Dergiler / Records of Natural Products / 2021 / Cilt: 15 - Sayı: 2

Isolation, Characterization and Antiproliferative Activity of Secondary Metabolites from Tanacetum alyssifolium (Bornm.) Grierson

Sayfa
122–129
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Sesquiterpene lactones; tatridin A (2), tamirin (4) and tanachin (5) were found to be the most cytotoxic molecules against MCF-7 cell line.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:Secondary metabolites of Tanacetum alyssifolium (Bornm.) Grierson (Asteraceae) were investigated for the first time.
📊
Temel Bulgular & Veri:Thirteen compounds including axillarin (1), Luteolin-7-O-β-glucoside (8) and rutin (13) as flavonoids, fraxetin (7), isofraxidin (9), isofraxidin-7-O-glucoside (11) and fraxidin (12) as coumarins, tatridin A (2), altissin (3), tamirin (4) and tanachin (5) as sesquiterpene lactones and 2,4-dihydroxy-6-methoxy acetophenone (6) and picein (10) as acetophenone derivatives were isolated from the methanol extract of the species.
💡
Sonuç & Katkı:Sesquiterpene lactones; tatridin A (2), tamirin (4) and tanachin (5) were found to be the most cytotoxic molecules against MCF-7 cell line.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Özet

Secondary metabolites of Tanacetum alyssifolium (Bornm.) Grierson (Asteraceae) were investigated for the first time. Thirteen compounds including axillarin (1), Luteolin-7-O-β-glucoside (8) and rutin (13) as flavonoids, fraxetin (7), isofraxidin (9), isofraxidin-7-O-glucoside (11) and fraxidin (12) as coumarins, tatridin A (2), altissin (3), tamirin (4) and tanachin (5) as sesquiterpene lactones and 2,4-dihydroxy-6-methoxy acetophenone (6) and picein (10) as acetophenone derivatives were isolated from the methanol extract of the species. The structures of all isolated compounds were elucidated by 1D and 2D-NMR techniques and by comparing with the literature data. In addition, in vitro cytotoxic activity of all isolated compounds was evaluated against breast cancer MCF-7 cell line by XTT assay. Sesquiterpene lactones; tatridin A (2), tamirin (4) and tanachin (5) were found to be the most cytotoxic molecules against MCF-7 cell line.

🔖

Bu Makaleye Atıf Yap

KÖKSAL, E., ULUTAŞ, Y., BAYRAKTAR, T., ALTAY, A., ÇATIR, M., ALP, C., ALEMDAR, M. B. A., ŞİMŞEK, S., DEMİRTAŞ, İ., KANDEMİR, A., AKŞİT, H. (2021). Isolation, Characterization and Antiproliferative Activity of Secondary Metabolites from Tanacetum alyssifolium (Bornm.) Grierson. Records of Natural Products, Cilt: 15 - Sayı: 2, 122–129. https://ajindex.com/articles/308200

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (15)

  1. M.J. Abad, P. Bermejo and A. Villar (1995). An approach to the genus Tanacetum L.(Compositae): phytochemical and pharmacological review, Phytother. Res. 9, 79-92
  2. E. Köksal (2011). Peroxidase from leaves of Spinach (Spinacia oleracea): Partial purification and some biochemical properties, Int. J. Pharmocol. 7, 135-139
  3. R.D. Lindsay (1996). Flavors in Food Chemistry 3rd edition ed.: Marcel Dekker Inc
  4. A. Bower, S. Marquez and E.G. de Mejia (2016). The health benefits of selected culinary herbs and spices found in the traditional Mediterranean diet, Crit. Rev. Food Sci. Nutr. 56, 2728-2746
  5. M.B. Bahadori, M. Eskandani, M. De Mieri, M. Hamburger and H. Nazemiyeh (2018). Anti-proliferative activity-guided isolation of clerodermic acid from Salvia nemorosa L.: Geno/cytotoxicity and hypoxiamediated mechanism of action, Food Chem. Toxicol. 120, 155-163
  6. T. Baytop (1999). Türkiye’de Bitkiler İle Tedavi İstanbul: Nobel Yayınları
  7. A. Güner (2012). Türkiye Bitkileri Listesi (Damarlı Bitkiler) İstanbul: ANG Vakfı
  8. A. Kandemir, M. Korkmaz and C.Ş.Ç Sevindi (2015). Erzincan (Türkiye)’a Özgü Endemik Bitki Taksonlarının IUCN Tehdit Kategorileri, Bağbahçe Bil. Derg. 2, 43-65
  9. Z.Q, Yin, C.L. Fan, W.C. Ye, R.W. Jiang, C.T. Che, T.C. Mak and X.S. Yao (2005). Acetophenone derivatives and sesquiterpene from Euphorbia ebracteolata, Planta Med. 71, 979-982
  10. J. Dou, W. Xu, J.J. Koivisto, J.K. Mobley, D. Padmakshan, M. Kögler and T. Vuorinen (2018). Characteristics of hot water extracts from the bark of cultivated willow (Salix sp.), ACS Sustain. Chem. Eng. 6, 5566-5573
  11. J. Hu, W. Ma, N. Li and K.J. Wang (2017). Antioxidant and anti-inflammatory flavonoids from the flowers of Chuju, a medical cultivar of Chrysanthemum morifolim Ramat, J. Mex. Chem. Soc. 61, 282-289
  12. Z. Özer, S. Çarıkçı, H. Yılmaz, T. Kılıç, T. Dirmenci and A.C. Gören (2020). Determination of secondary metabolites of Origanum vulgare subsp. hirtum and O. vulgare subsp. vulgare by LC-MS/MS, J. Chem. Metrol. 14, 24-35
  13. J.Y. Lallemand and M. Duteil (1977). 13C NMR spectra of quercetin and rutin, Org. Magn. Reson. 9, 179- 180
  14. R.E. Craig, J.A. Campbell, A.C. Craig, C.F. Campana and R.G. Kelsey (1990). Tatridin A from Artemisia arbuscula ssp. arbuscula: Crystal structure of tatridin A diacetate and the identification of deacetyltulirinol, J. Nat. Prod. 53, 1585-1586
  15. M. Konstantinopoulou, A. Karioti, S. Skaltsas and H. Skaltsa (2003). Sesquiterpene lacto