Affiliation:
1. Department of Chemistry Lomonosov Moscow State University Leninskie Gory, 1–3 Moscow 119991 Russia
2. Emanuel Institute of Biochemical Physics Russian Academy of Sciences 4 Kosygin st. Moscow 119334 Russia
Abstract
AbstractA simple two‐step protocol for the synthesis of 3‐aryl/hetaryl‐4‐nitro‐5‐styrylisoxazole was elaborated. A large series of novel 5‐styrylisoxazoles (36 compounds) containing various substituents at positions 3 and 5 of isoxazole cycle was obtained. The title compounds revealed fluorescent properties in visible region, possessing emission maximum up to 610nm. The effect of solvatochromism and chemosensor properties towards a number of metal cations were demonstrated. Cytotoxic activity against MCF‐7 (breast carcinoma), HCT‐116 (colon carcinoma), A549 (pulmonary carcinoma) and WI38 (fibroblasts from lung tissue) cell lines was tested and toxicity in the concentration range of 10–100 μM was found for several compounds.
Funder
Russian Science Foundation
Cited by
1 articles.
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