Synthesis, structural characterizations and in vitro cytotoxic activities of new sulfonamide-based Schiff base derivatives

被引:3
作者
Sahal, Hakan [1 ]
Oz, Samet [2 ]
Tekin, Suat [2 ]
Canpolat, Erdal [3 ]
机构
[1] Munzur Univ, Vocat Sch Tunceli, Dept Food Proc, TR-62000 Tunceli, Turkey
[2] Inonu Univ, Fac Med, Dept Physiol, Malatya, Turkey
[3] Firat Univ, Fac Educ, Dept Elementary Sci Educ, Elazig, Turkey
关键词
Sulfonamide derivative; Schiff base; spectroscopic; cytotoxic activity; cancer cell lines; DNA damage; RAPID COLORIMETRIC ASSAY; THERMAL CHARACTERIZATIONS; ANTIMICROBIAL ACTIVITY; ANTICANCER ACTIVITIES; CARBONIC-ANHYDRASE; INHIBITORS; GROWTH; SURVIVAL; SERIES;
D O I
10.1080/07391102.2022.2067237
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Synthesis of five different new compounds (1-5) were carried out. Their structures were characterized by spectroscopic methods such as Fourier transform infrared, Proton nuclear magnetic resonance, Carbon-13 nuclear magnetic resonance and Elemental analysis. Cytotoxic activities of five new sulfonamide based-Schiff base compounds were determined by MTT assay using A-2780 (human ovarian cancer) and MCF-7 (breast cancer) cell lines. LogIC(50) values of the sulfonamide derivates compounds were calculated by Graphpad Prism 12 programme after a 24-hour treatment for A2780 and MCF-7 cells. Comet assay experiments were performed to determine DNA damage using LogIC(50) concentrations of all compounds in A2780 and MCF-7 cells. All compounds significantly reduced A2780 and MCF-7 cell viability compared to control groups (p < 0.05). In addition, all compounds caused DNA damage in A2780 and MCF-7 cells (p < 0.05). These results show that the synthesized compounds exhibit cytotoxic effects against cancer cells and that the cause of cell death is due to DNA damage. Communicated by Ramaswamy H. Sarma
引用
收藏
页码:4361 / 4367
页数:7
相关论文
共 32 条
  • [1] Ahmed M, 2020, LAT AM J PHARM, V39, P38
  • [2] Discovering Some Novel 7-Chloroquinolines Carrying a Biologically Active Benzenesulfonamide Moiety as a New Class of Anticancer Agents
    Al-Dosari, Mohammed Salem
    Ghorab, Mostafa Mohamed
    Al-Said, Mansour Sulaiman
    Nissan, Yassin Mohammed
    [J]. CHEMICAL & PHARMACEUTICAL BULLETIN, 2013, 61 (01) : 50 - 58
  • [3] Alsaid M S, 2013, Drug Res (Stuttg), V63, P263, DOI 10.1055/s-0033-1337928
  • [4] Allicin from garlic strongly inhibits cysteine proteinases and cytopathic effects of Entamoeba histolytica
    Ankri, S
    Miron, T
    Rabinkov, A
    Wilchek, M
    Mirelman, D
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (10) : 2286 - 2288
  • [5] SULFONYLUREA RECEPTORS, ION CHANNELS, AND FRUIT-FLIES
    BOYD, AE
    [J]. DIABETES, 1988, 37 (07) : 847 - 850
  • [6] Sulfonamides and Sulfonylated Derivatives as Anticancer Agents
    Casini, Angela
    Scozzafava, Andrea
    Mastrolorenzo, Antonio
    Supuran, Claudiu T.
    [J]. CURRENT CANCER DRUG TARGETS, 2002, 2 (01) : 55 - 75
  • [7] Synthesis, Characterization, and Anticancer Activity of New Benzofuran Substituted Chalcones
    Coskun, Demet
    Tekin, Suat
    Sandal, Suleyman
    Coskun, Andmehmet Fatih
    [J]. JOURNAL OF CHEMISTRY, 2016, 2016
  • [8] RAPID COLORIMETRIC ASSAY FOR CELL-GROWTH AND SURVIVAL - MODIFICATIONS TO THE TETRAZOLIUM DYE PROCEDURE GIVING IMPROVED SENSITIVITY AND RELIABILITY
    DENIZOT, F
    LANG, R
    [J]. JOURNAL OF IMMUNOLOGICAL METHODS, 1986, 89 (02) : 271 - 277
  • [9] Impairment of the DNA repair and growth arrest pathways by p53R2 silencing enhances DNA damage-induced apoptosis in a p53-dependent manner in prostate cancer cells
    Devlin, Hong-Lin
    Mack, Phillip C.
    Burich, Rebekah A.
    Gumerlock, Paul H.
    Kung, Hsing-Jien
    Mudryj, Maria
    White, Ralph W. deVere
    [J]. MOLECULAR CANCER RESEARCH, 2008, 6 (05) : 808 - 818
  • [10] Dueke-Eze C. U., 2011, AFR J PURE APPL CHEM, V5, P13, DOI DOI 10.5897/AJPAC.9000160