Antimalarial Activity of Some Organotin(IV) Chlorobenzoate Compounds against Plasmodium falciparum
Abstract
This paper reported the comparative study on antimalarial activity of some organotin(IV) derivatives with some chlorobenzoic acid derivatives used as the ligands. The compounds were synthesized by reacting the intermediate products of dibutyltin(IV) oxide, diphenyltin(IV) dihydroxide and triphenyltin(IV) hydroxide, with chlorobenzoic acid. The antimalarial activity was performed against Plasmodium falciparum. The results showed that the IC50 of the compounds tested were about the same with the chloroquine (2 x 10-3 µg/mL) used as the positive control, but unlike chloroquine which has been known to have resistance as antimalarial, these organotin(IV) compounds prepared are not resistant to the Plasmodium. The result also showed that the derivative of triphenyltin(IV) has higher IC50respective to others.
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A. A. James, Mosquito molecular genetics: the hands that feed bite back, Science, 1992, 257 (5066), 37-38. https://doi.org/10.1126/science.1352413.
P. N. Harijanto, Radical change on the malaria treatment in Indonesia, Cermin Dunia Ked., 2006, 152, 30-36.
WHO, Roll Back Malaria program. Available at. http://www.who.int/malaria/en/. 2011. [Verified 20 April 2011].
A. Szorcsik, L. Nagy, K. Gadja-Schrantz, L. Pellerito, E. Nagy, E. T. Edelmann, Structural studies on organotin(IV) complexes formed with ligands containing {S, N, O} donor atoms, J Radioanal Nucl Chem., 2002, 252 (3), 523-530. https://doi.org/10.1023/A:1015802820423.
E. R. T. Tiekink, Structural Chemistry of Organotin Carboxylates: a Review of the Crystallographic Literature, App Organomet Chem., 1991, 5 (1), 1-23. https://doi.org/10.1002/aoc.590050102.
K. Shahid, S. Ali, S. Shahzadi, Z. Akhtar, Organotin(IV) Complexes on Aniline Derivatives Part-II-Synthesis and Spectroscopic Characterization of Organotin(IV) Derivatives of 2-[4 Bromoanailine)carboxyl]benzoic Acid, Turk J Chem., 2003, 27, 209-215.
L. Pellerito, L. Nagy, Organotin(IV)n+ complexes formed with biologically active ligands: equilibrium and structural studies, and some biological aspects, Coord Chem Rev., 2002, 224 (1-2), 111-150.
https://doi.org/10.1016/S0010-8545(01)00399-X.
B. Gleeson, J. Claffey, D. Ertler, M. Hogan, H. Müller-Bunz, F. Paradisi, D. Wallis, M. Tacke, Novel organotin antibacterial and anticancer drugs, Polyhedron, 2008, 27 (18), 3619-3624. https://doi.org/10.1016/j.poly.2008.09.009.
W. Rehman, A. Badshah, S. Khan, L. T. A. Tuyet, Synthesis, characterization, antimicrobial and antitumor screening of some diorganotin(IV) complexes of 2-[(9H-Purin-6-ylimino)]-phenol, Eur J Med Chem., 2009, 44 (10), 3981-3985. https://doi.org/10.1016/j.ejmech.2009.04.027.
S. Hadi, M. Rilyanti, Synthesis and in vitro anticancer activity of some organotin(IV) benzoate compounds, Orient J Chem., 2010, 26 (3), 775-779.
S. Hadi, M. Rilyanti, Suharso, In Vitro Activity and Comparative Studies Of Some Organotin(IV) Benzoate Derivatives Against Leukemia Cancer Cell: L-1210, Indo J Chem., 2012, 12 (2), 172-177.
S. Hadi, B. Irawan, Efri, The Antifungal Activity Test of Some Organotin(IV) Carboxylates, J Appl Sci Res., 2008, 4 (11), 1521-1525.
