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Penicillin biosynthesis: active site mapping with aminoadipoylcysteinylvaline variants
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1984
Year
Structural VariantsPenicillin BiosynthesisAntimicrobial ChemotherapyChemical BiologyPharmaceutical ChemistryDrug ResistanceMedicinal ChemistryBiosynthesisDiversity Oriented SynthesisAntimicrobial ResistanceBiochemistryDiversity-oriented SynthesisNatural Product SynthesisPharmacologyClinical MicrobiologyAntibioticsNatural SciencesAminoadipoly MoietyMicrobiologyNatural PrecursorMedicineSynthetic Chemistry
A series of structural variants on the aminoadipoly moiety of the natural precursor of penicillins, δ-(L-α-aminoadipoyl)-L-cysteinyl-D-valine, have been synthesised and their effectiveness as substrates for the enzyme isopenicillin N synthetase has been determined.