Add to ORKGQM/MM modelling of FAAH inactivation by O-biphenyl-3-yl carbamates identifies the deprotonation of Ser241 as the key reaction step, explaining why FAAH is insensitive to the electron-donor effect of conjugated substituents; this may aid design of new inhibitors with improved selectivity and in vivo potency
Fatty acid amide hydrolase (FAAH), a promising target for the treatment of several central and perip...
Fatty acid amide hydrolase (FAAH) is an enzyme responsible for the deactivating hydrolysis of fatty ...
Fatty acid amide hydrolase (FAAH), a promising target for the treatment of several central and perip...
QM/MM modelling of FAAH inactivation by O-biphenyl-3-yl carbamates identifies the deprotonation of S...
Modelling of the mechanism of covalent adduct formation by the inhibitor O-arylcarbamate URB524 in F...
Modelling of the mechanism of covalent adduct formation by the inhibitor O-arylcarbamate URB524 in F...
Carbamate and urea derivatives are important classes of fatty acid amide hydrolase (FAAH) inhibitors...
Carbamate and urea derivatives are important classes of fatty acid amide hydrolase (FAAH) inhibitors...
Modelling of the mechanism of covalent adduct formation by the inhibitor O-arylcarbamate URB524 in F...
FAAH (fatty acid amide hydrolase) is a promising target for the treatment of several central nervous...
Carbamate and urea derivatives are important classes of fatty acid amide hydrolase (FAAH) inhibitors...
Fatty acid amide hydrolase (FAAH) is a member of the amidase signature family and is responsible for...
Cyclohexylcarbamic acid aryl esters are a class of fatty acid amide hydrolase (FAAH) inhibitors, whi...
Cyclohexylcarbamic acid aryl esters are a class of fatty acid amide hydrolase (FAAH) inhibitors, whi...
Cyclohexylcarbamic acid aryl esters are a class of fatty acid amide hydrolase (FAAH) inhibitors, whi...
Fatty acid amide hydrolase (FAAH), a promising target for the treatment of several central and perip...
Fatty acid amide hydrolase (FAAH) is an enzyme responsible for the deactivating hydrolysis of fatty ...
Fatty acid amide hydrolase (FAAH), a promising target for the treatment of several central and perip...
QM/MM modelling of FAAH inactivation by O-biphenyl-3-yl carbamates identifies the deprotonation of S...
Modelling of the mechanism of covalent adduct formation by the inhibitor O-arylcarbamate URB524 in F...
Modelling of the mechanism of covalent adduct formation by the inhibitor O-arylcarbamate URB524 in F...
Carbamate and urea derivatives are important classes of fatty acid amide hydrolase (FAAH) inhibitors...
Carbamate and urea derivatives are important classes of fatty acid amide hydrolase (FAAH) inhibitors...
Modelling of the mechanism of covalent adduct formation by the inhibitor O-arylcarbamate URB524 in F...
FAAH (fatty acid amide hydrolase) is a promising target for the treatment of several central nervous...
Carbamate and urea derivatives are important classes of fatty acid amide hydrolase (FAAH) inhibitors...
Fatty acid amide hydrolase (FAAH) is a member of the amidase signature family and is responsible for...
Cyclohexylcarbamic acid aryl esters are a class of fatty acid amide hydrolase (FAAH) inhibitors, whi...
Cyclohexylcarbamic acid aryl esters are a class of fatty acid amide hydrolase (FAAH) inhibitors, whi...
Cyclohexylcarbamic acid aryl esters are a class of fatty acid amide hydrolase (FAAH) inhibitors, whi...
Fatty acid amide hydrolase (FAAH), a promising target for the treatment of several central and perip...
Fatty acid amide hydrolase (FAAH) is an enzyme responsible for the deactivating hydrolysis of fatty ...
Fatty acid amide hydrolase (FAAH), a promising target for the treatment of several central and perip...