Quinaldine derivatives: preparation and biological activity
Language English Country Netherlands Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Antifungal Agents chemical synthesis chemistry pharmacology MeSH
- Quinaldines chemical synthesis chemistry pharmacology MeSH
- Chlorella vulgaris chemistry drug effects MeSH
- Chlorophyll antagonists & inhibitors biosynthesis MeSH
- Chloroplasts drug effects MeSH
- Photosynthesis drug effects MeSH
- Herbicides chemical synthesis chemistry pharmacology MeSH
- Microbial Sensitivity Tests MeSH
- Oxidation-Reduction MeSH
- Spinacia oleracea chemistry MeSH
- Stereoisomerism MeSH
- In Vitro Techniques MeSH
- Electron Transport drug effects MeSH
- Structure-Activity Relationship MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Antifungal Agents MeSH
- Quinaldines MeSH
- Chlorophyll MeSH
- Herbicides MeSH
The series of quinaldine derivatives were prepared, some of them by means of novel synthetic methods. The synthetic approach, analytical and spectroscopic data of all newly synthesized compounds are presented. The prepared compounds were tested for their in vitro antifungal activity as well as for their photosynthesis-inhibiting activity (the inhibition of photosynthetic electron transport in spinach chloroplasts (Spinacia oleracea L.) and the reduction of chlorophyll content in Chlorella vulgaris Beij.). Structure-activity relationships among the chemical structure, the physical properties and the biological activities of the evaluated compounds are discussed in the article.
References provided by Crossref.org
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Ring-substituted 4-hydroxy-1H-quinolin-2-ones: preparation and biological activity
