Metabolomics Structure Database

 
MW REGNO: 62405
Common Name:beta-D-glucosyl crocetin
Systematic Name:1-O-[(2E,4E,6E,8E,10E,12E,14E)-15-carboxy-2,6,11-trimethylhexadeca-2,4,6,8,10,12,14-heptaenoyl]-beta-D-glucopyranose
Synonyms:all-trans-crocetin mono(beta-D-glucosyl) ester; crocetin beta-D-glucopyranosyl ester; crocetin beta-D-glucosyl ester; crocetin mono(beta-D-glucosyl) ester; trans-crocetin beta-D-glucosyl ester [PubChem Synonyms]
Exact Mass:
490.2203 (neutral)    Calculate m/z:
Formula:C26H34O9
InChIKey:ZVGODNZUEWDIPM-YXRLTKITSA-N
ClassyFire superclass:Lipids and lipid-like molecules
SMILES:C/C(=CC=CC=C(/C)C=CC=C(/C)C(=O)O[C@H]1[C@@H]([C@H]([C@@H]([C@@H](CO)O1)O)O)O)/C=C/C=C(C)/C(=O)O
Studies:Available studies(via PubChem CID)

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External database links:

PubChem CID:10368299
CHEBI ID:62765

References

LIPID MAPS classification: "Update of the LIPID MAPS comprehensive classification system for lipids", Fahy E, Subramaniam S, Murphy RC, Nishijima M, Raetz CR, Shimizu T, Spener F, van Meer G, Wakelam MJ, and Dennis EA, J. Lipid Res. (2009) 50: S9-S14. DOI: 10.1194/jlr.R800095-JLR200
ClassyFire classification: "ClassyFire: automated chemical classification with a comprehensive, computable taxonomy", Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS, J. Cheminformatics (2016) 8:61. DOI: 10.1186/s13321-016-0174-y
NPClassifier classification: "NPClassifier: A Deep Neural Network-Based Structural Classification Tool for Natural Products", Kim HW, Wang M, Leber CA, Nothias LF, Reher R, Kang KB, van der Hooft JJJ, Dorrestein PC, Gerwick WH and Cottrell GW. J Nat Prod. 2021 Nov 26;84(11):2795-2807.DOI: 10.1021/acs.jnatprod.1c00399.

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