Discovery of Benzo[d]isoxazol-3-amine

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Reference of 36216-80-5, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about Reference of 36216-80-5

Reference of 36216-80-5, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.36216-80-5, Name is Benzo[d]isoxazol-3-amine, molecular formula is C7H6N2O. In a Article£¬once mentioned of 36216-80-5

Heteroaryl urea inhibitors of fatty acid amide hydrolase: Structure-mutagenicity relationships for arylamine metabolites

The structure-activity relationships for a series of heteroaryl urea inhibitors of fatty acid amide hydrolase (FAAH) are described. Members of this class of inhibitors have been shown to inactivate FAAH by covalent modification of an active site serine with subsequent release of an aromatic amine from the urea electrophile. Systematic Ames II testing guided the optimization of urea substituents by defining the structure-mutagenicity relationships for the released aromatic amine metabolites. Potent FAAH inhibitors were identified having heteroaryl amine leaving groups that were non-mutagenic in the Ames II assay.

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Reference of 36216-80-5, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about Reference of 36216-80-5

Reference£º
Benzisoxazole – Wikipedia,
Benzisoxazole – an overview | ScienceDirect Topics