cysteinyl

Montelukast sodium (MK0476) is an orally available leukotriene receptor antagonist which is widely used for the prophylaxis and chronic treatment of asthma and has been linked to rare cases of clinically apparent liver injury.

Montelukast (Singular) is an orally available leukotriene receptor antagonist which is widely used for the prophylaxis and chronic treatment of asthma and has been linked to rare cases of clinically apparent liver injury.

N-[S-Trityl-L-cysteinyl]glycine is a cleavable ADC linker.

D-(L-a-Aminoadipoyl)-L-Cysteinyl-D-Isodehydrovaline-CoA is a derivative of coenzyme A.

Delta-(L-alpha-aminoadipoyl)-L-cysteinyl-D-vinylglycine-CoA (Delta-(L-alpha-aminoadipoyl)-L-cysteinyl-D-vinylglycine-coenzyme A) is a derivative of coenzyme A.

Gamma-glutamyl[S-(2-iodobenzyl)cysteinyl]glycine-CoA (Gamma-glutamyl[S-(2-iodobenzyl)cysteinyl]glycine-coenzyme A) is a derivative of coenzyme A.

L-D-(α-Aminoadipoyl)-L-cysteinyl-D-valine-CoA (L-D-(a-Aminoadipoyl)-L-cysteinyl-D-valine-coenzyme A) is a derivative of coenzyme A.

L-Glutathione reduced (Glutathione) is a naturally occurring tripeptide found in cells as an endogenous antioxidant that scavenges oxygen free radicals. L-Glutathione reduced is a cofactor for certain enzymes and is involved in the rearrangement of protein disulfide bonds and the reduction of peroxides.

Diflapolin is a highly active dual 5-lipoxygenase-activating protein (FLAP) and soluble epoxide hydrolase (sEH) inhibitor, exhibiting marked anti-inflammatory efficacy and high target selectivity.

S-(2-Hydroxyethyl)glutathione-d4 hydrochloride (Glycine, L-γ-glutamyl-S-(2-hydroxyethyl)-L-cysteinyl-d4) is the deuterium-labeled form of S-(2-Hydroxyethyl)glutathione hydrochloride.

Cysteinylglycine acetate (Cys-Gly Acetate) is an acetate salt of Cysteinylglycine. Cysteinylglycine is an endogenous metabolite. Cysteinylglycine is used in disease diagnosis.

Cysteinyltyrosine is a dipeptide composed of cysteine and tyrosine. It is an incomplete breakdown product of protein digestion or protein catabolism.

Cysteinylglycine (Cys-Gly), is a biologically important compound since it is formed during the γ-glutamyl cycle. It is a L-cysteinyl peptide, that can be used in the studies of many peptides and important proteins.

Cysteinylglycine TFA is an endogenous metabolite. It is used in disease diagnosis.

Cysteinylcysteine is a bioactive chemical.

Cysteinyllysine is a dipeptide composed of cysteine and lysine. It is an incomplete breakdown product of protein digestion or protein catabolism.

Homocysteinylpropachlor is a bioactive chemical.

2-S-Cysteinyldopa is a cross-linked compound that can be isolated from the byssal threads of P. canaliculus. Additionally, 2-S-Cysteinyldopa can be formed in vitro through the oxidation of pcFP-1 by mushroom tyrosinase.

Cysteinyldopa (5-S-Cysteinyldopa) is an endogenous metabolite and widely recognized as one of the most popular and well-known biomarkers for melanoma.

5-S-Cysteinyldopamine is a thioether metabolite of dopamine that can induce neurological damage by causing extensive oxidative stress and protein aggregation. This is characterized by protein carbonylation, glutathione depletion, and increased expression of α-synuclein (α-Syn) and ERp57 proteins. It is applicable in research on neurodegenerative diseases such as Parkinson's disease.

Paracetamol-cysteine TFA (APAP-Cys TFA) is a metabolite of Paracetamol, a biomarker of paracetamol metabolism.

Gemilukast (ONO-6950) is an orally active and potent dual inhibitor of cysteinyl leukotriene 1 and 2 receptors (CysLT1 and CysLT2), inhibits LTC 4-induced bronchoconstriction, and is inhibitory to human CysLT1 and CysLT2, and may be used in the treatment of asthma.

Triciribine phosphate (VD 002) is a highly selective AKT inhibitor that induces cell cycle arrest and cysteinyl asparagin-dependent apoptosis, inhibits neovascularization, and can be used in the study of leukemia.

Pobilukast (SKF 104353) is a selective cysteinyl leukotriene receptor antagonist that blocks phosphatidylinositol metabolism and leukotriene D-induced thromboxane synthesis, and can be used to study limiting myocardial damage in excessively myocardial reperfusion-injured (MI/R) rats.128-63-53-4