Fostamatinib (R788) disodium hexahydrate is the oral prodrug of the active compound R406.
Cediranib maleate (AZD-2171 maleate) is a highly potent, orally available VEGFR inhibitor with IC50s of
Cediranib maleate (AZD-2171 maleate) is a highly potent, orally available VEGFR inhibitor with IC50s of
Harringtonolide is a potent RACK1 inhibitor (IC50=39.66 μM in A375 cells). Harringtonolide inhibits the epithelial-mesenchymal transition (EMT) process and cell proliferation by affecting the interaction between FAK and RACK1.
Harringtonolide is a potent RACK1 inhibitor (IC50=39.66 μM in A375 cells). Harringtonolide inhibits the epithelial-mesenchymal transition (EMT) process and cell proliferation by affecting the interaction between FAK and RACK1.
Higenamine is a β2-AR agonist, used in the research of heart failure. Higenamine (Norcoclaurine) has anti-apoptotic effects.
Higenamine is a β2-AR agonist, used in the research of heart failure. Higenamine (Norcoclaurine) has anti-apoptotic effects.
Sultamicillin Tosylate is a semi-synthetic β-lactamase inhibitor with an IC50 of 0.8 μM.
Ceftiofur is a semisynthetic, beta-lactamase-stable, broad-spectrum cephalosporin with antibacterial activity.
WAY-297674 is a protein kinase (CK2) inhibitor (IC50=8.6 µM). It can be used in studies related to cancer, viral infections, and glomerulonephritis.