Development of novel effective agents from 1H-indolylammonium trifluoroacetates effective against conditionally pathogenic microorganisms

Q3 Pharmacology, Toxicology and Pharmaceutics Research Results in Pharmacology Pub Date : 2022-01-01 DOI:10.3897/rrpharmacology.8.73329
I. S. Stepanenko, S. A. Yamashkin, T. N. Platkova, A. I. Kiryutina, I. Sorokvasha
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Abstract

Introduction: The problem of antibiotic resistance of microorganisms is becoming more urgent in the twenty-first century. More and more pathogenic microbes are becoming resistant to two or more antibiotics. This problem has become worse into the COVID-19 pandemic. The search for new compounds with antimicrobial activity is one of the principles for overcoming the antibiotic resistance of microorganisms. Materials and methods: Methods for the preparation, isolation, and identification of salts of 2,3,5-trimethyl-, 1,2,3,5-tetramethyl-, 2,3-dimethyl-5-methoxy-, 5-methoxy-1,2,3-trimethyl-1H-indole-6-amines and trifluoroacetic acid were developed and laboratory microbiological studies of them for antimicrobial activity were carried out. Sensitivity of the test-strains of microorganisms to the new compounds was studied. A method of serial dilutions to determine the minimal inhibitory concentration (MIC) of the compounds under study was used in the study. Results and discussion: The compounds 5-8 showed a pronounced antibacterial activity against the test strains of microorganisms in vitro with MIC from 0.98 μg/mL to 125.0 μg/mL. The prospects for targeted synthesis of biologically active compounds which are derivatives of 1H-indolylamines with a trifluoromethyl group in the molecule were determined, and after additional studies, the compounds 5-8 may find application as water-soluble synthetic antimicrobial agents. Conclusion: The laboratory microbiological screening of showed that they have an antimicrobial effect that exceeds the activity of the reference drug, dioxidine. The presence of molecular mechanisms predicted in silico in the spectrum of biological activity of the studied compounds, such as Pseudolysin inhibitor, Omptin inhibitor, Undecaprenyldiphospho-muramoylpentapeptide beta-N-acetylglucosaminyltransferase inhibitor, UDP-epimerase inhibitor, Bacterial efflux pump inhibitor, suggests the presence of antimicrobial activity against gram-positive and gram-negative microorganisms. Trifluoroacetates 2,3,5-trimethyl-1H-indole-6-ammonium (5), 1,2,3,5-tetramethyl-1H-indole-6-ammonium (6), 2,3-dimethyl-5-methoxy-1H-indole-6-ammonium (7), 1,2,3-trimethyl-5-methoxy-1H-indole-6-ammonium (8), after additional studies, may find application as water-soluble synthetic antimicrobial agents.
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Development从h -吲哚胺三氟乙酸酯中提取的新型有效药物对条件致病性微生物有效
在21世纪,微生物的抗生素耐药性问题变得越来越紧迫。越来越多的致病微生物对两种或两种以上的抗生素产生耐药性。这一问题在COVID-19大流行中变得更加严重。寻找具有抗菌活性的新化合物是克服微生物抗生素耐药性的原则之一。材料与方法:建立了2,3,5-三甲基-、1,2,3,5-四甲基-、2,3-二甲基-5-甲氧基-、5-甲氧基-1,2,3-三甲基- 1h -吲哚-6-胺盐和三氟乙酸盐的制备、分离和鉴定方法,并对其抗菌活性进行了实验室微生物学研究。研究了受试菌对新化合物的敏感性。采用连续稀释法测定所研究化合物的最低抑菌浓度(MIC)。结果与讨论:化合物5 ~ 8对试验菌株的体外抑菌活性显著,MIC范围为0.98 ~ 125.0 μg/mL。确定了靶向合成具有生物活性的化合物的前景,这些化合物是分子中含有三氟甲基的1h -吲哚胺衍生物,经过进一步的研究,化合物5-8可能作为水溶性合成抗菌剂应用。结论:实验室微生物学筛选表明,它们的抑菌作用超过对照药二氧化二醇的活性。在所研究的化合物(如假溶血素抑制剂、Omptin抑制剂、十一戊烯基二磷酸-鼠戊基五肽-n -乙酰氨基葡萄糖转移酶抑制剂、udp -外聚酶抑制剂、细菌外排泵抑制剂)的生物活性谱中,硅预测了分子机制的存在,表明其对革兰氏阳性和革兰氏阴性微生物具有抗菌活性。三氟乙酸酯2,3,5-三甲基- 1h -吲哚-6-铵(5),1,2,3,5-四甲基- 1h -吲哚-6-铵(6),2,3-二甲基-5-甲氧基- 1h -吲哚-6-铵(7),1,2,3-三甲基-5-甲氧基- 1h -吲哚-6-铵(8),经进一步研究,可作为水溶性合成抗菌剂应用。
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来源期刊
Research Results in Pharmacology
Research Results in Pharmacology Medicine-Pharmacology (medical)
CiteScore
1.50
自引率
0.00%
发文量
32
审稿时长
12 weeks
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