Glutathione

Oglufanide (H-Glu-Trp-OH) is a dipeptide immunomodulator isolated from calf thymus. Oglufanide inhibits vascular endothelial growth factor (VEGF) . Oglufanide can stimulate the immune response to hepatitic C virus (HCV) and intracellular bacterial

Oglufanide (H-Glu-Trp-OH) is a dipeptide immunomodulator isolated from calf thymus. Oglufanide inhibits vascular endothelial growth factor (VEGF) . Oglufanide can stimulate the immune response to hepatitic C virus (HCV) and intracellular bacterial

Gamma-glutamyl transpeptidase (GGT: aka gamma-glutamyl transferase) cleaves the gamma-glutamyl bond of glutathione, making extracellular glutathione available for intracellular use. Elevated intracellular glutathione contributes to resistance of

A non-competitive inhibitor of &gamma-glutamyl transferase (GGT), exhibiting a Ki value of 17.6 &muM less toxic than the GGT inhibitor acivicin toward dividing cells.

A non-competitive inhibitor of &gamma-glutamyl transferase (GGT), exhibiting a Ki value of 17.6 &muM less toxic than the GGT inhibitor acivicin toward dividing cells.

A non-competitive inhibitor of &gamma-glutamyl transferase (GGT), exhibiting a Ki value of 17.6 &muM less toxic than the GGT inhibitor acivicin toward dividing cells.

A non-competitive inhibitor of &gamma-glutamyl transferase (GGT), exhibiting a Ki value of 17.6 &muM less toxic than the GGT inhibitor acivicin toward dividing cells.

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

General description This substance is a primary reference substance with assigned absolute purity (considering chromatographic purity, water, residual solvents, inorganic impurities). The exact value can be found on the certificate.

Rat GSTA1/Glutathione S Transferase Alpha 1 ELISA Kit

Rat Gsta4/Glutathione S-transferase alpha-4 ELISA Kit

InformationRemogliflozin etabonate (GSK189075) is an orally active, selective and low-affinity inhibitor ofsodium glucose cotransporter (SGLT2)with Ki of 1950 nM, 2140 nM, 43100 nM, 8570 nM for hSGLT2, rSGLT2, hSGLT1, rSGLT1, respectively.