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H-6 is a discovery-stage small molecule inhibitor developed by Shifa Biomedical for the treatment of dyslipidemia. It targets Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) by binding to the protein's surface at the site where the Epidermal Growth Factor-like domain A (EGF(A)) of the Low-Density Lipoprotein Receptor (LDLR) typically attaches. By inhibiting the PCSK9-LDLR interaction, H-6 prevents the lysosomal degradation of LDLR, thereby increasing the density of LDLR on the surface of hepatocytes and facilitating the clearance of LDL cholesterol from the bloodstream.
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