Synthesis, characterization and biological evaluation of dipicolylamine sulfonamide derivatized platinum complexes as potential anticancer agents

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dc.contributor.author Thushara, Nadini
dc.contributor.author Darshani, Taniya
dc.contributor.author Samarakoon, Sameera R.
dc.contributor.author Perera, Inoka C.
dc.contributor.author Fronczek, Frank R.
dc.contributor.author Sameera, Sameera
dc.contributor.author Perera, Theshini
dc.date.accessioned 2021-07-07T03:31:32Z
dc.date.available 2021-07-07T03:31:32Z
dc.date.issued 2021
dc.identifier.uri http://archive.cmb.ac.lk:8080/xmlui/handle/70130/5504
dc.description.abstract Three new Pt complexes, [PtCl2(N(SO2(2-nap))dpa)], [PtCl2(N(SO2(1-nap))dpa)] and [PtCl2(N(SO2pip)dpa)], containing a rare 8-membered ring were synthesized in good yield and high purity by utilizing the ligands N(SO2(2-nap))dpa, N(SO2(1-nap))dpa and N(SO2pip)dpa, which contain a dipicolylamine moiety. Structural studies of all three complexes confirmed that the ligands are bound in a bidentate mode via Pt–N(pyridyl) bonds forming a rare 8-membered ring. The intense fluorescence displayed by the ligands is quenched upon coordination to Pt. According to time dependent density functional theory (TDDFT) calculations, the key excitations of N(SO2(2-nap))dpa and [PtCl2(N(SO2(1-nap))dpa)] involve the 2-nap-ligand-centered π → π* excitations. While all six compounds have shown antiproliferative activity against human breast cancer cells (MCF-7), the N(SO2pip)dpa and N(SO2(2-nap))dpa ligands and [PtCl2((NSO2pip)dpa)] complex have shown significantly high cytotoxicity, directing them to be further investigated as potential anti-cancer drug leads. en_US
dc.language.iso en en_US
dc.title Synthesis, characterization and biological evaluation of dipicolylamine sulfonamide derivatized platinum complexes as potential anticancer agents en_US
dc.type Article en_US


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