Laboratory of Molecular Biology, Istituto di Ricerche Farmacologiche Mario Negri IRCCS, via La Masa 19, 20157 Milano, Italy.
Expert Opin Drug Discov. 2013 Jun;8(6):641-54. doi: 10.1517/17460441.2013.788497. Epub 2013 Apr 9.
Aldehyde oxidases (AOXs) are molybdo-flavoenzymes that oxidize aromatic aldehydes into the corresponding carboxylic acids and heterocycles into hydroxylated derivatives. AOXs have broad substrate specificity and are present in the liver of humans and many experimental animals. These enzymes play an important role in Phase I metabolism of drugs and xenobiotics of toxicological interest.
Preclinical studies on the AOX-dependent metabolism of new drug candidates are problematic. Furthermore, there is a general lack of reliable in silico methodologies to predict whether a new organic molecule is an AOX substrate. In vitro systems, for the design of high- or medium-throughput screening tests, to identify AOX substrates have many limitations. In vivo studies on AOX-dependent metabolism in animal models, on the other hand, are difficult because the complement of liver AOXs in humans and popular experimental animals is different. The authors discuss the possible ways to overcome all these problems.
The significance of AOXs as drug-metabolizing enzymes is increasing, as the current strategies of organic synthesis designed to avoid cytochrome P450 (CYP450)-dependent metabolism tend to enrich for new chemical structures efficiently oxidized by these enzymes. There is need for reliable methods to screen for, predict, and validate AOX-dependent metabolism of new drug candidates.
醛氧化酶(AOX)是一种钼黄素酶,可将芳香醛氧化成相应的羧酸,将杂环化合物氧化成羟基衍生物。AOX 具有广泛的底物特异性,存在于人和许多实验动物的肝脏中。这些酶在药物和毒理学感兴趣的外源化学物的 I 相代谢中起着重要作用。
关于 AOX 依赖性新候选药物代谢的临床前研究存在问题。此外,通常缺乏可靠的计算方法来预测新的有机分子是否为 AOX 底物。用于设计高通量或中通量筛选测试以鉴定 AOX 底物的体外系统存在许多局限性。另一方面,由于人和流行的实验动物的肝脏 AOX 组成不同,动物模型中 AOX 依赖性代谢的体内研究也很困难。作者讨论了克服所有这些问题的可能方法。
作为药物代谢酶,AOX 的重要性正在增加,因为目前旨在避免细胞色素 P450(CYP450)依赖性代谢的有机合成策略往往会富集可被这些酶有效氧化的新化学结构。需要可靠的方法来筛选、预测和验证新候选药物的 AOX 依赖性代谢。