Inhibition of human neutrophil respiratory burst by nimesulide metabolites is higher than that of the parent drug (2004)
- Authors:
- USP affiliated authors: SANTOS, ANTONIO CARDOZO DOS - FCFRP ; VALIM, YARA MARIA LUCISANO - FCFRP ; CURTI, CARLOS - FCFRP ; POLIZELLO, ANA CRISTINA MORSELI - FCFRP
- Unidade: FCFRP
- Subjects: FARMÁCIA; PRODUTOS NATURAIS; METABOLISMO; BIOENERGÉTICA
- Language: Inglês
- Imprenta:
- Publisher place: Buenos Aires
- Date published: 2004
- Source:
- Título: Free Radical Biology and Medicine
- ISSN: 0891-5849
- Volume/Número/Paginação/Ano: v. 36, suppl. 1, p. S94, res. P8-108, 2004
- Conference titles: Biennial Meeting of The International Society for Free Radical Research
-
ABNT
KANASHIRO, Alexandre et al. Inhibition of human neutrophil respiratory burst by nimesulide metabolites is higher than that of the parent drug. Free Radical Biology and Medicine. Buenos Aires: Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 31 dez. 2025. , 2004 -
APA
Kanashiro, A., Mingatto, F. E., Kabeya, L. M., Dorta, D. J., Polizello, A. C. M., Santos, A. C. dos, et al. (2004). Inhibition of human neutrophil respiratory burst by nimesulide metabolites is higher than that of the parent drug. Free Radical Biology and Medicine. Buenos Aires: Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo. -
NLM
Kanashiro A, Mingatto FE, Kabeya LM, Dorta DJ, Polizello ACM, Santos AC dos, Curti C, Lucisano-Valim YM. Inhibition of human neutrophil respiratory burst by nimesulide metabolites is higher than that of the parent drug. Free Radical Biology and Medicine. 2004 ; 36 S94.[citado 2025 dez. 31 ] -
Vancouver
Kanashiro A, Mingatto FE, Kabeya LM, Dorta DJ, Polizello ACM, Santos AC dos, Curti C, Lucisano-Valim YM. Inhibition of human neutrophil respiratory burst by nimesulide metabolites is higher than that of the parent drug. Free Radical Biology and Medicine. 2004 ; 36 S94.[citado 2025 dez. 31 ] - Potential mechanisms for mitochondrial 'Ca POT. 2+' efflux and permeability transition (MPT) evaluated with phenotiazinic drugs
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