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Phytochemical Content of Centaurea polypodiifolia boiss. var. polypodiifolia

Year 2017, Volume: 4 Issue: 3, Special Issue 2, 452 - 458, 20.12.2017
https://doi.org/10.21448/ijsm.376888

Abstract

Various solvents including hexane, CHCl3, EtOAc, and MeOH were used to extract the aerial parts of C. polypodiifolia Boiss. var. polypodiifolia. Hexane extract was analyzed by GC-MS and nonacosane and octacosane were determined as the main constituents. HPLC-TOF/MS analyses were carried out on CHCl3, EtOAc, and MeOH extracts. The main constituents of CHCl3 extract were detected as 4-hydroxybenzoic acid, vanilic acid, and gentisic acid. Gentisic acid, fumaric acid, chlorogenic acid, and vanilic acid were determined as the main compounds of EtOAc extract. Finally, main constituents of MeOH extract were found as fumaric acid, chlorogenic acid, quercetin-3-β-D-glucoside, gentisic acid and diosmin.

References

  • Dittrich, M. (1977). Cynareae systematic review. Biology and Chemistry of the Compositae.
  • Kargıoğlu, M., Cenkci, S., Serteser, A., Evliyaoğlu, N., Konuk, M., Kök, M. Ş., & Bağcı, Y. (2008). An ethnobotanical survey of inner-West Anatolia, Turkey. Human Ecology, 36(5), 763-777.
  • Reyhan, A., Küpeli, E., & Ergun, F. (2004). The biological activity of Centaurea L. species. Gazi University Journal of Science, 17(4), 149-164.
  • Bruno, M., Maggio, A., Paternostro, M. P., Rosselli, S., Arnold, N. A., & Herz, W. (2001). Sesquiterpene lactones and other constituents of three Cardueae from Cyprus. Biochemical systematics and ecology, 29(4), 433-435.
  • Bruno, M., Maggio, A., Rosselli, S., Gedris, T. E., & Herz, W. (2002). Sesquiterpene lactones and other constituents of Centaurea paniculata ssp. castellana. Biochemical systematics and ecology, 30(4), 379-381.
  • Bruno, M., Rosselli, S., Maggio, A., Raccuglia, R. A., & Arnold, N. A. (2005). Guaianolides from Centaurea babylonica. Biochemical systematics and ecology, 33(8), 817-825.
  • Cardona, M. L., Fernández, I., Pedro, J. R., & Pérez, B. (1991). Sesquiterpene lactones and flavonoids from Centaurea aspera. Phytochemistry, 30(7), 2331-2333.
  • Karamenderes, C., Konyalioglu, S., Khan, S., & Khan, I. A. (2007). Total phenolic contents, free radical scavenging activities and inhibitory effects on the activation of NF‐kappa B of eight Centaurea L. species. Phytotherapy Research, 21(5), 488-491.
  • Middleton, M., Cox, P. J., Jaspars, M., Kumarasamy, Y., Nahar, L., Reid, R., & Sarker, S. D. (2003). Dibenzylbutyrolactone lignans and indole alkaloids from the seeds of Centaurea nigra (Asteraceae). Biochemical systematics and ecology, 31(6), 653-656.
  • MacManus, S. M., Sarker, S. D., Shoeb, M., Majinda, R. R. T., & Jaspars, M. (2004). Epoxylignans from the seeds of Centaurea cyanus (Asteraceae).
  • Shoeb, M., MacManus, S. M., Kumarasamy, Y., Jaspars, M., Nahar, L., Thoo-Lin, P. K., & Sarker, S. D. (2006). Americanin, a bioactive dibenzylbutyrolactone lignan, from the seeds of Centaurea americana. Phytochemistry, 67(21), 2370-2375.
  • Akkal, S., Benayache, F., Bentamene, A., Medjroubi, K., Seguin, E., & Tillequin, F. (2003). Flavonoid aglycones from Centaurea napifolia. Chemistry of natural compounds, 39(2), 219-220.
  • Gonnet, J. F. (1993). Flavonoid glycoside variation in wild specimens of Centaurea triumfetti (Compositae) and comments on its relationships with Centaurea montana based on flavonoid fingerprints. Biochemical systematics and ecology, 21(3), 389-396.
  • Kaij-a-Kamb, M., Amoros, M., & Girre, L. (1992). The chemistry and biological activity the the genus Centaurea. Pharmaceutica Acta Helvetiae, 67(7), 178.
  • Balasundram, N., Sundram, K., & Samman, S. (2006). Phenolic compounds in plants and agri-industrial by-products: Antioxidant activity, occurrence, and potential uses. Food chemistry, 99(1), 191-203.
  • Maddox, C. E., Laur, L. M., & Tian, L. (2010). Antibacterial activity of phenolic compounds against the phytopathogen Xylella fastidiosa. Current microbiology, 60(1), 53.
  • Nitiema, L. W., Savadogo, A., Simpore, J., Dianou, D., & Traore, A. S. (2012). In vitro antimicrobial activity of some phenolic compounds (coumarin and quercetin) against gastroenteritis bacterial strains. Int J Microbiol Res, 3(3), 183-7.
  • Yanez, J., Vicente, V., Alcaraz, M., Castillo, J., Benavente-Garcia, O., Canteras, M., & Teruel, J. A. L. (2004). Cytotoxicity and antiproliferative activities of several phenolic compounds against three melanocytes cell lines: relationship between structure and activity. Nutrition and cancer, 49(2), 191-199.
  • Karimi, E., Oskoueian, E., Hendra, R., & Jaafar, H. Z. (2010). Evaluation of Crocus sativus L. stigma phenolic and flavonoid compounds and its antioxidant activity. Molecules, 15(9), 6244-6256.
  • Johnson, S. K., & Blanchard, A. (2006). Alternative medicine and herbal use among university students. Journal of American College Health, 55(3), 163-168.
  • Demirtas, I., Ayhan, B., Sahin, A., Aksit, H., Elmastas, M., & Telci, I. (2011). Antioxidant activity and chemical composition of Sideritis libanotica Labill. ssp. linearis (Bentham) Borm.(Lamiaceae). Natural product research, 25(16), 1512-1523.

