Metabolomics Structure Database

 
MW REGNO: 47494
Common Name:Furanodiene
Systematic Name:3,6,10-trimethyl-4H,7H,8H,11H-cyclodeca[b]furan
RefMet Name:Furanodiene
Synonyms: [PubChem Synonyms]
Exact Mass:
216.1514 (neutral)    Calculate m/z:
Formula:C15H20O
InChIKey:VMDXHYHOJPKFEK-IAVOFVOCSA-N
LIPID MAPS Category:Prenol Lipids
LIPID MAPS mainclass:Isoprenoids
LIPID MAPS subclass:C15 isoprenoids
SMILES:C/C/1=CCc2c(C)coc2C/C(=C/CC1)/C
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:636458
CHEBI ID:80824
HMDB ID:HMDB0036769
KEGG ID:C16959
Chemspider ID:10278459
Marine Natural Products DB:CMNPD1274
Plant Metabolite Hub(Pmhub):MS000025511

Calculated physicochemical properties (?):

Heavy Atoms: 16  
Rings: 2  
Aromatic Rings: 1  
Rotatable Bonds: 0  
van der Waals Molecular volume: 230.67 Å3 molecule-1  
Toplogical Polar Sufrace Area: 13.14 Å2 molecule-1  
Hydrogen Bond Donors: 0  
Hydrogen Bond Acceptors: 1  
logP: 4.36  
Molar Refractivity: 67.60  
Fraction sp3 Carbons: 0.47  
sp3 Carbons: 7  

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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