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Allosteric modulators Allosteric modulators typically attach to regions distinct from the orthosteric site of receptors, inducing conformational changes to regulate the affinity and/or efficacy of orthosteric ligands, or to directly modulate receptor activity with positive, negative, or neutral effects

In hypercholesterolemic mice, deletion of Arg2 or inhibition of arginase with BEC improves endothelial function and reduces atherosclerosis (Ryoo et al., 2008)

Newton, 2007

It accumulates predominantly in the liver and binds all major TR isoforms with similar affinity to T3 binding preferentially to TR relative to TR, and was initially studied as a lipid-lowering compound able to stimulate hepatic pathways with minimal side effects due to its hepatic tropism

Its a tripeptide three amino acids bonded together: cysteine, glycine, and glutamate

However, effects of BPC 157 on vascular tone and intracellular Src-Cav-1-eNOS signaling are still not understood