Phytochemical Content of Centaurea polypodiifolia boiss. var. polypodiifolia

Year 2017, Volume: 4 Issue: 3, Special Issue 2, 452 - 458, 20.12.2017
https://doi.org/10.21448/ijsm.376888

Abstract

Various solvents including hexane, CHCl3, EtOAc,
and MeOH were used to extract the aerial parts of C. polypodiifolia Boiss. var. polypodiifolia.
Hexane extract was analyzed by GC-MS and nonacosane and octacosane were determined
as the main constituents. HPLC-TOF/MS analyses were carried out on CHCl3,
EtOAc, and MeOH extracts. The main constituents of CHCl3 extract were
detected as 4-hydroxybenzoic acid, vanilic acid, and gentisic acid. Gentisic acid,
fumaric acid, chlorogenic acid, and vanilic acid were determined as the main compounds
of EtOAc extract. Finally, main constituents of MeOH extract were found as fumaric
acid, chlorogenic acid, quercetin-3-β-D-glucoside,
gentisic acid and diosmin.

References

  • Dittrich, M. (1977). Cynareae systematic review. Biology and Chemistry of the Compositae.
  • Kargıoğlu, M., Cenkci, S., Serteser, A., Evliyaoğlu, N., Konuk, M., Kök, M. Ş., & Bağcı, Y. (2008). An ethnobotanical survey of inner-West Anatolia, Turkey. Human Ecology, 36(5), 763-777.
  • Reyhan, A., Küpeli, E., & Ergun, F. (2004). The biological activity of Centaurea L. species. Gazi University Journal of Science, 17(4), 149-164.
  • Bruno, M., Maggio, A., Paternostro, M. P., Rosselli, S., Arnold, N. A., & Herz, W. (2001). Sesquiterpene lactones and other constituents of three Cardueae from Cyprus. Biochemical systematics and ecology, 29(4), 433-435.
  • Bruno, M., Maggio, A., Rosselli, S., Gedris, T. E., & Herz, W. (2002). Sesquiterpene lactones and other constituents of Centaurea paniculata ssp. castellana. Biochemical systematics and ecology, 30(4), 379-381.
  • Bruno, M., Rosselli, S., Maggio, A., Raccuglia, R. A., & Arnold, N. A. (2005). Guaianolides from Centaurea babylonica. Biochemical systematics and ecology, 33(8), 817-825.
  • Cardona, M. L., Fernández, I., Pedro, J. R., & Pérez, B. (1991). Sesquiterpene lactones and flavonoids from Centaurea aspera. Phytochemistry, 30(7), 2331-2333.
  • Karamenderes, C., Konyalioglu, S., Khan, S., & Khan, I. A. (2007). Total phenolic contents, free radical scavenging activities and inhibitory effects on the activation of NF‐kappa B of eight Centaurea L. species. Phytotherapy Research, 21(5), 488-491.
  • Middleton, M., Cox, P. J., Jaspars, M., Kumarasamy, Y., Nahar, L., Reid, R., & Sarker, S. D. (2003). Dibenzylbutyrolactone lignans and indole alkaloids from the seeds of Centaurea nigra (Asteraceae). Biochemical systematics and ecology, 31(6), 653-656.
  • MacManus, S. M., Sarker, S. D., Shoeb, M., Majinda, R. R. T., & Jaspars, M. (2004). Epoxylignans from the seeds of Centaurea cyanus (Asteraceae).
  • Shoeb, M., MacManus, S. M., Kumarasamy, Y., Jaspars, M., Nahar, L., Thoo-Lin, P. K., & Sarker, S. D. (2006). Americanin, a bioactive dibenzylbutyrolactone lignan, from the seeds of Centaurea americana. Phytochemistry, 67(21), 2370-2375.
