ABSTRACT
Protein kinases are hubs in oncogenic regulation that transmit messages of cell proliferation, survival, migration, and metastasis, and can hence be considered verified targets in cancerous treatment today. Nevertheless, the drawbacks of some of the already approved kinase inhibitors, like poor selectivity, dose-limiting toxicities, and resistance, remain to foster new scaffolds and ideal chemotypes. Oxazole is a privileged five-membered heteroaromatic ring comprised of nitrogen and oxygen that has found broad application in anticancer drug discovery due to its desirable electronic properties, drug-like nature and its ability to make key interactions with the kinase ATP-binding sites. We have reviewed in detail the recent advances in oxazoles and benzoxazole analogues that have been discovered as inhibitors of key cancer-relevant tyrosine kinases, such as VEGFR-2, EGFR, CDK2, MAPKs, and other receptor/non-receptor tyrosine-kinase targets. We also present synthetic strategies that are representative, a trend of structure-activity relationship (SAR), and molecular docking evidence that can be used to explain potency and selectivity, hinge bonding, and conserved residue binding that can be commonly seen in most targets. This review incorporates a combination of chemical design theory and biological performance by enumerating the role of oxazole-based hybrids and optimal patterns of replacement in enhancing antiproliferative action in various cancer cell entities. We conclude by finally highlighting areas of concern, as well as future opportunities of the translation of oxazole-derived kinase inhibitors, such as enhancing the selectivity of kinase activity, improving resistance to its activities, and enhancing the ADME/toxicity profiles, to clinically relevant anticancer candidates.
KEYWORDS: Cancer, Kinase protein, VEGFR inhibitors, EGFR inhibitors, CDK-2 inhibitors, MAP kinase inhibitors, RTKs inhibitors
2026 August -Bioorganic Chemistry
https://www.sciencedirect.com/science/article/pii/S0045206826005158