Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	2563
Common Name:	LTC4
Systematic Name:	5S-hydroxy,6R-(S-glutathionyl),7E,9E,11Z,14Z-eicosatetraenoic acid
RefMet Name:	LTC4
Synonyms:	Leukotriene C4 [PubChem Synonyms]
Exact Mass:	625.3033 (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:	C30H47N3O9S
InChIKey:	GWNVDXQDILPJIG-NXOLIXFESA-N
LIPID MAPS Category:	Fatty Acyls [FA]
LIPID MAPS mainclass:	Eicosanoids [FA03]
LIPID MAPS subclass:	Leukotrienes [FA0302]
Massbank MS spectra:	View MS spectra
SMILES:	CCCCC/C=CC/C=CC=CC=C[C@H]([C@H](CCCC(=O)O)O)SC[C@@H](C(=O)NCC(=O)O)NC(=O)CC[C@@H](C(=O)O)N
Studies:	Available studies (via RefMet name)

Select appropriate tab below to view additional details:

All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	5280493
LIPID MAPS ID:	LMFA03020003
CHEBI ID:	16978
HMDB ID:	HMDB0001198
KEGG ID:	C02166
Chemspider ID:	4444133
METLIN ID:	3681
MetaCyc ID:	LEUKOTRIENE-C4
Plant Metabolite Hub(Pmhub):	MS000008777

Calculated physicochemical properties (?):

Heavy Atoms:	43
Rings:	0
Aromatic Rings:	0
Rotatable Bonds:	25
van der Waals Molecular volume:	634.42 Å3 molecule-1
Toplogical Polar Sufrace Area:	216.35 Å2 molecule-1
Hydrogen Bond Donors:	7
Hydrogen Bond Acceptors:	9
logP:	4.49
Molar Refractivity:	169.51
Fraction sp3 Carbons:	0.57
sp3 Carbons:	17

Human Pathway links:

HMDB and KEGG pathways containing this metabolite

REACTOME pathways containing this metabolite

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