Isomyricitrin (BioDeep_00000270562)
Secondary id: BioDeep_00000228400
PANOMIX_OTCML-2023
代谢物信息卡片
化学式: C21H20O13 (480.090387)
中文名称: 杨梅素-3-O-Β-D-葡萄糖苷
谱图信息:
最多检出来源 unclassified Codonopsis(otcml) 97.83%
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)O)O)O)c1cc(c(c(c1)O)O)O)O)O
InChI: InChI=1S/C21H20O13/c22-5-12-15(28)17(30)18(31)21(33-12)34-20-16(29)13-8(24)3-7(23)4-11(13)32-19(20)6-1-9(25)14(27)10(26)2-6/h1-4,12,15,17-18,21-28,30-31H,5H2/t12-,15-,17+,18-,21+/m1/s1
描述信息
Myricetin 3-O-beta-D-glucopyranoside is a myricetin O-glucoside that is myricetin with a beta-D-glucosyl residue attached at position 3. It has a role as a plant metabolite. It is a myricetin O-glucoside, a beta-D-glucoside, a monosaccharide derivative and a pentahydroxyflavone. It is functionally related to a beta-D-glucose. It is a conjugate acid of a myricetin 3-O-beta-D-glucopyranoside(1-).
myricetin 3-O-beta-D-glucopyranoside is a natural product found in Saxifraga tricuspidata, Libocedrus yateensis, and other organisms with data available.
Myricetin 3-O-glucoside is a metabolite found in or produced by Saccharomyces cerevisiae.
A myricetin O-glucoside that is myricetin with a beta-D-glucosyl residue attached at position 3.
同义名列表
15 个代谢物同义名
5,7-Dihydroxy-3-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-2-(3,4,5-trihydroxyphenyl)-4H-chromen-4-one; 5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one; 4H-1-Benzopyran-4-one, 3-(beta-D-glucopyranosyloxy)-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-; 5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)-4H-chromen-3-yl beta-D-glucopyranoside; 5,7-Dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)-4H-1-benzopyran-3-yl hexopyranoside; myricetin 3-O-beta-D-glucopyranoside; Myricetin 3-beta-D-glucopyranoside; myricetin 3-O-beta-D-glucoside; Myricetin 3-beta-glucoside; Myricetin 3-O-D-glucoside; Myricetin 3-O-glucoside; Isomyricitrin; Isomericitrin; 3- [ (beta-D-Glucopyranosyl) oxy ] -3,4,5,5,7-pentahydroxyflavone; Myricetin 3-glucoside
数据库引用编号
9 个数据库交叉引用编号
- ChEBI: CHEBI:75813
- PubChem: 5318606
- ChEMBL: CHEMBL1221722
- ChemIDplus: 0019833126
- KNApSAcK: C00005729
- CAS: 19833-12-6
- medchemexpress: HY-N7906
- Flavonoid: FL5FAGGL0001
- MetaboLights: MTBLC75813
分类词条
相关代谢途径
Reactome(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)
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。
文献列表
- Bui Thi Thuy Luyen, Bui Huu Tai, Nguyen Phuong Thao, Kim Ji Eun, Ji Yun Cha, Ming Jie Xin, Young Mi Lee, Young Ho Kim. Anti-inflammatory components of Euphorbia humifusa Willd.
Bioorganic & medicinal chemistry letters.
2014 Apr; 24(8):1895-900. doi:
10.1016/j.bmcl.2014.03.014
. [PMID: 24679441] - Md Maniruzzaman Manir, Jeong Kee Kim, Byeong-Gon Lee, Surk-Sik Moon. Tea catechins and flavonoids from the leaves of Camellia sinensis inhibit yeast alcohol dehydrogenase.
Bioorganic & medicinal chemistry.
2012 Apr; 20(7):2376-81. doi:
10.1016/j.bmc.2012.02.002
. [PMID: 22377672] - Li-Wen Tian, Ying-Jun Zhang, Chang Qu, Yi-Fei Wang, Chong-Ren Yang. Phloroglucinol glycosides from the fresh fruits of Eucalyptus maideni.
Journal of natural products.
2010 Feb; 73(2):160-3. doi:
10.1021/np900530n
. [PMID: 20092288] - Huizheng Fu, Yongming Luo, Dongming Zhang. [Studies on chemical constituents of leaves of Psidium guajava].
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica.
2009 Mar; 34(5):577-9. doi:
. [PMID: 19526787]
- . .
.
. doi:
. [PMID: 19733370]