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Volumn 11, Issue 1, 2008, Pages 47-50

Synthesis, structure and cytotoxic activity evaluation of a dinuclear complex of Cd(II) with N′,N′2-bis[(1E)-1-(2-pyridyl)ethylidene]propanedi hydrazide

Author keywords

Cd(II) complex; Cytotoxic activity; Hydrazone ligand; X ray analysis

Indexed keywords


EID: 38049035877     PISSN: 13877003     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.inoche.2007.10.013     Document Type: Article
Times cited : (30)

References (14)
  • 7
    • 38049061455 scopus 로고    scopus 로고
    • note
    • -1.
  • 8
    • 38049084272 scopus 로고    scopus 로고
    • note
    • 2 = 0.1251 (on all data).
  • 10
    • 38049030049 scopus 로고    scopus 로고
    • G.M. Sheldrick, SHELXL-97: Program for Crystal Structure Refinement, University of Göttingen, Germany, 1997.
  • 12
    • 38049002919 scopus 로고    scopus 로고
    • note
    • 2 in the nutrient medium RPMI 1640 with HEPES (RPMI-1640 Medium, Sigma, Cat. No. R-4130) supplemented with 10%, heat-inactivated, fetal calf serum (Foetal Bovine Serum Standard Quality, PAA, Cat. No. A15-101), l-glutamine (3 mM), penicillin (192 U/mL), streptomycin (200 μg/mL). Exponentially growing cells were harvested with 0.5% trypsin (Institute for Immunology and Virusology Torlak, Belgrade). Evaluation of cytotoxic activity: For the evaluation of cytotoxic effect 100 μL of cell suspensions was seeded in triplicate in 96-well flat bottom microtiter plates (Nunc, Denmark) in density of 1200 (cells/well), and after an initial incubation period of 24 h was treated by tested compounds. Control wells were not treated with agents. Stock solutions of the complex were prepared in DMSO and afterwards diluted by growth medium. Diluted solution (50 μL) was added into the plate wells to appropriate final concentrations. After the continuous drug exposure times of 48 h and 72 h, the survival was determined by sulforhodamine B (SRB) assay (Sigma Chemicals Co., St. Louis, USA) which was performed as previously reported [13,14]. Absorbance of dissolved SRB in unbuffered 10 mM tris base was read in a microtiter plate reader at λ = 570 nm. The results of the measurements are expressed as the percentage of control growth PG (%) and were calculated according to Eq. (1). The cytotoxic activity was determined from Eq. (2)(1)PG (%) = frac(mean OD (optical density) of treated cells, mean OD of control cells) × 100 %(2)IC (%) = 100 % - PG (%).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.