Metabolomics Structure Database

 
MW REGNO: 51585
Common Name:Kanamycin B
Systematic Name:(1R,2S,3S,4R,6S)-4,6-diamino-3-(3-amino-3-deoxy-alpha-D-glucopyranosyloxy)-2-hydroxycyclohexyl 2,6-diamino-2,6-dideoxy-alpha-D-glucopyranoside
RefMet Name:Kanamycin B
Synonyms:2'-amino-2'-deoxykanamycin; Nebramycin V; O-3-amino-3-deoxy-alpha-D-glucopyranosyl-(1->4)-O-(2,6-diamino-2,6-dideoxy-alpha-D-glucopyranosyl-(1->6))-2-deoxy-D-streptamine [PubChem Synonyms]
Exact Mass:
483.2540 (neutral)    Calculate m/z:
Formula:C18H37N5O10
InChIKey:SKKLOUVUUNMCJE-FQSMHNGLSA-N
ClassyFire superclass:Organic oxygen compounds [C0004603]
ClassyFire class:Organooxygen compounds [C0000323]
ClassyFire subclass:Carbohydrates and carbohydrate conjugates [C0000011]
ClassyFire direct parent:4,6-disubstituted 2-deoxystreptamines [C0003574]
Massbank MS spectra:View MS spectra
SMILES:C1[C@@H]([C@H]([C@@H]([C@H]([C@@H]1N)O[C@@H]1[C@@H]([C@H]([C@@H]([C@@H](CO)O1)O)N)O)O)O[C@@H]1[C@@H]([C@H]([C@@H]([C@@H](CN)O1)O)O)N)N
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:439318
CHEBI ID:28098
KEGG ID:C00825
Natural Products Atlas ID:NP018696
EPA CompTox DB:DTXCID00197282
Plant Metabolite Hub(Pmhub):MS000009681

Calculated physicochemical properties (?):

Heavy Atoms: 33  
Rings: 3  
Aromatic Rings: 0  
Rotatable Bonds: 6  
van der Waals Molecular volume: 425.78 Å3 molecule-1  
Toplogical Polar Sufrace Area: 292.54 Å2 molecule-1  
Hydrogen Bond Donors: 11  
Hydrogen Bond Acceptors: 10  
logP: -2.46  
Molar Refractivity: 118.42  
Fraction sp3 Carbons: 1.00  
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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