sameAs
Ruthenium(II) p-cymene complex bearing 2,2'-dipyridylamine targets caspase 3 deficient MCF-7 breast cancer cells without disruption of antitumor immune response.Improved in vitro antitumor potential of (O,O'-Diisobutyl-ethylenediamine-N,N'-di-3-propionate)tetrachloridoplatinum(IV) complex under normoxic and hypoxic conditions.Reactions of (benzamidomethyl)triethylammonium chloride with some inorganic nucleophiles in aqueous media.The CellScan technology for in vitro studies on novel platinum complexes with organoarsenic ligands.Self-association of ruthenium(II) polypyridyl complexes and their interactions with calf thymus DNA.Conjugates of cisplatin and cyclooxygenase inhibitors as potent antitumor agents overcoming cisplatin resistance.Study of the cytotoxic activity of di and triphenyltin(IV) carboxylate complexes.Conjugation of cisplatin analogues and cyclooxygenase inhibitors to overcome cisplatin resistance.Synthesis and evaluation of carbaborane derivatives of indomethacin as cyclooxygenase inhibitors.Ortho-carbaborane derivatives of indomethacin as cyclooxygenase (COX)-2 selective inhibitorsMultidentate 2-pyridyl-phosphine ligands - towards ligand tuning and chirality.nido-Dicarbaborate Induces Potent and Selective Inhibition of Cyclooxygenase-22-Carbaborane-3-phenyl-1H-indoles--synthesis via McMurry reaction and cyclooxygenase (COX) inhibition activity.Antiproliferative activity of (η(6)-arene)ruthenacarborane sandwich complexes against HCT116 and MCF7 cell lines.Molecular Modeling of the Interactions between Carborane-Containing Analogs of Indomethacin and Cyclooxygenase-2.Metal-organic frameworks as competitive materials for non-linear optics.van der Waals Metal-Organic Framework as an Excitonic Material for Advanced Photonics.Gallium phosphinoarylbisthiolato complexes counteract drug resistance of cancer cells.Carbaborane-based alkynylphosphanes and phospholes.Antiproliferative effect of novel platinum(II) and palladium(II) complexes on hepatic tumor stem cells in vitro.Carbaboranes as pharmacophores: similarities and differences between aspirin and asborin.Synthesis and biological applications of ionic triphenyltin(IV) chloride carboxylate complexes with exceptionally high cytotoxicity.Cytotoxicity, apoptosis and study of the DNA-binding properties of bi- and tetranuclear gallium(III) complexes with heterocyclic thiolato ligands.Anticancer activity of dinuclear gallium(III) carboxylate complexes.Antiproliferative effect and genotoxicity of novel synthesized palladium complexes with organoarsenic ligands.Charge-Compensated Metallacarborane Building Blocks for Conjugation with Peptides.First representative of optically active P-L-menthyl-substituted (aminomethyl)phosphine and its borane and metal complexes.Soluble monometallic salen complexes derived from O-functionalised diamines as metalloligands for the synthesis of heterobimetallic complexes.Platinum(II) and palladium(II) complexes of chiral P-Cl functionalized bis-phosphino ortho-carbaboranes.Synthesis and reactivity of ortho-carbaborane-containing chiral aminohalophosphines.Synthesis, characterization, and crystal structures of novel intramolecularly base-stabilized borane derivatives with six- and seven-membered chelate rings.[Li(thf)3cyclo-(P4tBu4CH)]--synthesis, molecular structure and dynamic behaviour.New dinuclear nickel(II) complexes: synthesis, structure, electrochemical, and magnetic properties.Platinum(II) tetramesityltetraphosphane-1,4-diides.Asborin: the carbaborane analogue of aspirin.CarbORev-5901: The First Carborane-Based Inhibitor of the 5-Lipoxygenase Pathway.Different transmetallation behaviour of [M(P4HR4)] salts toward rhodium(I) and copper(I) (M = Na, K; R = Ph, Mes; Mes = 2,4,6-Me3C6H2).The reactivity of gallium-(I), -(II) and -(III) heterocycles towards Group 15 substrates: attempts to prepare gallium-terminal pnictinidene complexes.When arsine makes the difference: chelating phosphino and bridging arsinoarylthiolato gallium complexes.C2-Symmetric P,N Ligands Derived from Carborane-Based Diphosphetanes: Synthesis and Coordination Chemistry.
