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Compound 4d is a novel small molecule thiazoloquinoxaline derivative containing a sulfapyridine moiety, developed by researchers at the Egyptian Atomic Energy Authority as a targeted therapy for hepatocellular carcinoma (HCC). It functions as a potent inhibitor of Vascular Endothelial Growth Factor Receptor 2 (VEGFR-2), a critical receptor involved in tumor angiogenesis and progression. In preclinical studies, compound 4d demonstrated significant cytocidal activity against HepG2 liver cancer cells and effectively suppressed hepatic VEGF expression in vivo. A key advantage of this compound is its improved safety profile compared to the standard-of-care multi-kinase inhibitor sorafenib; it exhibits significantly lower cardiotoxicity, as evidenced by its reduced impact on myocardium cells and the maintenance of normal cardiac enzyme functions in animal models.
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