This work is licensed under a Creative Commons Attribution 4.0 International License.
Bioactive Flavonol C-Glycoside from Sida cordifolia L. and its Molecular Docking Study
Corresponding Author(s) : Ranajit Kumar Sutradhar
Asian Journal of Chemistry,
Vol. 35 No. 6 (2023): Vol 35 Issue 6, 2023
Abstract
Phytochemical studies of the aerial parts of Sida cordifolia L. has led to the isolation of a new flavonol C-glycoside, 3′-(3′′,7′′-dimethyl-2′′,6′′-octadiene)-8-C-β-D-glucosyl-kaempferol-3-O-β-D-galactoside (1) together with two known flavonoids, luteolin and quercetin. The structures of all the compounds were established on the basis of chemical and spectroscopic studies. Compound 1 was assessed to check the analgesic and anti-inflammatory activities and showed significant activities. Molecular docking study was conducted for compound 1 against 4O1Z protein receptor, which strongly support the in vitro biological findings.
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References
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E.M. Franzotti, C.V.F. Santos, H.M.S.L. Rodrigues, R.H.V. Mourão, M.R. Andrade and A.R. Antoniolli, J. Ethnopharmacol., 72, 273 (2000); https://doi.org/10.1016/s0378-8741(00)00205-1
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A. Saxena, D. Prasad, R. Haldhar, G. Singh and A. Kumar, J. Environ. Chem. Eng., 6, 694 (2018); https://doi.org/10.1016/j.jece.2017.12.064
M.A.M. Momin, S.F. Bellah, S.M.R. Rahman, A.A. Rahman, G.M.M. Murshid and T.B. Emran, Asian Pac. J. Trop. Biomed., 4, 18 (2014); https://doi.org/10.1016/S2221-1691(14)60202-1
A. Jain, S. Choubey, P.K. Singour, H. Rajak and R.S. Pawar, J. Appl. Pharm. Sci., 1, 23 (2011).
A. Galal, V. Raman and I.A. Khan, Curr. Tradit. Med., 1, 5 (2015); https://doi.org/10.2174/2215083801666141226215639
A.L. Gunatilaka, S. Sotheeswaran, S. Balasubramaniam, H.B. Sriyani and A.I. Chandrasekara, Planta Med., 39, 66 (1980); https://doi.org/10.1055/s-2008-1074904
S. Ghosal, A. Prakash and R.K. Varma, Phytochemistry, 43, 384 (1981).
B. Dinda, N. Das, S. Dinda, M. Dinda and I. SilSarma. J. Ethnopharm., 176, 176 (2015); https://doi.org/10.1016/j.jep.2015.10.027
M.M. Goyal and K.K. Rani, Indian Drugs, 25, 184 (1988).
N.S. Aminah, E.R. Laili, M. Rafi, A. Rochman, M. Insanu and K.N.W. Tune, Heliyon, 7, e06682 (2021); https://doi.org/10.1016/j.heliyon.2021.e06682
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S. Ghosal, R.B.P.S. Chauhan and R. Mehta, Phytochemistry, 14, 830 (1975); https://doi.org/10.1016/0031-9422(75)83057-3
B. Asha and N.R. Bannerjee, Curr. Sci., 54, 690 (1985).
R.K. Sutradhar, A.K.M.M. Rahman, M.U. Ahmad and S.C. Bachar, Phytochem. Lett., 1, 179 (2008); https://doi.org/10.1016/j.phytol.2008.09.004
R.K. Sutradhar, A.K.M.M. Rahman, M.U. Ahmad and A. Saha, Indian J. Chem., 46B, 1896 (2007).
R.K. Sutradhar, A.K.M.M. Rahman and M.U. Ahmad, J. Iran. Chem. Soc., 4, 175 (2007); https://doi.org/10.1007/BF03245964
M. Zimmermann, Pain, 16, 109 (1983); https://doi.org/10.1016/0304-3959(83)90201-4
A. Saha, M.A. Masud, S.C. Bachar, J.K. Kundu, B.K. Datt, L. Nahar and S.D. Sarker. Pharm. Biol., 45, 355 (2007); https://doi.org/10.1080/13880200701212973
C.A. Winter, E.A. Risley and G.W. Nuss, Exp. Biol. Med., 111, 544 (1962); https://doi.org/10.3181/00379727-111-27849
O.P. Agarwal, Chemistry of Organic Natural Products, Goel Publishing House, Meerut, India, vol. II, p. 212 (1993).
M. Dubois, K.A. Gilles, J.K. Hamilton, P.A. Rebers and F. Smith, Anal. Chem., 28, 350 (1956); https://doi.org/10.1021/ac60111a017
N. Yayli, H. Seymen and C. Baltaci, Phytochemistry, 58, 607 (2001); https://doi.org/10.1016/S0031-9422(01)00289-8
L.O.A. Manguro, I. Ugi, P. Lemmen and R. Hermann, Phytochemistry, 64, 891 (2003); https://doi.org/10.1016/S0031-9422(03)00374-1
M.M. Abou-Zaid, D.A. Lombardo, G.C. Kite, R.J. Grayer and N.C. Veitch, Phytochemistry, 58, 167 (2001); https://doi.org/10.1016/S0031-9422(01)00156-X
K. Yamaguchi, Spectral Data of Natural Products, Elsevier Publishing Company: Amsterdam, vol. 1, pp. 94-95 (1970).
K.R. Markham and T.J. Mabry, Phytochemistry, 7, 1197 (1968); https://doi.org/10.1016/S0031-9422(00)88270-9
H. Wagner, V.M. Chari and J. Sonnenbichler, Tetrahedron Lett., 17, 1799 (1976); https://doi.org/10.1016/S0040-4039(00)93787-0
A. Rauf, T. Abu-Izneid, F.A. Alhumaydhi, N. Muhammad, A.S.M. Aljohani, S. Naz, S. Bawazeer, A. Wadood and M.S. Mubarak, BMC Complement. Med. Ther., 20, 237 (2020); https://doi.org/10.1186/s12906-020-03030-2
M.S. Shah, M.M. Rahman, M.D. Islam, A. Al-Macktuf, J.U. Ahmed, H. Nishino and M.A. Haque, J. Mol. Struct., 1248, 131465 (2022); https://doi.org/10.1016/j.molstruc.2021.131465