Approaches for Designing new Potent Inhibitors of Farnesyl Pyrophosphate Synthase.
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Essential multimeric enzymes in kinetoplastid parasites: A host of potentially druggable protein-protein interactions.Detection and treatment of Trypanosoma cruzi: a patent review (2011-2015).Activity of Fluorine-Containing Analogues of WC-9 and Structurally Related Analogues against Two Intracellular Parasites: Trypanosoma cruzi and Toxoplasma gondii.α-Methylation enhances the potency of isoprenoid triazole bisphosphonates as geranylgeranyl diphosphate synthase inhibitors.Tetrazine Click Chemistry for the Modification of 1-Hydroxy-1,1-methylenebisphosphonic Acids: Towards Bio-orthogonal Functionalization of Gold Nanoparticles.Versatile “click” synthesis of 1-hydroxy-1,1-methylenebisphosphonic acids with thioalkoxy substituents for the preparation of stable gold nanoparticles
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Approaches for Designing new Potent Inhibitors of Farnesyl Pyrophosphate Synthase.
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Approaches for Designing new Potent Inhibitors of Farnesyl Pyrophosphate Synthase.
@en
type
label
Approaches for Designing new Potent Inhibitors of Farnesyl Pyrophosphate Synthase.
@en
prefLabel
Approaches for Designing new Potent Inhibitors of Farnesyl Pyrophosphate Synthase.
@en
P2860
P1476
Approaches for Designing new Potent Inhibitors of Farnesyl Pyrophosphate Synthase.
@en
P2093
Bruno N Falcone
P2860
P304
P356
10.1517/17460441.2016.1143814
P407
P577
2016-01-18T00:00:00Z