Tuberonic acid glucoside (BioCAD00000018985)
Metabolite Card
Formula: C18H28O9 (388.1733)
SMILES: OC[C@H]1O[C@@H](OCC\C=C/C[C@@H]2[C@@H](CC(O)=O)CCC2=O)[C@H](O)[C@@H](O)[C@@H]1O
Synonyms [en]
Tuberonic acid glucoside; (1R,2S)-3-oxo-2-(5'-O-beta-D-glucopyranosyloxy-2'Z-pentenyl)-cyclopentaneacetic acid; 12-Hydroxyjasmonic acid glucoside; tuberonic acid beta-D-glucoside; 12-hydroxyjasmonic acid 12-O-beta-D-glucoside; MEGxp0_000347
Last reviewed on 2024-06-28.
Cite this Page
Tuberonic acid glucoside. 数据之源,洞见之始. SMRUCC genomics institute, a synthetic life researcher from China.
https://biocad_registry.innovation.ac.cn/s/(-)-arctiin
(retrieved
2026-01-03) (CAD Registry RN: BioCAD00000018985). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Note
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.
DBLinks
- CAS Registry Number: 120399-24-8
- PubChem CID: 52922085
- ChEBI: 37419
- HMDB: HMDB0301837
- LipidMaps: LMFA13010032
- KEGG: C08558
- BioCyc:
- NCBI MeSH: tuberonic acid glucoside
- Wikipedia:
Other DBLinks
- CAS Registry Number: 120399-24-8
- CAS Registry Number: 124649-25-8
- PubChem: 133554324
- PubChem: 24066896
- PubChem: 5281204
- PubChem: 52922085
- PubChem: 86764688
- ChEBI: ChEBI:182264
- ChEBI: ChEBI:37419
- HMDB: HMDB0301837
- LipidMaps: LMFA13010032
- KEGG: C08558
- NCBI MeSH: tuberonic acid glucoside
- RefMet: RM0153873
- Metlin: METLIN_46606
- Coconut NaturalProduct: CNP0257421.1
- Coconut NaturalProduct: CNP0257421.2
- Coconut NaturalProduct: CNP0257421.4
- Coconut NaturalProduct: CNP0257421.5
- Coconut NaturalProduct: CNP0257421.6
Class / Ontology
- WishartLab ClassyFire: [Fatty acyl glycosides] Fatty acyl glycosides
- RefMet: [Fatty acyl glycosides] Fatty acyl glycosides
- LipidMaps: [Fatty acyl glycosides of mono- and disaccharides [FA1301]] Fatty acyl glycosides of mono- and disaccharides [FA1301]
- ChEBI: [CHEBI:37419] 12-hydroxyjasmonic acid 12-O-beta-D-glucoside
- Coconut NaturalProduct: [Fatty acyl glycosides of mono- and disaccharides] Fatty acyl glycosides of mono- and disaccharides
Taxonomy Source
- Aconitum leucostomum [ncbi taxid: 632164]
- Anarsia lineatella [ncbi taxid: 1101080]
- Apollonias barbujana [ncbi taxid: ]
- Aquilegia ecalcarata [ncbi taxid: 46965]
- Artemisia hanseniana [ncbi taxid: ]
- Blumea mollis [ncbi taxid: 119169]
- Ceanothus velutinus [ncbi taxid: 54785]
- Chlorophytum borivilianum [ncbi taxid: 503355]
- Dipterocarpus dyeri [ncbi taxid: 340441]
- Fragaria vesca [ncbi taxid: 57918]
- Garcinia scortechinii [ncbi taxid: 180116]
- Gardenia tubifera [ncbi taxid: 1240870]
- Ipomoea cairica [ncbi taxid: 129201]
- Isodon lophanthoides [ncbi taxid: 204133]
- Kopsia grandifolia [ncbi taxid: 1750995]
- Lasianthus fordii [ncbi taxid: 1406743]
- Ledebouria socialis [ncbi taxid: 34191]
- Lycopus europaeus [ncbi taxid: 260603]
- Panax innovans [ncbi taxid: ]
- Penicillium cinerascens [ncbi taxid: 70096]
- Perilla frutescens [ncbi taxid: 48386]
- Persea mexicana [ncbi taxid: ]
- Phyllanthus emblica [ncbi taxid: ]
- Rhodobacter sphaeroides [ncbi taxid: ]
- Solanum tuberosum [ncbi taxid: 4113]
- Sordaria araneosa [ncbi taxid: 573841]
- Thymus vulgaris [ncbi taxid: 49992]
- Phyllanthus emblica [ncbi taxid: ]
- Salanum tuberosum [ncbi taxid: ]
- Solanum tuberosum [ncbi taxid: 4113]
- Artemisia vulgaris [ncbi taxid: 4220]
Pathway Synthetic
| pathway id | name |
|---|