WebAll the newly synthesized chalcone derivatives were examined for their in vitro antiproliferative inhibitory activity using, A-375, MCF-7, A-549, HT-29, and H-460 human cancer cell lines. Cisplatin and foretinib were used as a positive control. WebJun 1, 2024 · One of the synthesized thiophene‐chalcone derivative 15 e displayed an IC50 value of 6.3±0.9 μM and also induced apoptosis in A549 cells. This strategy is …
α‐Substituted Chalcones: A Key Review - Al‐Rifai - 2024 ...
WebThe fluoro-substituted tris-chalcone derivatives were synthesized from phloroglucinol and benzaldehyde in three steps (Scheme 1) [5]. The tris-chalcones have shown inhibition of hCA I and II isoenzymes, acetylcholinesterase, butyrylcholinesterase. The base-catalyzed Claisen- Schmidt condensation reaction between aromatic aldehydes and ketones ... WebThe pyrazoline, oxazine, thiazine and pyrimidine derivatives of chalcones can be produced through the condensation of their α,β-unsaturated carbonyl moiety. The heterocyclic chalcones were refluxed with hydrazine hydrate and anhydrous sodium acetate in glacial acetic acid to obtain their N-acetylated pyrazoline derivatives. set review strixhaven
Recent Developments on the Synthetic and Biological …
WebMay 27, 2024 · New thiophene chalcones 3, 6 and thiophene Schiff base-chalcone derivatives 4a–4d, 7a–7d are synthesized. Structures of the compounds are confirmed by 1H and 13C NMR, and IR spectra. According to antimicrobial and antileishmanial tests, the compounds 4c–7c demonstrate efficient antileishmanial and antimicrobial activities. … WebThiophene-derived compounds are interesting in chemistry, biology and pharmacology because of their various pharmacological activities. Complex compounds with metals have also been prepared and studied. It is stated that the structure and conformation of the molecule significantly alter the biological activities [1]. Webapplication of chalcone derivatives as synthons in organic syn-thesis, has led to the synthesis of thiophene analogues of chal-cone and their subsequent heterocyclics. The thiophene heteroaryl ring is important owing to elemental sulphur having antifungal properties, while chalcones bearing sulphur either setrevstartsize is not defined