Enzyme inhibitors and enzyme substrates

α-Naphthyl Acid Phosphate, Monosodium Salt, a product of kinase-mediated phosphorylation of 1-naphthol in the cell, is recognized as an alkaline, acid, and protein phosphatase inhibitor. This compound has also been shown to dephosphorylate the

α-Naphthyl Acid Phosphate, Monosodium Salt, a product of kinase-mediated phosphorylation of 1-naphthol in the cell, is recognized as an alkaline, acid, and protein phosphatase inhibitor. This compound has also been shown to dephosphorylate the

2-((2-(Bis(4-methoxyphenyl)(phenyl)methoxy)ethyl)(phenyl)amino)ethan-1-ol (DMTr-N-phenyldiethanolamine).

2-amino-2-methylpropane-1,3-diol,(5-bromo-4-chloro-1H-indol-3-yl)phosphonic acid.

Product description：SU3327 is a potent, selective and substrate-competitive JNK inhibitor with an IC50 of 0.7 μM. SU3327 also inhibits protein-protein interactions between JNK and JNK Interacting Protein (JIP) with an IC50 of 239 nM. SU3327 shows

Product description：SU3327 is a potent, selective and substrate-competitive JNK inhibitor with an IC50 of 0.7 μM. SU3327 also inhibits protein-protein interactions between JNK and JNK Interacting Protein (JIP) with an IC50 of 239 nM. SU3327 shows

Product description：SU3327 is a potent, selective and substrate-competitive JNK inhibitor with an IC50 of 0.7 μM. SU3327 also inhibits protein-protein interactions between JNK and JNK Interacting Protein (JIP) with an IC50 of 239 nM. SU3327 shows

Product description：SU3327 is a potent, selective and substrate-competitive JNK inhibitor with an IC50 of 0.7 μM. SU3327 also inhibits protein-protein interactions between JNK and JNK Interacting Protein (JIP) with an IC50 of 239 nM. SU3327 shows

2-Ethyl-3-hydroxy-6-methylpyridine.

2-Ethyl-3-hydroxy-6-methylpyridine.

2-Ethyl-3-hydroxy-6-methylpyridine.

2-Methoxy-5-methyl-4-(4-methyl-2-nitro-phenylazo)-phenylamine.