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Ternifolipyrons A–J: new cytotoxic α-pyrones from Isodon ternifolius (D. Don) Kudô

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 chemica...

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Autores principales: Elshamy, Abdelsamed I., Mohamed, Tarik A., Swapana, Ningombam, Kasai, Yusuke, Noji, Masaaki, Efferth, Thomas, Imagawa, Hiroshi, Hegazy, Mohamed-Elamir F., Umeyama, Akemi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10309080/
https://www.ncbi.nlm.nih.gov/pubmed/37396835
http://dx.doi.org/10.1039/d3ra03146b
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author Elshamy, Abdelsamed I.
Mohamed, Tarik A.
Swapana, Ningombam
Kasai, Yusuke
Noji, Masaaki
Efferth, Thomas
Imagawa, Hiroshi
Hegazy, Mohamed-Elamir F.
Umeyama, Akemi
author_facet Elshamy, Abdelsamed I.
Mohamed, Tarik A.
Swapana, Ningombam
Kasai, Yusuke
Noji, Masaaki
Efferth, Thomas
Imagawa, Hiroshi
Hegazy, Mohamed-Elamir F.
Umeyama, Akemi
author_sort Elshamy, Abdelsamed I.
collection PubMed
description 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 IC(50) 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 IC(50) values of 8.37, 18.04, and 18.93 μM, respectively.
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spelling pubmed-103090802023-06-30 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 RSC Adv Chemistry 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 IC(50) 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 IC(50) values of 8.37, 18.04, and 18.93 μM, respectively. The Royal Society of Chemistry 2023-06-29 /pmc/articles/PMC10309080/ /pubmed/37396835 http://dx.doi.org/10.1039/d3ra03146b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Elshamy, Abdelsamed I.
Mohamed, Tarik A.
Swapana, Ningombam
Kasai, Yusuke
Noji, Masaaki
Efferth, Thomas
Imagawa, Hiroshi
Hegazy, Mohamed-Elamir F.
Umeyama, Akemi
Ternifolipyrons A–J: new cytotoxic α-pyrones from Isodon ternifolius (D. Don) Kudô
title Ternifolipyrons A–J: new cytotoxic α-pyrones from Isodon ternifolius (D. Don) Kudô
title_full Ternifolipyrons A–J: new cytotoxic α-pyrones from Isodon ternifolius (D. Don) Kudô
title_fullStr Ternifolipyrons A–J: new cytotoxic α-pyrones from Isodon ternifolius (D. Don) Kudô
title_full_unstemmed Ternifolipyrons A–J: new cytotoxic α-pyrones from Isodon ternifolius (D. Don) Kudô
title_short Ternifolipyrons A–J: new cytotoxic α-pyrones from Isodon ternifolius (D. Don) Kudô
title_sort ternifolipyrons a–j: new cytotoxic α-pyrones from isodon ternifolius (d. don) kudô
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10309080/
https://www.ncbi.nlm.nih.gov/pubmed/37396835
http://dx.doi.org/10.1039/d3ra03146b
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