Metabolomics Structure Database

 
MW REGNO: 41950
Common Name:Maltohexaose
Systematic Name:(2R,3R,4S,5S,6R)-2-{[(2R,3S,4R,5R,6R)-6-{[(2R,3S,4R,5R,6R)-6-{[(2R,3S,4R,5R,6R)-6-{[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-{[(2R,3S,4R,5R,6S)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}oxan-3-yl]oxy}-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol
RefMet Name:Maltohexaose
Synonyms: [PubChem Synonyms]
Exact Mass:
990.3275 (neutral)    Calculate m/z:
Formula:C36H62O31
InChIKey:OCIBBXPLUVYKCH-QXVNYKTNSA-N
ClassyFire superclass:Organic oxygen compounds [C0004603]
ClassyFire class:Organooxygen compounds [C0000323]
ClassyFire subclass:Carbohydrates and carbohydrate conjugates [C0000011]
ClassyFire direct parent:Oligosaccharides [C0000198]
SMILES:C([C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)O[C@@H]1[C@@H](CO)O[C@@H]([C@@H]([C@H]1O)O)O[C@@H]1[C@@H](CO)O[C@@H]([C@@H]([C@H]1O)O)O[C@@H]1[C@@H](CO)O[C@@H]([C@@H]([C@H]1O)O)O[C@@H]1[C@@H](CO)O[C@@H]([C@@H]([C@H]1O)O)O[C@@H]1[C@@H](CO)O[C@@H]([C@@H]([C@H]1O)O)O)O)O)O)O
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:5288409
CHEBI ID:61953
HMDB ID:HMDB0012253
KEGG ID:C01936
Chemspider ID:4450599
MetaCyc ID:MALTOHEXAOSE
Plant Metabolite Hub(Pmhub):MS000017399

Calculated physicochemical properties (?):

Heavy Atoms: 67  
Rings: 6  
Aromatic Rings: 0  
Rotatable Bonds: 16  
van der Waals Molecular volume: 829.69 Å3 molecule-1  
Toplogical Polar Sufrace Area: 518.55 Å2 molecule-1  
Hydrogen Bond Donors: 20  
Hydrogen Bond Acceptors: 31  
logP: -3.80  
Molar Refractivity: 217.45  
Fraction sp3 Carbons: 1.00  
sp3 Carbons: 36  

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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