Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	57682
Common Name:	2-amino-2,3,7-trideoxy-D-lyxo-hept-6-ulosonic acid
Systematic Name:	2-amino-2,3,7-trideoxy-D-lyxo-hept-6-ulosonic acid
RefMet Name:	2-Amino-2,3,7-trideoxy-D-threo-hept-6-ulosonic acid
Synonyms:	2-Amino-3,7-dideoxy-D-threo-hept-6-ulosonic acid [PubChem Synonyms]
Exact Mass:	191.0794 (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:	C7H13NO5
InChIKey:	IFMHGOADXGYWMO-KVQBGUIXSA-N
LIPID MAPS Category:	Fatty Acyls [FA]
LIPID MAPS mainclass:	Fatty Acids and Conjugates [FA01]
LIPID MAPS subclass:	Hydroxy fatty acids [FA0105]
SMILES:	CC(=O)[C@H]([C@@H](C[C@@H](C(=O)O)N)O)O
Studies:	Available studies (via RefMet name)

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All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	25137912
LIPID MAPS ID:	LMFA01050473
CHEBI ID:	51282
KEGG ID:	C16850
MetaCyc ID:	CPD-10792
Plant Metabolite Hub(Pmhub):	MS000025437

Calculated physicochemical properties (?):

Heavy Atoms:	13
Rings:	0
Aromatic Rings:	0
Rotatable Bonds:	5
van der Waals Molecular volume:	179.33 Å3 molecule-1
Toplogical Polar Sufrace Area:	120.85 Å2 molecule-1
Hydrogen Bond Donors:	4
Hydrogen Bond Acceptors:	5
logP:	-1.04
Molar Refractivity:	44.46
Fraction sp3 Carbons:	0.71
sp3 Carbons:	5

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