| Literature DB >> 24900455 |
Amy B Dounay1, Marie Anderson1, Bruce M Bechle1, Brian M Campbell1, Michelle M Claffey1, Artem Evdokimov1, Edelweiss Evrard1, Kari R Fonseca1, Xinmin Gan1, Somraj Ghosh1, Matthew M Hayward1, Weldon Horner1, Ji-Young Kim1, Laura A McAllister1, Jayvardhan Pandit1, Vanessa Paradis1, Vinod D Parikh1, Matthew R Reese1, SuoBao Rong1, Michelle A Salafia1, Katherine Schuyten1, Christine A Strick1, Jamison B Tuttle1, James Valentine1, Hong Wang1, Laura E Zawadzke1, Patrick R Verhoest1.
Abstract
Kynurenine aminotransferase (KAT) II has been identified as a potential new target for the treatment of cognitive impairment associated with schizophrenia and other psychiatric disorders. Following a high-throughput screen, cyclic hydroxamic acid PF-04859989 was identified as a potent and selective inhibitor of human and rat KAT II. An X-ray crystal structure and (13)C NMR studies of PF-04859989 bound to KAT II have demonstrated that this compound forms a covalent adduct with the enzyme cofactor, pyridoxal phosphate (PLP), in the active site. In vivo pharmacokinetic and efficacy studies in rat show that PF-04859989 is a brain-penetrant, irreversible inhibitor and is capable of reducing brain kynurenic acid by 50% at a dose of 10 mg/kg (sc). Preliminary structure-activity relationship investigations have been completed and have identified the positions on this scaffold best suited to modification for further optimization of this novel series of KAT II inhibitors.Entities:
Keywords: KAT II; hydroxamic acid; kynurenic acid; kynurenine aminotransferase
Year: 2012 PMID: 24900455 PMCID: PMC4025856 DOI: 10.1021/ml200204m
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345