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This work is licensed under a Creative Commons Attribution 4.0 International License.
Phytochemical Analysis, Pharmacological Activities, Isolation and Characterization of Bioactive Compounds from the Roots of Sterculia urens Roxb.
Corresponding Author(s) : K.R.S. Prasad
Asian Journal of Chemistry,
Vol. 34 No. 2 (2022): Vol 34 Issue 2
Abstract
The present study was intended to explore the pharmacological significance of the crude root extract of Sterculia urens Roxb. Further the bio-active compounds were isolated and characterized using chromatographic and spectroscopic techniques. Soxhlet extraction apparatus was utilized for isolation of the chemical constituents from the root using a series of solvents such as n-hexane, ethyl acetate, methanol and water. The pharmacological activities such as inhibition of DPPH radical, α-amylase enzyme activity, albumin denaturation along with antibacterial and thrombolytic activities. The isolation of purified bioactive constituents was carried using preparative HPLC technique and the purified compounds were characterized using spectroscopic techniques like NMR, IR and mass. Among the crude root extracts, methanolic extract shows high DPPH radical scavenging activity with IC50 concentration of 26.74 ± 0.08 μg/mL. The IC50 concentrations in α-amylase enzyme inhibition activity was 263.96 ± 0.90, 127.73 ± 1.23 and 223.54 ± 4.76 μg/mL, respectively for ethyl acetate, methanol and water extracts, respectively. The methanolic extract shows high albumin denaturation inhibition assay than other extracts with IC50 concentration as 137.09 ± 0.20 μg/mL, which is very close to standard ascorbic acid. The methanolic extract also shows high % clot lysis than other extracts and results were comparable with 100 μL of streptokinase standard. The preparative HPLC followed by spectral analysis confirm that two known alkaloids (Sterculinine I & II) and three known flavonoids (gossypetin, apigenin and 6-hydroxyluteolin) were purified and characterized from the root methanol of Sterculia urens Roxb. The purified and identified compounds were reported for the first time in Sterculia urens Roxb.
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- G. Miliauskas, P.R. Venskutonis and T.A. Van Beek, Food Chem., 85, 231 (2004); https://doi.org/10.1016/j.foodchem.2003.05.007
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- T.Y. Kristoferson Lulan, S. Fatmawati, M. Santoso and T. Ersam, Free Radic. Antioxid., 8, 96 (2018); https://doi.org/10.5530/fra.2018.2.15
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Y. Cai, Q. Luo, M. Sun and H. Corke, Life Sci., 74, 2157 (2004); https://doi.org/10.1016/j.lfs.2003.09.047
F. Berrino, A. Verdecchia, J.M. Lutz, C. Lombardo, A. Micheli and R. Capocaccia, Eur. J. Cancer, 45, 901 (2009); https://doi.org/10.1016/j.ejca.2009.01.018
M.T. Olivier, F.M. Muganza, L.J. Shai, S.S. Gololo and L.D. Nemutavhanani, S. Afr. J. Bot., 108, 41 (2017); https://doi.org/10.1016/j.sajb.2016.09.014
T. Kanoje and K. Sharma, Int. J. Dev. Res., 7, 14185 (2017).
M.O. Ilomuanya, R.F. Elesho, A.N. Amenaghawon, A.O. Adetuyi, V. Velusamy and A.S. Akanmu, Future J. Pharm. Sci., 6, 1 (2020); https://doi.org/10.1186/s43094-019-0015-8
M.M. Gouda, R.A. Shabaraya and S.M.S. Kumar, Int. Curr. Pharm. J., 1, 376 (2012); https://doi.org/10.3329/icpj.v1i11.12064
J. Redfern, M. Kinninmonth, D. Burdass and J. Verran, J. Microbiol. Biol. Educ., 15, 45 (2014); https://doi.org/10.1128/jmbe.v15i1.656
A. Kathirvel and V. Sujatha, Arab. J. Chem., 9, 1435 (2016); https://doi.org/10.1016/j.arabjc.2012.03.018
J.B. Harborne, Phytochemical Methods, An Guide to Modern Techniques of Plant Analysis, Chapman and Hall Ltd.: London (1973).
E. Iqbal, K.A. Salim and L.B.L. Lim, J. King Saud Univ. Sci., 27, 224 (2015); https://doi.org/10.1016/j.jksus.2015.02.003
R. Maria, M. Shirley, C. Xavier, S. Jaime, V. David, S. Rosa and D. Jodie, J. King Saud Univ. Sci., 30, 500 (2018); https://doi.org/10.1016/j.jksus.2017.03.009
H. Noreen, N. Semmar, M. Farman and J.S.O. McCullagh, Asian Pac. J. Trop. Med., 10, 792 (2017); https://doi.org/10.1016/j.apjtm.2017.07.024
S.S. Pawar and D. Dasgupta, J. King Saud Univ. Sci., 30, 293 (2018); https://doi.org/10.1016/j.jksus.2016.09.002
A.M. Adeosun, S.O. Oni, O.M. Ighodaro, O.H. Durosinlorun and O.M. Oyedele, J. Taibah Univ. Med. Sci., 11, 1 (2016); https://doi.org/10.1016/j.jtumed.2015.11.006
R. Batool, M.R. Khan, M. Sajid, S. Ali and Z. Zahra, BMC Chem., 13, 32 (2019); https://doi.org/10.1186/s13065-019-0549-z
D.D. Sylvie, P.C. Anatole, B.P. Cabral and P.B. Veronique, Asian Pac. J. Trop. Biomed., 4, S625 (2014); https://doi.org/10.12980/APJTB.4.201414B168
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S. Murthuza and B.K. Manjunatha, Beni-Seuf Univ. J. Basic Appl. Sci., 7, 719 (2018); https://doi.org/10.1016/j.bjbas.2018.10.001
I. Hasan, S. Hussain, S. Millat, N. Sen, A. Rahman, A. Rahman, S. Islam and M.R. Moghal, J. Tradit. Complement. Med., 8, 107 (2018); https://doi.org/10.1016/j.jtcme.2017.03.005
S.J.B. Dalir, H. Djahaniani, F. Nabati and M. Hekmati, Heliyon, 6, e03624 (2020); https://doi.org/10.1016/j.heliyon.2020.e03624
I. Jallali, P. waffo Téguo, A. Smaoui, J.-M. Mérillon, C. Abdelly and R. Ksouri, Arab. J. Chem., 13, 2680 (2020); https://doi.org/10.1016/j.arabjc.2018.06.020
M.V.N. Rinaldi, I.E.C. Díaz, I.B. Suffredini and P.R.H. Moreno, Rev. Bras. Farmcog., 27, 77 (2017); https://doi.org/10.1016/j.bjp.2016.08.006
M. Atlabachew, B.S. Chandravanshi and M. Redi-Abshiro, Chem. Cent. J., 11, 107 (2017); https://doi.org/10.1186/s13065-017-0337-6
T.Y. Kristoferson Lulan, S. Fatmawati, M. Santoso and T. Ersam, Free Radic. Antioxid., 8, 96 (2018); https://doi.org/10.5530/fra.2018.2.15
T. Murningsih, P. Praptiwi, L. Liana and A. Fathoni, Nusantara Biosci., 11, 44 (2019); https://doi.org/10.13057/nusbiosci/n110108
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