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Ukr Biokhim Zh (1999) ; 83(1): 30-7, 2011.
Article in Russian | MEDLINE | ID: mdl-21800646

ABSTRACT

A series of 5-amino-1H-pyrazoles was synthesized and studied as inhibitors of furin. The most potent compound, 5-amino-4-acetylamino-3-(4-methylphenylamino)1H-pyrazole, was found to retard the activity of furin by mixed-type inhibition with K = 288 microM. These findings permit to plan new ways for chemical modifications of the 5-amino-1H-pyrazole structure and design more potent furin inhibitors of non-peptide nature.


Subject(s)
Enzyme Inhibitors/chemical synthesis , Furin/antagonists & inhibitors , Pyrazoles/chemical synthesis , Enzyme Inhibitors/chemistry , Enzyme Inhibitors/pharmacology , Furin/chemistry , Molecular Structure , Pyrazoles/chemistry , Pyrazoles/pharmacology , Structure-Activity Relationship
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