Screening of anxiolytic properties and analysis of structure-activity relationship of new derivatives of 6-(4-methoxy)-7H-[1,2,4]triazolo[3,4-a][2,3]benzodiazepine under the code RD

Introduction: Searching for new compounds with anti-anxiety activity resulting from the combination of privileged scaffolds is a promising direction in medicinal chemistry and in the development of new drugs. Anxiolytic potential and cytotoxic properties of previously synth...

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Main Authors: Maria O. Skripka, Alexander A. Spasov, Dmitriy V. Maltsev, Mikhail V. Miroshnikov, Dmitriy S. Yakovlev, Kira T. Sultanova, Maxim A. Kochergin, Lyudmila N. Divaeva
Format: Article
Language:English
Published: Pensoft Publishers 2021-06-01
Series:Research Results in Pharmacology
Online Access:https://rrpharmacology.pensoft.net/article/67499/download/pdf/
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spelling doaj-664c982eb558401abd9dc9147f715f2d2021-09-28T14:35:59ZengPensoft PublishersResearch Results in Pharmacology2658-381X2021-06-0172313710.3897/rrpharmacology.7.6749967499Screening of anxiolytic properties and analysis of structure-activity relationship of new derivatives of 6-(4-methoxy)-7H-[1,2,4]triazolo[3,4-a][2,3]benzodiazepine under the code RDMaria O. Skripka0Alexander A. Spasov1Dmitriy V. Maltsev2Mikhail V. Miroshnikov3Dmitriy S. Yakovlev4Kira T. Sultanova5Maxim A. Kochergin6Lyudmila N. Divaeva7Volgograd State Medical UniversityVolgograd Medical Research CenterVolgograd Medical Research CenterVolgograd State Medical UniversityVolgograd Medical Research CenterVolgograd Medical Research CenterVolgograd State Medical UniversitySouthern Federal University Introduction: Searching for new compounds with anti-anxiety activity resulting from the combination of privileged scaffolds is a promising direction in medicinal chemistry and in the development of new drugs. Anxiolytic potential and cytotoxic properties of previously synthesized molecules, containing fragments of 2,3-benzodiazepine and 1,2,4-triazole – 6-(4-methoxyphenyl)-7H-[1,2,4]triazolo[3,4-A][2,3]benzodiazepines under the generic code RD were studied. Materials and methods: Screening for anxiolytic activity was performed on elevated plus maze (EPM) and open field (OF) test models. Structural and functional analysis of the anti-anxiety activity of the studied substances was carried out. A degree of muscle relaxant effect of the substances was assessed in the tests Grid, Wire, and Rotarod. A cytotoxicity study of RD compounds was carried out using an MTT assay on human hepatocellular carcinoma cells HepG2. Results and discussion: For a number of novel triazolo[3,4-a][2,3]benzodiazepine derivatives, a prominent anxiolytic activity was manifested in terms of EPM test. The results of OF test were consistent with the obtained data and confirmed the presence of the sought activity in the leading compounds. There was no significant effect on muscle tone for the compounds under study. It was observed that RD compounds possessed no cytotoxic properties and were safe for further studies in vivo. Conclusion: Among the new derivatives of 6-(4-methoxyphenyl)-7H-[1,2,4]triazolo[3,4-a][2,3]benzodiazepine under the code RD, substances (RD-4, 12, 13) with a high anxiolytic activity comparable to diazepam and tofisopam were found. The most promising compound is RD-4 due to its pronounced anxiolytic and low cytotoxic properties. https://rrpharmacology.pensoft.net/article/67499/download/pdf/
collection DOAJ
language English
format Article
sources DOAJ
author Maria O. Skripka
Alexander A. Spasov
Dmitriy V. Maltsev
Mikhail V. Miroshnikov
Dmitriy S. Yakovlev
Kira T. Sultanova
Maxim A. Kochergin
Lyudmila N. Divaeva
