PFK-158 is an inhibitor of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatases (PFK-2/FBPase) isoform 3 (PFKFB3) and derivative of 3-(3-pyridinyl)-1-[4-pyridinyl]-2-propen-1-one (3PO), with potential antineoplastic activity.
More Information Supplier PagePFK-158 is an inhibitor of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatases (PFK-2/FBPase) isoform 3 (PFKFB3) and derivative of 3-(3-pyridinyl)-1-[4-pyridinyl]-2-propen-1-one (3PO), with potential antineoplastic activity.
More Information Supplier PagePFK-158 is an inhibitor of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatases (PFK-2/FBPase) isoform 3 (PFKFB3) and derivative of 3-(3-pyridinyl)-1-[4-pyridinyl]-2-propen-1-one (3PO), with potential antineoplastic activity.
More Information Supplier PageIndoximod is a methylated tryptophan with anti-immunosuppressive activity.
More Information Supplier PageIndoximod is a methylated tryptophan with anti-immunosuppressive activity.
More Information Supplier PageCB-839 an is orally bioavailable inhibitor of glutaminase, with potential antineoplastic activity.
More Information Supplier PageCB-839 an is orally bioavailable inhibitor of glutaminase, with potential antineoplastic activity.
More Information Supplier PageCB-839 an is orally bioavailable inhibitor of glutaminase, with potential antineoplastic activity.
More Information Supplier PageAMG 232 is a highly potent, selective and orally bioavailable piperidinone inhibitor of the MDM2-p53 interaction((SPR KD= 0.045 nM, SJSA-1 EdU IC50=9.1 nM).
More Information Supplier PageSAR156497 is an exquisitely selective Aurora A, B, and C inhibitor with in vitro and in vivo efficacy with IC50 = 0.5 nM (Aurora A), 1 nM (Aurora B / incenp), 3 nM (Aurora C / incenp) respectively SAR156497 combines high in vitro potency with satisfactory metabolic stability and limited CYP 3A4 and PDE3 inhibition.
More Information Supplier Page
