Benzyl alcohol beta-D-rutinoside (BioDeep_00000896478)

human metabolite

代谢物信息卡片

(2R,3R,4R,5R,6S)-2-{[(2R,3S,4S,5R,6R)-6-(benzyloxy)-3,4,5-trihydroxyoxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol

化学式: C19H28O10 (416.16823880000004)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)O)O
InChI: InChI=1S/C19H28O10/c1-9-12(20)14(22)16(24)18(28-9)27-8-11-13(21)15(23)17(25)19(29-11)26-7-10-5-3-2-4-6-10/h2-6,9,11-25H,7-8H2,1H3/t9-,11+,12-,13+,14+,15-,16+,17+,18+,19+/m0/s1

描述信息

Benzyl alcohol beta-d-rutinoside is a member of the class of compounds known as O-glycosyl compounds. O-glycosyl compounds are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. Benzyl alcohol beta-d-rutinoside is soluble (in water) and a very weakly acidic compound (based on its pKa). Benzyl alcohol beta-d-rutinoside can be found in common grape, which makes benzyl alcohol beta-d-rutinoside a potential biomarker for the consumption of this food product.

同义名列表

5 个代谢物同义名

(2R,3R,4R,5R,6S)-2-{[(2R,3S,4S,5R,6R)-6-(benzyloxy)-3,4,5-trihydroxyoxan-2-yl]methoxy}-6-methyloxane-3,4,5-triol; Benzyl alcohol beta-D-rutinoside; Benzyl alcohol b-D-rutinoside; Benzyl alcohol β-D-rutinoside; hydrangeifolin I

数据库引用编号

5 个数据库交叉引用编号

PubChem: 10549806
HMDB: HMDB0303057
ChEMBL: CHEMBL511744
foodb: FDB007542
chemspider: 8725197

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)

9 个相关的物种来源信息

179731 Itoa orientalis: 10.1021/NP800014S
167387 Castanopsis fissa: 10.1016/J.PHYTOCHEM.2011.07.007
39297 Dracocephalum ruyschiana: 10.1021/NP300609U
171213 Acer nikoense: 10.1248/CPB.51.62
345127 Parthenocissus tricuspidata: 10.1248/CPB.51.62
77057 Idesia polycarpa: 10.1016/J.BMCL.2013.04.011
270431 Erica arborea: 10.1002/HLCA.200800379
484842 Coussarea hydrangeifolia: 10.1016/J.PHYTOCHEM.2005.06.019
9606 Homo sapiens: -

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

Mina Lee, Hyang Hwa Lee, Jin-Ku Lee, Sang-Kyu Ye, Seung Hyun Kim, Sang Hyun Sung. Anti-adipogenic activity of compounds isolated from Idesia polycarpa on 3T3-L1 cells. Bioorganic & medicinal chemistry letters. 2013 Jun; 23(11):3170-4. doi: 10.1016/j.bmcl.2013.04.011. [PMID: 23628332]
Erdenechimeg Selenge, Toshihiro Murata, Kyoko Kobayashi, Javzan Batkhuu, Fumihiko Yoshizaki. Flavone tetraglycosides and benzyl alcohol glycosides from the Mongolian medicinal plant Dracocephalum ruyschiana. Journal of natural products. 2013 Feb; 76(2):186-93. doi: 10.1021/np300609u. [PMID: 23356964]
Yongxin Li, Shanjiang Yu, Dong Liu, Peter Proksch, Wenhan Lin. Inhibitory effects of polyphenols toward HCV from the mangrove plant Excoecaria agallocha L. Bioorganic & medicinal chemistry letters. 2012 Jan; 22(2):1099-102. doi: 10.1016/j.bmcl.2011.11.109. [PMID: 22196120]
Xing Yun Chai, Yue Lin Song, Zheng Ren Xu, Hai Ming Shi, Chang Cai Bai, Dan Bi, Jing Wen, Fei Fei Li, Peng Fei Tu. Itosides J-N from Itoa orientalis and structure - anti-COX-2 activity relationship of phenolic glycosides. Journal of natural products. 2008 May; 71(5):814-9. doi: 10.1021/np800014s. [PMID: 18412396]