GDE3 inhibitors encompass chemicals that, although not directly targeting GDE3, modulate the broader realm of lipid metabolism in which GDE3 operates. These chemicals act on various nodes of lipid processing and signaling, offering potential indirect control over GDE3 activity. For instance, Orlistat inhibits lipases, enzymes pivotal for breaking down fats in the diet, offering a link to GDE3's metabolic environment. Similarly, Fenofibrate and Rosiglitazone, through their agonism of PPAR receptors, offer a broader modulation of lipid metabolism pathways that can indirectly interface with GDE3's domain of operations.
Further, the suite of statins - Atorvastatin, Simvastatin, and Lovastatin - throw light on another facet of lipid metabolism: cholesterol synthesis. By inhibiting HMG-CoA reductase, they disrupt the mevalonate pathway, indirectly influencing multiple lipid-modifying enzymes, including potentially GDE3. On a similar note, inhibitors like GGTI-298 and FTI-277 obstruct specific lipid modifications in proteins, which might create a ripple effect across lipid metabolism processes where GDE3 is implicated.