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• W2095967387 abstract "A range of penicillins have been examined as competitive reversible inhibitors of enkephalinase (neutral endopeptidase; EC 3.4.24.11). Carfecillin (Ki = 0.18μM) was the most potent inhibitor in the series, whereas cloxacillin (27.5 μM), ampicillin (41.0 μM), nafcillin (58.7 μM) and carbenicillin (158 μM) had moderate potency and benzyl penicillin (885 μM), mezlocillin (473μM) and azlocillin (556 μM) were weak inhibitors. Structure-activity relationships within the series have been rationalised from a consideration of molecular graphics analysis of the match between receptor binding groups with thiorphan as well as log P values." @default.
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• W2095967387 date "1992-01-01" @default.
• W2095967387 modified "2023-09-27" @default.
• W2095967387 title "Novel Inhibitors of Enkephalin-Degrading Enzymes IV: Structure-Activity Relationships within the Penicillins as Enkephalinase Inhibitors" @default.
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• W2095967387 doi "https://doi.org/10.3109/14756369209040748" @default.
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