Bojarova, Pavla published the artcileAryl sulfamates are broad spectrum inactivators of sulfatases: Effects on sulfatases from various sources, Recommanded Product: Potassium 4-nitrophenyl sulfate, the publication is Bioorganic & Medicinal Chemistry Letters (2009), 19(2), 477-480, database is CAplus and MEDLINE.
Aryl sulfamates were originally developed as inhibitors of steroid sulfatase, and have recently been shown to be powerful inactivators of a bacterial sulfatase, PaAtsA from Pseudomonas aeruginosa. We demonstrate that a simple aryl sulfamate, 3-nitrophenyl sulfamate, can inactivate sulfatases from various sources including snail, limpet and abalone. In each case inactivation was time-dependent and active-site directed, as demonstrated by protection against inactivation by substrate. These results suggest that such easily acquired aryl sulfamates can be used as reliable biochem. reagents for the study of sulfatases from a diverse array of sources.
Bioorganic & Medicinal Chemistry Letters published new progress about 6217-68-1. 6217-68-1 belongs to esters-buliding-blocks, auxiliary class Salt,Nitro Compound,Sulfonate,Benzene, name is Potassium 4-nitrophenyl sulfate, and the molecular formula is C6H4KNO6S, Recommanded Product: Potassium 4-nitrophenyl sulfate.
Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics