Source: Molecular Diversity. Unidades: FCF, IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, PRODUTOS NATURAIS, RELAÇÕES QUANTITATIVAS ENTRE ESTRUTURA QUÍMICA E ATIVIDADE BIOLÓGICA, DOENÇAS INFECCIOSAS, DOENÇAS (TRATAMENTO), TUBERCULOSE
ABNT
ANDRADE, Carolina H. et al. Fragment-based and classical quantitative structure-activity relationships for a series of hydrazides as antituberculosis agents. Molecular Diversity, v. 12, n. 1, p. 47-59, 2008Tradução . . Disponível em: https://doi.org/10.1007/s11030-008-9074-z. Acesso em: 03 out. 2024.APA
Andrade, C. H., Salum, L. B., Castilho, M. S., Pasqualoto, K. F. M., Ferreira, E. I., & Andricopulo, A. D. (2008). Fragment-based and classical quantitative structure-activity relationships for a series of hydrazides as antituberculosis agents. Molecular Diversity, 12( 1), 47-59. doi:10.1007/s11030-008-9074-zNLM
Andrade CH, Salum LB, Castilho MS, Pasqualoto KFM, Ferreira EI, Andricopulo AD. Fragment-based and classical quantitative structure-activity relationships for a series of hydrazides as antituberculosis agents [Internet]. Molecular Diversity. 2008 ; 12( 1): 47-59.[citado 2024 out. 03 ] Available from: https://doi.org/10.1007/s11030-008-9074-zVancouver
Andrade CH, Salum LB, Castilho MS, Pasqualoto KFM, Ferreira EI, Andricopulo AD. Fragment-based and classical quantitative structure-activity relationships for a series of hydrazides as antituberculosis agents [Internet]. Molecular Diversity. 2008 ; 12( 1): 47-59.[citado 2024 out. 03 ] Available from: https://doi.org/10.1007/s11030-008-9074-z