Metabolomics Structure Database

 
MW REGNO: 133897
Common Name:Neosolaniol
Systematic Name:[(1S,2R,4S,7R,9R,10R,11S,12S)-11-acetyloxy-4,10-dihydroxy-1,5-dimethylspiro[8-oxatricyclo[7.2.1.02,7]dodec-5-ene-12,2'-oxirane]-2-yl]methyl acetate
Synonyms: [PubChem Synonyms]
Exact Mass:
382.1628 (neutral)    Calculate m/z:
Formula:C19H26O8
InChIKey:TVZHDVCTOCZDNE-WVJYZQHISA-N
ClassyFire superclass:Lipids and lipid-like molecules
ClassyFire class:Prenol lipids
ClassyFire subclass:Sesquiterpenoids
ClassyFire direct parent:Trichothecenes
Massbank MS spectra:View MS spectra
SMILES:CC1=C[C@@H]2[C@@](C[C@@H]1O)(COC(=O)C)[C@@]1(C)[C@@H]([C@H]([C@H]([C@]31CO3)O2)O)OC(=O)C
Studies:Available studies(via PubChem CID)

Select appropriate tab below to view additional details:

External database links:

PubChem CID:13818797
CHEMBL ID:CHEMBL422680
Plant Metabolite Hub(Pmhub):MS000004155

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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