Journal
BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH
Volume 56, Issue -, Pages -Publisher
ASSOC BRAS DIVULG CIENTIFICA
DOI: 10.1590/1414-431X2023e12404
Keywords
Terezine E; 14-Hydroxyterezine D; Cytotoxicity; Antimicrobial activity; Molecular docking
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Secondary metabolites produced by endophytes are valuable sources of biologically active compounds. The newly discovered natural products terezine E and 14-hydroxyterezine D exhibited anti-cancer activity in our study, and their affinity for binding to specific enzymes was evaluated using molecular docking. Furthermore, their cytotoxicity, antimicrobial activity, and minimum inhibitory concentration values were assessed. Terezine E showed higher cytotoxicity and antimicrobial activity than 14-hydroxyrerezine D.
Secondary metabolites produced by endophytes are an excellent source of biologically active compounds. The newly isolated natural products terezine E and 14-hydroxyterezine D are endophytic metabolites exhibiting anticancer activity recently identified by our team (https://doi.org/10.1080/14786419.2018.1489393). In our current study, we evaluated their affinity for binding to the active site of histone deacetylase (PDB ID: 4CBT) and matrix metalloproteinase 9 (PDB ID: 4H3X) by molecular docking using AutoDock Vina software after having tested their cytotoxic activities on three cell lines (human ductal breast epithelial tumor cells (T47D)-HCC1937), human hepatocarcinoma cell line (HepG2)-HB8065), and human colorectal carcinoma cells (HCT-116)-TCP1006, purchased from ATCC, USA)). Additionally, their antimicrobial activities were investigated, and their minimum inhibitory concentration (MIC) values were determined against P. notatum and S. aureus by the broth microdilution method. Higher cytotoxicity was observed for terezine E against all tested cell lines compared to 14-hydroxyterezine D. Molecular docking results supported the high cytotoxicity of terezine E and showed higher binding affinity with 4CBT with an energy score of 9 kcal/mol. Terezine E showed higher antibacterial and antifungal activities than 14-hydroxyrerezine D: MIC values were 15.45 and 21.73 mu g/mL against S. aureus and 8.61 and 11.54 mu g/mL against P. notatum, respectively.
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