about
8-Hydroxyquinolines: a review of their metal chelating properties and medicinal applicationsEffect of Zn...Zn separation on the hydrolytic activity of model dizinc phosphodiesterases.Metallotherapeutics: novel strategies in drug design.Self-activating nuclease and anticancer activities of copper(II) complexes with aryl-modified 2,6-di(thiazol-2-yl)pyridine.DNA binding and unwinding by self-assembled supramolecular hetero-bimetallacycles.Artificial ribonucleases.Carbohydrate linked organotin(IV) complexes as human topoisomerase Iα inhibitor and their antiproliferative effects against the human carcinoma cell line.Copper(II) complexes with 2NO and 3N donor ligands: synthesis, structures and chemical nuclease and anticancer activities.DNA targeting polyaza macrobicyclic dizinc(II) complexes promoting high in vitro caspase dependent anti-proliferative activity against human carcinoma cancer cells.Potent oxidative DNA cleavage by the di-copper cytotoxin: [Cu2(μ-terephthalate)(1,10-phen)4]2+.On the binding modes of metal NHC complexes with DNA secondary structures: implications for therapy and imaging.Covalently attached oligodeoxyribonucleotides induce RNase activity of a short peptide and modulate its base specificity.DNA Binding and Photocleavage Studies of Cobalt(III) Ethylenediamine Pyridine Complexes: [Co(en)2(py)2]3+ and [Co(en)2(mepy)2]3+.Synthesis, characterization, and photoactivated DNA cleavage by copper (II)/cobalt (II) mediated macrocyclic complexes.Synthesis, physico-chemical investigations of Co(II), Ni(II) and Cu(II) complexes and their in vitro microbial, cytotoxic, DNA cleavage studies.DNA cleavage and in vitro antimicrobial studies of Co(II), Ni(II), and Cu(II) complexes with ONNO donor Schiff bases: synthesis, spectral characterization, and electrochemical studies.Hydrolytic cleavage of DNA-model substrates promoted by polyoxovanadates.Mononuclear Co(III) and Ni(II) complexes with polypyridyl ligands, [Co(phen)2(taptp)]3+ and [Ni(phen) 2(taptp)]2+: synthesis, photocleavage and DNA-binding.Macrocyclic amines as catalysts of the hydrolysis of the triphosphate bridge of the mRNA 5'-cap structure.Methionine sustituted polyamides are RNAse mimics that inhibit translation.Synthesis of new OBAN's and further studies on positioning of the catalytic group.Synthesis, structure and comparison of the DNA cleavage ability of metal complexes M(II)L with the N-(2-ethoxyethanol)-bis(2-picolyl)amine ligand L (M = Co, Ni, Cu and Zn).When structural and electronic analogy leads to reactivity: the unprecedented phosphodiesterase activity of vanadates.DNA hydrolytic cleavage catalyzed by synthetic multinuclear metallonucleases.Triazolopyridopyrimidines: an emerging family of effective DNA photocleavers. DNA binding. Antileishmanial activity.Multinuclear diffusion NMR spectroscopy and DFT modeling: a powerful combination for unraveling the mechanism of phosphoester bond hydrolysis catalyzed by metal-substituted polyoxometalates.Synthesis, characterization, DNA binding, cleavage activity and cytotoxicity of copper(II) complexes.UV-C radiation induced conformational relaxation of pMTa4 DNA in Escherichia coli may be the cause of single strand breaks.Synthesis and characterization of FeIII(μ-OH)ZnII complexes: effects of a second coordination sphere and increase in the chelate ring size on the hydrolysis