2005
DOI: 10.1016/j.jorganchem.2005.07.046
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Crystal structure, antitumor activities and DNA-binding properties of the La(III) complex with Phthalazin-1(2H)-one prepared by a novel route

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Cited by 19 publications
(11 citation statements)
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“…Although the mechanism which the La-complex selectively affects L 1210 is still unclear, its special structure is vital. Lots of other heterocyclic Schiff's bases Lanthanum complexes often appear similar biological and pharmaceutical activities, for example, Lanthanum complexes with both 4 0 ,5,7-trihydroxy-flavanoe benzoyl hydrazone [11] and phthalazin-1(2H)-one [12] have considerable cytotoxic activity against two kinds of tumor cells (human leukemia HL-60 and lung adenocarinoma A-549), the two complexes can strongly bind with calf thymus DNA, the intrinsic binding constants of their complexes with DNA are 1.83 · 10 7 and 1.4 · 10 7 M À1 , respectively. This is an interesting phenomenon, which also show that the interaction between the complex molecules and DNA can cause DNA damage in tumor cells, blocking the division of tumor cells and resulting in the cell death [8,9].…”
Section: Cytotoxic Activitiesmentioning
confidence: 99%
“…Although the mechanism which the La-complex selectively affects L 1210 is still unclear, its special structure is vital. Lots of other heterocyclic Schiff's bases Lanthanum complexes often appear similar biological and pharmaceutical activities, for example, Lanthanum complexes with both 4 0 ,5,7-trihydroxy-flavanoe benzoyl hydrazone [11] and phthalazin-1(2H)-one [12] have considerable cytotoxic activity against two kinds of tumor cells (human leukemia HL-60 and lung adenocarinoma A-549), the two complexes can strongly bind with calf thymus DNA, the intrinsic binding constants of their complexes with DNA are 1.83 · 10 7 and 1.4 · 10 7 M À1 , respectively. This is an interesting phenomenon, which also show that the interaction between the complex molecules and DNA can cause DNA damage in tumor cells, blocking the division of tumor cells and resulting in the cell death [8,9].…”
Section: Cytotoxic Activitiesmentioning
confidence: 99%
“…After refluxing for 30 min, triethylamine (0.020 g, 0.2 mmol) was added into the reaction mixtures dropwise to deprotonate the phenolic hydroxyl substituent of 8-hydroxyquinolinato unit. Then, the mixtures were refluxed and stirred continuously for 8 h. After cooling to room temperature, the precipitate was centrifugalized, washed adequately with hot methanol and dried in vacuum over 48 …”
Section: Preparation Of the Eu(iii) Complexesmentioning
confidence: 99%
“…In fact, some groove binders of Hoechst 33,258 family can also present red shifts or even blue shifts of absorption bands when they bind to DNA helix through groove binding modes, especially for multiple binders [45,46]. After all, hydrodynamic measurements that are sensitive to length change of DNA (i.e., viscosity and sedimentation) are regarded as the least ambiguous and the most critical criterions for binding modes in solution in absence of crystallographic structural data [47,48].…”
Section: Uv-vis Spectroscopy Studymentioning
confidence: 99%
“…In fact, some groove binders of Hoechst 33,258 family can also present red shifts or even blue shifts of absorption bands when they bind to DNA helix by groove binding modes, especially for multiple binders (Behrens et al 2001;Frau et al 1997). After all, hydrodynamic measurements that are sensitive to length change of DNA (i.e., viscosity and sedimentation) are regarded as the least ambiguous and the most critical criterions for binding modes in solution in absence of crystallographic structural data (Sigman et al 1993;Wang et al 2005). …”
Section: Ultraviolet-visible (Uv-vis) Spectroscopy Study For Dna Bindmentioning
confidence: 99%