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Medicinal chemistry approaches to avoid aldehyde oxidase metabolism
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
Affiliation:Worldwide Medicinal Chemistry, Dynamics and Metabolism, Pfizer Global Research and Development, Sandwich Laboratories, Sandwich, Kent, UK. David.Pryde@pfizer.com
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.
Keywords:
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