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3-芳硫基和3-环己硫基拉帕醌衍生物高效催化氧化制备新型磺酰基衍生物及其抗菌活性评价

Efficient Catalytic Oxidation of 3-Arylthio- and 3-Cyclohexylthio-lapachone Derivatives to New Sulfonyl Derivatives and Evaluation of Their Antibacterial Activities.

作者信息

Cardoso Mariana F do C, Gomes Ana T P C, Moreira Caroline Dos S, Simões Mário M Q, Neves Maria G P M S, da Rocha David R, da Silva Fernando de C, Moreirinha Catarina, Almeida Adelaide, Ferreira Vitor F, Cavaleiro José A S

机构信息

Department of Chemistry and QOPNA, University of Aveiro, Aveiro 3810-193, Portugal.

Departamento de Química Orgânica, Instituto de Química, Universidade Federal Fluminense, Niterói 24020-150, RJ, Brazil.

出版信息

Molecules. 2017 Feb 16;22(2):302. doi: 10.3390/molecules22020302.

DOI:10.3390/molecules22020302
PMID:28212345
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6155948/
Abstract

New sulfonyl-lapachones were efficiently obtained through the catalytic oxidation of arylthio- and cyclohexylthio-lapachone derivatives with hydrogen peroxide in the presence of a Mn(III) porphyrin complex. The antibacterial activities of the non-oxidized and oxidized lapachone derivatives against the Gram-negative bacteria and the Gram-positive bacteria were evaluated after their incorporation into polyvinylpyrrolidone (PVP) micelles. The obtained results show that the PVP-formulations of the lapachones - and of the sulfonyl-lapachones and reduced the growth of .

摘要

通过在锰(III)卟啉配合物存在下用过氧化氢催化氧化芳硫基和环己硫基拉帕醌衍生物,高效地获得了新型磺酰基拉帕醌。将未氧化和氧化的拉帕醌衍生物掺入聚乙烯吡咯烷酮(PVP)胶束后,评估了它们对革兰氏阴性菌和革兰氏阳性菌的抗菌活性。所得结果表明,拉帕醌以及磺酰基拉帕醌的PVP制剂减少了[具体细菌名称未给出]的生长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6af7/6155948/913a86fcf91e/molecules-22-00302-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6af7/6155948/91785df57d9c/molecules-22-00302-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6af7/6155948/2e71ecbdd21e/molecules-22-00302-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6af7/6155948/f9ea6a753ae8/molecules-22-00302-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6af7/6155948/d0716e1cbb3d/molecules-22-00302-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6af7/6155948/913a86fcf91e/molecules-22-00302-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6af7/6155948/91785df57d9c/molecules-22-00302-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6af7/6155948/2e71ecbdd21e/molecules-22-00302-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6af7/6155948/f9ea6a753ae8/molecules-22-00302-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6af7/6155948/d0716e1cbb3d/molecules-22-00302-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6af7/6155948/913a86fcf91e/molecules-22-00302-g004.jpg

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