Copyright (c) 2022 AJC
This work is licensed under a Creative Commons Attribution 4.0 International License.
Analysis of Diospyrin: A Short Review
Corresponding Author(s) : Madhushree Das Sarma
Asian Journal of Chemistry,
Vol. 34 No. 3 (2022): Vol 34 Issue 3, 2022
Abstract
Various analytical techniques are developed for detection, separation and quantification of a specific phytochemical or a component in a biological sample, particularly in relation to their therapeutic aspects. Diospyrin, a bis hydroxy naphthoquinonoid, is an important bioactive constituent of several Diospyros and Euclea spp. This compound has been identified as a prospective ‘lead molecule’ for novel chemotherapy for its significant in vivo and in vitro pharmacological activities. In this short review, some chromatographic and potentiometric methods of detection and quantitative estimation of diospyrin have been discussed.
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- D.J. Newman and G.M. Cragg, J. Nat. Prod. Chem., 83, 770 (2020); https://doi.org/10.1021/acs.jnatprod.9b01285
- R. Cooper and J.J. Deakin, Botanical Miracles: Chemistry of Plants That Changed the World, CRC Press, US (2016).
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J. Guo, H. Lin, J. Wang, Y. Lin, T. Zhang and Z. Jiang, J. Pharm. Biomed. Anal., 165, 182 (2019); https://doi.org/10.1016/j.jpba.2018.12.009
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A. Joubert, F. Kooy, J.J.M. Meyer and N. Lall, Chromatographia, 64, 399 (2006); https://doi.org/10.1365/s10337-006-0055-z
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B. Hazra, J. Golenser, O. Nechemiya, S. Bhattacharya, T. Azzam, A. Domb and S. Frankenburg, Indian J. Pharmacol., 34, 422 (2002).
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B. Hazra, P. Sur, D. Roy, B. Sur and A. Banerjee, Planta Med., 50, 295 (1984); https://doi.org/10.1055/s-2007-969713
B. Hazra, A.K. Saha, R. Ray, D.K. Roy, P. Sur and A. Banerjee, Trans. R. Soc. Trop. Med. Hyg., 81, 738 (1987); https://doi.org/10.1016/0035-9203(87)90013-7
M.R. Khan, S.L. Mutasa, G. Ndaalio and H. Wevers, Pak. J. Sci. Ind. Res., 21, 197 (1978).
F. van der Kooy, J.J.M. Meyer and N. Lall, S. Afr. J. Bot., 72, 349 (2006); https://doi.org/10.1016/j.sajb.2005.09.009
R.S. Kapil and M.M. Dhar, J. Sci. Ind. Res., 20B, 498 (1961).
U. Sanyal, S. Bhattacharyya, A. Patra and B. Hazra, J. Chromatogr. A, 1017, 225 (2003); https://doi.org/10.1016/j.chroma.2003.08.008
G.S. Sidhu and M. Pardhasaradhi, Tetrahedron Lett., 8, 4263 (1967); https://doi.org/10.1016/S0040-4039(00)73011-5
A.L. Fallas and R.H. Thomson, J. Chem. Soc. C, 2279 (1968); https://doi.org/10.1039/j39680002279
T.J. Lillie, O.C. Musgrave and D. Skoyles, J. Chem. Soc. Perkin Trans. I, 2155 (1976); https://doi.org/10.1039/p19760002155
M. Yoshida and K. Mori, Eur. J. Org. Chem., 1313 (2000); https://doi.org/10.1002/1099 0690(200004)2000:7<1313::AIDEJOC1313>3.0.CO;2-I
G.A. Pullella, D. Vuong, E. Lacey and M.J. Piggott, J. Nat. Prod., 83, 3623 (2020); https://doi.org/10.1021/acs.jnatprod.0c00800
W.T.A. Harrison and O.C. Musgrave, Acta Crystallogr. C, 60, 399 (2004); https://doi.org/10.1107/S0108270104007826
M.N. Ravishankara, N. Shrivastava, M.G. Jayathirtha, H. Padh and M. Rajani, J. Chromatogr. B Biomed. Sci. Appl., 744, 257 (2000); https://doi.org/10.1016/S0378-4347(00)00277-2
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