Journal of Heterocyclic Chemistry · 2018 · 40 citations · 17 references
PharmacyMedicinal ChemistryPharmacologyCancer PharmacologyDrug DesignDrug DiscoveryLead Compound DesignOncology PharmacologyStructure-activity Relationship AnalysisAnticancer ActivityAnticancer ChemotherapyAnticancer Compound ScreeningMass Spectral Data AnalysisMedicinal Chemistry ApplicationsPyrimidine AnalogsPyrimidine AnaloguesPyrimidine Chemistry
Novel spiro [pyrimido[5,4‐b]quinoline‐10,5′‐pyrrolo[2,3‐d]pyrimidine] derivatives were designed and synthesized, and their chemical structures were confirmed by IR, NMR, elemental analysis, and mass spectral analysis. The anticancer activities of the newly synthesized compounds were evaluated in vitro against four human cancer cell lines including A431, PC‐3, MCF‐7, and MCF‐10A by MTT assay. The screening results showed that three compounds ( 4m , 4q , and 4s ) exhibited potent cytotoxic activities with IC 50 values between 7.82 and 9.88 μM against human breast cancer cell line (MCF‐7). Further in vitro studies revealed that inhibition of Sunitinib could be the possible mechanism of action of these molecules.
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