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Aromatic organic heterocyclic compounds that consist of a five-membered ring with four carbon atoms and one nitrogen atom that forms an amine functional group.
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Elbasvir (MK8742) is an NS5A inhibitor preventing hepatitis C viral RNA replication and virion assembly Median EC50 values range from 0 2 to 3600 pmol/L based on genotype
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Quisinostat (JNJ-26481585) 2HCl is a novel second-generation HDAC inhibitor with highest potency for HDAC1 with IC50 of 0 11 nM in a cell-free assay modest potent to HDACs 2 4 10 and 11 greater than 30-fold selectivity against HDACs 3 5 8 and 9 and lowest potency to HDACs 6 and 7 Phase 2
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Ac-YVAD-cmk (Caspase-1 Inhibitor II) is a selective IL-1β converting enzyme (ICE) inhibitor with neuroprotective and anti-inflammatory effects, effectively suppresses the expression of IL-1β and IL-18.
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Indoximod a methylated tryptophan acts as an IDO (indoleamine-(2 3)-dioxygenase) pathway inhibitor and reverses IDO-mediated immune suppression Phase 2 This product has poor solubility animal experiments are available cell experiments please choose carefully
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Atorvastatin Calcium is an inhibitor of HMG-CoA reductase used as a cholesterol-lowering medication that blocks the production of cholesterol Atorvastatin Calcium induces apoptosis and autophagy
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Bromoenol lactone((6E)-Bromoenol lactone) is a selective irreversible potent inhibitor of calcium-independent phospholipase A2 (iPLA2 ) with an IC50 value of 7 M It prevents antigen-stimulated exocytosis in mast cells without hindering Ca2 influx
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Atorvastatin Calcium is an inhibitor of HMG-CoA reductase used as a cholesterol-lowering medication that blocks the production of cholesterol Atorvastatin Calcium induces apoptosis and autophagy
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Sunitinib malate is a multi-targeted RTK inhibitor targeting VEGFR2 (Flk-1) and PDGFR with IC50 of 80 nM and 2 nM in cell-free assays and also inhibits c-Kit Sunitinib Malate effectively inhibits autophosphorylation of Ire1 Sunitinib Malate increases both death receptor and mitochondrial-dependent apoptosis
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