Journals / Turkish Journal of Chemistry / 2006 / Cilt: 30 - Sayı: 3

Secondary Metabolites from Phlomis syriaca and Their Antioxidant Activities

Pages
383–390
Publication Date
2006-03-01
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Free radical scavenging activity of the isolated compounds was determined using the radical 2,2-diphenyl-1-picrylhydrazyl (DPPH), spectroscopically.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:An iridoid glucoside, lamiide (1); 4 phenylethanoid glycosides, acteoside (2), b-OH acteoside (3), leucosceptoside A (4) and samioside (5); a caffeic acid ester, chlorogenic acid (6); 2 flavone glucosides, luteolin-7-O-glucopyranoside (7) and chrysoeriol-7-O-glucopyranoside (8); and a flavanone aglycone, naringenin (9), were isolated from the aerial parts of Phlomis syriaca.
📊
Key Findings & Data:The structures of the isolated compounds were elucidated by means of spectroscopic (UV, IR, 1D- and 2D-NMR, and FAB-MS) methods.
💡
Conclusion & Impact:Free radical scavenging activity of the isolated compounds was determined using the radical 2,2-diphenyl-1-picrylhydrazyl (DPPH), spectroscopically.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Phlomis syriaca · Lamiaceae · Iridoid glucosides

Abstract

An iridoid glucoside, lamiide (1); 4 phenylethanoid glycosides, acteoside (2), b-OH acteoside (3), leucosceptoside A (4) and samioside (5); a caffeic acid ester, chlorogenic acid (6); 2 flavone glucosides, luteolin-7-O-glucopyranoside (7) and chrysoeriol-7-O-glucopyranoside (8); and a flavanone aglycone, naringenin (9), were isolated from the aerial parts of Phlomis syriaca. The structures of the isolated compounds were elucidated by means of spectroscopic (UV, IR, 1D- and 2D-NMR, and FAB-MS) methods. Free radical scavenging activity of the isolated compounds was determined using the radical 2,2-diphenyl-1-picrylhydrazyl (DPPH), spectroscopically.

Özet

An iridoid glucoside, lamiide (1); 4 phenylethanoid glycosides, acteoside (2), b-OH acteoside (3), leucosceptoside A (4) and samioside (5); a caffeic acid ester, chlorogenic acid (6); 2 flavone glucosides, luteolin-7-O-glucopyranoside (7) and chrysoeriol-7-O-glucopyranoside (8); and a flavanone aglycone, naringenin (9), were isolated from the aerial parts of Phlomis syriaca. The structures of the isolated compounds were elucidated by means of spectroscopic (UV, IR, 1D- and 2D-NMR, and FAB-MS) methods. Free radical scavenging activity of the isolated compounds was determined using the radical 2,2-diphenyl-1-picrylhydrazyl (DPPH), spectroscopically.

🔖

Cite This Article

HARPUT, Ü. Ş., ÇALIŞ, İ., SARACOĞLU, İ., DÖNMEZ, A. A., NAGATSU, A. (2006). Secondary Metabolites from Phlomis syriaca and Their Antioxidant Activities. Turkish Journal of Chemistry, Cilt: 30 - Sayı: 3, 383–390. https://ajindex.com/articles/218010

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (14)

  1. A. Huber Morath, Phlomis, in “Flora of Turkey and the East Aegean Islands”, ed.: P.H.Davis. Vol. 7, pp 102-126,
  2. Edinburg University Press,
  3. Edinburgh (1982), T. Baytop, “Therapy with Medicinal Plants in Turkey (Past and Present)” 2nded. pp. 193, Nobel Tıp Kitapevleri, ˙Istanbul (1999). E. Ye¸silada, Biodiversity in Turkish Folk Medicine in “Biomolecular Aspects of Biodiversity and Inno- vative Utilization” Ed. B.Sener, Kluwer Academic, Pleum Publishers,
  4. London (2002). ˙I. C¸ alı¸s, A.A. Ba¸saran, ˙I. Saraco˘glu, O. Sticher and P. R¨uedi, Phytochemistry 29, 1253-1257 (1990). ˙I. Saraco˘glu, M. Varel, ˙I. C¸ alı¸s and A.A. D¨onmez, Turk. J. Chem. 27, 739-747 (2003). T. Ers¨oz, ˙I. Saraco˘glu, D. Ta¸sdemir, H. Kırmızıbekmez, A.A. D¨onmez, C.M. Ireland and ˙I. C¸ alı¸s, Z. Natur- forsch., 57c, 221-225 (2002). ˙I. Saraco˘glu, ¨U.S¸. Harput, ˙I. C¸ alı¸s and Y. Ogihara, Turk. J. Chem. 26, 133-142 (2002). ˙I. C¸ alı¸s, H. Kırmızıbekmez, D. Ta¸sdemir and P. R¨uedi, Helv. Chim. Acta. 87, 611-619 (2004).
  5. T. Hatano, R. Edamatsu, M. Hiramatsu, A. Mori, Y. Fujita, T. Yasuhara, T. Yoshida and T. Okuda T. Chem. Pharm. Bull. 37, 2016-2021 (1989).
  6. A. Bianco, C. Bonini, G. Guiso, C. Iavarone and C. Tragola, Gazz. Chim. Ital. 107, 67-69 (1977).
  7. C. Andary, R. Wylde, C. Laffite, G. Privat and F. Winternitz, Phytochemistry, 21, 1123-1127 (1982).
  8. S. Kitagawa, H. Tsukamoto, S. Hisade and S. Nishibe, Chem. Pharm. Bull. 32, 1209-1213 (1984).
  9. T. Miyase, A. Koizumi, A. Ueno, T. Noro, M. Kuroyanagi, S. Fukushima, Y. Akiyama and T. Takemoto, Chem. Pharm. Bull. 30, 2732-2737 (1982). F.N. Yal¸cın, T. Ers¨oz, P. Akbay, ˙I. C¸ alı¸s, A.A. D¨onmez and O. Sticher, Turk J. Chem. 27, 295-306 (2003).
  10. K.R. Markham and V.M. Chari, The Flavonoids: Advances in Research, eds: J.B. Harborne and T.J. Mabry, Chapman and Hall, London (1982).
  11. K.R. Markham and H. Geiger, The Flavonoids: Advances in Research since 1986, ed: J.B. Harborne, Chapman and Hill, London (1994).
  12. X.L. Piao, I.H. Park, S.H. Baek, H.Y. Kim, M.K. Park and J.H. Park, J. Ethnopharmacol. 93, 243-246 (2004).
  13. H. Kırmızıbekmez, S. Piacenta, C. Pizza, A.A. D¨onmez, ˙I. C¸ alı¸s, Z. Naturforsch. 59b, 609-613 (2004). SBAG2304, Chemotaxonomy of the Genus Phlomis in Turkey (2004). ˙I. Saraco˘glu, M. Inoue, ˙I. C¸ alı¸s and Y. Ogihara, Biol. Pharm. Bull. 18, 1396-1400 (1995). ˙I. C¸ alı¸s, H. Kırmızıbekmez, J.A. Beutler, A.A. D¨onmez, F.N. Yal¸cın, E. Kılı¸c, M. ¨Ozalp, P. R¨uedi and D. Ta¸sdemir, Turk. J. Chem. 29, 71-81 (2005).
  14. P. Montoro, A. Br