2026-04-17T18:54:54Zhttps://recercat.cat/oai/request

oai:recercat.cat:2445/2180572025-12-04T21:15:50Zcom_2072_1057col_2072_478781col_2072_478917

00925njm 22002777a 4500 dc S. P. Moura, Sara P. author Marín Martínez, Silvia author Rufino, Ismael author Guedes, Rita C. author Cascante i Serratosa, Marta author Salvador, Jorge A. R. author 2025-01-28T12:45:30Z 2025-01-28T12:45:30Z 2024-12-12 2025-01-28T12:45:30Z A series of novel carnosic acid 1 derivatives incorporating urea moieties at the C-20 position was synthesized and evaluated for their antiproliferative activity against the HCT116 colorectal cancer cell line. Most derivatives demonstrated enhanced antiproliferative activity compared to that of carnosic acid 1. The most promising derivatives were tested in other colorectal cancer cell lines (SW480, SW620, and Caco-2), melanoma (A375), and pancreatic cancer (MiaPaca-2). Derivative 14 consistently demonstrated the highest activity across all tested cancer cell lines, showing selectivity for cancer cells over normal cells. Further investigation of the mechanism of action in SW480 cells revealed that compound 14 induced cell cycle arrest at the G0/G1 phase by downregulating CDK4 and CDK6. Molecular docking studies revealed that compound 14 established several interactions with key residues in the active site of CDK6. Additionally, compound 14 also reduced ROS production. In summary, our results strongly indicate that compound 14 has potential as a lead compound in the development of innovative anticancer drugs. Cicle cel·lular Urea Cèl·lules canceroses Cell cycle Urea Cancer cells Design, Synthesis, and Biological Evaluation of Novel Urea-Containing Carnosic Acid Derivatives with Anticancer Activity