Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	62060
Common Name:	Biotin sulfoxide
Systematic Name:	5-[(3aS,4S,6aR)-5-oxido-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl]pentanoic acid
RefMet Name:	Biotin sulfoxide
Synonyms:	biotin S-oxide [PubChem Synonyms]
Exact Mass:	260.0831 (neutral)    Calculate m/z: (Choose adduct) [M+H]+ [M+H-H2O]+ [M.]+ [M+2H]2+ [M+3H]3+ [M+4H]4+ [M+K]+ [M+2K]2+ [M-H+2K]+ [M+Na]+ [M+2Na]2+ [M-H+2Na]+ [M+Li]+ [M+2Li]2+ [M+NH4]+ [M-H]- [M-2H]2- [M-3H]3- [M-4H]4- [M+Cl]- [M+OAc]- [M+HCOO]- M(neutral)
Formula:	C10H16N2O4S
InChIKey:	KCSKCIQYNAOBNQ-YBSFLMRUSA-N
ClassyFire superclass:	Organoheterocyclic compounds [C0000002]
ClassyFire class:	Biotin and derivatives [C0000244]
ClassyFire subclass:	Biotin and derivatives [C0000244]
ClassyFire direct parent:	Aliphatic heteropolycyclic compounds
SMILES:	C(CCC(=O)O)C[C@H]1[C@@H]2[C@H](CS1=O)NC(=O)N2
Studies:	Available studies (via RefMet name)

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External database links:

PubChem CID:	83833
CHEBI ID:	62193
HMDB ID:	HMDB0249229

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