P50
Q30316086-1F96869D-130A-4830-AD51-E48CBE6159B9Q30316613-D2BA639C-F899-4787-B857-374BD9C281CDQ31134320-9651D3DB-398A-461A-ADEA-2A030766767DQ33383881-0AD140D7-C183-47CC-A8D6-A558D6103758Q33574710-861DBD60-BCC1-4D7A-8D31-78968062B67CQ34060461-FC4A0163-8619-4F5C-8474-6497D7A8B3A2Q34818345-F7A5BCA7-EE7E-483C-B5D0-368B6ACD1331Q35334366-D7572BFD-B205-47A5-8DC4-0C9DA05DB566Q36105949-2F31C098-448C-4041-AB32-911E270349EEQ36129926-90D18531-BD72-4C27-A76C-E7256755EB26Q36230206-2223A4ED-CD52-4786-98A2-91738CE7AC04Q36987287-42EFC709-239A-4532-8863-08462FE92732Q37361431-DC6FE9AB-AD8C-4240-A0B5-4047995E5C6EQ38695135-F2009FD6-4247-41FD-B0B4-9F923096A3CFQ38717483-8EE99378-676B-44F9-A2B5-57954A29C4DEQ38814195-0C77CB70-ECF5-4D23-B14F-8FF00FA22F5CQ39005842-726E2995-BF7C-4803-9989-B702CC71FF49Q39035304-3F22FDE1-7C92-4585-A1DD-74D722141784Q39095869-E6A7B85E-85E9-43FB-9E43-FCC5CCA7A2B0Q39401735-853B458D-19FC-4E69-B12F-E7B93CA37AB5Q39589505-D5169334-3080-4B2C-9F8E-594AE6E63504Q39632707-F16947A7-3A3D-4AAF-BABA-8901E2D4FC64Q39704042-2CA1D851-525A-4D38-AC52-A7877ACD90D6Q39772626-EC95E7BA-CC27-4814-8CA4-826B0C529349Q39783253-52FBB6FF-8D79-4B6C-AF26-E6C7A783618AQ40216495-44B3F979-A914-4732-9F2E-95CF1904039CQ43053873-F43572C6-8192-4EB5-8BB9-460E7B8FFA22Q43100630-935298F6-0F3F-43CF-AD24-4836056CD617Q43297817-359E1933-1EA0-48E4-9EEF-14CE84AA3B9BQ43594652-6F0FF4F0-E1B0-4063-A2FD-1752364A6178Q45120556-A1C49615-796B-4A82-B6C4-35A5A9B17158Q45150361-435B51BB-506D-4CCC-84FC-9C1A82672E56Q45573687-9837DD10-300A-4649-93BD-D8C18F33FE62Q46057703-976B0F5B-B1F7-4413-9FF5-B820AA6CC6ABQ46072092-FC38C2C8-712B-4845-99EB-FFA003EA87B6Q46358059-62E08B5F-7ECD-4FC6-920D-7EA66799CE10Q46669212-6FD8ACD3-63F8-4020-A506-CA65B28D3B04Q46853752-7E88ACEF-D4ED-42D1-8776-071C21AA7381Q47252270-CA3FEA85-8D7C-4B14-B215-0EB3F925E9E3Q48160878-B26028AF-B25F-4D61-843C-C3CA21A02031
P50
description
German inorganic chemist and professor at Leipzig University
@en
Professorin für Anorganische Chemie an der Universität Leipzig
@de
scheikundige
@nl
name
Evamarie Hey-Hawkins
@ast
Evamarie Hey-Hawkins
@de
Evamarie Hey-Hawkins
@en
Evamarie Hey-Hawkins
@es
Evamarie Hey-Hawkins
@nl
Evamarie Hey-Hawkins
@sl
type
label
Evamarie Hey-Hawkins
@ast
Evamarie Hey-Hawkins
@de
Evamarie Hey-Hawkins
@en
Evamarie Hey-Hawkins
@es
Evamarie Hey-Hawkins
@nl
Evamarie Hey-Hawkins
@sl
prefLabel
Evamarie Hey-Hawkins
@ast
Evamarie Hey-Hawkins
@de
Evamarie Hey-Hawkins
@en
Evamarie Hey-Hawkins
@es
Evamarie Hey-Hawkins
@nl
Evamarie Hey-Hawkins
@sl
P1015
P227
P1015
P1053
H-2278-2012
P106
P19
P2080
P21
P214
2696149068402965730006
P227
1158518234
P31
P3829
P496
0000-0003-4267-0603
P569
1957-01-01T00:00:00Z
P7859
lccn-n2018009481