about
Differential cytotoxic activity of a novel palladium-based compound on prostate cell lines, primary prostate epithelial cells and prostate stem cellsSynthesis, structures and biomolecular interactions of new silver(i) 5,5-diethylbarbiturate complexes of monophosphines targeting Gram-positive bacteria and breast cancer cells.trans-Bis[2-(piperazin-1-yl)-ethan-amine]-bis-(saccharinato)cobalt(II)Palladium(II) saccharinate complexes with bis(2-pyridylmethyl)amine induce cell death by apoptosis in human breast cancer cells in vitro.In vitro DNA binding studies of the sweetening agent saccharin and its copper(II) and zinc(II) complexes.Anti-growth effect of a novel trans-dichloridobis[2-(2-hydroxyethyl)pyridine]platinum (II) complex via induction of apoptosis on breast cancer cell lines.The role of cell cycle progression for the apoptosis of cancer cells induced by palladium(II)-saccharinate complexes of terpyridine.Cytotoxic and apoptotic effects of the combination of palladium (II) 5,5-diethylbarbiturate complex with bis(2-pyridylmethyl)amine and curcumin on non small lung cancer cell lines.New palladium(II) and platinum(II) 5,5-diethylbarbiturate complexes with 2-phenylpyridine, 2,2'-bipyridine and 2,2'-dipyridylamine: synthesis, structures, DNA binding, molecular docking, cellular uptake, antioxidant activity and cytotoxicity.Cytotoxic activity of novel palladium-based compounds on leukemia cell lines.Biochemical and proteomic analysis of a potential anticancer agent: Palladium(II) Saccharinate complex of terpyridine acting through double strand break formation.Synthesis, crystal structures, in vitro DNA binding, antibacterial and cytotoxic activities of new di- and polynuclear silver(I) saccharinate complexes with tertiary monophosphanes.Di- and polynuclear silver(I) saccharinate complexes of tertiary diphosphane ligands: synthesis, structures, in vitro DNA binding, and antibacterial and anticancer properties.Synthesis, structural characterization and cell death-inducing effect of novel palladium(II) and platinum(II) saccharinate complexes with 2-(hydroxymethyl)pyridine and 2-(2-hydroxyethyl)pyridine on cancer cells in vitro.Evaluation of the molecular mechanisms of a palladium(II) saccharinate complex with terpyridine as an anticancer agent.Synthesis, crystal structures, DNA binding and cytotoxicity of two novel platinum(II) complexes containing 2-(hydroxymethyl)pyridine and pyridine-2-carboxylate ligands.Anti-cancer activity of a novel palladium(II) complex on human breast cancer cells in vitro and in vivo.Cell death-inducing effect of novel palladium(II) and platinum(II) complexes on non-small cell lung cancer cells in vitro.Cationic Pd(II)/Pt(II) 5,5-diethylbarbiturate complexes with bis(2-pyridylmethyl)amine and terpyridine: Synthesis, structures,DNA/BSA interactions, intracellular distribution, cytotoxic activity and induction of apoptosis.Bis(triethanolamine)cadmium(II) and -mercury(II) saccharinates: seven-coordinate complexes containing both tri- and tetradentate triethanolamine ligands.N-(2-hydroxyethyl)ethylenediammonium hydrogenphosphate monohydrate.Bis(2-pyridylmethanol)bis(saccharinato)zinc(II) and -cadmium(II) at 120 K: three-dimensional structures containing both N-and O-coordinated ambidentate saccharinate ligands.2-(hydroxymethyl)pyridinium dihydrogenphosphate.1,3-Dibenzoylimidazolidine-2-thione and 1,3-dibenzoyl-3,4,5,6-tetrahydropyrimidine-2(1H)-thione.C-H...O, C-H...pi and pi-pi interactions in three benzofuran-2-yl ketone derivatives.A palladium(II)-saccharinate complex of terpyridine exerts higher anticancer potency and less toxicity than cisplatin in a mouse allograft model.Structures and biochemical evaluation of silver(I) 5,5-diethylbarbiturate complexes with bis(diphenylphosphino)alkanes as potential antimicrobial and anticancer agents.Anti-angiogenic effect of a Palladium(II)-Saccharinate Complex of Terpyridine in vitro and in