Metabolomics Structure Database

 
MW REGNO: 51881
Common Name:Coenzyme B
Systematic Name:N-(7-sulfanylheptanoyl)-L-threonine 3-(dihydrogen phosphate)
RefMet Name:Coenzyme B
Synonyms:(2S,3R)-2-[(7-mercaptoheptanoyl)amino]-3-(phosphonooxy)butanoic acid; (2S,3R)-3-phosphonooxy-2-[(7-sulfanylheptanoyl)amino]butanoic acid; 7-mercaptoheptanoyl-O-phospho-L-threonine; 7-mercaptoheptanoylthreonine phosphate; 7-thioheptanoyl-threonine O-phosphate; MHTP; N-(7-mercaptoheptanoyl)-L-threonine 3-O-phosphate; N-(7-sulfanylheptanoyl)-3-O-phosphono-L-threonine; N-(7-sulfanylheptanoyl)-3-phospho-L-threonine [PubChem Synonyms]
Exact Mass:
343.0855 (neutral)    Calculate m/z:
Formula:C11H22NO7PS
InChIKey:JBJSVEVEEGOEBZ-SCZZXKLOSA-N
ClassyFire superclass:Organic acids and derivatives [C0000264]
ClassyFire class:Carboxylic acids and derivatives [C0000265]
ClassyFire subclass:Amino acids, peptides, and analogues [C0000013]
ClassyFire direct parent:N-acyl-alpha amino acids [C0002402]
SMILES:C[C@H]([C@@H](C(=O)O)NC(=O)CCCCCCS)OP(=O)(O)O
Studies:Available studies (via RefMet name)

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External database links:

PubChem CID:5462265
CHEBI ID:28890
HMDB ID:HMDB0304798
KEGG ID:C04628
Plant Metabolite Hub(Pmhub):MS000018430

Calculated physicochemical properties (?):

Heavy Atoms: 21  
Rings: 0  
Aromatic Rings: 0  
Rotatable Bonds: 11  
van der Waals Molecular volume: 304.45 Å3 molecule-1  
Toplogical Polar Sufrace Area: 133.16 Å2 molecule-1  
Hydrogen Bond Donors: 4  
Hydrogen Bond Acceptors: 7  
logP: 2.13  
Molar Refractivity: 80.34  
Fraction sp3 Carbons: 0.82  
sp3 Carbons: 9  

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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