HPLC-HRESI-MSn Characterization of Polyphenolic Compounds in the Stem Bark of Chlorophora regia A. Chev (Moraceae)

Authors

  • James Oppong-Kyekyeku Department of Pharmaceutical Chemistry, Kwame Nkrumah University of Science and Technology, Kumasi https://orcid.org/0000-0001-7181-6793
  • Samuel Oppong Bekoe Department of Pharmaceutical Chemistry, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana
  • Edmund Ekuadzi Department of Pharmacognosy, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana
  • John Nii Adotey Addotey Department of Pharmaceutical Chemistry, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana
  • Samuel Asare-Nkansah Department of Pharmaceutical Chemistry, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana

DOI:

https://doi.org/10.25026/jtpc.v6i2.419

Keywords:

Chlorophora regia, polyphenolic compounds, HPLC-HRESI-MS/MS, fragmentation pattern

Abstract

Isolation and identification of secondary metabolites from medicinal plants could be tedious and time consuming. Therefore, any technique that could be used to confirm the identity of medicinal plant constituents without isolating them will save time and resources. Chlorophora similar to many genera in the Moraceae family have been demonstrated to be rich sources of polyphenolic compounds with important biological activities. The current study was designed to employ HRESI-MSn analyses to qualitatively examine isolated polyphenolic compounds from the stem bark of Chlorophora regia. Based on the HRESI-MSn data obtained, the fragmentation patterns of the compounds under study will be proposed and could be used in their identification in a matrix. Five polyphenolic compounds were successfully isolated and purified using various chromatographic techniques including column chromatography, thin-layer chromatography (TLC) and preparative HPLC. The structures of the isolated compounds were elucidated by in-depth analyses of their 1D and 2D NMR and mass spectroscopic data. HRESI-MS/MS was further used to characterize the isolated compounds. Five polyphenolic compounds including three Diels-Alder type adducts: sanggenon C, kuwanol E and chalcomoracin; two stilbene derivatives: chlorophorin and isochlorophorin were isolated from the stem bark. The tandem MS fragmentation patterns of the compounds in positive mode, were successfully proposed. The fragments obtained and proposed fragmentation patterns of the isolated compounds could be employed qualitatively in the identification of the studied polyphenolic compounds in a matrix.

Downloads

Download data is not yet available.

References

M. Royer, G. Herbette, V. Eparvier, J. Beauchêne, B. Thibaut, D. Stien, Secondary metabolites of Bagassa guianensis Aubl. wood: a study of the chemotaxonomy of the Moraceae family, Phytochemistry, 71 (2010) 1708-1713.

R. Naik, D.S. Harmalkar, X. Xu, K. Jang, K. Lee, Bioactive benzofuran derivatives: Moracins A–Z in medicinal chemistry, Eur J Med Chem, 90 (2015) 379-393.

R. Tsao, R. Yang, J.C. Young, Antioxidant isoflavones in osage orange, Maclura pomifera (Raf.) Schneid, J Agr Food Chem, 51 (2003) 6445-6451.

A. Groweiss, J.H. Cardellina, M.R. Boyd, HIV-Inhibitory prenylated xanthones and flavones from Maclura tinctoria, J Nat Prod, 63 (2000) 1537-1539.

T. Padayachee, B. Odhav, Antimicrobial activity of plant phenols from Chlorophora excelsa and Virgilia oroboides, Afr J Biotechnol, 12 (2013) 17.

K. Shimizu, S. Yasutake, R. Kondo, A new stilbene with tyrosinase inhibitory activity from Chlorophora excelsa, Chem Pharm Bull, 51 (2003) 318-319.

G. Cioffi, L.M. Escobar, A. Braca, N. De Tommasi, Antioxidant Chalcone Glycosides and Flavanones from Maclura (Chlorophora) tinctoria. J Nat Prod, 66 (2003) 1061-1064.

J. Li, G. Strobel, J. Harper, E. Lobkovsky, J. Clardy, Cryptocin, a potent tetramic acid antimycotic from the endophytic fungus Cryptosporiopsis cf. quercina. Org Lett, 2 (2000) 767-770.

J.O. Kyekyeku, S. Kusari, R.K. Adosraku, S. Zühlke, M. Spiteller, Prenylated 2-arylbenzofuran derivatives with potent antioxidant properties from Chlorophora regia (Moraceae). Fitoterapia, 108 (2016) 41-47.

Y.-Q. Shi, T. Fukai, H. Sakagami, W.-J. Chang, P.-Q. Yang, F.-P. Wang, T. Nomura, Cytotoxic Flavonoids with Isoprenoid Groups from Morus mongolica, J Nat Prod, 64 (2001) 181-188.

Y. Hano, T. Nomura, S. Ueda, Two new Diels-Alder type adducts, mulberrofuran T and kuwanol E, from callus tissues of Morus alba L. Heterocycles, 29, (1989) 2035-2041.

M. Takasugi, S. Nagao, T. Masamune, A. Shirata, K. TakahashI, Chalcomoracin, a natural Diels-Alder adduct from diseased mulberry, Chem Lett, (1980) 1573-1576.

L.P. Christensen, J. Lam, T. Sigsgaard, A novel stilbene from the wood of Chlorophora excelsa, Phytochemistry, 27 (1988) 3014-3016.

S. Maneechai, W. De-Eknamkul, K. Umehara, H. Noguchi, K. Likhitwitayawuid, Flavonoid and stilbenoid production in callus cultures of Artocarpus lakoocha. Phytochemistry, 81 (2012) 42-49.

Downloads

Additional Files

Published

2022-11-22

How to Cite

Oppong-Kyekyeku, J., Bekoe, S. O., Ekuadzi, E., Addotey, J. N. A., & Asare-Nkansah, S. (2022). HPLC-HRESI-MSn Characterization of Polyphenolic Compounds in the Stem Bark of Chlorophora regia A. Chev (Moraceae). Journal of Tropical Pharmacy and Chemistry, 6(2), 133–143. https://doi.org/10.25026/jtpc.v6i2.419

Most read articles by the same author(s)