Oleanolic Acid Glycosides from Scabiosa caucasica and Scabiosa ochroleuca: Structural Analysis and Cytotoxicity

Author:

Nazaryan Samvel12ORCID,Bruguière Antoine1,Hovhannisyan Nelli2,Miyamoto Tomofumi3,Dias Alexandre M. M.4,Bellaye Pierre-Simon5,Collin Bertrand6,Briand Loïc1,Mitaine-Offer Anne-Claire1

Affiliation:

1. Center for Taste and Feeding Behavior (CSGA), CNRS, INRAE, Agro Institute, Université de Bourgogne, 21000 Dijon, France

2. Center of Excellence in Applied Biosciences, Yerevan State University (YSU), Yerevan 0025, Armenia

3. Graduate School of Pharmaceutical Sciences, Kyushu University, Fukuoka 819-0395, Japan

4. Plateforme d’Imagerie et de Radiothérapie Précliniques, Service de Médecine Nucléaire, Centre Georges-François Leclerc, 21000 Dijon, France

5. Plateforme d’Imagerie et de Radiothérapie Précliniques, Service de Médecine Nucléaire, Centre Georges-François Leclerc, UMR INSERM, Université de Bourgogne, Institut Agro 1231, 21000 Dijon, France

6. Plateforme d’Imagerie et de Radiothérapie Précliniques, Service de Médecine Nucléaire, Centre Georges-François Leclerc, ICMUB, UMR CNRS, Université de Bourgogne 6302, 21000 Dijon, France

Abstract

In the field of research on medicinal plants from the Armenian flora, the phytochemical study of two Scabiosa L. species, S. caucasica M. Bieb. and S. ochroleuca L. (Caprifoliaceae), has led to the isolation of five previously undescribed oleanolic acid glycosides from an aqueous-ethanolic extract of the roots: 3-O-α-L-rhamnopyranosyl-(1→3)-β-D-glucopyranosyl-(1→4)-β-D-glucopyranosyl-(1→4)-β-D-xylopyranosyl-(1→3)-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyloleanolic acid 28-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester, 3-O-β-D-xylopyranosyl-(1→2)-[α-L-rhamnopyranosyl-(1→4)]-β-D-glucopyranosyl-(1→4)-β-D-glucopyranosyl-(1→4)-β-D-xylopyranosyl-(1→3)-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyloleanolic acid 28-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester, 3-O-β-D-xylopyranosyl-(1→2)-[α-L-rhamnopyranosyl-(1→4)]-β-D-glucopyranosyl-(1→4)-β-D-glucopyranosyl-(1→4)-β-D-xylopyranosyl-(1→3)-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyloleanolic acid, 3-O-β-D-xylopyranosyl-(1→2)-[α-L-rhamnopyranosyl-(1→4)]-β-D-xylopyranosyl-(1→4)-β-D-glucopyranosyl-(1→4)-β-D-xylopyranosyl-(1→3)-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyloleanolic acid 28-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester, 3-O-α-L-rhamnopyranosyl-(1→4)-β-D-glucopyranosyl-(1→4)-β-D-glucopyranosyl-(1→4)-β-D-xylopyranosyl-(1→3)-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyloleanolic acid 28-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester. Their full structural elucidation required extensive 1D and 2D NMR experiments, as well as mass spectrometry analysis. For the biological activity of the bidesmosidic saponins and the monodesmosidic saponin, their cytotoxicity on a mouse colon cancer cell line (MC-38) was evaluated.

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

Reference13 articles.

1. International Agency for Research on Cancer (IARC), World Health Organization (2023, March 28). Cancer Today: GLOBOCAN 2020 Estimates, Available online: https://gco.iarc.fr/today/home.

2. Overview of Cancer Control in Armenia and Policy Implications;Bedirian;Front. Oncol.,2022

3. Synthesis and antitumor activities of naturally occurring oleanolic acid triterpenoid saponins and their derivatives;Liu;Eur. J. Med. Chem.,2013

4. Oleanolic acid and hederagenin glycosides from Weigela stelzneri;Rezgui;Phytochemistry,2016

5. Cytotoxic glycosides from Weigela × “Bristol Ruby”;Nguyen;Fitoterapia,2019

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