Antiparasitic evaluation of salicylate and salicylamide derivatives
DOI:
https://doi.org/10.34119/bjhrv6n4-156Keywords:
natural products, salicylic acid, neglected diseases, Leishmania, TrypanosomaAbstract
In the present study, twelve salicylic acid derivatives were obtained through Fischer esterification, the Mitsunobu reaction, and the acid chloride reactions. The products were structurally characterized using infrared, 1H NMR, 13C NMR spectroscopy, and high resolution mass spectrometry of three unpublished compounds. Then they were evaluated against the parasites Leishmania braziliensis, Trypanosoma cruzi, and Plasmodium falciparum. Some compounds were weakly bioactive against L. braziliensis amastigotes, such as N-cyclohexyl-2-hydroxybenzamide (10), EC50 = 15.60 ± 2.69 µM and SI = 2.67, and against T. cruzi such as 4-methoxybenzyl 2-hydroxybenzoate (8) EC50 > 23.23 µM and SI < 2.41. The compounds did not present significant activity against P. falciparum. The data obtained indicate that salicylic acid derivatives can be structurally modified for the synthesis of more potent and selective compounds against parasites that cause several neglected diseases.
References
ANTWI, C. A.; AMISIGO, C. M.; ADJIMANI, J. P.; & GWIRA, T. M. In vitro activity and mode of action of phenolic compounds on Leishmania donovani. PLoS neglected tropical diseases, v. 13, n. 2, e0007206, 2019.
BAMOHARRAM, F. F.; HERAVI, M. M.; ROSHANI, M.; JAHANGIR, M.; & GHARIB, A. Preyssler catalyst,[NaP5W30O110] 14−: A green, efficient and reusable catalyst for esterification of salicylic acid with aliphatic and benzylic alcohols. Applied Catalysis A: General, v. 302, n. 1, 42-47, 2006.
BUCKNER, F. S.; VERLINDE, C. L.; LA FLAMME, A. C.; VAN VOORHIS, W. C. Efficient technique for screening drugs for activity against Trypanosoma cruzi using parasites expressing beta-galactosidase. Antimicrobial Agents and Chemotherapy. v. 40, 1996.
CHAPADO, L.; LINARES-PALOMINO, P. J.; SALIDO, S.; ALTAREJOS, J.; ROSADO, J. A.; SALIDO, G. M. Synthesis and evaluation of the platelet antiaggregant properties of phenolic antioxidants structurally related to rosmarinic acid. Bioorganic Chemistry, v. 38, p. 108-114, 2010.
DEV, D.; PALAKURTHY, N. B.; THALLURI, K.; CHANDRA, J.; & MANDAL, B. Ethyl 2-Cyano-2-(2-nitrobenzenesulfonyloxyimino) acetate (o-NosylOXY): a recyclable coupling reagent for racemization-free synthesis of peptide, amide, hydroxamate, and ester. The Journal of Organic Chemistry, v. 79 n. 12, 5420-5431, 2014.
EISENMANN, J. L. Process of making hydroxy ester compounds. United States. Patented 3.028.417 - April 3, 1962.
FIGUEREDO, A. S., ASSENÇO, J. N. F., DA COSTA, A. A. C., LÓPEZ, R. E. DA S., & DA SILVA, M. C. P. (2022). Protease inhibitor activity of plant natural products as leishmanicine agents / Atividade de inibidores de proteases de produtos naturais contra agentes leishmanicidas. Brazilian Journal of Development, 8(4), 23608–23632. https://doi.org/10.34117/bjdv8n4-059
FINNEY, D. J. Statistical Method in Biological Assay (Mathematics in Medicine series) – November 23, 1978.
GAO, B.; CHEN, K.; BI, X.; & WANG, J. Intramolecular functionalization of C (sp3) H bonds adjacent to an amide nitrogen atom: Metal-free synthesis of 2-hydroxy-benzoxazinone derivatives. Tetrahedron, v. 73, n. 50, 7005-7010, 2017.
INSUASTY, D.; ROBLEDO, S. M.; VÉLEZ, I. D.; CUERVO, P., INSUASTY, B., QUIROGA, J., NOGUERAS, M., COBO, J., ABONIA, R. A Schmidt rearrangement-mediated synthesis of novel tetrahydro-benzo[1,4]diazepin-5-ones as potential anticancer and antiprotozoal agents. European Journal of Medicinal Chemistry. 2017.
ISLAN, G. A.; DURÁN, M.; CACICEDO M. L.; NAKAZATO, G.; KOBAYASHI, R. K. T.; MARTINEZ, D. S. T.; CASTRO, G. R.; DURÁN, N. Nanopharmaceuticals as a solution to neglected diseases: Is it possible?. Acta tropica, v. 170, p. 16-42, 2017.
JI, X. Y.; WANG, H. Q.; HAO, L. H.; HE, W. Y.; GAO, R. M.; LI, Y. P.; LI, Y. H.; JIANG, J. D.; LI, Z. R. Synthesis and antiviral activity of N-phenylbenzamide derivatives, a novel class of enterovirus 71 inhibitors. Molecules, v. 18, n. 3, p. 3630-3640, 2013.
LEAL, S. M.; AMADO, D. F.; KOUZNETSOV, V. V.; ESCOBA, P. In Vitro Antileishmanial, Trypanocidal, and Mammalian Cell Activities of Diverse N,N'-Dihetaryl Substituted Diamines and Related Compounds. Scientia Pharmaceutica, v. 81, n. 1, p. 43-56, 2013.
