Metabolism by aldehyde oxidase: drug design and complementary approaches to challenges in drug discovery

N Manevski, L King, WR Pitt, F Lecomte… - Journal of Medicinal …, 2019 - ACS Publications
Aldehyde oxidase (AO) catalyzes oxidations of azaheterocycles and aldehydes, amide
hydrolysis, and diverse reductions. AO substrates are rare among marketed drugs, and …

Targeting MET: discovery of small molecule inhibitors as non-small cell lung cancer therapy

C Wang, X Lu - Journal of Medicinal Chemistry, 2023 - ACS Publications
MET has been considered as a promising drug target for the treatment of MET-dependent
diseases, particularly non-small cell lung cancer (NSCLC). Small molecule MET inhibitors …

[HTML][HTML] Anticancer activities of tetra-, penta-, and hexacyclic phenothiazines modified with quinoline moiety.

M Jeleń, B Morak-Młodawska, R Korlacki - Journal of Molecular Structure, 2023 - Elsevier
The quinoline molecule is a chemical motif showing a highly promising pharmacological
potential. Its numerous derivatives introduced into medicine revolutionized in the treatment …

High Affinity and FAP-Targeted Radiotracers: A Potential Design Strategy to Improve the Pharmacokinetics and Tumor Uptake for FAP Inhibitors

Y Wang, H Yuan, N Liu, S Tang, Y Feng… - Journal of Medicinal …, 2023 - ACS Publications
Fibroblast activation protein (FAP) is overexpressed in cancer-associated fibroblasts,
making it an attractive target for both imaging and therapy of malignancy. This study …

Roles of selected non-P450 human oxidoreductase enzymes in protective and toxic effects of chemicals: review and compilation of reactions

SP Rendić, RD Crouch, FP Guengerich - Archives of Toxicology, 2022 - Springer
This is an overview of the metabolic reactions of drugs, natural products, physiological
compounds, and other (general) chemicals catalyzed by flavin monooxygenase (FMO) …

Applications of artificial intelligence in drug design: opportunities and challenges

M Thomas, A Boardman, M Garcia-Ortegon… - Artificial Intelligence in …, 2022 - Springer
Artificial intelligence (AI) has undergone rapid development in recent years and has been
successfully applied to real-world problems such as drug design. In this chapter, we review …

Quinoline-based molecules targeting c-Met, EGF, and VEGF receptors and the proteins involved in related carcinogenic pathways

A Martorana, G La Monica, A Lauria - Molecules, 2020 - mdpi.com
The quinoline ring system has long been known as a versatile nucleus in the design and
synthesis of biologically active compounds. Currently, more than one hundred quinoline …

Unlocking c-MET: A comprehensive journey into targeted therapies for breast cancer

PJ Kaboli, HF Chen, A Babaeizad, KR Geraylow… - Cancer Letters, 2024 - Elsevier
Breast cancer is the most common malignancy among women, posing a formidable health
challenge worldwide. In this complex landscape, the c-MET (cellular-mesenchymal …

Aldehyde oxidase mediated drug metabolism: an underpredicted obstacle in drug discovery and development

SNR Gajula, TN Nathani, RM Patil… - Drug Metabolism …, 2022 - Taylor & Francis
Aldehyde oxidase (AO) has garnered curiosity as a non-CYP metabolizing enzyme in drug
development due to unexpected consequences such as toxic metabolite generation and …

The drug-drug interaction between erlotinib and OSI-930 is mediated through aldehyde oxidase inhibition

LWT Tang, Y Shi, R Sharma, RS Obach - Drug Metabolism and Disposition, 2024 - Elsevier
The propensity for aldehyde oxidase (AO) substrates to be implicated in drug-drug
interactions (DDIs) is not well understood due to the dearth of potent inhibitors that elicit in …