| Texto completo | |
| Autor(es): |
Fontes, Josielle, V
;
Santos, Igor A.
;
Rosa, Leticia B.
;
Lima, Rochanna L. A.
;
Jardim, Ana C. G.
;
Miguel, Danilo C.
;
Abbehausen, Camilla
Número total de Autores: 7
|
| Tipo de documento: | Artigo Científico |
| Fonte: | CHEMISTRYSELECT; v. 7, n. 31, p. 10-pg., 2022-08-19. |
| Resumo | |
Neglected tropical diseases such as Leishmaniasis and Chikungunya fever are worldwide public health challenges mainly affecting tropical and subtropical countries. One cationic [Cu-(1)(NHC)(2)](+) (4) and two neutral [Cu(I)(NHC)CI] complexes, where NHC=1,3-bis(mesityl)imidazole-2-ylidene (IMes) (5) or 1,3-bis-(2,6-diisopropylphenyl)imidazole-2-ylidene (IPr) (6), had their in vitro activity evaluated towards Leishmonia ornozonensis and Chikungunya virus (CHIKV). The compound (6) inhibited 95% of L. omozonensis infection in RAW macrophages at 10 mu M and 90% of the CHIKV replication at 2 mu M in BHK-21 cells. Otherwise, the other compounds showed higher cytotoxicity in BHK-21 and RAW or lower antiparasitic or antiviral activities. The best activity of compound 6 can be explained by slower ligand exchange with solvent molecules measured by H-1 NMR technique and the best hydrophilic/lipophilic balance (log P= -0.684 +/- 0.055) in the series determined by shake flask method. Antioxidant activity measured by reduction of DPPH revealed a moderate redox ability of all complexes. The binding constant of (6) with bovine serum albumin (BSA) represents the weakest in the series (10(3)). The chemical and in vitro evaluation reported here represent a novel application and chemical insights for the design of [Cu(I)(NHC)L] metallodrugs for these infectious diseases. (AU) | |
| Processo FAPESP: | 19/16904-2 - Metalofármacos direcionados a alvos específicos para o tratamento de leishmaniose |
| Beneficiário: | Camilla Abbehausen |
| Modalidade de apoio: | Auxílio à Pesquisa - Regular |
| Processo FAPESP: | 14/21129-4 - O papel das proteínas ligantes de ácidos graxos na infecção de macrófagos por Leishmania: um alvo potencial para novas drogas contra leishmaniose |
| Beneficiário: | Danilo Ciccone Miguel |
| Modalidade de apoio: | Auxílio à Pesquisa - Jovens Pesquisadores |