501-96-2 - Search Results | AbMole BioScience

About 5 results found for searched term "501-96-2" (0.274 seconds)

Cat.No.	Name	Target
M13552	CTX1	p53
	CTX1 is a p53 activator that overcomes HdmX-mediated p53 repression. CTX1 exhibits potent anti-cancer activity in a mouse acute myeloid leukemia (AML) model system.
M17174	(-)-Rhododendrol	Phenols
	(-)-Rhododendrol
M21409	FN-1501	CDK
	LT-171-861
	FN-1501 is a potent inhibitor of Fms-like receptor tyrosine kinase 3 (FLT3) and cyclin-dependent kinase (CDK), and the IC50 for CDK2/cyclin A, CDK4/cyclin D1, CDK6/cyclin D1 and FLT3 with IC50s of 2.47, 0.85, 1.96 and 0.28 nM, respectively.
M29780	BAY 2965501	DGK
	BAY 2965501 is a potent and selective diacylglycerol kinase zeta (DGKζ) inhibitor that enhances T cell initiation of suboptimal tumor antigens by inhibiting DGKζ. In addition, BAY 2965501 induces pERK activation.BAY 2965501 can be used in cancer research.
M45317	(S)-BAY 2965501	DGK
	(S)-BAY 2965501 is the left-handed isomer of BAY 2965501 (HY-153343).BAY 2965501 is a potent and selective diacylglycerol kinase zeta (DGKz) inhibitor and induces pERK activation. BAY 2965501 is a potent and selective inhibitor of diacylglycerol kinase zeta (DGKz) and induces pERK activation.