As part of a continuing search for new potential anticancer candidates, we describe the synthesis, cytotoxicity and mechanistic evaluation of a series of 4-oxoquinoline-3-carboxamide derivatives as novel anticancer agents. The inhibitory activity of compounds 10–18 was determined against three cancer cell lines using the MTT colorimetric assay. The screening revealed that derivatives 16b and 17b exhibited significant cytotoxic activity against the gastric cancer cell line but was not active against a normal cell line, in contrast to doxorubicin, a standard chemotherapeutic drug in clinical use. Interestingly, no hemolytical activity was observed when the toxicity of 16b and 17b was tested against blood cells. The in silico and in vitro mech...
AbstractThe design of molecules that recognize the specific sequence of the DNA double helix or thos...
New cytotoxic quinoline derivatives were designed, synthesized and evaluated in vitro as anti-tumor ...
Synthesis of ethyl 7-hydroxy-1-azacoumarin-3-carboxylate (3) was developed using ethyl-7-hydroxy cou...
As part of a continuing search for new potential anticancer candidates, we describe the synthesis, ...
Abstract: As part of a continuing search for new potential anticancer candidates, we describe the s...
Novel nineteen compounds based on a 4-aminoquinoline scaffold were designed and synthesized as poten...
This letter describes the preparation of quinoline derivatives and their cytotoxic potentials toward...
In this study, a new series of N-(di or trimethoxyaryl)-5-arylisoxazole-3-carboxamide derivatives we...
International audienceWe report a novel series of quinoxaline derivatives from which agents with ant...
The quinoxaline scaffold is a promising platform for the discovery of active chemotherapeutic agents...
Quinone-based small molecules are the promising structures for antiproliferative drug design and can...
A series of 2-aroyl and 2-aryl-5,6,7-trimethoxyquinoline and 4-aroyl-6,7,8-trimethoxyquinoline combr...
International audienceThe quinoxaline core is a promising scaffold in medicinal chemistry. Multiple ...
10The combination of two pharmacophores into a single molecule represents one of the methods that ca...
Okten, Salih/0000-0001-9656-1803; OZCAN, Evrencan/0000-0002-3662-6190WOS:000532595000001PubMed: 3240...
AbstractThe design of molecules that recognize the specific sequence of the DNA double helix or thos...
New cytotoxic quinoline derivatives were designed, synthesized and evaluated in vitro as anti-tumor ...
Synthesis of ethyl 7-hydroxy-1-azacoumarin-3-carboxylate (3) was developed using ethyl-7-hydroxy cou...
As part of a continuing search for new potential anticancer candidates, we describe the synthesis, ...
Abstract: As part of a continuing search for new potential anticancer candidates, we describe the s...
Novel nineteen compounds based on a 4-aminoquinoline scaffold were designed and synthesized as poten...
This letter describes the preparation of quinoline derivatives and their cytotoxic potentials toward...
In this study, a new series of N-(di or trimethoxyaryl)-5-arylisoxazole-3-carboxamide derivatives we...
International audienceWe report a novel series of quinoxaline derivatives from which agents with ant...
The quinoxaline scaffold is a promising platform for the discovery of active chemotherapeutic agents...
Quinone-based small molecules are the promising structures for antiproliferative drug design and can...
A series of 2-aroyl and 2-aryl-5,6,7-trimethoxyquinoline and 4-aroyl-6,7,8-trimethoxyquinoline combr...
International audienceThe quinoxaline core is a promising scaffold in medicinal chemistry. Multiple ...
10The combination of two pharmacophores into a single molecule represents one of the methods that ca...
Okten, Salih/0000-0001-9656-1803; OZCAN, Evrencan/0000-0002-3662-6190WOS:000532595000001PubMed: 3240...
AbstractThe design of molecules that recognize the specific sequence of the DNA double helix or thos...
New cytotoxic quinoline derivatives were designed, synthesized and evaluated in vitro as anti-tumor ...
Synthesis of ethyl 7-hydroxy-1-azacoumarin-3-carboxylate (3) was developed using ethyl-7-hydroxy cou...