Genistein 8-c-glucoside (BioDeep_00000000979)

PANOMIX_OTCML-2023

代谢物信息卡片

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

化学式: C21H20O10 (432.105642)
中文名称: 染料木素 8-C-葡萄糖苷
谱图信息: 最多检出来源 Chinese Herbal Medicine(otcml) 88.24%

分子结构信息

SMILES: C(C(O)1)(c(c(O)4)c(c(c(O)c4)3)OC=C(C3=O)c(c2)ccc(O)c2)OC(CO)C(O)C1O
InChI: InChI=1S/C21H20O10/c22-6-13-17(27)18(28)19(29)21(31-13)15-12(25)5-11(24)14-16(26)10(7-30-20(14)15)8-1-3-9(23)4-2-8/h1-5,7,13,17-19,21-25,27-29H,6H2

描述信息

Genistein 8-C-glucoside is a C-glycosyl compound that is genistein substituted by a beta-D-glucopyranosyl residue at position 8 via a C-glucosidic linkage. It has a role as a plant metabolite. It is a C-glycosyl compound and a member of 7-hydroxyisoflavones. It is functionally related to a genistein.
Genistein 8-C-glucoside is a natural product found in Dalbergia sissoo, Genista ephedroides, and other organisms with data available.
A C-glycosyl compound that is genistein substituted by a beta-D-glucopyranosyl residue at position 8 via a C-glucosidic linkage.

同义名列表

6 个代谢物同义名

5,7-dihydroxy-3-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one; (1S)-1,5-anhydro-1-[5,7-dihydroxy-3-(4-hydroxyphenyl)-4-oxo-4H-1-benzopyran-8-yl]-D-glucitol; Genistein 8-c-glucoside; G8CG; 5,7,4-Trihydroxyisoflavone 8-C-glucoside; 3-Genistein-8-C-glucoside

数据库引用编号

17 个数据库交叉引用编号

ChEBI: CHEBI:5304
KEGG: C10420
PubChem: 5281757
PubChem: 5472471
Metlin: METLIN47675
ChEMBL: CHEMBL1945734
ChEMBL: CHEMBL1975213
LipidMAPS: LMPK12050163
KNApSAcK: C00006118
CAS: 66026-80-0
medchemexpress: HY-N6882
PMhub: MS000011575
Flavonoid: FLIAAACS0002
MetaboLights: MTBLC5304
PubChem: 12606
3DMET: B03829
NIKKAJI: J535.048D

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)

13 个相关的物种来源信息

1978221 - Crotalaria thebaica: 10.21608/BFSA.2000.66404
1265830 - Dalbergia nitidula: 10.1016/S0031-9422(01)00195-9
1265830 - Dalbergia nitidula: 10.1039/P19800002463
107308 - Dalbergia sissoo:
107308 - Dalbergia sissoo: 10.1039/P19800002463
49820 - Genista cinerea: 10.1080/10575639508043160
123905 - Genista ephedroides: 10.1021/NP980112S
3873 - Lupinus luteus: 10.1248/CPB.41.394
359571 - Podocytisus caramanicus: 10.1055/S-2007-990248
3892 - Pueraria: 10.1248/CPB.35.4846
3893 - Pueraria montana var. lobata:
3893 - Pueraria montana var. lobata: 10.1080/10286021003745445
49838 - Retama sphaerocarpa: 10.1007/S10600-007-0207-X

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

Bingrui Liu, Kenneth T Kongstad, Sun Qinglei, Nils T Nyberg, Anna K Jäger, Dan Staerk. Dual high-resolution α-glucosidase and radical scavenging profiling combined with HPLC-HRMS-SPE-NMR for identification of minor and major constituents directly from the crude extract of Pueraria lobata. Journal of natural products. 2015 Feb; 78(2):294-300. doi: 10.1021/np5009416. [PMID: 25679337]
Preety Dixit, Raju Chillara, Vikram Khedgikar, Jyoti Gautam, Priyanka Kushwaha, Avinash Kumar, Divya Singh, Ritu Trivedi, Rakesh Maurya. Constituents of Dalbergia sissoo Roxb. leaves with osteogenic activity. Bioorganic & medicinal chemistry letters. 2012 Jan; 22(2):890-7. doi: 10.1016/j.bmcl.2011.12.036. [PMID: 22212722]
Yasufumi Katagiri, Yasuyuki Hashidoko, Satoshi Tahara. Localization of flavonoids in the yellow lupin seedlings and their UV-B-absorbing potential. Zeitschrift fur Naturforschung. C, Journal of biosciences. 2002 Sep; 57(9-10):811-6. doi: 10.1515/znc-2002-9-1010. [PMID: 12440717]