Journal of Chemistry · 2015 · 26 citations · 38 references
MedicineMedicinal ChemistryPharmacologyDrug DiscoveryStructure-activity RelationshipsSynthetic Medicinal ChemistryAntibacterial AgentsAntibacterial PharmacologyAntifungal AgentsAntimicrobial MetabolitesCandida Albicans InfectionMedicinal Chemistry ApplicationsNatural Antifungal CompoundsNew Antifungal AgentsNovel Antifungal Drug Development
A series of 2‐arylamino‐3‐chloro‐1,4‐naphthoquinone derivatives ( 3a – h ) by the reaction of 2,3‐dichloro‐1,4‐naphthoquinone with aryl amines ( 2a – h ) and benzo[ b ]phenazine‐6,11‐dione derivatives ( 4a – c ) by the treatment of 2‐arylamino‐3‐chloro‐1,4‐naphthoquinone derivatives ( 3a – h ) with sodium azide were synthesized and tested for their in vitro antibacterial and antifungal activities. The results suggest that compounds 3d and 3g had potent antifungal activity against Candida albicans (MIC = 78.12 μ g/mL). All synthesized compounds ( 3a – h , 4a – c ) possessed activity against E. faecalis with MIC values of between 312.5 and 1250 μ g/mL. Benzo[ b ]phenazine‐6,11‐dione derivatives ( 4a – c ) were mostly active against Gram‐positive bacteria. The structures of the new members of the series were established on the basis of their spectral properties (IR, 1 H NMR, 13 C NMR, and mass spectrometry).
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Journal of Molecular Structure
Christer B. Aakeröy · Journal of Chemical Crystallography · 1997 · 1.1K citations · Full text
Vishnu K. Tandon, Hardesh K. Maurya, Nripendra N. Mishra et al. · European Journal of Medicinal Chemistry · 2009 · 128 citations