MCTR1 Chemical Properties

Boiling point:

987.7±65.0 °C(Predicted)

Density 

1.224±0.06 g/cm3(Predicted)

storage temp. 

Store at -20°C

solubility 

DMF: 50 mg/ml; DMSO: 50 mg/ml; Ethanol: 1 mg/ml; PBS (pH 7.2): 100μg/ml

pka

2.21±0.10(Predicted)

MCTR1 Usage And Synthesis

Uses

L-γ-Glutamyl-S-[(1R,2E,4E,6Z,9Z)-12-carboxy-1-[(1S,3Z,6Z)-1-hydroxy-3,6-nonadien-1-yl]-2,4,6,9-dodecatetraen-1-yl]-L-cysteinylglycine is a related compound of S-?[(1R,?2E,?4E,?6Z,?9Z)?-?12-Carboxy-?1-?[(1S,?3Z,?6Z)?-?1-?hydroxy-?3,?6-?nonadien-?1-?yl]?-?2,?4,?6,?9-?dodecatetraen-?1-?yl]?-?L-?cysteinyl-glycine (C178710), which is synthesized from omega-3 essential fatty acids and utilized by macrophages for tissue regeneration and inflammation.

Definition

ChEBI: (13R)-S-glutathionyl-(14S)-hydroxy-(4Z,7Z,9E,11E,16Z,19Z)-docosahexaenoic acid is a docosanoid that is (14S)-hydroxy-(4Z,7Z,9E,11E,16Z,19Z)-docosahexaenoic acid in which a glutathionyl group is attached at position 13R via a sulfide linkage. It has a role as a human metabolite. It is a docosanoid, an organic sulfide, a tricarboxylic acid, a secondary alcohol and a glutathione conjugate. It is a conjugate acid of a (13R)-S-glutathionyl-(14S)-hydroxy-(4Z,7Z,9E,11E,16Z,19Z)-docosahexaenoate(2-).