A photoreversible covalent inhibitor of PTPs; binds the catalytic domain of SHP-1 (Ki = 184 μM) and covalently reacts with free thiols, a reaction that is reversible with irradiation (350 nm)
Size
10 mg
Concentration
n/a
Applications
n/a
Other Names
Protein Tyrosine Phosphatase Inhibitor III|α-Bromo-4-(carboxymethoxy)acetophenone