A series of substituted chalcones and their corresponding pyrazoles were synthesized and evaluated for in vitro cytotoxic activity against a panel of human cancer cell lines. Out of 93 compounds screened, 8 compounds, 1s, 3i,j,n, 4i,j,n and 4s, showed marked activity. Compounds 4j,n and 4s were found to be the most promising in this study. SAR is also discussed
AbstractA series of ten novel chalcone incorporated quinazoline derivatives (11a–11j) were designed ...
A new series of N-(4-(1-Phenyl-5-aryl-4,5-dihydro-1H-pyrazol-3-yl)phenyl)-4-substitutedbenzamide der...
In an effort to develop new potent antimicrobial and anticancer agents, new pyrrole-based chalcones ...
Several chalcones were synthesized and their<em> in vitro </em>cytotoxicity against vari...
Despite having the second highest mortality associated with cancer, currently Sorafenib is the only ...
A new series of chalcones (3a-j) were synthesized by condensation of simple aldehydes with substitut...
A series of chalcones a1–20 bearing a 4-OMe groups on the A-ring were initially synthesized and thei...
A series of new chalcones substituted with azide/triazole groups were designed and synthesized, and ...
A novel series of triazin-chalcones (7,8)a-g and triazin-N-(3,5-dichlorophenyl)pyrazolines (9,10)a-g...
Despite having the second highest mortality associated with cancer, currently Sorafenib is the only ...
Chemically diverse heterocyclic chalcones were prepared and evaluated for cytotoxicity, aiming to pu...
Objectives: Several pyrazoline derivatives have been developed as chemotherapeutic agents and have f...
A series of 59 chalcones was prepared and evaluated for the antimitotic effect against K562 leukemia...
A combinatorial synthesis of small libraries of a variety of amino chalcones has been carried out in...
A series of ten novel chalcone incorporated quinazoline derivatives (11a–11j) were designed and synt...
AbstractA series of ten novel chalcone incorporated quinazoline derivatives (11a–11j) were designed ...
A new series of N-(4-(1-Phenyl-5-aryl-4,5-dihydro-1H-pyrazol-3-yl)phenyl)-4-substitutedbenzamide der...
In an effort to develop new potent antimicrobial and anticancer agents, new pyrrole-based chalcones ...
Several chalcones were synthesized and their<em> in vitro </em>cytotoxicity against vari...
Despite having the second highest mortality associated with cancer, currently Sorafenib is the only ...
A new series of chalcones (3a-j) were synthesized by condensation of simple aldehydes with substitut...
A series of chalcones a1–20 bearing a 4-OMe groups on the A-ring were initially synthesized and thei...
A series of new chalcones substituted with azide/triazole groups were designed and synthesized, and ...
A novel series of triazin-chalcones (7,8)a-g and triazin-N-(3,5-dichlorophenyl)pyrazolines (9,10)a-g...
Despite having the second highest mortality associated with cancer, currently Sorafenib is the only ...
Chemically diverse heterocyclic chalcones were prepared and evaluated for cytotoxicity, aiming to pu...
Objectives: Several pyrazoline derivatives have been developed as chemotherapeutic agents and have f...
A series of 59 chalcones was prepared and evaluated for the antimitotic effect against K562 leukemia...
A combinatorial synthesis of small libraries of a variety of amino chalcones has been carried out in...
A series of ten novel chalcone incorporated quinazoline derivatives (11a–11j) were designed and synt...
AbstractA series of ten novel chalcone incorporated quinazoline derivatives (11a–11j) were designed ...
A new series of N-(4-(1-Phenyl-5-aryl-4,5-dihydro-1H-pyrazol-3-yl)phenyl)-4-substitutedbenzamide der...
In an effort to develop new potent antimicrobial and anticancer agents, new pyrrole-based chalcones ...