A novel pyrimido-pyridazine derivative for developing anticancer agents was synthesized via Ullmann arylation using an efficient Cu(OAc) catalyst. Compounds were investigated for their anticancer potential, against human breast adenocarcinoma cells, viz. MCF-7, MDA-MB-231 and normal cell line HEK-293. Further, an study was conducted on lymphoma-bearing mice while analysis was carried out for molecular interactions. Compound displayed significant antitumor activity towards MDA-MB-231 cells through induction of apoptosis and arresting cells in S-phase , while it significantly increased the lifespan and reduced tumor growth . An  study revealed potent tyrosine-protein kinase inhibitors. Taken together the molecule has the potential to become an effective therapeutic treatment for breast cancer.

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http://dx.doi.org/10.4155/fmc-2022-0199DOI Listing

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A novel pyrimido-pyridazine derivative for developing anticancer agents was synthesized via Ullmann arylation using an efficient Cu(OAc) catalyst. Compounds were investigated for their anticancer potential, against human breast adenocarcinoma cells, viz. MCF-7, MDA-MB-231 and normal cell line HEK-293.

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