## Abstract The synthesized compounds are screened for their antibacterial activity, but only three of the tested substances show weak potency against Gram‐positive bacteria.
Synthesis and in vitro antibacterial evaluation of 1-substituted-4-ethoxycarbonylmethylthiosemicarbazides and products of their dehydrocyclization
✍ Scribed by Agata Siwek; Joanna Stefańska; Irena Wawrzycka-Gorczyca; Monika Wujec
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 180 KB
- Volume
- 21
- Category
- Article
- ISSN
- 1042-7163
- DOI
- 10.1002/hc.20597
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✦ Synopsis
Abstract
A series of s‐triazoles and thiohydantoines were synthesized by dehydrocyclization of 1‐substituted‐4‐ethoxycarbonylmethylthiosemicarbazides. The molecular structure proposed for s‐triazoles was confirmed by the X‐ray crystal structure analysis of one compound that was prone to crystallization. All compounds were tested in vitro for their antibacterial activity. Some of them showed low levels of activity against Gram‐positive species, MIC range 100–400 μg/mL or higher. © 2010 Wiley Periodicals, Inc. Heteroatom Chem 21:131–138, 2010; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20597
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The synthesis and antibacterial evaluation of a number of 2-(substituted phenylureido)-4-thiocyanatobenzothiazoles are described. The more active compounds against the test organisms in vitro generally were those substituted with halogens on the phenyl and benzothiazole rings.
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