Synthesis and In Vitro Antitumor Activity of Novel Chromenones Bearing Benzothiazole Moiety
El-Helw, EAE; Derbala, HA; El-Shahawi, MM; Salem MS,; Ali, MM;
Abstract
Abstract: 6-(Benzo[d]thiazol-2-yl)-4-oxo-(4H)-chromene-3-carbaldehyde was utilized to construct a novel series of fused chromone bearing benzothiazole moiety, namely chromeno[2,3-b]azetol, benzo[c]chromene, and chromeno[2,3-c]pyrazole derivatives, as well as, non-fused chromones, such as thiazolidinone, pyrazolone, and pyridine derivatives. The in vitro antitumor activities of the synthesized products against six cancer cell lines, including A594, HCT-116, MCF-7, HepPG2, PC3, and HFB4, were evaluated. Some compounds exhibited significant anticancer activities against both lung and colon cancer cells very close to that of a standard drug doxorubicin.
Other data
Title | Synthesis and In Vitro Antitumor Activity of Novel Chromenones Bearing Benzothiazole Moiety | Authors | El-Helw, EAE ; Derbala, HA ; El-Shahawi, MM ; Salem MS, ; Ali, MM | Keywords | benzothiazole;;3-formylchromone;antitumoractivity;thiazolidinone;pyrazole;ANTICANCER ACTIVITY EVALUATION;;BIOLOGICAL EVALUATION;PYRAZOLE;AMIDES;DESIGN;DERIVATIVES;CYTOTOXICITY | Issue Date | 2019 | Publisher | MAIK NAUKA/INTERPERIODICA/SPRINGER | Journal | RUSSIAN JOURNAL OF BIOORGANIC CHEMISTRY | Volume | 45 | Start page | 42 | End page | 53 | ISSN | 1068-1620 | DOI | 10.1134/S1068162019010047 | Scopus ID | 2-s2.0-85065427839 | Web of science ID | WOS:000471969900006 |
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