In the study, a series of twelve ring-substituted 4-hydroxy-1H-quinolin-2- one derivatives were prepared. The procedures for synthesis of the compounds are presented. The compounds were analyzed using RP-HPLC to determine lipophilicity and tested for their photosynthesis-inhibiting activity using spinach (Spinacia oleracea L.) chloroplasts. All the synthesized compounds were also evaluated for antifungal activity using in vitro screening with eight fungal strains. For all the compounds, the relationships between the lipophilicity and the chemical structure of the studied compounds are discussed, as well as their structure-activity relationships (SAR)
Quinolone derivatives have recently been introduced as inhibitors of eukaryotic topisomerase-II with...
With an objective of synthesizing some novel, potent and broad spectrum antifungal activity having c...
In this study, series of ring-substituted 2-styrylquinazolin-4(3H)-one and 4-chloro-2-styrylquinazol...
In the study, a series of twelve ring-substituted 4-hydroxy-1H-quinolin-2-one derivatives were prepa...
In this study, a series of fourteen ring-substituted 8-hydroxyquinoline derivatives were prepared. T...
* Authors to whom correspondence should be addressed. Abstract: The series of twelve ring-substitute...
In this study, series of ring-substituted 2-styrylquinazolin-4(3H)-one and 4-chloro-2-styrylquinazol...
In this study, series of ring-substituted 2-styrylquinazolin-4(3H)-one and 4-chloro-2-styrylquinazol...
In this study, a series of fourteen ring-substituted 8-hydroxyquinoline derivatives were prepared. T...
This research article reports the synthesis of a series of 4-methyl-2-(p-substitutedphenyl)quinoline...
Abstract: The series of quinoline derivatives were prepared. The synthetic procedures of compounds a...
In this study, a series of thirty-five substituted quinoline-2-carboxamides and thirty-three substit...
In this study, a series of twelve ring-substituted salicylanilides and carbamoylphenylcarbamates wer...
Two series of thiosemicarbazone-based iron chelators (twenty-seven compounds) were designed and synt...
In this study, a series of twenty-five ring-substituted 4-arylamino-7-chloroquinolinium chlorides we...
Quinolone derivatives have recently been introduced as inhibitors of eukaryotic topisomerase-II with...
With an objective of synthesizing some novel, potent and broad spectrum antifungal activity having c...
In this study, series of ring-substituted 2-styrylquinazolin-4(3H)-one and 4-chloro-2-styrylquinazol...
In the study, a series of twelve ring-substituted 4-hydroxy-1H-quinolin-2-one derivatives were prepa...
In this study, a series of fourteen ring-substituted 8-hydroxyquinoline derivatives were prepared. T...
* Authors to whom correspondence should be addressed. Abstract: The series of twelve ring-substitute...
In this study, series of ring-substituted 2-styrylquinazolin-4(3H)-one and 4-chloro-2-styrylquinazol...
In this study, series of ring-substituted 2-styrylquinazolin-4(3H)-one and 4-chloro-2-styrylquinazol...
In this study, a series of fourteen ring-substituted 8-hydroxyquinoline derivatives were prepared. T...
This research article reports the synthesis of a series of 4-methyl-2-(p-substitutedphenyl)quinoline...
Abstract: The series of quinoline derivatives were prepared. The synthetic procedures of compounds a...
In this study, a series of thirty-five substituted quinoline-2-carboxamides and thirty-three substit...
In this study, a series of twelve ring-substituted salicylanilides and carbamoylphenylcarbamates wer...
Two series of thiosemicarbazone-based iron chelators (twenty-seven compounds) were designed and synt...
In this study, a series of twenty-five ring-substituted 4-arylamino-7-chloroquinolinium chlorides we...
Quinolone derivatives have recently been introduced as inhibitors of eukaryotic topisomerase-II with...
With an objective of synthesizing some novel, potent and broad spectrum antifungal activity having c...
In this study, series of ring-substituted 2-styrylquinazolin-4(3H)-one and 4-chloro-2-styrylquinazol...