LE, T. B.; BEAUFAY, C.; BONNEAU, N.; MINGEOT-LECLERCQ, M. P.; & QUETIN-LECLERCQ, J. Anti-protozoal activity of essential oils and their constituents against Leishmania, Plasmodium and Trypanosoma. Phytochimie, v. 1, p. 1-33, 2018.
LOPES, S. P.; CASTILLO, Y. P.; MONTEIRO, M. L.; MENEZES, R. R. D.; ALMEIDA, R. N.; MARTINS, A. M.; SOUSA, D. P. D. Trypanocidal Mechanism of Action and in silico Studies of p-Coumaric Acid Derivatives. International journal of molecular sciences, v. 20, n. 23, p. 5916, 2019.
MADASAMY, K.; BALAKRISHNAN, M. H.; KORIVI, R.; & MANNATHAN, S. Trifluoroacetic Acid-Mediated Denitrogenative ortho-Hydroxylation of 1, 2, 3-Benzotriazin-4 (3H)-ones: A Metal-Free Approach. The Journal of Organic Chemistry, v. 87, n. 13, 8752-8756, 2022.
MASETTO, E. V.; LAZAROTO, A. C.; OLEINIK, G.; LIMA, F. O.; GALLINA, A. L.; & SOARES, L. C. Salicilatos como inibidores do processo oxidativo mediado por cobre e ferro no biodiesel B100. Química Nova, v. 45, 1053-1059, 2022.
MONZOTE, L.; HERRERA, I.; SATYAL, P.; & SETZER, W. N. In-Vitro evaluation of 52 commercially-available essential oils against Leishmania amazonensis. Molecules, v. 24, n.7, 1248, 2019.
NÓBREGA, F. R.; SILVA, L. V.; BEZERRA FILHO, C. D. S. M.; LIMA, T. C.; CASTILLO, Y. P.; BEZERRA, D. P.; TAMIRES, C. L.; YUNIERKIS, P. C.; DANIEL, P. B.; TATJANA, K. S. L.; SOUSA, D. P. D. Design, Antileishmanial Activity, and QSAR Studies of a Series of Piplartine Analogues. Journal of Chemistry, 2019.
PULIDO, S. A.; MUN~OZ, D.L.; RESTREPO, A.M.; MESA, C.V.; ALZATE J.F.; VELEZ, I.D.; S.M. ROBLEDO. Improvement of the green fluorescent protein reporter system in Leishmania spp. for the in vitro and in vivo screening of antileishmanial drugs, Acta Tropica. v. 122, 2012.
SANDERSON, J. T.; CLABAULT, H.; PATTON, C.; LASSALLE-CLAUX, G.; JEAN-FRANÇOIS, J.; PARÉ, A. F.; HÉBERT, M. J.; SURETTE, M. E.; TOUAIBIA, M. Antiproliferative, antiandrogenic and cytotoxic effects of novel caffeic acid derivatives in LNCaP human androgen-dependent prostate cancer cells. Bioorganic & Medical Chemistry, v. 21, n. 22, p. 7182–7193, 2013.
SCARIM, C. B.; JORNADA, D. H.; MACHADO, M. G. M.; FERREIRA, C. M. R.; DOS SANTOS, J. L.; CHUNG, M. C. Thiazole, thio and semicarbazone derivatives against tropical infective diseases: Chagas disease, human African trypanosomiasis (HAT), leishmaniasis, and malaria. European journal of medicinal chemistry, v. 162, p. 378-395, 2019.
TAYLOR, V. M.; CEDEN~O, D. L.; MUN~OZ, D. L.; JONES, M. A.; LASH, T. D.; YOUNG, A. M.; CONSTANTINO, M. H.; ESPOSITO, N.; VELEZ, I. D.; ROBLEDO, S. M. In Vitro and in Vivo studies of the utility of dimethyl and diethyl carbaporphyrin ketals in treat- ment of cutaneous leishmaniasis, Antimicrob. Agents Chemother. v. 55 2011.
URBANIAK, M. D.; CAPES, A. S.; CROSSMAN, A.; O’NEILL, S.; THOMPSON, S.; GILBERT, I. H.; FERGUSON, M. A. J. Fragment screening reveals salicylic hydroxamic acid as an inhibitor of Trypanosoma brucei GPI GlcNAc-PI de-N-acetylase. Carbohydrate Research, v. 387, p. 54–58, 2014.
VILLA, C.; BALDASSARI, S.; GAMBARO, R.; MARIANI, E.; & LOUPY, A. Eco‐friendly methodologies for the synthesis of some aromatic esters, well‐known cosmetic ingredients. International journal of cosmetic science, v. 27, n. 1, 11-16, 2005.
YAMADA, K.; YOSHIDA, S.; FUJITA, H.; KITAMURA, M.; & KUNISHIMA, M. O‐Benzylation of Carboxylic Acids Using 2, 4, 6‐Tris (benzyloxy)‐1, 3, 5‐triazine (TriBOT) under Acidic or Thermal Conditions. European Journal of Organic Chemistry, v. 36, 7997-8002, 2015.
ZHAO, Q., CHU, J., JIANG, T., & YIN, H. Synthesis of isoamyl salicylate using a novel mesoporous titania superacid as a catalyst. Korean Journal of Chemical Engineering, v. 25, 1008-1013, 2008.


