Structure-activity relationships of new Schiff bases derived from diaminomaleonitrile as new agents for the treatment of Chagas disease (2019)
- Authors:
- USP affiliated authors: ANDRICOPULO, ADRIANO DEFINI - IFSC ; SALCEDO, DAVID LEANDRO PALOMINO - IFSC ; OLIVEIRA, ALDO SENA DE - IFSC
- Unidade: IFSC
- Subjects: TRYPANOSOMA CRUZI; DOENÇA DE CHAGAS; PLANEJAMENTO DE FÁRMACOS
- Keywords: Drug design; Schiff bases; QSAR; Molecular docking; Cruzain
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título: Anais eletrônicos
- Conference titles: Brazilian Symposium on Medicinal Chemistry - BrazMedChem
-
ABNT
SALCEDO, David Leandro Palomino et al. Structure-activity relationships of new Schiff bases derived from diaminomaleonitrile as new agents for the treatment of Chagas disease. 2019, Anais.. Campinas: Galoá, 2019. Disponível em: https://proceedings.science/p/107073. Acesso em: 27 dez. 2025. -
APA
Salcedo, D. L. P., Oliveira, A. S. de, Mello, L. dos S., Cruz Junior, J. W. da, Dockal, E. R., & Andricopulo, A. D. (2019). Structure-activity relationships of new Schiff bases derived from diaminomaleonitrile as new agents for the treatment of Chagas disease. In Anais eletrônicos. Campinas: Galoá. Recuperado de https://proceedings.science/p/107073 -
NLM
Salcedo DLP, Oliveira AS de, Mello L dos S, Cruz Junior JW da, Dockal ER, Andricopulo AD. Structure-activity relationships of new Schiff bases derived from diaminomaleonitrile as new agents for the treatment of Chagas disease [Internet]. Anais eletrônicos. 2019 ;[citado 2025 dez. 27 ] Available from: https://proceedings.science/p/107073 -
Vancouver
Salcedo DLP, Oliveira AS de, Mello L dos S, Cruz Junior JW da, Dockal ER, Andricopulo AD. Structure-activity relationships of new Schiff bases derived from diaminomaleonitrile as new agents for the treatment of Chagas disease [Internet]. Anais eletrônicos. 2019 ;[citado 2025 dez. 27 ] Available from: https://proceedings.science/p/107073 - Structure-activity relationships of β-chalcogenamines: synthesis, enzyme inhibition, molecular docking and QSAR studies
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