Borges Keyller Bastos, Borges Warley De Souza, Pupo Mônica Tallarico, Bonato Pierina Sueli
Departament of Physics and Chemistry, Faculty of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, Brazil.
Appl Microbiol Biotechnol. 2007 Dec;77(3):669-74. doi: 10.1007/s00253-007-1171-x. Epub 2007 Sep 18.
The stereoselective kinetic biotransformation of thioridazine, a phenothiazine neuroleptic drug, by endophytic fungi was investigated. In general, the sulfur of lateral chain (position 2) or the sulfur of phenothiazinic ring (position 5) were oxidated yielding the major human metabolites thioridazine-2-sulfoxide and thioridazine-5-sulfoxide. The quantity of metabolites biosynthesized varied among the 12 endophytic fungi evaluated. However, mono-2-sulfoxidation occurred in higher ratio and frequency. Among the 12 fungi evaluated, 4 of them deserve prominence for presenting an evidenced stereoselective biotransformation: Phomopsis sp. (TD2), Glomerella cingulata (VA1), Diaporthe phaseolorum (VR4), and Aspergillus fumigatus (VR12). Both enantiomers of thioridazine were consumed by the fungi; however, the 2-sulfoxidation yielded preferentially the R configuration at the sulfur atom.
研究了内生真菌对吩噻嗪类抗精神病药物硫利达嗪的立体选择性动力学生物转化。一般来说,侧链的硫(位置2)或吩噻嗪环的硫(位置5)被氧化,生成主要的人体代谢物硫利达嗪-2-亚砜和硫利达嗪-5-亚砜。在所评估的12种内生真菌中,生物合成的代谢物数量各不相同。然而,单-2-亚砜氧化的发生率和频率更高。在所评估的12种真菌中,有4种因其呈现出明显的立体选择性生物转化而值得关注:拟茎点霉属(TD2)、炭疽菌(VA1)、菜豆壳球孢(VR4)和烟曲霉(VR12)。硫利达嗪的两种对映体均被真菌消耗;然而,2-亚砜氧化在硫原子处优先产生R构型。