KC7F2 20mg | Purity Not Available
Selleck Chemicals
KC7F2 is a selective HIF-1α translation inhibitor with IC50 of 20 μM in a cell-based assay.
More Information Supplier PageKC7F2 is a selective HIF-1α translation inhibitor with IC50 of 20 μM in a cell-based assay.
More Information Supplier PageO4I2 is a potent Oct3/4 inducer, which is suitable for iPSC generation.
More Information Supplier PageBioymifi, a small-molecule death receptor 5 (DR5) agonist, binds to the extracellular domain(ECD) of DR5 with a Kd of 1.2 μM but showed little binding affinity to the DR4 ECD. It induces DR5 clustering and aggregation, leading to apoptosis.
More Information Supplier PageBioymifi, a small-molecule death receptor 5 (DR5) agonist, binds to the extracellular domain(ECD) of DR5 with a Kd of 1.2 μM but showed little binding affinity to the DR4 ECD. It induces DR5 clustering and aggregation, leading to apoptosis.
More Information Supplier PageNCT-501 is a potent and selective inhibitor of Aldehyde Dehydrogenase 1A1 (ALDH1A1) with IC50 of 40 nM.
More Information Supplier PageNCT-501 is a potent and selective inhibitor of Aldehyde Dehydrogenase 1A1 (ALDH1A1) with IC50 of 40 nM.
More Information Supplier PageMRT67307 is a potent and dual IKKϵ and TBK1 inhibitor with IC50 of 160 and 19 nM, respectively. MRT67307 potently inhibits ULK1 and ULK2 and blocks autophagy.
More Information Supplier PageBEC HCl is a slow-binding, and competitive arginase inhibitor with Ki of 0.31 μM (pH7.5) and 0.4-0.6 μM for Arginase II and rat Arginase I, respectively.
More Information Supplier PageBrdU (Bromodeoxyuridine) is a nucleoside analog that competes with thymidine for incorporation into DNA, and used in the detection of proliferating cells.
More Information Supplier Page