spellingShingle Maria O. Skripka
Alexander A. Spasov
Dmitriy V. Maltsev
Mikhail V. Miroshnikov
Dmitriy S. Yakovlev
Kira T. Sultanova
Maxim A. Kochergin
Lyudmila N. Divaeva
Screening of anxiolytic properties and analysis of structure-activity relationship of new derivatives of 6-(4-methoxy)-7H-[1,2,4]triazolo[3,4-a][2,3]benzodiazepine under the code RD
Research Results in Pharmacology
author_facet Maria O. Skripka
Alexander A. Spasov
Dmitriy V. Maltsev
Mikhail V. Miroshnikov
Dmitriy S. Yakovlev
Kira T. Sultanova
Maxim A. Kochergin
Lyudmila N. Divaeva
author_sort Maria O. Skripka
title Screening of anxiolytic properties and analysis of structure-activity relationship of new derivatives of 6-(4-methoxy)-7H-[1,2,4]triazolo[3,4-a][2,3]benzodiazepine under the code RD
title_short Screening of anxiolytic properties and analysis of structure-activity relationship of new derivatives of 6-(4-methoxy)-7H-[1,2,4]triazolo[3,4-a][2,3]benzodiazepine under the code RD
title_full Screening of anxiolytic properties and analysis of structure-activity relationship of new derivatives of 6-(4-methoxy)-7H-[1,2,4]triazolo[3,4-a][2,3]benzodiazepine under the code RD
title_fullStr Screening of anxiolytic properties and analysis of structure-activity relationship of new derivatives of 6-(4-methoxy)-7H-[1,2,4]triazolo[3,4-a][2,3]benzodiazepine under the code RD
title_full_unstemmed Screening of anxiolytic properties and analysis of structure-activity relationship of new derivatives of 6-(4-methoxy)-7H-[1,2,4]triazolo[3,4-a][2,3]benzodiazepine under the code RD
title_sort screening of anxiolytic properties and analysis of structure-activity relationship of new derivatives of 6-(4-methoxy)-7h-[1,2,4]triazolo[3,4-a][2,3]benzodiazepine under the code rd
publisher Pensoft Publishers
series Research Results in Pharmacology
issn 2658-381X
publishDate 2021-06-01
description Introduction: Searching for new compounds with anti-anxiety activity resulting from the combination of privileged scaffolds is a promising direction in medicinal chemistry and in the development of new drugs. Anxiolytic potential and cytotoxic properties of previously synthesized molecules, containing fragments of 2,3-benzodiazepine and 1,2,4-triazole – 6-(4-methoxyphenyl)-7H-[1,2,4]triazolo[3,4-A][2,3]benzodiazepines under the generic code RD were studied. Materials and methods: Screening for anxiolytic activity was performed on elevated plus maze (EPM) and open field (OF) test models. Structural and functional analysis of the anti-anxiety activity of the studied substances was carried out. A degree of muscle relaxant effect of the substances was assessed in the tests Grid, Wire, and Rotarod. A cytotoxicity study of RD compounds was carried out using an MTT assay on human hepatocellular carcinoma cells HepG2. Results and discussion: For a number of novel triazolo[3,4-a][2,3]benzodiazepine derivatives, a prominent anxiolytic activity was manifested in terms of EPM test. The results of OF test were consistent with the obtained data and confirmed the presence of the sought activity in the leading compounds. There was no significant effect on muscle tone for the compounds under study. It was observed that RD compounds possessed no cytotoxic properties and were safe for further studies in vivo. Conclusion: Among the new derivatives of 6-(4-methoxyphenyl)-7H-[1,2,4]triazolo[3,4-a][2,3]benzodiazepine under the code RD, substances (RD-4, 12, 13) with a high anxiolytic activity comparable to diazepam and tofisopam were found. The most promising compound is RD-4 due to its pronounced anxiolytic and low cytotoxic properties.
url https://rrpharmacology.pensoft.net/article/67499/download/pdf/
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