Synthesis of novel acrylyl pyranochromen-2-one derivatives and their antibacterial activity evaluation
By: Prasad, Suchita.
Contributor(s): Mittal, Ayushi.
Publisher: New Delhi CSIR 2019Edition: Vol.58(B), April.Description: 482-496p.Subject(s): GENERAL CHEMISTRYOnline resources: Click here In: Indian journal of chemistry (Section B)Summary: A series of fourteen pyranochromen-2-one acrylate derivatives has been synthesized by acid-catalyzed esterification reaction of the corresponding pyranochromen-2-one acrylic acids with various alcohols under reflux conditions. In order to have comparison of the activity profiles of esters and amides, the synthesis of ten pyranochromen-2-one acrylamides from corresponding acrylic acids using different coupling agents has also been carried out. All of the synthesized compounds have been fully characterized from their spectral data and evaluated for antibacterial activity against both Gram-positive (Bacillus cereus and Staphylococcus aureus) and Gram-negative bacteria (Pseudomonas aeruginosa and Escherichia coli). It is inferred form the results that the presence of hydroxyl group along with longer hydrophobic alkyl chain is favorable for a compound to inhibit bacterial growth, which can be used to design and develop the next generation of compounds with higher antibacterial efficacy.Item type | Current location | Call number | Status | Date due | Barcode | Item holds |
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Articles Abstract Database | School of Pharmacy Archieval Section | Not for loan | 2022-0319 |
A series of fourteen pyranochromen-2-one acrylate derivatives has been synthesized by acid-catalyzed esterification reaction of the corresponding pyranochromen-2-one acrylic acids with various alcohols under reflux conditions. In order to have comparison of the activity profiles of esters and amides, the synthesis of ten pyranochromen-2-one acrylamides from corresponding acrylic acids using different coupling agents has also been carried out. All of the synthesized compounds have been fully characterized from their spectral data and evaluated for antibacterial activity against both Gram-positive (Bacillus cereus and Staphylococcus aureus) and Gram-negative bacteria (Pseudomonas aeruginosa and Escherichia coli). It is inferred form the results that the presence of hydroxyl group along with longer hydrophobic alkyl chain is favorable for a compound to inhibit bacterial growth, which can be used to design and develop the next generation of compounds with higher antibacterial efficacy.
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