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Synthesis, characterization and antitumor activity of novel tetrapodal 1,4-dihydropyridines: p53 induction, cell cycle arrest and low damage effect on normal cells induced by genotoxic factor H<sub>2</sub>O<sub>2</sub>
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Citations
64
References
2016
Year
Organic ChemistryChemistryPharmaceutical ChemistryTumor BiologyMedicinal ChemistryNovel TetrakisAnti-cancer AgentRadiation OncologyP53 InductionCell Cycle ArrestPharmacologyEnantioselective SynthesisAntitumor ActivitiesNatural SciencesAcid-catalyzed CondensationNormal CellsMedicineSynthetic ChemistrySmall MoleculesDrug Discovery
Synthesis of novel tetrakis(2,6-dimethyl-4-phenyl-1,4-dihydropyridinyl)methanes<bold>5a–d</bold>by acid-catalyzed condensation of the tetrakis-aldehydes<bold>6a–d</bold>with eight equivalents of 3-aminobut-2-enenitrile<bold>2</bold>is reported. Antitumor activities of compounds<bold>5a–d</bold>were also investigated.
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