Sodium thiosalicylate

A membrane active peptide antibiotic of the peptaibol class that strongly induces helical peptide structures and forms voltage-gated ion channels in the lipid bilayers of cell membranes often used to study ion channel assembly, voltage gating, and

3-thia TDA is an analog of the 14-carbon saturated fatty acid myristic acid, wherein the C-3 carbon has been replaced by sulfur in a thioether linkage. When chronically administered to rats, 3-thia TDA acts as a peroxisome inducer (PPAR ligand),

A synthetic intermediate for pharmaceutical synthesis.

A chromophoric substrate that is used to quantify inorganic phosphate (Pi) in the presence of purine nucleoside phosphorylase, followed by continuous spectrophotometry at an absorbance of 355-360 nm used to measure changes in Pi levels in coupled

A form of the sugar Neu5Ac O-linked with the nucleotide CMP serves as the substrate for sialyltransferases, which transfer Neu5Ac from CMP-sialic acid to various acceptor substrates, most commonly at terminal positions of the oligosaccharide

A dual MET/AXL inhibitor.

A PAF receptor agonist with potency comparable to PAF C-18 and PAF C-16 chromogenic substrate used in Cayman&rsquos PAF-AH Assay Kit (Item No. 760901).

A synthetic intermediate useful for pharmaceutical synthesis.

A colorimetric substrate for KIAA1363, a 2-acetyl monoacylglyceryl ether hydrolase critical to the survival and proliferation of many cancer cell lines.

A phospholipid containing palimitoyl (16:0) and oleoyl (18:1) acyl substituents at the sn-1 and sn-2 positions, respectively, that been used to generate lipid membrane bilayers with controlled permeability and may be useful for various surfactant

An inhibitor of Ras-mediated signaling that functions by dislodging Ras from the cell membrane thereby rendering it susceptible to proteolytic degradation inhibits the growth of human Ha-ras-transformed Rat1 fibroblasts with an IC50 value of 7.5

A first generation quinoxaline derivative that acts as a noncompetitive antagonist of mGluR1 and mGluR5 (IC50s = 5.2 and 82 nM, respectively).