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In Vitro and In Vivo Evaluation of an Adamantyl-Based Phenyl Sulfonyl Acetamide against Cutaneous Leishmaniasis Models of Leishmania amazonensis.
Santos, Camila C; Zhang, Huaisheng; Batista, Marcos M; de Oliveira, Gabriel M; Demarque, Kelly C; da Silva-Gomes, Natália L; Moreira, Otacílio C; Ogungbe, Ifedayo Victor; Soeiro, Maria de Nazaré C.
Affiliation
  • Santos CC; Laboratory of Cellular Biology (LBC), Oswaldo Cruz Institute (IOC/Fiocruz), Rio de Janeiro, Rio de Janeiro, Brazil.
  • Zhang H; Department of Chemistry, Physics and Atmospheric Science, Jackson State University, Jackson, Mississippi, USA.
  • Batista MM; Laboratory of Cellular Biology (LBC), Oswaldo Cruz Institute (IOC/Fiocruz), Rio de Janeiro, Rio de Janeiro, Brazil.
  • de Oliveira GM; Laboratory of Cellular Biology (LBC), Oswaldo Cruz Institute (IOC/Fiocruz), Rio de Janeiro, Rio de Janeiro, Brazil.
  • Demarque KC; Laboratory of Cellular Biology (LBC), Oswaldo Cruz Institute (IOC/Fiocruz), Rio de Janeiro, Rio de Janeiro, Brazil.
  • da Silva-Gomes NL; Laboratory of Molecular Biology and Endemic Diseases, Oswaldo Cruz Institute (IOC/Fiocruz), Rio de Janeiro, Rio de Janeiro, Brazil.
  • Moreira OC; Laboratory of Molecular Biology and Endemic Diseases, Oswaldo Cruz Institute (IOC/Fiocruz), Rio de Janeiro, Rio de Janeiro, Brazil.
  • Ogungbe IV; Department of Chemistry, Physics and Atmospheric Science, Jackson State University, Jackson, Mississippi, USA ifedayo.v.ogungbe@jsums.edu soeiro@ioc.fiocruz.br.
  • Soeiro MNC; Laboratory of Cellular Biology (LBC), Oswaldo Cruz Institute (IOC/Fiocruz), Rio de Janeiro, Rio de Janeiro, Brazil ifedayo.v.ogungbe@jsums.edu soeiro@ioc.fiocruz.br.
Antimicrob Agents Chemother ; 64(12)2020 11 17.
Article in En | MEDLINE | ID: mdl-32928731
ABSTRACT
Phenotypic assay against Leishmania amazonensisin vitro and in vivo led to identification of an adamantyl-based phenyl sulfonyl acetamide (compound 1) as a promising antileishmanial agent. Compound 1 inhibited the growth of intracellular forms of L. amazonensis (50% inhibitory concentration [IC50] = 4 µM) and exhibited low toxicity to host cells, with a selectivity index (SI) of >125. However, in a cutaneous leishmaniasis (CL) mouse model, compound 1 did not reduce lesions and parasite load when administered as monotherapy or when given simultaneously with a suboptimal dose of miltefosine.
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Full text: 1 Database: MEDLINE Main subject: Leishmania mexicana / Leishmaniasis, Cutaneous / Leishmania / Antiprotozoal Agents Limits: Animals Language: En Year: 2020 Type: Article

Full text: 1 Database: MEDLINE Main subject: Leishmania mexicana / Leishmaniasis, Cutaneous / Leishmania / Antiprotozoal Agents Limits: Animals Language: En Year: 2020 Type: Article