  • Akkal, S., Benayache, F., Bentamene, A., Medjroubi, K., Seguin, E., & Tillequin, F. (2003). Flavonoid aglycones from Centaurea napifolia. Chemistry of natural compounds, 39(2), 219-220.
  • Gonnet, J. F. (1993). Flavonoid glycoside variation in wild specimens of Centaurea triumfetti (Compositae) and comments on its relationships with Centaurea montana based on flavonoid fingerprints. Biochemical systematics and ecology, 21(3), 389-396.
  • Kaij-a-Kamb, M., Amoros, M., & Girre, L. (1992). The chemistry and biological activity the the genus Centaurea. Pharmaceutica Acta Helvetiae, 67(7), 178.
  • Balasundram, N., Sundram, K., & Samman, S. (2006). Phenolic compounds in plants and agri-industrial by-products: Antioxidant activity, occurrence, and potential uses. Food chemistry, 99(1), 191-203.
  • Maddox, C. E., Laur, L. M., & Tian, L. (2010). Antibacterial activity of phenolic compounds against the phytopathogen Xylella fastidiosa. Current microbiology, 60(1), 53.
  • Nitiema, L. W., Savadogo, A., Simpore, J., Dianou, D., & Traore, A. S. (2012). In vitro antimicrobial activity of some phenolic compounds (coumarin and quercetin) against gastroenteritis bacterial strains. Int J Microbiol Res, 3(3), 183-7.
  • Yanez, J., Vicente, V., Alcaraz, M., Castillo, J., Benavente-Garcia, O., Canteras, M., & Teruel, J. A. L. (2004). Cytotoxicity and antiproliferative activities of several phenolic compounds against three melanocytes cell lines: relationship between structure and activity. Nutrition and cancer, 49(2), 191-199.
  • Karimi, E., Oskoueian, E., Hendra, R., & Jaafar, H. Z. (2010). Evaluation of Crocus sativus L. stigma phenolic and flavonoid compounds and its antioxidant activity. Molecules, 15(9), 6244-6256.
  • Johnson, S. K., & Blanchard, A. (2006). Alternative medicine and herbal use among university students. Journal of American College Health, 55(3), 163-168.
  • Demirtas, I., Ayhan, B., Sahin, A., Aksit, H., Elmastas, M., & Telci, I. (2011). Antioxidant activity and chemical composition of Sideritis libanotica Labill. ssp. linearis (Bentham) Borm.(Lamiaceae). Natural product research, 25(16), 1512-1523.
There are 21 citations in total.

Details

Primary Language English
Subjects Structural Biology
Journal Section Articles
Authors

Ferda Eser This is me

Ayse Sahin Yaglioglu This is me

Ebru Aktas This is me

Adem Onal

İbrahim Demirtas

Publication Date December 20, 2017
Submission Date May 4, 2017
Published in Issue Year 2017 Volume: 4 Issue: 3, Special Issue 2

Cite

APA Eser, F., Sahin Yaglioglu, A., Aktas, E., Onal, A., et al. (2017). Phytochemical Content of Centaurea polypodiifolia boiss. var. polypodiifolia. International Journal of Secondary Metabolite, 4(3, Special Issue 2), 452-458. https://doi.org/10.21448/ijsm.376888
International Journal of Secondary Metabolite

e-ISSN: 2148-6905