Aurones and Analogues: Promising Heterocyclic Scaffolds for Development of Antioxidant and Antimicrobial Agents


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Аннотация

Synthesis of some new multi-functional analogues of 2′-hydroxy chalcone containing isoxazole and pyrazole functions were synthesized, and their pharmacological activity was tested. Chalcone derivatives were synthesized by the reaction of 2′-hydroxy acetophenone with various substituted benzaldehydes in a basic medium. Aurones were isolated upon treatment with mercuric acetate. Synthesized chalcones and aurones were converted into the corresponding isoxazole and pyrazole derivatives upon their reaction with hydroxylamine hydrochloride or hydrazine hydrate, respectively. Structures of the compounds were confirmed by spectroscopic methods. All synthesized compounds were tested for antioxidant and antibacterial potential. Some of those demonstrated excellent antioxidant activity, and one product was identified as a promising antimicrobial candidate.

Об авторах

M. Irshad

Department of Chemistry, Division of Science and Technology

Автор, ответственный за переписку.
Email: misbahchatha@hotmail.com
Пакистан, Lahore, 54770

Q. Ali

Department of Chemistry, Division of Science and Technology

Email: misbahchatha@hotmail.com
Пакистан, Lahore, 54770

F. Iram

Department of Chemistry

Email: misbahchatha@hotmail.com
Пакистан, Lahore, 75500

S. Ahamad

Department of Chemistry

Email: misbahchatha@hotmail.com
Пакистан, Lahore, 75500

M. Saleem

Department of Chemistry

Email: misbahchatha@hotmail.com
Пакистан, Dera Ghazi Khan, 32200

M. Saadia

Department of Biochemistry

Email: misbahchatha@hotmail.com
Пакистан, Sargodha, 40100

M. Batool

Department of Chemistry

Email: misbahchatha@hotmail.com
Пакистан, Lahore, 54590

A. Kanwal

Department of Chemistry, Division of Science and Technology

Email: misbahchatha@hotmail.com
Пакистан, Lahore, 54770

S. Tabassum

Department of Chemistry, Division of Science and Technology

Email: misbahchatha@hotmail.com
Пакистан, Lahore, 54770


© Pleiades Publishing, Ltd., 2019

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