Literature DB >> 33519927

Dehydrobufotenin extracted from the Amazonian toad Rhinella marina (Anura: Bufonidae) as a prototype molecule for the development of antiplasmodial drugs.

Felipe Finger Banfi1, Gabriela Camila Krombauer1, Amanda Luisa da Fonseca2, Renata Rachide Nunes2, Silmara Nunes Andrade2, Millena Alves de Rezende2, Mariana Helena Chaves3, Evaldo Dos Santos Monção3, Alex Guterres Taranto2, Domingos de Jesus Rodrigues4, Gerardo Magela Vieira3, Whocely Victor de Castro5, Fernando de Pilla Varotti2, Bruno Antonio Marinho Sanchez1.   

Abstract

BACKGROUND: The resistance against antimalarial drugs represents a global challenge in the fight and control of malaria. The Brazilian biodiversity can be an important tool for research and development of new medicinal products. In this context, toxinology is a multidisciplinary approach on the development of new drugs, including the isolation, purification, and evaluation of the pharmacological activities of natural toxins. The present study aimed to evaluate the cytotoxicity, as well as the antimalarial activity in silico and in vitro of four compounds isolated from Rhinella marina venom as potential oral drug prototypes.
METHODS: Four compounds were challenged against 35 target proteins from P. falciparum and screened to evaluate their physicochemical properties using docking assay in Brazilian Malaria Molecular Targets (BraMMT) software and in silico assay in OCTOPUS® software. The in vitro antimalarial activity of the compounds against the 3D7 Plasmodium falciparum clones were assessed using the SYBR Green I based assay (IC50). For the cytotoxic tests, the LD50 was determined in human pulmonary fibroblast cell line using the [3(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] (MTT) assay.
RESULTS: All compounds presented a ligand-receptor interaction with ten Plasmodium falciparum-related protein targets, as well as antimalarial activity against chloroquine resistant strain (IC50 = 3.44 μM to 19.11 μM). Three of them (dehydrobufotenine, marinobufagin, and bufalin) showed adequate conditions for oral drug prototypes, with satisfactory prediction of absorption, permeability, and absence of toxicity. In the cell viability assay, only dehydrobufotenin was selective for the parasite.
CONCLUSIONS: Dehydrobufotenin revealed to be a potential oral drug prototype presenting adequate antimalarial activity and absence of cytotoxicity, therefore should be subjected to further studies.

Entities:  

Keywords:  Antimalarial drug Docking; Bufadienolides; Natural compounds

Year:  2021        PMID: 33519927      PMCID: PMC7812938          DOI: 10.1590/1678-9199-JVATITD-2020-0073

Source DB:  PubMed          Journal:  J Venom Anim Toxins Incl Trop Dis        ISSN: 1678-9180


  54 in total

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Authors:  C A Lipinski; F Lombardo; B W Dominy; P J Feeney
Journal:  Adv Drug Deliv Rev       Date:  2001-03-01       Impact factor: 15.470

2.  Antimalarial activity of medicinal plants used in traditional medicine in S. Tomé and Príncipe islands.

Authors:  Maria do Céu de Madureira; Ana Paula Martins; Milene Gomes; Jorge Paiva; António Proença da Cunha; Virgílio do Rosário
Journal:  J Ethnopharmacol       Date:  2002-06       Impact factor: 4.360

Review 3.  Homology models in docking and high-throughput docking.

Authors:  Claudio N Cavasotto
Journal:  Curr Top Med Chem       Date:  2011       Impact factor: 3.295

4.  DataWarrior: an open-source program for chemistry aware data visualization and analysis.

Authors:  Thomas Sander; Joel Freyss; Modest von Korff; Christian Rufener
Journal:  J Chem Inf Model       Date:  2015-02-02       Impact factor: 4.956

5.  Identification of novel antiplasmodial compound by hierarquical virtual screening and in vitro assays.

Authors:  David Bacelar Costa Júnior; Janay Stefany Carneiro Araújo; Larissa de Mattos Oliveira; Flávio Simas Moreira Neri; Paulo Otávio Lourenço Moreira; Alex Gutterres Taranto; Amanda Luisa Fonseca; Fernando de Pilla Varotti; Franco Henrique Andrade Leite
Journal:  J Biomol Struct Dyn       Date:  2020-05-13

6.  Octopus: a platform for the virtual high-throughput screening of a pool of compounds against a set of molecular targets.

Authors:  Eduardo Habib Bechelane Maia; Vinícius Alves Campos; Bianca Dos Reis Santos; Marina Santos Costa; Iann Gabriel Lima; Sandro J Greco; Rosy I M A Ribeiro; Felipe M Munayer; Alisson Marques da Silva; Alex Gutterres Taranto
Journal:  J Mol Model       Date:  2017-01-07       Impact factor: 1.810

7.  Cytotoxic profile of natural and some modified bufadienolides from toad Rhinella schneideri parotoid gland secretion.

Authors:  Geraldino A Cunha-Filho; Inês S Resck; Bruno C Cavalcanti; Cláudia O Pessoa; Manoel O Moraes; José R O Ferreira; Felipe A R Rodrigues; Maria L Dos Santos
Journal:  Toxicon       Date:  2010-04-08       Impact factor: 3.033

8.  Structure-activity relationships of analogs of pentamidine against Plasmodium falciparum and Leishmania mexicana amazonensis.

Authors:  C A Bell; J E Hall; D E Kyle; M Grogl; K A Ohemeng; M A Allen; R R Tidwell
Journal:  Antimicrob Agents Chemother       Date:  1990-07       Impact factor: 5.191

9.  New bufadienolides extracted from Rhinella marina inhibit Na,K-ATPase and induce apoptosis by activating caspases 3 and 9 in human breast and ovarian cancer cells.

Authors:  Israel José Pereira Garcia; Gisele Capanema de Oliveira; Jéssica Martins de Moura Valadares; Felipe Finger Banfi; Silmara Nunes Andrade; Túlio Resende Freitas; Evaldo Dos Santos Monção Filho; Hérica de Lima Santos; Gerardo Magela Vieira Júnior; Mariana Helena Chaves; Domingos de Jesus Rodrigues; Bruno Antonio Marinho Sanchez; Fernando P Varotti; Leandro Augusto Barbosa
Journal:  Steroids       Date:  2019-09-06       Impact factor: 2.668

Review 10.  How can natural products serve as a viable source of lead compounds for the development of new/novel anti-malarials?

Authors:  Eric Guantai; Kelly Chibale
Journal:  Malar J       Date:  2011-03-15       Impact factor: 2.979

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