spacer Human dCK C4S-S74E mutant in complex with UDP and the DI-43 inhibitor
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Title Development of new deoxycytidine kinase inhibitors and noninvasive in vivo evaluation using positron emission tomography.
Authors Murphy, J.M.search; Armijo, A.L.search; Nomme, J.search; Lee, C.H.search; Smith, Q.A.search; Li, Z.search; Campbell, D.O.search; Liao, H.I.search; Nathanson, D.A.search; Austin, W.R.search; Lee, J.T.search; Darvish, R.search; Wei, L.search; Wang, J.search; Su, Y.search; Damoiseaux, R.search; Sadeghi, S.search; Phelps, M.E.search; Herschman, H.R.search; Czernin, J.search; Alexandrova, A.N.search; Jung, M.E.search; Lavie, A.search; Radu, C.G.search
Journal J.MED.CHEM.search vol:56, pag:6696-6708 (2013), Identifiers: PubMed ID (23947754)search DOI (10.1021/jm400457y)
Abstract Combined inhibition of ribonucleotide reductase and deoxycytidine kinase (dCK) in multiple cancer cell lines depletes deoxycytidine triphosphate pools leading to DNA replication stress, cell cycle arrest, and apoptosis. Evidence implicating dCK in cancer cell proliferation and survival stimulated our interest in developing small molecule dCK inhibitors. Following a high throughput screen of a diverse chemical library, a structure-activity relationship study was carried out. Positron Emission Tomography (PET) using (18)F-L-1-(2'-deoxy-2'-FluoroArabinofuranosyl) Cytosine ((18)F-L-FAC), a dCK-specific substrate, was used to rapidly rank lead compounds based on their ability to inhibit dCK activity in vivo. Evaluation of a subset of the most potent compounds in cell culture (IC50 = ∼1-12 nM) using the (18)F-L-FAC PET pharmacodynamic assay identified compounds demonstrating superior in vivo efficacy.
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Other entries described in this publication 4jlk
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