BMS-1 25mg | Purity Not Available
Selleck Chemicals
BMS-1 is a small-molecule inhibitor of PD-1/PD-L1 interaction with IC50 of 6 nM.
More Information Supplier PageBMS-1 is a small-molecule inhibitor of PD-1/PD-L1 interaction with IC50 of 6 nM.
More Information Supplier PageBMS-1 is a small-molecule inhibitor of PD-1/PD-L1 interaction with IC50 of 6 nM.
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 PageDEL-22379 is a water-soluble ERK dimerization inhibitor with IC50 of ∼0.5 μM.
More Information Supplier PageTiplaxtinin(PAI-039) is an orally efficacious and selective plasminogen activator inhibitor-1 (PAI-1) inhibitor with IC50 of 2.7 μM.
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 PageDASA-58 is a specific and potent Pyruvate kinase M2 (PKM2) activator.
More Information Supplier PageDASA-58 is a specific and potent Pyruvate kinase M2 (PKM2) activator.
More Information Supplier PageWZB117 is an inhibitor of Glucose Transporter 1 (GLUT1). It inhibited cell proliferation in lung cancer A549 cells and breast cancer MCF7 cells with an IC50 of approximately 10 μM.
More Information Supplier PageWZB117 is an inhibitor of Glucose Transporter 1 (GLUT1). It inhibited cell proliferation in lung cancer A549 cells and breast cancer MCF7 cells with an IC50 of approximately 10 μM.
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