Synthesis, characterization and in silico studies of coumarin-chalcone derivatives and their cytotoxicity activity against breast cancer cells

被引:1
作者
Rahama, Muhammad Sulaiman [1 ,3 ]
Khairuddean, Melati [1 ]
Ismail, Noor Zafirah [1 ]
Al-Amin, Mohammad [2 ]
Salhimi, Salizawati Muhamad [2 ]
机构
[1] Univ Sains Malaysia, Sch Chem Sci, George Town 11800, Penang, Malaysia
[2] Univ Sains Malaysia, Sch Pharmaceut Sci, George Town 11800, Penang, Malaysia
[3] Umaru Musa Yaradua Univ, Dept Chem, Katsina, Nigeria
关键词
In silico study; Coumarin-chalcone; Cytotoxicity activity; Breast cancer cells; MOLECULAR DOCKING; BIOLOGICAL EVALUATION; DRUG DISCOVERY; ANTICANCER; PERFORMANCE; SOLUBILITY; INDUCTION; APOPTOSIS; DESIGN; LINES;
D O I
10.1016/j.molstruc.2024.140341
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Breast carcinoma disease is the most common ailment affecting women globally. Despite relentless efforts by scientists, numerous scientific strategies have been blocked by the aggressive nature of cancer cells, impeding their invasion, and spread to neighbouring tissues. This study aimed on evaluating the cytotoxic effects of newly synthesized coumarin chalcone compounds on breast cancer cell lines (MCF-7). The findings were compared with computational data derived from computer-assisted software and the Swiss ADME web tool. Molecular docking analyses indicated that all the synthesized compounds satisfied Lipinski's criteria. Furthermore, results from cytotoxicity assays demonstrated that compounds 5A, 5B, and 7A displayed significant efficacy against MCF-7 cells with IC50 (6.44 f 0.64 mu M, 8.48 f 1.06 mu M, 9.02 f 0.96 mu M), this finding indicated that the compounds highlighted above demonstrated greater cytotoxic effects against human breast cancer cells MCF-7 than the control drug Tamoxifen (IC50 = 17.42 f 1.48 mu M). Therefore, compounds 5A, 5B, and 7A could be considered promising compounds against MCF-7.
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页数:16
相关论文
共 62 条
[51]  
Rizvi SMD, 2013, EXCLI J, V12, P831
[52]   Advances in Lung Cancer Treatment Using Nanomedicines [J].
Sharma, Akshansh ;
Shambhwani, Devanshi ;
Pandey, Sadanand ;
Singh, Jay ;
Lalhlenmawia, Hauzel ;
Kumarasamy, Murali ;
Singh, Sachin Kumar ;
Chellappan, Dinesh Kumar ;
Gupta, Gaurav ;
Prasher, Parteek ;
Dua, Kamal ;
Kumar, Deepak .
ACS OMEGA, 2023, 8 (01) :10-41
[53]   An ongoing journey of chalcone analogues as single and multi-target ligands in the field of Alzheimer's disease: A review with structural aspects [J].
Sharma, Pratibha ;
Singh, Manjinder .
LIFE SCIENCES, 2023, 320
[54]   Long non-coding RNAs in drug resistance across the top five cancers: Update on their roles and mechanisms [J].
Shi, Yue ;
Adu-Amankwaah, Joseph ;
Zhao, Qizhong ;
Li, Xin ;
Yu, Qianxue ;
Bushi, Aisha ;
Yuan, Jinxiang ;
Tan, Rubin .
HELIYON, 2024, 10 (05)
[55]  
Tosun A, 2009, Z NATURFORSCH C, V64, P56
[56]  
van de Waterbeemd H, 2009, CHEM BIODIVERS, V6, P1760, DOI 10.1002/cbdv.200900056
[57]   A gap analysis of UK biobank publications reveals SNPs associated with intrinsic subtypes of breast cancer [J].
van den Driest, Lisa ;
Kelly, Patricia ;
Marshall, Alan ;
Johnson, Caroline H. ;
Lasky-Su, Jessica ;
Lannigan, Alison ;
Rattray, Zahra ;
Rattray, Nicholas J. W. .
COMPUTATIONAL AND STRUCTURAL BIOTECHNOLOGY JOURNAL, 2024, 23 :2200-2210
[58]   Review on Natural Coumarin Lead Compounds for Their Pharmacological Activity [J].
Venugopala, K. N. ;
Rashmi, V. ;
Odhav, B. .
BIOMED RESEARCH INTERNATIONAL, 2013, 2013
[59]   Selective cytotoxicity and apoptosis induction in glioma cell lines by 5-oxygenated-6,7-methylenedioxycoumarins from Pterocaulon species [J].
Vianna, D. R. ;
Hamerski, L. ;
Figueiro, F. ;
Bernardi, A. ;
Visentin, L. C. ;
Pires, E. N. S. ;
Teixeira, H. F. ;
Salbego, C. G. ;
Eifler-Lima, V. L. ;
Battastini, A. M. O. ;
von Poser, G. L. ;
Pinto, A. C. .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2012, 57 :268-274
[60]   Dietary Compound Isoliquiritigenin Inhibits Breast Cancer Neoangiogenesis via VEGF/VEGFR-2 Signaling Pathway [J].
Wang, Zhiyu ;
Wang, Neng ;
Han, Shouwei ;
Wang, Dongmei ;
Mo, Suilin ;
Yu, Linzhong ;
Huang, Hui ;
Tsui, Kamchuen ;
Shen, Jiangang ;
Chen, Jianping .
PLOS ONE, 2013, 8 (07)