12-Hydroxyjasmonic acid glucoside (BioDeep_00000004053)

Main id: BioDeep_00000019123

human metabolite

代谢物信息卡片

2-[(1R,2R)-3-oxo-2-[(2Z)-5-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}pent-2-en-1-yl]cyclopentyl]acetic acid

化学式: C18H28O9 (388.17332380000005)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1CC(=O)C(C1CC(=O)O)CC=CCCOC2C(C(C(C(O2)CO)O)O)O
InChI: InChI=1S/C18H28O9/c19-9-13-15(23)16(24)17(25)18(27-13)26-7-3-1-2-4-11-10(8-14(21)22)5-6-12(11)20/h1-2,10-11,13,15-19,23-25H,3-9H2,(H,21,22)/b2-1-/t10-,11-,13+,15-,16+,17-,18-/m1/s1

描述信息

12-hydroxyjasmonic acid glucoside, also known as tuberonic acid beta-D-glucoside, is a member of the class of compounds known as fatty acyl glycosides of mono- and disaccharides. Fatty acyl glycosides of mono- and disaccharides are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol. 12-hydroxyjasmonic acid glucoside is slightly soluble (in water) and a weakly acidic compound (based on its pKa). 12-hydroxyjasmonic acid glucoside can be found in potato, which makes 12-hydroxyjasmonic acid glucoside a potential biomarker for the consumption of this food product.

同义名列表

6 个代谢物同义名

2-[(1R,2R)-3-oxo-2-[(2Z)-5-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}pent-2-en-1-yl]cyclopentyl]acetic acid; 2-[(1R,2R)-3-oxo-2-[(2Z)-5-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}pent-2-en-1-yl]cyclopentyl]acetate; (1R,2S)-3-oxo-2-(5-O-beta-D-glucopyranosyloxy-2Z-pentenyl)-cyclopentaneacetic acid; 12-Hydroxyjasmonic acid glucoside; 12-Hydroxyjasmonate glucoside; Tuberonic acid glucoside

数据库引用编号

12 个数据库交叉引用编号

KEGG: C08558
PubChem: 5281204
HMDB: HMDB0301837
Metlin: METLIN46606
KNApSAcK: C00001326
foodb: FDB001489
chemspider: 4444622
CAS: 120399-24-8
ChEBI: CHEBI:37419
PubChem: 10751
LipidMAPS: LMFA02020207
NIKKAJI: J759.874B

分类词条

Fatty acyl glycosides of mono- and disaccharides

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)

21 个相关的物种来源信息

497761 Origanum dictamnus: 10.1021/JF904596M
296036 Phyllanthus emblica: 10.1248/CPB.50.841
48386 Perilla frutescens: 10.1271/BBB.60.732
319561 Breynia vitis-idaea: 10.1080/10286021003745452
296042 Breynia fruticosa: 10.1016/J.PHYTOCHEM.2009.10.002
1219483 Breynia rostrata: 10.1016/J.PHYTOCHEM.2009.10.002
216479 Euphorbia maculata: 10.1248/CPB.57.840
526203 Euphorbia supina: 10.1248/CPB.57.840
39352 Origanum vulgare: 10.1021/JF061477I
4113 Solanum tuberosum: 10.1016/0031-9422(96)00333-0
497761 Origanum dictamnus: 10.1021/JF904596M
296036 Phyllanthus emblica: 10.1248/CPB.50.841
48386 Perilla frutescens: 10.1271/BBB.60.732
319561 Breynia vitis-idaea: 10.1080/10286021003745452
296042 Breynia fruticosa: 10.1016/J.PHYTOCHEM.2009.10.002
1219483 Breynia rostrata: 10.1016/J.PHYTOCHEM.2009.10.002
216479 Euphorbia maculata: 10.1248/CPB.57.840
526203 Euphorbia supina: 10.1248/CPB.57.840
39352 Origanum vulgare: 10.1021/JF061477I
4113 Solanum tuberosum: 10.1016/0031-9422(96)00333-0
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

Yanling Hua, Watsamon Ekkhara, Sompong Sansenya, Chantragan Srisomsap, Sittiruk Roytrakul, Wataru Saburi, Ryosuke Takeda, Hideyuki Matsuura, Haruhide Mori, James R Ketudat Cairns. Identification of rice Os4BGlu13 as a β-glucosidase which hydrolyzes gibberellin A4 1-O-β-d-glucosyl ester, in addition to tuberonic acid glucoside and salicylic acid derivative glucosides. Archives of biochemistry and biophysics. 2015 Oct; 583(?):36-46. doi: 10.1016/j.abb.2015.07.021. [PMID: 26241499]
Rosa Quirantes-Piné, David Arráez-Román, Antonio Segura-Carretero, Alberto Fernández-Gutiérrez. Characterization of phenolic and other polar compounds in a lemon verbena extract by capillary electrophoresis-electrospray ionization-mass spectrometry. Journal of separation science. 2010 Sep; 33(17-18):2818-27. doi: 10.1002/jssc.201000228. [PMID: 20715141]
Shinji Wakuta, Shigeki Hamada, Hiroyuki Ito, Hideyuki Matsuura, Kensuke Nabeta, Hirokazu Matsui. Identification of a beta-glucosidase hydrolyzing tuberonic acid glucoside in rice (Oryza sativa L.). Phytochemistry. 2010 Aug; 71(11-12):1280-8. doi: 10.1016/j.phytochem.2010.04.025. [PMID: 20570296]
Fanjiang Kong, Xiquan Gao, Kyong-Hee Nam, Kosaku Takahashi, Hideyuki Matsuura, Teruhiko Yoshihara. Inhibition of stem elongation in spinach by theobroxide. Journal of plant physiology. 2006 Mar; 163(5):557-61. doi: 10.1016/j.jplph.2005.05.005. [PMID: 16473660]
Hideyuki Matsuura, Teruhiko Yoshihara. Metabolism of deuterium-labeled jasmonic acid and OPC 8:0 in the potato plant (Solanum tuberosum L.). Bioscience, biotechnology, and biochemistry. 2003 Sep; 67(9):1903-7. doi: 10.1271/bbb.67.1903. [PMID: 14519974]
H Matsuura, F Ohmori, M Kobayashi, A Sakurai, T Yoshihara. Qualitative and quantitative analysis of endogenous jasmonoids in potato plant (Solanum tuberosum L.). Bioscience, biotechnology, and biochemistry. 2000 Nov; 64(11):2380-7. doi: 10.1271/bbb.64.2380. [PMID: 11193405]
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