Medicinal chemistry approaches to avoid aldehyde oxidase metabolism |
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Authors: | Pryde David C Tran Thien-Duc Jones Peter Duckworth Jonathan Howard Martin Gardner Iain Hyland Ruth Webster Rob Wenham Tracey Bagal Sharan Omoto Kiyoyuki Schneider Richard P Lin Jian |
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Affiliation: | Worldwide Medicinal Chemistry, Dynamics and Metabolism, Pfizer Global Research and Development, Sandwich Laboratories, Sandwich, Kent, UK. David.Pryde@pfizer.com |
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Abstract: | ![]() Aldehyde oxidase (AO) is a molybdenum-containing enzyme distributed throughout the animal kingdom and capable of metabolising a wide range of aldehydes and N-heterocyclic compounds. Although metabolism by this enzyme in man is recognised to have significant clinical impact where human AO activity was not predicted by screening in preclinical species, there is very little reported literature offering real examples where drug discoverers have successfully designed away from AO oxidation. This article reports on some strategies adopted in the Pfizer TLR7 agonist programme to successfully switch off AO metabolism that was seen principally in the rat. |
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