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J Med Chem ; 45(11): 2185-96, 2002 May 23.
Article in English | MEDLINE | ID: mdl-12014956

ABSTRACT

We report the inhibition of a human recombinant geranylgeranyl diphosphate synthase (GGPPSase) by 23 bisphosphonates and six azaprenyl diphosphates. The IC50 values range from 140 nM to 690 microM. None of the nitrogen-containing bisphosphonates that inhibit farnesyl diphosphate synthase were effective in inhibiting the GGPPSase enzyme. Using three-dimensional quantitative structure-activity relationship/comparative molecular field analysis (CoMFA) methods, we find a good correlation between experimental and predicted activity: R2 = 0.938, R(cv)2 = 0.900, R(bs)2 = 0.938, and F-test = 86.8. To test the predictive utility of the CoMFA approach, we used three training sets of 25 compounds each to generate models to predict three test sets of three compounds. The rms pIC50 error for the nine predictions was 0.39. We also investigated the pharmacophore of these GGPPSase inhibitors using the Catalyst method. The results demonstrated that Catalyst predicted the pIC50 values for the nine test set compounds with an rms error of 0.28 (R2 between experimental and predicted activity of 0.948).


Subject(s)
Alkyl and Aryl Transferases/antagonists & inhibitors , Diphosphonates/chemical synthesis , Enzyme Inhibitors/chemical synthesis , Organophosphates/chemical synthesis , Alkyl and Aryl Transferases/chemistry , Antiparasitic Agents/chemical synthesis , Antiparasitic Agents/chemistry , Bone Resorption/drug therapy , Diphosphonates/chemistry , Enzyme Inhibitors/chemistry , Farnesyltranstransferase , Humans , Models, Molecular , Organophosphates/chemistry , Quantitative Structure-Activity Relationship , Recombinant Proteins/antagonists & inhibitors , Recombinant Proteins/chemistry
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