about
sameAs
Synthesis, characterization, cytotoxicity, and hydrolytic behavior of C2- and C1-symmetrical Ti(IV) complexes of tetradentate diamine bis(phenolato) ligands: a new class of antitumor agents.Different ortho and para electronic effects on hydrolysis and cytotoxicity of diamino bis(phenolato) "salan" Ti(IV) complexes.Synthetic models for non-heme carboxylate-bridged diiron metalloproteins: strategies and tactics.The MXCXXC class of metallochaperone proteins: model studies.Insights into molecular mechanism of action of salan titanium(IV) complex with in vitro and in vivo anticancer activity.Selenocysteine containing analogues of Atx1-based peptides protect cells from copper ion toxicity.Specific Design of Titanium(IV) Phenolato Chelates Yields Stable and Accessible, Effective and Selective Anticancer Agents.Anticancer metal complexes: synthesis and cytotoxicity evaluation by the MTT assay.Highly Effective and Hydrolytically Stable Vanadium(V) Amino Phenolato Antitumor Agents.Highly Stable Tetra-Phenolato Titanium(IV) Agent Formulated into Nanoparticles Demonstrates Anti-Tumoral Activity and Selectivity.Anti-proliferative activity of nano-formulated phenolato titanium(IV) complexes against cancer cells.Heteroleptic titanium(IV) catecholato/piperazine systems and their anti-cancer properties.High antitumor activity of highly resistant salan-titanium(IV) complexes in nanoparticles: an identified active species.Cytotoxic salan-titanium(IV) complexes: high activity toward a range of sensitive and drug-resistant cell lines, and mechanistic insights.Cytotoxicity and hydrolysis of trans-Ti(IV) complexes of salen ligands: structure-activity relationship studies.Unexpected influence of stereochemistry on the cytotoxicity of highly efficient Ti(IV) salan complexes: new mechanistic insights.Major impact of N-methylation on cytotoxicity and hydrolysis of salan Ti(IV) complexes: sterics and electronics are intertwined.Markedly different cytotoxicity of the two enantiomers of C(2)-symmetrical Ti(IV) phenolato complexes; mechanistic implications.Antitumor reactivity of non-metallocene titanium complexes of oxygen-based ligands: is ligand lability essential?Structure and coordination determination of peptide-metal complexes using 1D and 2D ¹H NMRCoordination chemistry of amine bis(phenolate) titanium complexes: tuning complex type and structure by ligand modification.Catalytic oxidation by a carboxylate-bridged non-heme diiron complex.A comparative chemical-biological evaluation of titanium(IV) complexes with a salan or cyclopentadienyl ligand.Living polymerization and block copolymerization of alpha-olefins by an amine bis(phenolate) titanium catalyst.Peptide models of Cu(I) and Zn(II) metallochaperones: the effect of pH on coordination and mechanistic implications.Catalytic oxidative ring opening of THF promoted by a carboxylate-bridged diiron complex, triarylphosphines, and dioxygen.Synthesis and conformational analysis of constrained ethylene-bridged bis(hydroxylamino-1,3,5-triazine) compounds as tetradentate ligands; structure of rigid dinuclear Ti(IV) complex.Effective Inhibition of Cellular ROS Production by MXCXXC-Type Peptides: Potential Therapeutic Applications in Copper-Homeostasis Disorders.C1-symmetrical titanium(IV) complexes of salan ligands with differently substituted aromatic rings: enhanced cytotoxic activity.Fluorescent antitumor titanium(iv) salen complexes for cell imaging.Unbound position II in MXCXXC metallochaperone model peptides