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Ternifolipyrons A-J: new cytotoxic α-pyrones from Isodon ternifolius (D. Don) Kudô.
Elshamy, Abdelsamed I; Mohamed, Tarik A; Swapana, Ningombam; Kasai, Yusuke; Noji, Masaaki; Efferth, Thomas; Imagawa, Hiroshi; Hegazy, Mohamed-Elamir F; Umeyama, Akemi.
Affiliation
  • Elshamy AI; Chemistry of Natural Compounds Department, National Research Centre 33 El Bohouth St., Dokki Giza 12622 Egypt elshamynrc@yahoo.com.
  • Mohamed TA; Chemistry of Medicinal Plants Department, National Research Centre 33 El-Bohouth St., Dokki Giza 12622 Egypt mohegazy@uni-mainz.de.
  • Swapana N; Faculty of Pharmaceutical Sciences, Tokushima Bunri University Yamashiro-cho Tokushima 770-8514 Japan umeyama@ph.bunri-u.ac.jp.
  • Kasai Y; Department of Chemistry, Manipur Technical University Takyelpat Imphal 795004 Manipur India.
  • Noji M; Faculty of Pharmaceutical Sciences, Tokushima Bunri University Yamashiro-cho Tokushima 770-8514 Japan umeyama@ph.bunri-u.ac.jp.
  • Efferth T; Faculty of Pharmaceutical Sciences, Tokushima Bunri University Yamashiro-cho Tokushima 770-8514 Japan umeyama@ph.bunri-u.ac.jp.
  • Imagawa H; Department of Pharmaceutical Biology, Institute of Pharmaceutical and Biomedical Sciences, University of Mainz Staudinger Weg 5 55128 Mainz Germany.
  • Hegazy MF; Faculty of Pharmaceutical Sciences, Tokushima Bunri University Yamashiro-cho Tokushima 770-8514 Japan umeyama@ph.bunri-u.ac.jp.
  • Umeyama A; Chemistry of Medicinal Plants Department, National Research Centre 33 El-Bohouth St., Dokki Giza 12622 Egypt mohegazy@uni-mainz.de.
RSC Adv ; 13(29): 19710-19720, 2023 Jun 29.
Article in En | MEDLINE | ID: mdl-37396835
ABSTRACT
Isodon ternifolius (D.Don) Kudô is an important Asian herb used in traditional medicine against several diseases. Nineteen compounds were isolated from the dichloromethane-methanol (1 1) extract of I. ternifolius roots, including ten new α-pyrone derivatives, named ternifolipyrons A-J. The chemical structures of the isolates were determined by a combination of 1D and 2D NMR, along with LR- and HRMS spectroscopy. The absolute configurations of the α-pyrone derivatives were constructed based upon the X-ray signal crystal of the bromobenzoyl derivative of 1 as well as the electronic circular dichroism (ECD). All isolates (1-19) were investigated for their growth-inhibitory potential towards CCRF-CEM-leukemia cells at a fixed concentration of 30 µM. The compounds which exerted more than 50% inhibition at this concentration, compounds (7, 10, 12, 15-17), were tested at a different concentration range to determine their IC50 values in CCRF-CEM leukemia, MDA-MB-231 triple-negative breast cancer, and MCF7 breast cancer cell lines. Ursolic acid (16) showed the most potent activity against the three cancer cell lines with IC50 values of 8.37, 18.04, and 18.93 µM, respectively.