MALOŇ, M., Z. TRÁVNÍČEK, M. MARYŠKO, R. ZBOŘIL, M. MAŠLÁŇ, Jaromír MAREK, K. DOLEŽAL, J. ROLČÍK, V. KRYŠTOF a M. STRNAD. Metal complexes as anticancer agents 2. Iron(III) and copper(II) bio-active complexes with N-6-benzylaminopurine derivatives. Inorganica Chimica Acta. Oxford, UK: Elsevier Science, 2001, roč. 323, 1-2, s. 119-129. ISSN 0020-1693.
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Základní údaje
Originální název Metal complexes as anticancer agents 2. Iron(III) and copper(II) bio-active complexes with N-6-benzylaminopurine derivatives
Autoři MALOŇ, M., Z. TRÁVNÍČEK, M. MARYŠKO, R. ZBOŘIL, M. MAŠLÁŇ, Jaromír MAREK, K. DOLEŽAL, J. ROLČÍK, V. KRYŠTOF a M. STRNAD.
Vydání Inorganica Chimica Acta, Oxford, UK, Elsevier Science, 2001, 0020-1693.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 10402 Inorganic and nuclear chemistry
Stát vydavatele Velká Británie a Severní Irsko
Utajení není předmětem státního či obchodního tajemství
Impakt faktor Impact factor: 1.394
Kód RIV RIV/00216224:14310/01:00004987
Organizační jednotka Přírodovědecká fakulta
UT WoS 000172077100015
Klíčová slova anglicky ron(III) and copper(II) complexes; 6-benzylaminopurine derivatives; cytotoxic activity; CDK inhibitor; magnetic properties; crystal structures
Štítky 6-benzylaminopurine derivatives, CDK inhibitor, crystal structures, cytotoxic activity, magnetic properties, ron(III) and copper(II) complexes
Změnil Změnil: doc. RNDr. Jaromír Marek, Ph.D., učo 1989. Změněno: 11. 12. 2001 11:52.
Anotace
Iron(III) complexes with 2-(3-hydroxypropylamino)-6-benzylaniino-9-isopropylpurine (Bohemin, HL1), in its protonized form, of the composition (H+HL1)(2)[FeCl5]. 2H(2)O (1), (H+HL1)(2)[FeCl5]. 3H(2)O (2) have been prepared by two different routes. A new way for synthesis of copper(II) complex with 6-(2-chlorobenzylamino)purine (HL2), [Cu-2(mu -Cl)(2)(mu -HL2)(2)(HL2)(2)Cl-2]. 2H(2)O (3), together with the preparation of copper(II) complex with 6-(3-chlorobenzylamino)purine (HL3), [Cu-2(mu -Cl)(2)(mu -HL3)(2)Cl-2] (4), is also reported. The characterization have been based on elemental analysis, electronic, infrared, ES + mass and Fe-57 Mossbauer spectra, conductivity data and magnetic susceptibility temperature measurements over the 4.5-300 K for 1-3, and 35-300 K for 4. temperature range, respectively. Molecular structure of an electroneutral form of the HL2 ligand, (HL2. 2H(2)O), and a protonized form of the HL3 ligand, (H+HL3-Cl), have been determined by a single-crystal X-ray analysis. A mononuclear trigonal-bipyramidal (for 1 and 2), binuclear octahedral (for 3) and binuclear trigonal-bipyramidal (for 4) structures of the complexes were proposed mainly on the basis of spectral and magnetic properties. An S = 3/2-5/2 spin-admixed state in 1 and 2 was found to be related to the presence of [FeCl5](2-) (S = 3/2) and [FeCl5(H2O)](2-) (S = 5/2) complex anions in I and 2, as found by Fe-57 Mossbauer spectroscopy. Cytotoxic activity of the complexes was determined by a calcein AM assay and IC50 values were also estimated. For testing, human malignant melanoma cell line G-361. human osteogenic sarcoma cell line HOS, human chronic myelogenous leukaemia K-562 and human breast adenocarcinoma cell line MCF7 were used. The inhibition of p34(cdc2) kinase by the complexes I and 2, which is known to be one of the important mechanisms responsible for cytotoxicity of cytokinin-derived compounds, was also studied.
Návaznosti
GA203/00/0152, projekt VaVNázev: Syntéza, studium a biologická aktivita komplexních sloučenin vybraných přechodných kovů s purinovými deriváty
MSM 143100008, záměrNázev: Genomy a jejich funkce
Investor: Ministerstvo školství, mládeže a tělovýchovy ČR, Genomy a jejich funkce
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