Triazoles in medicinal chemistry: physicochemical properties, bioisosterism, and application

Q Guan, S **ng, L Wang, J Zhu, C Guo… - Journal of Medicinal …, 2024‏ - ACS Publications
Triazole demonstrates distinctive physicochemical properties, characterized by weak
basicity, various dipole moments, and significant dual hydrogen bond acceptor and donor …

Biotransformation reactions of five-membered aromatic heterocyclic rings

DK Dalvie, AS Kalgutkar… - Chemical research in …, 2002‏ - ACS Publications
Organic compounds containing five-membered aromatic heterocyclic rings are widely
distributed in nature and often play an important role in various biochemical processes …

Cytochromes P450 for engineering herbicide tolerance

D Werck-Reichhart, A Hehn, L Didierjean - Trends in plant science, 2000‏ - cell.com
In recent years, genome sequencing has revealed that cytochromes P450 (P450s) constitute
the largest family of enzymatic proteins in higher plants. P450s are mono-oxygenases that …

The conduct of in vitro studies to address time-dependent inhibition of drug-metabolizing enzymes: a perspective of the pharmaceutical research and manufacturers of …

SW Grimm, HJ Einolf, SD Hall, K He, HK Lim… - Drug Metabolism and …, 2009‏ - Elsevier
Time-dependent inhibition (TDI) of cytochrome P450 (P450) enzymes caused by new
molecular entities (NMEs) is of concern because such compounds can be responsible for …

Biodegradation of the gasoline oxygenates methyl tert-butyl ether, ethyl tert-butyl ether, and tert-amyl methyl ether by propane-oxidizing bacteria

RJ Steffan, K McClay, S Vainberg… - Applied and …, 1997‏ - journals.asm.org
Several propane-oxidizing bacteria were tested for their ability to degrade gasoline
oxygenates, including methyl tert-butyl ether (MTBE), ethyl tert-butyl ether (ETBE), and tert …

Mechanism-based inactivation (MBI) of cytochrome P450 enzymes: structure–activity relationships and discovery strategies to mitigate drug–drug interaction risks

STM Orr, SL Ripp, TE Ballard… - Journal of medicinal …, 2012‏ - ACS Publications
1. INTRODUCTION Cytochrome P450s (CYPs) constitute a superfamily of hemecontaining
enzymes that catalyze the oxidative metabolism of structurally diverse molecules including …

Flavin-containing monooxygenases: catalytic mechanism and substrate specificities

DM Ziegler - Drug metabolism reviews, 1988‏ - Taylor & Francis
Studies from several laboratories over the past two decades have shown that mammalian
tissues contain a flavoprotein that catalyzes NADPH-and oxygendependent oxidation of a …

Role of 20-hydroxyeicosatetraenoic acid (20-HETE) in vascular system

N Miyata, RJ Roman - Journal of Smooth Muscle Research, 2005‏ - jstage.jst.go.jp
Abstract Cytochrome P450s (P450) metabolize arachidonic acid (AA) to
hydroxyeicosatetraenoic acids (HETEs) and epoxyeicosatrienoic acids (EETs). Among these …

Enzymatic activation of chemicals to toxic metabolites

FP Guengerich, DC Liebler, DL Reed - CRC Critical Reviews in …, 1985‏ - Taylor & Francis
In the 1940s and 1950s the hypothesis first developed that many drugs, industrial chemicals,
pesticides, pollutants, and other materials are not toxic per se but elicit their effects only after …

Mechanism-based inactivation of cytochrome P450 enzymes: chemical mechanisms, structure-activity relationships and relationship to clinical drug-drug interactions …

AS Kalgutkar, RS Obach, TS Maurer - Current drug metabolism, 2007‏ - ingentaconnect.com
Cytochrome P450 constitute a superfamily of heme-containing enzymes that catalyze the
oxidative biotransformation of structurally diverse xenobiotics including drugs. Inhibition of …