impacts metal binding mode and reactivity: Distinct similarities to whole proteins.Diverse Structure−Activity Trends in Amine Bis(phenolate) Titanium Polymerization CatalystsHigh Molecular Weight Atactic Polypropylene prepared by Zirconium Complexes of an Amine Bis(phenolate) LigandIsospecific Living Polymerization of 1-Hexene by a Readily Available NonmetalloceneC2-Symmetrical Zirconium CatalystNovel zirconium complexes of amine bis(phenolate) ligands. Remarkable reactivity in polymerization of hex-1-ene due to an extra donor armIn Vivo Anticancer Activity of a Nontoxic Inert Phenolato Titanium Complex: High Efficacy on Solid Tumors Alone and Combined with Platinum Drugscombinations of inert phenolato Ti(iv) complexes with clinically employed anticancer chemotherapy: synergy with oxaliplatin on colon cellsHighly cytotoxic vanadium(v) complexes of salan ligands; insights on the role of hydrolysisA Marked Synergistic Effect in Antitumor Activity of Salan Titanium(IV) Complexes Bearing Two Differently Substituted Aromatic RingsNMR characterization of a Cu(i)-bound peptide model of copper metallochaperones: Insights on the role of methionine
P50
Q33401312-5330CE2B-9648-4EC2-B589-207801D6A403Q33788213-D8E3E148-A997-482A-BAAE-00CF16C29C99Q35660899-A1512A86-6CEF-4A7B-B25F-8B2D65F9D76BQ37892959-837A390F-F2C0-4A80-B4BC-6E091B38CE72Q38733687-4B0AD043-D4E9-4696-A213-B6A1EE722797Q38761519-2EB51C90-AB74-4BB1-95F2-77B88594F1C1Q38763409-9897B545-4329-4B61-A1C4-54B892FC7562Q38795822-C1509C24-BA36-47EA-BF7C-5B2071B6F866Q38809463-116F43C9-11CB-4C90-AE9A-FAC609D80AB0Q38827449-FB15FB70-CF0E-450C-BD69-E6FAAACACCC4Q39010679-C4DF5477-A301-4A7D-A484-D0A2F98F78D5Q39066077-1E7964B9-BFF2-49C5-9298-07F3383D0C57Q39282611-67D4E322-09D9-49C0-BE94-00C8C794C878Q39409301-E670E4C2-A5C0-47C1-9072-1D6EF4FEE280Q39417261-3793A09D-0F09-4E34-B9DE-D8EE52A7CEF9Q39444431-E97153E8-CE69-48EB-BD34-72029CFB4390Q39483013-639800F4-A59B-40FC-95D0-11DD7A8A3927Q39747437-A756FEED-F932-47C7-918B-4642C6F0DD06Q40136294-AE20FACA-79C9-42E6-945E-FC18DDCF531DQ40760206-BC4F9A90-10C9-4D46-BC49-2B68FD3A41BAQ43696985-B6C531D6-BD3F-431A-A777-76287A067A88Q43915436-FD35A61A-0754-45E5-B895-3CED90014C71Q43930810-7E1285B4-9922-48DF-8F18-42E9F02623CAQ44143777-7DF87220-F73E-439A-BEA8-B74E9449105CQ44493166-0338EB2F-1C05-4D00-9E50-D39CD4869191Q44965636-2924CB96-CA91-42E7-94C4-E54EB733FB10Q46524008-4388955D-27A9-496E-A579-5F9FED66C6C9Q46556611-117EED57-F824-4B79-A72A-5A881A8832E2Q46924827-95E8828E-1D35-4909-A03A-C2DC03C039F1Q49938063-EAA9F74A-9201-4E84-B18E-B92191C1EEFAQ53240374-3B74B1DD-91E6-46ED-AED9-7978F6903424Q57505502-1BDCB8FF-6733-43E5-9E9A-5E8B1A92D270Q57505554-E5BB5A91-46AF-47DA-9EBF-66A55F8A59AEQ57505564-709147BE-2A70-4FAD-8CAD-0FF89D5247AFQ57505567-9D25E436-4DEC-4C9C-9B18-5EB8A1AAEC38Q62598252-CD38594A-4EDB-4F18-809B-2801C163C750Q62598254-697032B8-24E0-4B12-B639-185823B17BEAQ62598292-06167A7A-4E10-4079-8C06-0FCBEFD3BC47Q62598294-5FD62467-4236-42B3-BD80-CE54A61806C1Q62598303-4E59D45F-FE58-4A84-A99B-71DF5B44B9B2
P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
ricercatrice
@it
հետազոտող
@hy
name
Edit Y Tshuva
@ast
Edit Y Tshuva
@en
Edit Y Tshuva
@es
Edit Y Tshuva
@sl
type
label
Edit Y Tshuva
@ast
Edit Y Tshuva
@en
Edit Y Tshuva
@es
Edit Y Tshuva
@sl
altLabel
Edit Yehudit Tshuva
@en
Tshuva EY
@en
prefLabel
Edit Y Tshuva
@ast
Edit Y Tshuva
@en
Edit Y Tshuva
@es
Edit Y Tshuva
@sl
P108
P214
P1053
B-5229-2015
P106
P21
P214
P31
P3829
P496
0000-0001-7452-3611
P569
1975-01-01T00:00:00Z
P735
P7859
viaf-298599470