Date published: 2025-10-26

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ORP-1 Inhibitors

Chemical classes known as ORP-1 inhibitors would encompass compounds that directly or indirectly modulate the activity of the ORP-1 protein. ORP-1 is part of the oxysterol-binding protein (OSBP) family, which is involved in lipid transport and cellular signaling pathways that regulate lipid metabolism, including cholesterol homeostasis. The ORP-1 protein specifically has been implicated in the transfer of sterols between cellular membranes. Direct inhibitors of ORP-1 would be molecules that bind to the protein and prevent its normal function, potentially by occupying the sterol-binding domain or by allosteric modulation. However, since direct inhibitors are not established, the focus is on chemicals that impact the protein's activity through interaction with metabolic pathways. For example, statins such as simvastatin, atorvastatin, and rosuvastatin are known to lower cholesterol biosynthesis by inhibiting HMG-CoA reductase, an upstream enzyme in the mevalonate pathway. This can indirectly influence ORP-1 activity by altering the intracellular concentration of cholesterol and potentially other lipids that ORP-1 might transfer. On the other hand, compounds like GW3965 and T0901317 are agonists of liver X receptors (LXRs), which regulate the expression of genes involved in cholesterol efflux and transport, possibly altering ORP-1's lipid transfer activity. Cholesterol transport inhibitors like U18666A and cholesterol absorption inhibitors like ezetimibe may also change the distribution and availability of cholesterol within cells, thereby affecting ORP-1's role in cholesterol homeostasis.

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