Dammarane-type triterpenoid saponins from Salvia russellii Benth. (April 2021)
- Record Type:
- Journal Article
- Title:
- Dammarane-type triterpenoid saponins from Salvia russellii Benth. (April 2021)
- Main Title:
- Dammarane-type triterpenoid saponins from Salvia russellii Benth.
- Authors:
- Hafez Ghoran, Salar
Firuzi, Omidreza
Asadollahi, Mojtaba
Stuppner, Hermann
Alilou, Mostafa
Jassbi, Amir Reza - Abstract:
- Abstract: Three undescribed dammarane-type saponins, russelliinosides A-C, together with a common sterol (β-sitosterol), an abietane diterpenoid (18-hydroxyferruginol), two oleane triterpenoids (daturaolone and oleanolic acid), an ursane triterpenoid (ursolic acid) as well as three 5-hydroxyflavones (cirsimaritin, eupatorin, and salvigenin) were isolated from a dichloromethane extract of the aerial parts of Salvia russellii Benth. The chemical structures of the aforementioned compounds were characterized, using detailed spectroscopic analyses, including high-resolution mass spectrometry and 1D and 2D NMR ( 1 H– 1 H COSY, TOCSY, HSQC, HMBC and NOESY) spectroscopy as well as physicochemical properties. Cytotoxic effects of S. russellii extract and the three isolated russelliinosides were tested against MCF-7 human breast and A549 lung cancer, as well as non-cancer NIH/3T3 cells using MTT reduction assay. Russelliinosides A and B exhibited cytotoxic activities with IC50 values of 7.1 and 30.7 μg/ml against MCF-7 and 33.9 and 69.4 μg/ml against A549 cells, respectively, while russelliinoside C did not show cytotoxicity against cancer cells. On the other hand, russelliinoside A showed an IC50 value of 31.5 μg/ml against NIH/3T3 cells, while russelliinosides B and C had no effect on the viability of these non-cancer cells. Graphical abstract: Image 1 Highlights: Three cytotoxic dammarane triterpene saponins were isolated from Salvia russellii. Three 5-hydoxyl-polymethoxy flavones,Abstract: Three undescribed dammarane-type saponins, russelliinosides A-C, together with a common sterol (β-sitosterol), an abietane diterpenoid (18-hydroxyferruginol), two oleane triterpenoids (daturaolone and oleanolic acid), an ursane triterpenoid (ursolic acid) as well as three 5-hydroxyflavones (cirsimaritin, eupatorin, and salvigenin) were isolated from a dichloromethane extract of the aerial parts of Salvia russellii Benth. The chemical structures of the aforementioned compounds were characterized, using detailed spectroscopic analyses, including high-resolution mass spectrometry and 1D and 2D NMR ( 1 H– 1 H COSY, TOCSY, HSQC, HMBC and NOESY) spectroscopy as well as physicochemical properties. Cytotoxic effects of S. russellii extract and the three isolated russelliinosides were tested against MCF-7 human breast and A549 lung cancer, as well as non-cancer NIH/3T3 cells using MTT reduction assay. Russelliinosides A and B exhibited cytotoxic activities with IC50 values of 7.1 and 30.7 μg/ml against MCF-7 and 33.9 and 69.4 μg/ml against A549 cells, respectively, while russelliinoside C did not show cytotoxicity against cancer cells. On the other hand, russelliinoside A showed an IC50 value of 31.5 μg/ml against NIH/3T3 cells, while russelliinosides B and C had no effect on the viability of these non-cancer cells. Graphical abstract: Image 1 Highlights: Three cytotoxic dammarane triterpene saponins were isolated from Salvia russellii. Three 5-hydoxyl-polymethoxy flavones, β-sitosterol ursolic and oleanolic acid were isolated from S. russellii. Chemical structures of the undescribed compounds were elucidated by 1D, 2D-NMR, and HRESI-MS analyses. … (more)
- Is Part Of:
- Phytochemistry. Volume 184(2021)
- Journal:
- Phytochemistry
- Issue:
- Volume 184(2021)
- Issue Display:
- Volume 184, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 184
- Issue:
- 2021
- Issue Sort Value:
- 2021-0184-2021-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-04
- Subjects:
- Salvia russellii Benth. -- Lamiaceae -- Dammarane triterpenes -- Russelliinosides -- Cytotoxic activity
Botanical chemistry -- Periodicals
Biochemistry -- Periodicals
Botany -- Periodicals
Chimie végétale -- Périodiques
572.2 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00319422 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.phytochem.2020.112653 ↗
- Languages:
- English
- ISSNs:
- 0031-9422
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6489.800000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 25120.xml