatus: 10.1016/0305-1978(94)90048-5
- 2036009 - Ranunculus moseleyi: 10.1016/0305-1978(94)90048-5
- 286982 - Ranunculus pseudotrullifolius: 10.1016/0305-1978(94)90048-5
- 74632 - Rosa gallica: 10.1021/JF903515F
- 1341699 - Senegalia pennata: 10.1021/NP1000818
- 72402 - Senna alexandrina: 10.1016/S0031-9422(00)89592-8
- 210369 - Tribulus terrestris: 10.1016/0031-9422(82)83030-6
- 329212 - Turnera diffusa: 10.1021/NP060253R
- 138046 - Vachellia tortilis: 10.1016/0031-9422(91)80106-B
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
- Edward Owen Norman, Stuart Hombsch, James Lever, Robert Brkljača, Jonathan White, Robin B Gasser, Aya C Taki, Sylvia Urban. Phytochemical Profiling and Biological Testing of the Constituents of the Australian Plant Haemodorum brevisepalum.
Journal of natural products.
2021 11; 84(11):2832-2844. doi:
10.1021/acs.jnatprod.1c00509
. [PMID: 34780692] - Yusnita Rifai, Midori A Arai, Takashi Koyano, Thaworn Kowithayakorn, Masami Ishibashi. Terpenoids and a flavonoid glycoside from Acacia pennata leaves as hedgehog/GLI-mediated transcriptional inhibitors.
Journal of natural products.
2010 May; 73(5):995-7. doi:
10.1021/np1000818
. [PMID: 20450170] - X Lozoya, M Meckes, M Abou-Zaid, J Tortoriello, C Nozzolillo, J T Arnason. Quercetin glycosides in Psidium guajava L. leaves and determination of a spasmolytic principle.
Archives of medical research.
1994; 25(1):11-5. doi:
"
. [PMID: 8019108]