Journal of Medicinal Chemistry · 1998 · 28 citations · 11 references
PharmacyMedicinal ChemistryMicrobiologyAntimicrobial PharmacologyAntimicrobial ResistanceStructure-activity RelationshipsQuantitative Structure-activity RelationshipsStructure-activity Relationship AnalysisCapacity Factor EstimationLipophilicity PredictionLipophilicity RelationshipsMolecular Property-based DesignPartition Coefficient PredictionPartition Coefficient RelationshipsQuaternary Ammonium CompoundsSubstituent Effects On Lipophilicity
A new class of antimicrobial, "soft", quaternary ammonium l-carnitine esters, of the type (CH3)3N+-CH2-CHOCO(R1)-CH2-COO(R2) Cl-, has been designed, with R1 and R2 being in general long-chain alkyl substituents. The series shows good activity against a wide range of bacteria, yeasts, and fungi. Lipophilicity has been measured by RP-HPLC method to give the logarithm of the experimental capacity factor (log k'), and a quantitative relationship has been determined between log k' and the theoretical partition coefficient (CLOGP); also, bond-dipole descriptors have been introduced into calculations by accounting for polar moieties present within the apolar cores of the molecules, giving a more refined calculated capacity factor (log k'calcd). Finally the latter has been related to the antimicrobial activity (MIC values). The proposed models are predictive for the best broad-spectrum antimicrobial compound within the series.
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Comprehensive Medicinal Chemistry
Quantitative Structure-Activity Relationships · 1991 · 749 citations
Soft drugs. 3. A new class of anticholinergic agents
Nicholas Bodor, Ross Woods, C. Raper et al. · Journal of Medicinal Chemistry · 1980 · 67 citations