S. Hadi, M. Rilyanti, Nurhasanah, Comparative Study on the Antifungal Activity of Some Di- and Tributyltin(IV) Carboxylate Compounds, Modern Appl Sci., 2009, 3 (2), 12-17.
R. Singh, P. Chaudary, N. K. Khausik, A Review: Organotin Compounds in Corrosion Inhibition, Rev Inorg Chem., 2010, 30 (4), 275-294. https://doi.org/10.1515/REVIC.2010.30.4.275.
N. N. Hazani, Y. Mohd, S. A. I. S. M. Ghazali, Y. Farina, N. N. Dzulkifli, Electrochemical Studies on Corrosion Inhibition Behaviour of Synthesised 2-acetylpyridine 4-ethyl-3-thiosemicarbazone and it is Tin(IV) Complex for Mild Steel in 1 M HCl Solution, J Electrochem Sci Technol., 2019, 10 (1), 29-36. https://doi.org/10.5229/JECST.2019.10.1.29.
H. Kurniasiah, M. Nurissalam, B. Iswantoro, H. Afriyani, H. I. Qudus, S. Hadi, The Synthesis, Characterization and Comparative Anticorrosion Study of Some Organotin(IV) 4-Chlorobenzoates, Orient J Chem., 2015, 31 (4), 2377-2383. http://dx.doi.org/10.13005/ojc/310467.
S. Hadi, H. Afriyani, W. D. Anggraini, H. I. Qudus, T. Suhartati, The Synthesis and Potency Study of Some Dibutyltin(IV) Dinitrobenzoate Compounds as Corrosion Inhibitors for Mild Steel HRP in DMSO-HCl Solution, Asian J Chem., 2015, 27 (4), 1509-1512. https://doi.org/10.14233/ajchem.2015.18590.
S. Hadi, Noviany, M. Rilyanti, In Vitro Antimalarial Activity of Some Organotin(IV) 2-Nitrobenzoate Compounds Against Plasmodium falciparum, Macedon J Chem Chem Eng., 2018, 37 (2), 185-191.
https://doi.org/10.5229/JECST.2019.10.1.29.
C. Hansch, R. P. Verma, Larvicidal activities of some organotin compounds on mosquito larvae: A QSAR study, Eur J Med Chem., 2009, 44 (1), 260-273. https://doi.org/10.1016/j.ejmech.2008.02.040.
Sudjadi, The Structure Determination of Organic Compounds. Ghalia Publishers, 1985, pp. 45-51. (In Indonesian).
S. Hadi, T. G. Appleton, G. A. Ayoko, Reactions of fac-[PtMe2(OMe)(H2O)3]+ with halide ions: effect of halide trans effect on methoxide hydrolysis, Inorg Chim Acta, 2003, 352, 201-207.
https://doi.org/10.1016/S0020-1693(03)00137-3.
S. Hadi, T. G. Appleton, Reactions of cisplatin hydrolytes, cis-[Pt(15NH3)2(H2O)2] 2+, with N-acetyl-L-cysteine, Russ J Inorg Chem., 2010, 55 (2), 223-228. https://doi.org/10.1134/S0036023610020142.
Z. H. Chohan, A. Rauf, Some Biologically Active Mixed Ligand Complexes of Co(II), Cu(II) and Ni(II) with ONO, NNO and SNO Donor Nicotinoylhydrazine-Derived Ligands, Synth. React Inorg Met-Org Chem., 1996, 26, 591-604. https://doi.org/10.1080/00945719608004764.
H. Gershon, Antifungal Activity of Bischelates of 5-, 7-, and 5,7-halogenated 8-quinols with copper(II). Determination of the long and short access of the pores in the fungal spore wall, J Med Chem., 1974, 17, 824-827.
A. J. Crowe, The antitumour activity of tin compounds; in Gielen M., Ed. Metal-Based Drugs, 1989, 1, 103-149. https://doi.org/10.1007/978-3-642-74191-3_2.
DOI: http://dx.doi.org/10.13171/mjc0200312162sh
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