Zamora, Ana Pérez, Sergio A. Rodríguez, Venancio Janiak, Christoph Yellol, Gorakh S. Ruiz, José Dual Antitumor and Antiangiogenic Activity of Organoplatinum(II) Complexes A library of over 20 cycloplatinated compounds of the type [Pt­(dmba-R)­LCl] (dmba-R = C,N-dimethylbenzylamine-like ligand; R being MeO, Me, H, Br, F, CF<sub>3</sub>, and NO<sub>2</sub> substituents in the R<sub>5</sub> or R<sub>4</sub> position of the phenyl ring; L = DMSO and P­(C<sub>6</sub>H<sub>4</sub>CF<sub>3</sub>-p)<sub>3</sub>) has been prepared. All compounds are active in both human ovarian carcinoma A2780 cells and cisplatin-resistant A2780cisR cells, with most of the DMSO platinum complexes exhibiting IC<sub>50</sub> values in the submicromolar range in the A2780 cell line. Interestingly, DMSO platinum complexes show low cytotoxicity in the nontumorigenic kidney cell line BGM and therefore high selectivity factors SF. In addition, some of the DMSO platinum complexes effectively inhibit angiogenesis in the human umbilical vein endothelial cell line EA.hy926. These are the first platinum­(II) complexes reported to inhibit angiogenesis at a close concentration to their IC<sub>50</sub> in A2780 cells, turning them into dual cytotoxic and antiangiogenic compounds. 2780 cells;R 4 position;IC 50 values;DMSO platinum complexes;selectivity factors SF;2780 cell line;DMSO platinum complexes show;CF;cell line EA.hy 926.;20 cycloplatinated compounds;nontumorigenic kidney cell line BGM 2015-12-17
    https://acs.figshare.com/articles/journal_contribution/Dual_Antitumor_and_Antiangiogenic_Activity_of_Organoplatinum_II_Complexes/2048103
10.1021/jm501662b.s003