Metabolomics Structure Database

 
MW REGNO: 28035
Common Name:Jasmolin II
Systematic Name:(1S)-2-methyl-4-oxo-3-[(2Z)-pent-2-en-1-yl]cyclopent-2-en-1-yl (1R,3R)-3-[(1E)-3-methoxy-2-methyl-3-oxoprop-1-en-1-yl]-2,2-dimethylcyclopropanecarboxylate
Synonyms:Jasmolin II [PubChem Synonyms]
Exact Mass:
374.2093 (neutral)    Calculate m/z:
Formula:C22H30O5
InChIKey:WKNSDDMJXANVMK-XIGJTORUSA-N
LIPID MAPS Category:Prenol Lipids [PR]
LIPID MAPS mainclass:Isoprenoids [PR01]
LIPID MAPS subclass:C10 isoprenoids (monoterpenes) [PR0102]
LIPID MAPS level4class:Cyclopropane and cyclobutane monoterpenoids [LMPR010206]
SMILES:CC/C=CCC1=C(C)[C@H](CC1=O)OC(=O)[C@@H]1[C@@H](/C=C(C)/C(=O)OC)C1(C)C
Studies:Available studies(via PubChem CID)

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External database links:

PubChem CID:12304690
LIPID MAPS ID:LMPR0102060005
CHEBI ID:39114
KEGG ID:C16781
EPA CompTox DB:DTXCID20809779
Plant Metabolite Hub(Pmhub):MS000025382

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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