Vieira Tatiana M, Dos Santos Isabella A, Silva Thayná S, Martins Carlos H G, Crotti Antônio E M
Departamento de Química, Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, Av. Bandeirantes, 3900, CEP 14040-901, Ribeirão Preto, SP, Brazil.
Laboratório de Pesquisa em Microbiologia Aplicada, Universidade de Franca, Av. Dr. Armando Salles de Oliveira, 201 - Parque Universitário, CEP 14404600, Franca, SP, Brazil.
Chem Biodivers. 2018 Aug;15(8):e1800216. doi: 10.1002/cbdv.201800216. Epub 2018 Jul 15.
We evaluated the antimicrobial activity of 25 monoketone curcuminoids (MKCs) against a representative panel of cariogenic bacteria in terms of their minimum inhibitory concentration (MIC) values. Curcumin A (10) displayed promising activity against Streptococcus mutans (MIC = 50 μg/ml) and Streptococcus mitis (MIC = 50 μg/ml) as well as moderate activity against S. sanguinis (MIC = 100 μg/ml), Lactobacillus casei (MIC = 100 μg/ml), and Streptococcus salivarius (MIC = 200 μg/ml). Results indicated higher activity of compound 10 than that of its bis-β-diketone analog. Additionally, compounds 3a (1,5-bis(4-methylphenyl)pentan-3-one) and 7b (1,5-bis(4-bromophenyl)pentan-3-ol) were moderately active against S. mitis (MIC = 100 μg/ml) and S. salivarus (MIC = 200 μg/ml).
我们根据最低抑菌浓度(MIC)值,评估了25种单酮类姜黄素(MKC)对一组代表性致龋菌的抗菌活性。姜黄素A(10)对变形链球菌(MIC = 50μg/ml)和缓症链球菌(MIC = 50μg/ml)显示出有前景的活性,对血链球菌(MIC = 100μg/ml)、干酪乳杆菌(MIC = 100μg/ml)和唾液链球菌(MIC = 200μg/ml)显示出中等活性。结果表明化合物10的活性高于其双β-二酮类似物。此外,化合物3a(1,5-双(4-甲基苯基)戊-3-酮)和7b(1,5-双(4-溴苯基)戊-3-醇)对缓症链球菌(MIC = 100μg/ml)和唾液链球菌(MIC = 200μg/ml)具有中等活性。