vivo.Apoptosis-inducing effect of a palladium(II) saccharinate complex of terpyridine on human breast cancer cells in vitro and in vivo.Synthesis, Spectroscopic, Structural and Quantum Chemical Studies of a New Imine Oxime and Its Palladium(II) Complex: Hydrolysis Mechanism.Sonochemical synthesis of nano-scale mixed-ligands lead(II) coordination polymers as precursors for preparation of PbO and PbBr(OH) nano-structures; thermal, structural and X-ray powder diffraction studies(3-Hydroxy-2-pyridylmethyl)dimethylammonium dihydrogenphosphateSynthesis, experimental and theoretical characterization of palladium(II) and platinum(II) saccharinate complexes with 2-(2-pyridyl)benzimidazoleAddition of niclosamide to palladium(II) saccharinate complex of terpyridine results in enhanced cytotoxic activity inducing apoptosis on cancer stem cells of breast cancerDNA binding and cleavage studies of two palladium(II) saccharinate complexes with terpyridineNi(ii)/Cu(ii)/Zn(ii) 5,5-diethylbarbiturate complexes with 1,10-phenanthroline and 2,2'-dipyridylamine: synthesis, structures, DNA/BSA binding, nuclease activity, molecular docking, cellular uptake, cytotoxicity and the mode of cell deathA combined experimental and theoretical investigation of a new imineoxime and its palladium(II) and platinum(II) complexes: synthesis, structural characterization and spectroscopic propertiesPalladium(ii) and platinum(ii) saccharinate complexes with bis(diphenylphosphino)methane/ethane: synthesis, S-phase arrest and ROS-mediated apoptosis in human colon cancer cellsZn(ii), Cd(ii) and Hg(ii) saccharinate complexes with 2,6-bis(2-benzimidazolyl)pyridine as promising anticancer agents in breast and lung cancer cell lines via ROS-induced apoptosis
P50
Q28487918-975B74ED-B8D2-456D-B607-F59B20004519Q32175273-38DDA572-ACDB-4013-8FB7-890AD0ADFE0AQ34040354-ABAC1D10-A11C-4026-A0C3-928CABDCF68FQ34678349-2F9A28B7-BD49-4F3C-A657-10F391FAE5A3Q35062325-40DA62AB-4D84-475E-BD75-E5C29877925DQ35682842-250C4B17-9F79-4FC9-B57C-991DA9BA03D9Q38716516-FC8C82F0-2051-4CBA-A620-E9559F013EB8Q38716898-C76E5B79-EDA7-441D-9C5A-26CEBD079AD5Q38899965-3378883B-2B30-4578-964E-DC29F4585B72Q38950850-CA356541-F017-4912-BCAE-B8A89BDB0748Q38957535-C6A8729A-B4DA-484A-AB31-2B548ECD98E9Q39028935-6FB249AB-3614-4EF4-888D-30FFFB763668Q39077625-63ACB218-373E-452B-A5B3-7C57FF8F8C34Q39093673-97B2E96E-DD81-4559-981E-C9438288F636Q39094578-8C5A1FB4-CEA2-45AB-89E2-A32722A154CCQ39189986-4897452E-337A-4096-944D-777F5496FC0AQ39480780-B852961F-58BC-49BB-9D24-A43B7CB7CCA2Q39496583-7AFC5F65-DAC0-46E6-87AA-CB99388A5E11Q40574188-1A0615F3-1695-4559-AC8C-B7127BAB627EQ43820282-A90B7DFE-E741-4648-9997-BEBC13A24EFDQ44047781-01CFCE4B-97A3-4426-B6C7-8C4849869CB6Q44087260-F9E1B7FE-3C26-4EAE-81B3-91538FFA014BQ44509920-9EB0AE3A-3336-4802-A888-08B5E54BB665Q46523139-5E2520BC-824E-412D-AD5D-BF9B6C6D8AA3Q46582930-8533C663-902C-4F89-AD1D-65AA8A4DF50DQ47978264-F70B4F9E-08A3-47A8-8508-9B3B66C9A1ABQ50206172-8A9E748D-AF06-4B13-9FA8-D9751AEF2438Q52858584-E441E0C1-24F5-4461-943E-51825955E486Q53032864-23664C8E-08CE-4801-BA61-83CFCC7EF309Q53298342-E4B7D56E-F7C3-4CE1-8915-79842029AE05Q82293316-97069DCA-6757-4931-99CC-FAF9B5B4DD0EQ83103752-A4C3DF88-DCA7-48C6-A56E-9A438716E872Q84338658-EBE34F38-CE82-4990-B39D-1C0BBA73803FQ85699600-EE95F022-DAD1-401A-AB08-484B198D68CFQ86324414-D82ED0F3-B7BE-46DD-8877-79AEC2081C6FQ87586277-469DFF1E-A239-41F1-96BE-15080F342CA0Q88080342-8197A089-FE36-4B82-B630-B71D458B66D8Q90653995-D8E5794A-A549-47EB-AB49-92BF65C60220Q95940468-F085AFEF-BE93-4C69-B8AE-C4A468D03FDE
P50
description
researcher ORCID ID = 0000-0002-2849-3332
@en
wetenschapper
@nl
name
Veysel T Yilmaz
@ast
Veysel T Yilmaz
@en
Veysel T Yilmaz
@es
Veysel T Yilmaz
@nl
type
label
Veysel T Yilmaz
@ast
Veysel T Yilmaz
@en
Veysel T Yilmaz
@es
Veysel T Yilmaz
@nl
prefLabel
Veysel T Yilmaz
@ast
Veysel T Yilmaz
@en
Veysel T Yilmaz
@es
Veysel T Yilmaz
@nl
P106
P1153
7006269202
P31
P496
0000-0002-2849-3332