Metabolomics Structure Database

 
MW REGNO: 63207
Common Name:Carbovir diphosphate
Systematic Name:[(1S,4R)-4-(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)cyclopent-2-en-1-yl]methyl trihydrogen diphosphate
Synonyms:(-)-carbovir 5'-diphosphate; (-)-carbovir diphosphate; carbovir 5'-diphosphate [PubChem Synonyms]
Exact Mass:
407.0396 (neutral)    Calculate m/z:
Formula:C11H15N5O8P2
InChIKey:LBDJPXUIKREEKI-RQJHMYQMSA-N
ClassyFire superclass:Nucleosides, nucleotides, and analogues [C0000289]
ClassyFire class:Nucleoside and nucleotide analogues [C0003737]
ClassyFire subclass:Nucleoside and nucleotide analogues [C0003737]
ClassyFire direct parent:Aromatic heteropolycyclic compounds
SMILES:C1=C[C@@H](C[C@@H]1COP(=O)(O)OP(=O)(O)O)n1cnc2c1nc(N)[nH]c2=O
Studies:-

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Calculated physicochemical properties (?):

Heavy Atoms: 26  
Rings: 3  
Aromatic Rings: 2  
Rotatable Bonds: 6  
van der Waals Molecular volume: 291.76 Å3 molecule-1  
Toplogical Polar Sufrace Area: 202.88 Å2 molecule-1  
Hydrogen Bond Donors: 5  
Hydrogen Bond Acceptors: 11  
logP: 1.58  
Molar Refractivity: 87.87  
Fraction sp3 Carbons: 0.36  
sp3 Carbons: 4  

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

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