Synthesis, cytotoxic and antimicrobial activities of novel cobalt and zinc complexes of benzimidazole derivatives

被引:49
作者
Apohan, Elif [1 ]
Yilmaz, Ulku [2 ,3 ]
Yilmaz, Ozgur [4 ]
Serindag, Ayfer [4 ]
Kucukbay, Hasan [3 ]
Yesilada, Ozfer [1 ]
Baran, Yusuf [5 ,6 ]
机构
[1] Inonu Univ, Art & Sci Fac, Dept Biol, Malatya, Turkey
[2] Inonu Univ, Battalgazi Vocat Sch, Battalgazi, Malatya, Turkey
[3] Inonu Univ, Art & Sci Fac, Dept Chem, Malatya, Turkey
[4] Inonu Univ, Inst Sci, Dept Biol, Malatya, Turkey
[5] Izmir Inst Technol, Fac Sci, Dept Mol Biol & Genet, Izmir, Turkey
[6] Abdullah Gul Univ, Fac Life & Nat Sci, Mol Biol & Genet Kayseri, Kayseri, Turkey
关键词
Benzimidazole complexes; Cytotoxic; Lung cancer; Antimicrobial; CELL LUNG-CANCER; SUBSTITUTED BENZIMIDAZOLE; STRUCTURAL-CHARACTERIZATION; BIOLOGICAL EVALUATION; METAL-COMPLEXES; IN-VITRO; ANTICANCER; IMIDAZOLE; APOPTOSIS; DESIGN;
D O I
10.1016/j.jorganchem.2016.11.020
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
In this study fourteen novel cobalt (II) or zinc (II) complexes of benzimidazoles were synthesized from the 1-(4-substitutedbenzyl)-1H-benzimidazoles and CoCl2.6H(2)O or ZnCl2. Cytotoxic activities of novel complexes were investigated against lung cancer cells (A549) and BEAS-2B. Three of the examined compounds (1, 4 and 5) showed high cytotoxic activity against A549. While the IC50 of the cisplatin was 2.56 pg/mL for A549 cells at 72 h, the IC50 values of compounds 1, 4 and 5 were 1.97, 1.87 and 1.9 mu g/mL, respectively. IC50 values of these compounds for BEAS-2B cells were higher than the IC50 values for A549. While the IC50 values for BEAS-2B cells were 59.8, 24.5 and 32.67 mu g/mL, respectively, the IC50 of the cisplatin was determined as 2.53 pgimL in the present work. Three of the compounds have also high antimicrobial activity against all the microorganisms used. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:52 / 58
页数:7
相关论文
共 56 条
[1]   5-Nitro-5′-hydroxy-indirubin-3′-oxime (AGM130), an indirubin-3′-oxime derivative, inhibits tumor growth by inducing apoptosis against non-small cell lung cancer in vitro and in vivo [J].
Ahn, Mee-Young ;
Kim, Tae-Hyung ;
Kwon, Seong-Min ;
Yoon, Hyo-Eun ;
Kim, Hyung-Sik ;
Kim, Jae-Il ;
Kim, Yong-Chul ;
Kang, Keon-Wook ;
Ahn, Sang-Gun ;
Yoon, Jung-Hoon .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2015, 79 :122-131
[2]   ISONICOTINAMIDE COMPLEXES WITH SOME METAL(II) HALIDES AND PSEUDOHALIDES [J].
AHUJA, IS ;
PRASAD, I .
INORGANIC & NUCLEAR CHEMISTRY LETTERS, 1976, 12 (10) :777-784
[3]   Benzimidazole-based silver(I)-N-heterocyclic carbene complexes as anti-bacterials: synthesis, crystal structures and nucleic acids interaction studies [J].
Asekunowo, Patrick O. ;
Haque, Rosenani A. ;
Razali, Mohd. R. ;
Budagumpi, Srinivasa .
APPLIED ORGANOMETALLIC CHEMISTRY, 2015, 29 (03) :126-137
[4]   Biological approach of anticancer activity of new benzimidazole derivatives [J].
Blaszczak-Swiatkiewicz, Katarzyna ;
Olszewska, Paulina ;
Mikiciuk-Olasik, Elzbieta .
PHARMACOLOGICAL REPORTS, 2014, 66 (01) :100-106
[5]   Novel structure's derived from 2-[[(2-Pyridyl)methyl]thio]-1H-benzimidazole as anti-Helicobacter pylori agents, part 2 [J].
Carcangue, D ;
Shue, YK ;
Wuonola, MA ;
Uria-Nickelsen, M ;
Joubran, C ;
Abedi, JK ;
Jones, J ;
Kühler, TC .
JOURNAL OF MEDICINAL CHEMISTRY, 2002, 45 (19) :4300-4309
[6]   Glycoproteomic Approach Identifies KRAS as a Positive Regulator of CREG1 in Non-small Cell Lung Cancer Cells [J].
Clark, David J. ;
Mei, Yuping ;
Sun, Shisheng ;
Zhang, Hui ;
Yang, Austin J. ;
Mao, Li .
THERANOSTICS, 2016, 6 (01) :65-77
[7]  
CRONSTEIN BN, 1995, ANNU REV PHARMACOL, V35, P449, DOI 10.1146/annurev.pharmtox.35.1.449
[8]   Direct Binding of Glyceraldehyde 3-Phosphate Dehydrogenase to Telomeric DNA Protects Telomeres against Chemotherapy-Induced Rapid Degradation [J].
Demarse, Neil A. ;
Ponnusamy, Suriyan ;
Spicer, Eleanor K. ;
Apohan, Elif ;
Baatz, John E. ;
Ogretmen, Besim ;
Davies, Christopher .
JOURNAL OF MOLECULAR BIOLOGY, 2009, 394 (04) :789-803
[9]   Synthesis and anticancer and anti-HIV testing of some pyrazino[1,2-a]benzimidazole derivatives [J].
Demirayak, S ;
Abu Mohsen, U ;
Karaburun, AÇ .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2002, 37 (03) :255-260
[10]   POTENTIAL ANTITUMOR AGENTS .59. STRUCTURE-ACTIVITY-RELATIONSHIPS FOR 2-PHENYLBENZIMIDAZOLE-4-CARBOXAMIDES, A NEW CLASS OF MINIMAL DNA-INTERCALATING AGENTS WHICH MAY NOT ACT VIA TOPOISOMERASE-II [J].
DENNY, WA ;
REWCASTLE, GW ;
BAGULEY, BC .
JOURNAL OF MEDICINAL CHEMISTRY, 1990, 33 (02) :814-819