Isolation of a Major Metabolite (i-OHAP) of Aprindine and Its Identification as N-(3-(N,N-Diethylamino)propyl)-N-phenyl-2-aminoindan-5-ol.

Cytochromes P450 (CYPs) are a superfamily of enzymes that metabolize the majority of xenobiotics in humans. This review presents a structure-based outline of CYP-catalyzed biotransformations of selected substrates, representing diverse structural classes of chemicals, ranging from drugs to toxicants. Data are presented in a tabular format for easy reference, with visual representations of all substrates and sites-of-attack. The major metabolites, isozymes responsible, chemical classification, and other information related to the biotransformation are provided. Pharmacophores proposed for the major CYP isozymes are discussed. This visual combination of substrates and biotransformation sites can serve as a useful reference for researchers.

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Isolation of a Major Metabolite (i-OHAP) of Aprindine and Its Identification as N-(3-(N,N-Diethylamino)propyl)-N-phenyl-2-aminoindan-5-ol.

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Synthesis and asymmetric resolution of a dopaminergic compound: 2-amino-5-methoxyindane

Synthesis and asymmetric resolution of a dopaminergic compound: 2-amino-5-methoxyindane

Chiral bioanalysis

Cytochromes P450: A Structure-Based Summary of Biotransformations Using Representative Substrates

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