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Future Microbiol ; 14: 235-245, 2019 02.
Article in English | MEDLINE | ID: mdl-30663901

ABSTRACT

AIM: Novel 4-methoxy-naphthalene derivatives were synthesized based on hits structures in order to evaluate the antifungal activity against Paracoccidioides spp. METHODS: Antifungal activity of compounds was evaluated against P. brasiliensis and most promising compounds 2 and 3 were tested against eight clinically important fungal species. RESULTS: Compound 3 was the more active compound with MIC 8 to 32 µg.ml-1 for Paracoccidioides spp without toxicity monkey kidney and murine macrophagecells. Carbohydrazide 3 showed good synergistic antifungal activity with amphotericin B against P. brasiliensis specie. Titration assay of carbohydrazide 3 with PbHSD enzyme demonstrates the binding ligand-protein. Molecular dynamics simulations show that ligand 3 let the PbHSD protein more stable. CONCLUSION: New carbohydrazide 3 is an attractive lead for drug development to treat paracoccidioidomycoses.


Subject(s)
Antifungal Agents/pharmacology , Naphthalenes/pharmacology , Paracoccidioides/drug effects , Paracoccidioidomycosis/drug therapy , Amphotericin B/pharmacology , Animals , Antifungal Agents/therapeutic use , Chlorocebus aethiops , Drug Combinations , Drug Synergism , Homoserine Dehydrogenase/metabolism , Hydrazines/pharmacology , Macrophages/drug effects , Mice , Microbial Sensitivity Tests , Molecular Dynamics Simulation , Naphthalenes/chemical synthesis , Naphthalenes/therapeutic use , Paracoccidioides/pathogenicity , Protein Stability , Vero Cells/drug effects
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