Bafilomycin A1 prevents maturation of autophagic vacuoles by inhibiting fusion between autophagosomes and lysosomes in rat hepatoma cell line, H-4-II-E cells.
More Information Supplier PageLY 2183240 acts both as a potent inhibitor of the reuptake of the endocannabinoid anandamide, and as an inhibitor of fatty acid amide hydrolase (FAAH), the primary enzyme responsible for degrading anandamide.
More Information Supplier PageLY 2183240 acts both as a potent inhibitor of the reuptake of the endocannabinoid anandamide, and as an inhibitor of fatty acid amide hydrolase (FAAH), the primary enzyme responsible for degrading anandamide.
More Information Supplier PageLY 2183240 acts both as a potent inhibitor of the reuptake of the endocannabinoid anandamide, and as an inhibitor of fatty acid amide hydrolase (FAAH), the primary enzyme responsible for degrading anandamide.
More Information Supplier PageGW2580 is a small-molecule, ATP-competitive inhibitor of cFMS kinase.
More Information Supplier PageGW2580 is a small-molecule, ATP-competitive inhibitor of cFMS kinase.
More Information Supplier PageCI-994 is a histone deacetylase (HDAC) inhibitor and induces histone hyperacetylation in living cells.
More Information Supplier PageCI-994 is a histone deacetylase (HDAC) inhibitor and induces histone hyperacetylation in living cells.
More Information Supplier Page
