Publication | Open Access
Identification of a Potent Botulinum Neurotoxin A Protease Inhibitor Using in Situ Lead Identification Chemistry
113
Citations
13
References
2006
Year
ToxinologyLead IdentificationChemical BiologyPharmaceutical ChemistryMolecular PharmacologyMedicinal ChemistryMicrom Lead CompoundBioanalysisToxicologyProteomicsDisease BotulismInhibitory ActivityBiochemistryPharmacologyNatural SciencesRational Drug DesignDeadly FoodMedicineDrug Discovery
[reaction: see text] Botulinum neurotoxins (BoNTs), etiological agents of the deadly food poisoning disease botulism, are the most toxic proteins currently known. By using in situ lead identification chemistry, we have uncovered the first class of inhibitors that displays nanomolar potency. From a 15 microM lead compound, structure-activity relationship studies were performed granting the most potent BoNT/A inhibitor reported to date that displays an inhibition constant of 300 nM.
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