| Literature DB >> 15544793 |
Filippo Minutolo1, Michela Antonello, Silvia Barontini, Simone Bertini, Laura Betti, Romano Danesi, Gianbattista Gervasi, Gino Giannaccini, Chiara Papi, Giorgio Placanica, Simona Rapposelli, Marco Macchia.
Abstract
The diphosphate moiety of geranylgeranyldiphosphate (GGdP) was replaced with metabolically and hydrolytically stable analogous polar portions, in an attempt to obtain new geranylgeranyltransferase (GGTase) inhibitors, which could also be selective over congener enzyme farnesyltransferase (FTase). In particular, the phosphonomethylphosphorylmethoxy derivative showed the highest inhibition potency, accompanied by a satisfactory GGTase/FTase selectivity.Entities:
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Year: 2004 PMID: 15544793 DOI: 10.1016/j.farmac.2004.08.002
Source DB: PubMed Journal: Farmaco ISSN: 0014-827X