Synthesis, cytotoxicity, and molecular docking of substituted 3‐(2‐methylbenzofuran‐3‐yl)‐5‐(phenoxymethyl)‐1,2,4‐oxadiazoles
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DOI: 10.1002/ardp.202000006
Abstract: A series of new benzofuran/oxadiazole hybrids (8a–n) was synthesized from 2H‐chromene‐3‐carbonitriles (3a–c) through the multistep synthetic methodology, and these hybrids are known to exhibit anticancer activities. All the compounds were evaluated for their in vitro… read more here.
Keywords: synthesis cytotoxicity; cytotoxicity molecular; docking substituted; activity ... See more keywords
Structural, cytotoxicity and molecular docking studies of some quinoline schiff bases and their Pd(II), Mn(II) and Ru(II) complexes
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DOI: 10.1016/j.molstruc.2020.128778
Abstract: Abstract Mononuclear Pd(II), Mn(II) and Ru(II) complexes have been synthesized from neutral bidentate ligands 1,5-dimethyl-2-phenyl-4-((quinolin-3-ylmethylene)amino)-1,2-dihydro-3H-pyrazol-3-one(QuAP), and 4-((2,6-dimethoxyquinolin-3-yl)methyleneamino)-1,5-dimethyl-2-phenyl-1,2-dihydro-3H-pyrazol-3-one (MeOQuAP) respectively. The structures of the isolated products are proposed by the elemental analyses, IR, UV–Vis., 1H NMR,… read more here.
Keywords: structural cytotoxicity; quinoline schiff; docking studies; cytotoxicity molecular ... See more keywords