SYNTHESIS OF ANTIBACTERIAL CINNAMAMIDES
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14160%2F23%3A00131719" target="_blank" >RIV/00216224:14160/23:00131719 - isvavai.cz</a>
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
SYNTHESIS OF ANTIBACTERIAL CINNAMAMIDES
Original language description
Substituted N-phenyl amides of 3,4-dichlorocinnamic acid have been the subject of earlier studies. Some derivatives have shown excellent antimicrobial and antimalarial activity. The newly synthesized compounds that are the subject of this study are direct structural analogues differing in phenyl substitution. 40 derivatives with multiple substitution of both electron-donating and electron-accepting groups were synthesized and characterized, and the antimicrobial activity against Gram-positive bacteria of the genus Staphylococcus was determined. Some derivatives shown excellent activity comparable to the clinically used antibiotics ampicillin and ciprofloxacin.
Czech name
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Czech description
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Classification
Type
O - Miscellaneous
CEP classification
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OECD FORD branch
30104 - Pharmacology and pharmacy
Result continuities
Project
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Continuities
S - Specificky vyzkum na vysokych skolach
Others
Publication year
2023
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů