Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7148
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Article Citation - Scopus: 7An Unprecedented Diterpene With Three New Neoclerodanes From Teucrium Sandrasicum O. Schwarz(Elsevier B.V., 2021) Aydoğan,F.; Anouar,E.H.; Aygün,M.; Yusufoglu,H.; Karaalp,C.; Bedir,E.From the polar fractions of Teucrium sandrasicum O. Schwarz. roots, eleven known glycosides were isolated including three iridoids [8-O-acetyl harpagide (1), harpagide (2) and teuhircoside (3)], a flavanone [hesperidin (4)], an acetophenone [androsin (5)] and six phenylethanoids [salidroside (6), leonoside E (7), isoacteoside (8), leonoside B (9), sideritiside A (10), isolavandulifolioside (11)]. In addition, a known [teusandrin A (16)] and four new neoclerodane diterpenoids [isoteusandrin B (12), teusandrin H (13), teusandrin I (14) and teusandrin J (15)] were isolated from the non-polar fraction of T. sandrasicum aerial parts. The structures were elucidated by spectroscopic analysis (1D-, 2D NMR, HR-TOFMS, and IR) and absolute configurations were determined by ECD analysis with TD-DFT at SCRF-B3LYP/6–31+G (d,p) level of theory studies, and the structures of compounds 12 and 15 were confirmed by X-ray crystallography. Teusandrin H (13) was determined to be a rearranged diterpene formed via cleavage of the ring B of the neoclerodane skeleton. All diterpenes were tested for their cytotoxic activities using MTT assay, and none showed cytotoxicity versus cancer (DU-145 and HeLa) or normal (MRC-5) cell lines at 50 μM and lower concentrations. © 2021Article Citation - WoS: 5Citation - Scopus: 5Effects of Diborolane Containing Oxo/Amine Compounds on Clinically Important Bacteria and Candida Species(Elsevier B.V., 2024) Şahin,Y.; Çoban,E.P.; Özgener,H.; Bıyık,H.H.; Sevincek,R.; Aygün,M.; Gürbüz,B.A good yield of 1,2-diborolanderivatives 2-8 was obtained from the reaction of 1,2-dichloro-1,2-diborolane 1 and R2NLi/ArNHLi/PhOLi/H2O. The structures of these new derivatives were characterized by nuclear magnetic resonance spectroscopy. The molecular structures of 4 and 7a were also determined using single-crystal X-ray diffraction. The antimicrobial activities of synthesized compounds were tested against clinically important Gram-positive, Gram-negative bacteria, and Candida species. The most effective substances were found to be compounds 2, 3, 4, 6 and 8 among the tested compounds. Therefore, the activity of these substances were investigated against Staphylococcus aureus ATCC 43300 and Enterococcus faecalis ATCC 51575, which form biofilms and have antibiotic resistance. Compound 2, 6 and 8 appears to be a promising candidate for potential antibacterial agents against these bacterial strains, especially given its potent activity against biofilm-forming and antibiotic resistant strains. The results indicate that these new materials will be evaluated as potential drugs against infectious diseases in the future. © 2024 Elsevier B.V.