Matches in SemOpenAlex for { <https://semopenalex.org/work/W4220794713> ?p ?o ?g. }
- W4220794713 endingPage "100856" @default.
- W4220794713 startingPage "100856" @default.
- W4220794713 abstract "A new series of various substituted aryl and hetero aryl amide derivatives of benzoxazole linked imidazo[2,1-b][1,3,4]thiadiazole (11a-j) were synthesized and their structures confirmed by spectral data. These newly synthesized compounds (11a-j) were evaluated for their anticancer profile towards human prostate cancer (PC3 and DU-145), lung cancer (A549) and breast cancer (MCF-7) cell lines by used of MTT assay and etoposide was chosen as positive control. Most of the derivatives displayed good to moderate antiproliferative activities with respective cell lines. Among the evaluated compounds, four compounds (11a, 11b, 11c and 11d) demonstrated more potent anticancer activity. Particularly, compound 11a showed strongest activity as etoposide." @default.
- W4220794713 created "2022-04-03" @default.
- W4220794713 creator A5001858298 @default.
- W4220794713 creator A5043836263 @default.
- W4220794713 creator A5046332104 @default.
- W4220794713 creator A5048723860 @default.
- W4220794713 date "2022-06-01" @default.
- W4220794713 modified "2023-10-16" @default.
- W4220794713 title "Synthesis and biological evaluation of amide derivatives of benzoxazole linked Imidazo[2,1-b][1,3,4]thiadiazole as antiproliferative agents" @default.
- W4220794713 cites W1065968067 @default.
- W4220794713 cites W1969321633 @default.
- W4220794713 cites W1972277565 @default.
- W4220794713 cites W1981096020 @default.
- W4220794713 cites W1987117203 @default.
- W4220794713 cites W1995214249 @default.
- W4220794713 cites W1999616220 @default.
- W4220794713 cites W1999816998 @default.
- W4220794713 cites W2008062014 @default.
- W4220794713 cites W2034629146 @default.
- W4220794713 cites W2043569527 @default.
- W4220794713 cites W2047351554 @default.
- W4220794713 cites W2047380695 @default.
- W4220794713 cites W2047527113 @default.
- W4220794713 cites W2059398392 @default.
- W4220794713 cites W2061505401 @default.
- W4220794713 cites W2080633817 @default.
- W4220794713 cites W2090289458 @default.
- W4220794713 cites W2093221020 @default.
- W4220794713 cites W2095395178 @default.
- W4220794713 cites W2112442086 @default.
- W4220794713 cites W2178742677 @default.
- W4220794713 cites W2732157431 @default.
- W4220794713 doi "https://doi.org/10.1016/j.cdc.2022.100856" @default.
- W4220794713 hasPublicationYear "2022" @default.
- W4220794713 type Work @default.
- W4220794713 citedByCount "1" @default.
- W4220794713 countsByYear W42207947132022 @default.
- W4220794713 crossrefType "journal-article" @default.
- W4220794713 hasAuthorship W4220794713A5001858298 @default.
- W4220794713 hasAuthorship W4220794713A5043836263 @default.
- W4220794713 hasAuthorship W4220794713A5046332104 @default.
- W4220794713 hasAuthorship W4220794713A5048723860 @default.
- W4220794713 hasConcept C121608353 @default.
- W4220794713 hasConcept C126322002 @default.
- W4220794713 hasConcept C178790620 @default.
- W4220794713 hasConcept C185592680 @default.
- W4220794713 hasConcept C202751555 @default.
- W4220794713 hasConcept C21951064 @default.
- W4220794713 hasConcept C2776694085 @default.
- W4220794713 hasConcept C2777752112 @default.
- W4220794713 hasConcept C2778047396 @default.
- W4220794713 hasConcept C2778119113 @default.
- W4220794713 hasConcept C2778439535 @default.
- W4220794713 hasConcept C2780192828 @default.
- W4220794713 hasConcept C2780263894 @default.
- W4220794713 hasConcept C2780783641 @default.
- W4220794713 hasConcept C2781076698 @default.
- W4220794713 hasConcept C2994372470 @default.
- W4220794713 hasConcept C2994423619 @default.
- W4220794713 hasConcept C54355233 @default.
- W4220794713 hasConcept C55493867 @default.
- W4220794713 hasConcept C62112901 @default.
- W4220794713 hasConcept C71240020 @default.
- W4220794713 hasConcept C71924100 @default.
- W4220794713 hasConcept C81885089 @default.
- W4220794713 hasConcept C86803240 @default.
- W4220794713 hasConcept C96232424 @default.
- W4220794713 hasConceptScore W4220794713C121608353 @default.
- W4220794713 hasConceptScore W4220794713C126322002 @default.
- W4220794713 hasConceptScore W4220794713C178790620 @default.
- W4220794713 hasConceptScore W4220794713C185592680 @default.
- W4220794713 hasConceptScore W4220794713C202751555 @default.
- W4220794713 hasConceptScore W4220794713C21951064 @default.
- W4220794713 hasConceptScore W4220794713C2776694085 @default.
- W4220794713 hasConceptScore W4220794713C2777752112 @default.
- W4220794713 hasConceptScore W4220794713C2778047396 @default.
- W4220794713 hasConceptScore W4220794713C2778119113 @default.
- W4220794713 hasConceptScore W4220794713C2778439535 @default.
- W4220794713 hasConceptScore W4220794713C2780192828 @default.
- W4220794713 hasConceptScore W4220794713C2780263894 @default.
- W4220794713 hasConceptScore W4220794713C2780783641 @default.
- W4220794713 hasConceptScore W4220794713C2781076698 @default.
- W4220794713 hasConceptScore W4220794713C2994372470 @default.
- W4220794713 hasConceptScore W4220794713C2994423619 @default.
- W4220794713 hasConceptScore W4220794713C54355233 @default.
- W4220794713 hasConceptScore W4220794713C55493867 @default.
- W4220794713 hasConceptScore W4220794713C62112901 @default.
- W4220794713 hasConceptScore W4220794713C71240020 @default.
- W4220794713 hasConceptScore W4220794713C71924100 @default.
- W4220794713 hasConceptScore W4220794713C81885089 @default.
- W4220794713 hasConceptScore W4220794713C86803240 @default.
- W4220794713 hasConceptScore W4220794713C96232424 @default.
- W4220794713 hasLocation W42207947131 @default.
- W4220794713 hasOpenAccess W4220794713 @default.
- W4220794713 hasPrimaryLocation W42207947131 @default.
- W4220794713 hasRelatedWork W2358524133 @default.
- W4220794713 hasRelatedWork W2362645172 @default.
- W4220794713 hasRelatedWork W2370855104 @default.