Antibacterial and antifungal activity of derivatives 3-(alkylthio)-4-R-5-(thiophen-2-ylmethyl)-4H-1,2,4-triazole

The amount of antibiotics has increased over the past decade. This also resulted in increase of microorganisms’ resistance to this class of drugs. Therefore, the synthesis of new compounds that have exhibited antimicrobial and antifungal activity and low level of side effects is an important issue...

Full description

Bibliographic Details
Main Authors: O. A. Suhak, O. І. Panasenko, Ye. G. Knysh, O. M. Kamyshny
Format: Article
Language:English
Published: Zaporozhye State Medical University 2015-12-01
Series:Aktualʹnì Pitannâ Farmacevtičnoï ì Medičnoï Nauki ta Praktiki
Subjects:
Online Access:http://pharmed.zsmu.edu.ua/article/view/52625/49803
id doaj-c77be8f3cb424615b1ea229f110c650b
record_format Article
spelling doaj-c77be8f3cb424615b1ea229f110c650b2020-11-24T22:20:46ZengZaporozhye State Medical UniversityAktualʹnì Pitannâ Farmacevtičnoï ì Medičnoï Nauki ta Praktiki2306-80942409-29322015-12-013677010.14739/2409-2932.2015.3.52625Antibacterial and antifungal activity of derivatives 3-(alkylthio)-4-R-5-(thiophen-2-ylmethyl)-4H-1,2,4-triazoleO. A. SuhakO. І. PanasenkoYe. G. KnyshO. M. Kamyshny The amount of antibiotics has increased over the past decade. This also resulted in increase of microorganisms’ resistance to this class of drugs. Therefore, the synthesis of new compounds that have exhibited antimicrobial and antifungal activity and low level of side effects is an important issue of modern pharmacy. The 1,2,4-triazole system is very promising in this aspect. The aim was to study the antimicrobial and antifungal activity of 4-R-5-(thiophen-2-ylmethyl)-4H-1,2,4-triazole-3-thiol and 3-(alkylthio)-4-R-5-(thiophen-2-ylmethyl)-4H-1,2,4-triazole. Methods and results. In the study "serial dilutions" method has been used. The criteria for the activity of given compound was the minimum inhibitory concentration (MIC) which is the lowest concentration of drug that inhibits the growth of the test culture and the minimum bactericidal concentration (MBC) which is the lowest concentration of drug that causes bactericidal effect. Test compounds are derivatives of 4-R-5-(thiophen-2-ylmethyl)-4H-1,2,4-triazole-3-thiol and 3-(alkyl-thio)-4-R-5-(thiophene-2-ylmethyl)-4H-1,2,4-triazole which exhibit antifungal and antimicrobial activity. Conclusion. The most active of the studied 1,2,4-triazole derivatives is 4 (4-methyl-3-(octylthio)-5-(thiophen-2-ylmethyl)-4H-1,2,4-triazole), which manifests as antifungal and antimicrobial activity. Some regularity between structure and action has been investigated. http://pharmed.zsmu.edu.ua/article/view/52625/49803Anti-Microbial AgentsAntifangal Agents1 2 4-triazole
collection DOAJ
language English
format Article
sources DOAJ
author O. A. Suhak
O. І. Panasenko
Ye. G. Knysh
O. M. Kamyshny
spellingShingle O. A. Suhak
O. І. Panasenko
Ye. G. Knysh
O. M. Kamyshny
Antibacterial and antifungal activity of derivatives 3-(alkylthio)-4-R-5-(thiophen-2-ylmethyl)-4H-1,2,4-triazole
Aktualʹnì Pitannâ Farmacevtičnoï ì Medičnoï Nauki ta Praktiki
Anti-Microbial Agents
Antifangal Agents
1 2 4-triazole
author_facet O. A. Suhak
O. І. Panasenko
Ye. G. Knysh
O. M. Kamyshny
author_sort O. A. Suhak
title Antibacterial and antifungal activity of derivatives 3-(alkylthio)-4-R-5-(thiophen-2-ylmethyl)-4H-1,2,4-triazole
title_short Antibacterial and antifungal activity of derivatives 3-(alkylthio)-4-R-5-(thiophen-2-ylmethyl)-4H-1,2,4-triazole
title_full Antibacterial and antifungal activity of derivatives 3-(alkylthio)-4-R-5-(thiophen-2-ylmethyl)-4H-1,2,4-triazole
title_fullStr Antibacterial and antifungal activity of derivatives 3-(alkylthio)-4-R-5-(thiophen-2-ylmethyl)-4H-1,2,4-triazole
title_full_unstemmed Antibacterial and antifungal activity of derivatives 3-(alkylthio)-4-R-5-(thiophen-2-ylmethyl)-4H-1,2,4-triazole
title_sort antibacterial and antifungal activity of derivatives 3-(alkylthio)-4-r-5-(thiophen-2-ylmethyl)-4h-1,2,4-triazole
publisher Zaporozhye State Medical University
series Aktualʹnì Pitannâ Farmacevtičnoï ì Medičnoï Nauki ta Praktiki
issn 2306-8094
2409-2932
publishDate 2015-12-01
description The amount of antibiotics has increased over the past decade. This also resulted in increase of microorganisms’ resistance to this class of drugs. Therefore, the synthesis of new compounds that have exhibited antimicrobial and antifungal activity and low level of side effects is an important issue of modern pharmacy. The 1,2,4-triazole system is very promising in this aspect. The aim was to study the antimicrobial and antifungal activity of 4-R-5-(thiophen-2-ylmethyl)-4H-1,2,4-triazole-3-thiol and 3-(alkylthio)-4-R-5-(thiophen-2-ylmethyl)-4H-1,2,4-triazole. Methods and results. In the study "serial dilutions" method has been used. The criteria for the activity of given compound was the minimum inhibitory concentration (MIC) which is the lowest concentration of drug that inhibits the growth of the test culture and the minimum bactericidal concentration (MBC) which is the lowest concentration of drug that causes bactericidal effect. Test compounds are derivatives of 4-R-5-(thiophen-2-ylmethyl)-4H-1,2,4-triazole-3-thiol and 3-(alkyl-thio)-4-R-5-(thiophene-2-ylmethyl)-4H-1,2,4-triazole which exhibit antifungal and antimicrobial activity. Conclusion. The most active of the studied 1,2,4-triazole derivatives is 4 (4-methyl-3-(octylthio)-5-(thiophen-2-ylmethyl)-4H-1,2,4-triazole), which manifests as antifungal and antimicrobial activity. Some regularity between structure and action has been investigated.
topic Anti-Microbial Agents
Antifangal Agents
1 2 4-triazole
url http://pharmed.zsmu.edu.ua/article/view/52625/49803
work_keys_str_mv AT oasuhak antibacterialandantifungalactivityofderivatives3alkylthio4r5thiophen2ylmethyl4h124triazole
AT oípanasenko antibacterialandantifungalactivityofderivatives3alkylthio4r5thiophen2ylmethyl4h124triazole
AT yegknysh antibacterialandantifungalactivityofderivatives3alkylthio4r5thiophen2ylmethyl4h124triazole
AT omkamyshny antibacterialandantifungalactivityofderivatives3alkylthio4r5thiophen2ylmethyl4h124triazole
_version_ 1725774040179671040