S-Octylglutathione

Modify Date: 2025-09-18 09:24:01

S-Octylglutathione Structure
S-Octylglutathione structure
Common Name S-Octylglutathione
CAS Number 24435-27-6 Molecular Weight 419.53600
Density N/A Boiling Point N/A
Molecular Formula C18H33N3O6S Melting Point N/A
MSDS USA Flash Point N/A

 Use of S-Octylglutathione


S-Octylglutathione is a competitive glutathione S-transferase (GST) inhibitor[1].

 Names

Name S-Octylglutathione
Synonym More Synonyms

 S-Octylglutathione Biological Activity

Description S-Octylglutathione is a competitive glutathione S-transferase (GST) inhibitor[1].
Related Catalog

 Chemical & Physical Properties

Molecular Formula C18H33N3O6S
Molecular Weight 419.53600
Exact Mass 419.20900
PSA 184.12000
LogP 2.43990
InChIKey MJWCZWAVSJZQNL-UHFFFAOYSA-N
SMILES CCCCCCCCSCC(NC(=O)CCC(N)C(=O)O)C(=O)NCC(=O)O

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
RIDADR NONH for all modes of transport

 Articles6

More Articles
Crystallographic and thermodynamic analysis of the binding of S-octylglutathione to the Tyr 7 to Phe mutant of glutathione S-transferase from Schistosoma japonicum.

Biochemistry 44 , 1174-1183, (2005)

Glutathione S-transferases are a family of multifunctional enzymes involved in the metabolism of drugs and xenobiotics. Two tyrosine residues, Tyr 7 and Tyr 111, in the active site of the enzyme play ...

An XAS investigation of product and inhibitor complexes of Ni-containing GlxI from Escherichia coli: mechanistic implications.

Biochemistry 40(15) , 4569-82, (2001)

Escherichia coli glyoxalase I (GlxI) is a metalloisomerase that is maximally activated by Ni(2+), unlike other known GlxI enzymes which are active with Zn(2+). The metal is coordinated by two aqua lig...

Effects of phenol compounds, glutathione analogues and a diuretic drug on glutathione S-transferase, glutathione reductase and glutathione peroxidase from canine erythrocytes.

Comp. Biochem. Physiol.,. B. 103(4) , 863-7, (1992)

1. Phenol compounds (ellagic acid, quercetin and purpurogallin), glutathione analogues (S-hexylglutathione and S-octylglutathione) and a diuretic drug (ethacrynic acid) were compared for their inhibit...

 Synonyms

(S)-2-Amino-4-[(R)-1-(carboxymethyl-carbamoyl)-2-octylsulfanyl-ethylcarbamoyl]-butyric acid
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