of a phosphate diester and DNA.Catalytic Metallodrugs: Substrate-Selective Metal Catalysts as Therapeutics.Synthesis and crystal structures of novel copper(II) complexes with glycine and substituted phenanthrolines: reactivity towards DNA/BSA and in vitro cytotoxic and antimicrobial evaluation.Structural analysis of zinc-finger (TTK) + [Cu(BPA)]2+ /[Cu(IDB)]2+ + DNA complexes: an investigation by molecular dynamics simulation.Synthesis, characterization, and DNA-binding and -cleavage properties of dinuclear Cu(II) --salophen/salen complexes.Cleavage of RNA phosphodiester bonds by small molecular entities: a mechanistic insight.Electrospray ionization mass spectrometric studies on the characteristic fragmentation of Asp/cyclen conjugates.The interface makes a difference: lanthanide ion coated vesicles hydrolyze phosphodiesters.Biocatalysis, DNA-protein interactions, cytotoxicity and molecular docking of Cu(II), Ni(II), Zn(II) and V(IV) Schiff base complexesWater-soluble bis(1,10-phenanthroline) octanedioate Cu2+ and Mn2+ complexes with unprecedented nano and picomolar in vitro cytotoxicity: promising leads for chemotherapeutic drug development
P2860
Q28389539-56F2552C-5307-4EAB-9713-B1E0EC936F27Q33214803-9D7B2136-A1E0-42B9-A46B-A1389A6B17E8Q34775956-8B096137-634F-4A76-BE04-9A52B04E0E7DQ34811353-E802C5E6-589A-4B3D-9FA5-33020010A6E9Q35612552-13133760-B819-4D6E-BC08-4A32A37FF6F0Q36343596-33C2366D-B46B-40CA-A401-B7F96CD51846Q39047919-908A21BE-24B3-477E-BA6E-8E52330C2872Q39161624-328DBFC8-A517-4687-8AEE-6C9B6A23DDD9Q39275712-98FB77B6-6B24-4E00-AFF7-376A3BF2031DQ39335872-05F8A2DA-BDAF-46C9-B8A2-F9CE8DFD5BF4Q39399932-58B42914-B806-450B-8963-C9C282FD96A3Q40773418-3F7D0C7A-8D1F-42D3-8C3F-79A163112AEAQ41917700-9B64DAB9-3300-4434-BFD3-8B985CB36D66Q43100086-00DD655C-E5B9-400A-ABED-26B82F018F60Q43108501-8AEBAED3-8B24-4BC8-8547-2B8C75531559Q43210241-E7AB4708-ECD0-4DB6-A4E5-174A7F39ADCCQ43214035-CEC1F83E-610A-4BDB-BE6F-3B9CDA90AF1CQ44462295-4A548F20-351C-4607-BB54-66D4CA282D44Q44636267-D75632C9-94E3-4A7B-BBC5-4654DE078093Q44941758-E04BF96A-BDF2-49F2-BAD3-ECD615D2C88CQ44959061-220C432B-86F4-44DE-9C89-B9B22DFCAD0BQ44977660-71F04A7A-6F5C-463B-A31B-B47BF9899F01Q46123363-5841FD5C-5C5D-4488-BD85-118AB69C24D5Q46194657-0A3DC06D-D989-4717-8D52-CFC1587C27BEQ46753251-E51E57D2-B237-4631-90F1-F98CFB3EFCD4Q46777436-91D058E5-F039-4A14-A9F5-E1156AB8F58CQ46959731-35685AA9-4A0C-4962-888C-0C5E22D49A3BQ46981209-586FB249-48C4-4500-A2FE-73B83E52BD46Q47193853-23D6CD93-B908-44D8-AC71-8DF9ABE8DDDFQ48157762-9EEE1262-5E69-48EB-B74B-6425F870D272Q50550654-A55F5595-CA78-4DBF-B5F6-8003DC3099B9Q53209418-B1A0C469-3797-40AC-82A7-F68A0D7DB3B3Q53232302-A41B43AE-ADA9-4289-B5C1-73DFE401CBD3Q53273073-0B1434A8-BE37-4AAC-A725-E0F70CA8B9E3Q53621884-17C02A3D-C837-45B6-B56B-D38FD1324078Q54463624-C06128A4-8A38-46D6-A107-390BCD4CA046Q57816439-5616675B-5047-4E98-B449-EA6810D7CC16Q58838382-76D2DB93-11C9-48EB-A2C7-8E552F52C745
P2860
description
2001 nî lūn-bûn
@nan
2001 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Chemical nucleases.
@ast
Chemical nucleases.
@en
Chemical nucleases.
@nl
type
label
Chemical nucleases.
@ast
Chemical nucleases.
@en
Chemical nucleases.
@nl
prefLabel
Chemical nucleases.
@ast
Chemical nucleases.
@en
Chemical nucleases.
@nl
P1476
Chemical nucleases.
@en
P2093
P304
P356
10.1016/S1367-5931(01)00259-9
P577
2001-12-01T00:00:00Z