Abstract
In this study novel thiosemicarbazides bearing piperidine moiety were synthesized in order to investigate their possible antibacterial and antifungal activities. A structure-activity relationship (SAR) study including conformational analysis and some physicochemical descriptors was carried out to provide the guidance for further synthetic work. The significant molecular descriptors related to the compounds with antifungal activity were: electrostatic potential surface, the highest occupied molecular orbital energy, surface area, volume, and hydration energy.
Keywords: Antibacterial activity, antifungal activity, conformational analysis, physicochemical descriptors, piperidine derivatives, thiosemicarbazide derivatives, electrostatic potential surface, bacterial pathogens, antibiotics point, cationic polypeptides
Medicinal Chemistry
Title: Antimicrobial Activity and SAR Study of Some Novel Thiosemicarbazide Derivatives Bearing Piperidine Moiety
Volume: 7 Issue: 6
Author(s): Agata Siwek and Joanna Stefanska
Affiliation:
Keywords: Antibacterial activity, antifungal activity, conformational analysis, physicochemical descriptors, piperidine derivatives, thiosemicarbazide derivatives, electrostatic potential surface, bacterial pathogens, antibiotics point, cationic polypeptides
Abstract: In this study novel thiosemicarbazides bearing piperidine moiety were synthesized in order to investigate their possible antibacterial and antifungal activities. A structure-activity relationship (SAR) study including conformational analysis and some physicochemical descriptors was carried out to provide the guidance for further synthetic work. The significant molecular descriptors related to the compounds with antifungal activity were: electrostatic potential surface, the highest occupied molecular orbital energy, surface area, volume, and hydration energy.
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Cite this article as:
Siwek Agata and Stefanska Joanna, Antimicrobial Activity and SAR Study of Some Novel Thiosemicarbazide Derivatives Bearing Piperidine Moiety, Medicinal Chemistry 2011; 7 (6) . https://dx.doi.org/10.2174/157340611797928406
DOI https://dx.doi.org/10.2174/157340611797928406 |
Print ISSN 1573-4064 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6638 |
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