Publication | Closed Access
The Chemistry of Pseudomonic Acid. 15. Synthesis and Antibacterial Activity of a Series of 5-Alkyl, 5-Alkenyl, and 5-Heterosubstituted Oxazoles
50
Citations
11
References
1996
Year
Bioorganic Chemistry5-Heterosubstituted OxazolesAntibacterial ActivityNatural SciencesOrganic ChemistryPseudomonic AcidAntibacterial AgentSynthetic ChemistryAntimicrobial CompoundChemistryPharmacologyPharmaceutical ChemistryGreater Chain LengthAcid FunctionalityDrug Resistance
The synthesis of a range of 5-alkyl, 5-alkenyl, and 5-heterosubstituted 2-(1-normon-2-yl) oxazoles is described. The antibacterial activity was determined as the minimum inhibitory concentration against a range of Gram-positive and Gram-negative organisms using a standard Agar dilution procedure. Compounds possessing an acid functionality directly on, or close to, the ring were found to be of greatly decreased potency, while increasing lipophilicity with greater chain length led to increased potency of these derivatives.
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