An asymmetric synthesis of a series of novel 4-methyl-(3\u27S,4\u27S)-cis-khellactone derivatives 3a–o is reported for the first time. Their structures were confirmed by 1H-NMR, 13C-NMR and MS. Their cytotoxic activity was evaluated by the MTT assay against three selected human cancer cell lines: HEPG-2 (human liver carcinoma), SGC-7901 (human gastric carcinoma), LS174T (human colon carcinoma). Some compounds showed high inhibitory activity against these human cancer cell lines. Among them, compound 3a exhibited strong cytotoxicity, with IC50 values ranging from 8.51 to 29.65 μM. The results showed that 4-methyl-cis-khellactone derivatives with S,S configuration could be a potential antitumor agents
In this report, we present efficient and stereoselective syntheses of 2,6-disubstituted trans-3-meth...
In the search for new anticancer agents, a library of variously substituted 3-methylidenechroman-4-o...
Forty-four novel chalcone-inspired analogs having a 3-aryl-2-propenoyl moiety derived from alicyclic...
An asymmetric synthesis of a series of novel 4-methyl-(3'S,4'S)-cis-khellactone derivative...
There was a major interest in the last years in the design of anticancer agents containing the 1,5-d...
As part of the studies in our laboratories aimed at improving the cytotoxicity of combretastatins an...
In the present work few novel 2-(4-methylbenzenesulphonamido)pentanedioic acid amide derivatives and...
Medicinal plant extracts have been used for medical purposes throughout human history. In this study...
In the present work few novel 2-(4-methylbenzenesulphonamido)pentanedioic acid amide derivatives and...
In the present work few novel 2-(4-methylbenzenesulphonamido)pentanedioic acid bis amide derivatives...
Chromone has emerged as one of the most important synthetic scaffolds for antitumor activity, which ...
The synthesis of a series of \u3b1-methylene-\u3b3-butyrolactones (compounds 4a, 4b, 6\u201312, 16, ...
In this study, a series of novel β‑hydroxy ketone derivatives 3a-o were designed, synthesized, and e...
In the present work few novel 2-(4-methylbenzenesulphonamido)pentanedioic acid amide derivatives and...
In the present work few novel 2-(4-methylbenzenesulphonamido)pentanedioic acid bis amide derivatives...
In this report, we present efficient and stereoselective syntheses of 2,6-disubstituted trans-3-meth...
In the search for new anticancer agents, a library of variously substituted 3-methylidenechroman-4-o...
Forty-four novel chalcone-inspired analogs having a 3-aryl-2-propenoyl moiety derived from alicyclic...
An asymmetric synthesis of a series of novel 4-methyl-(3'S,4'S)-cis-khellactone derivative...
There was a major interest in the last years in the design of anticancer agents containing the 1,5-d...
As part of the studies in our laboratories aimed at improving the cytotoxicity of combretastatins an...
In the present work few novel 2-(4-methylbenzenesulphonamido)pentanedioic acid amide derivatives and...
Medicinal plant extracts have been used for medical purposes throughout human history. In this study...
In the present work few novel 2-(4-methylbenzenesulphonamido)pentanedioic acid amide derivatives and...
In the present work few novel 2-(4-methylbenzenesulphonamido)pentanedioic acid bis amide derivatives...
Chromone has emerged as one of the most important synthetic scaffolds for antitumor activity, which ...
The synthesis of a series of \u3b1-methylene-\u3b3-butyrolactones (compounds 4a, 4b, 6\u201312, 16, ...
In this study, a series of novel β‑hydroxy ketone derivatives 3a-o were designed, synthesized, and e...
In the present work few novel 2-(4-methylbenzenesulphonamido)pentanedioic acid amide derivatives and...
In the present work few novel 2-(4-methylbenzenesulphonamido)pentanedioic acid bis amide derivatives...
In this report, we present efficient and stereoselective syntheses of 2,6-disubstituted trans-3-meth...
In the search for new anticancer agents, a library of variously substituted 3-methylidenechroman-4-o...
Forty-four novel chalcone-inspired analogs having a 3-aryl-2-propenoyl moiety derived from alicyclic...