Metabolomics Structure Database

 
MW REGNO: 36127
Common Name:(20R)-1alpha,25-dihydroxy-20-phenyl-16,17-didehydro-21-norvitamin D3 / (20R)-1alpha,25-dihydroxy-20-phenyl-16,17-didehydro-21-norcholecalciferol
Systematic Name:(5Z,7E)-(1S,3R,20R)-20-phenyl-21-nor-9,10-seco-5,7,10(19),16-cholestatetraene-1,3,25-triol
Synonyms: [PubChem Synonyms]
Exact Mass:
476.3290 (neutral)    Calculate m/z:
Formula:C32H44O3
InChIKey:VYGZKNHJYRSENF-SUAJYVKGSA-N
LIPID MAPS Category:Sterol Lipids [ST]
LIPID MAPS mainclass:Secosteroids [ST03]
LIPID MAPS subclass:Vitamin D3 and derivatives [ST0302]
SMILES:C=C1/C(=CC=C/CCC[C@@]3(C)[C@H]2CC=C3[C@H](CCCC(C)(C)O)c2ccccc2)/C[C@H](C[C@@H]1O)O
Studies:Available studies(via PubChem CID)

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External database links:

PubChem CID:9547680
LIPID MAPS ID:LMST03020585

Calculated physicochemical properties (?):

Heavy Atoms: 35  
Rings: 4  
Aromatic Rings: 1  
Rotatable Bonds: 7  
van der Waals Molecular volume: 509.71 Å3 molecule-1  
Toplogical Polar Sufrace Area: 60.69 Å2 molecule-1  
Hydrogen Bond Donors: 3  
Hydrogen Bond Acceptors: 3  
logP: 7.63  
Molar Refractivity: 145.57  
Fraction sp3 Carbons: 0.56  
sp3 Carbons: 18  

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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