Synthesis, carbonic anhydrase inhibition and cytotoxic activity of novel chromone-based sulfonamide derivatives-Reference-Cited by-同舟云学术

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Synthesis, carbonic anhydrase inhibition and cytotoxic activity of novel chromone-based sulfonamide derivatives

Published:2015-05 Issue: Volume:96 Page:425-435
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Awadallah Fadi M.,El-Waei Tamer A.,Hanna Mona M.,Abbas Safinaz E.,Ceruso Mariangela,Oz Beyza Ecem,Guler Ozen Ozensoy,Supuran Claudiu T.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference54 articles.

1. Synthesis, antimicrobial activity and bleaching effect of some reaction products of 4-oxo-4H-benzopyran-3-carboxaldehydes with aminobenzothiazoles and hydrazides

2. Antibacterial, antifungal and cytotoxic properties of some sulfonamide-derived chromones

3. Synthesis and anticancer activity of chromone-based analogs of lavendustin A

4. Synthesis and antitumor activity of novel dithiocarbamate substituted chromones

5. Synthesis and Evaluation of Antirhinovirus Activity of 3-Hydroxy and 3-Methoxy 2-Styrylchromones

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2. Natural products-isoxazole hybrids: A review of developments in medicinal chemistry;Arabian Journal of Chemistry;2024-06

3. Chemistry of heterocycles as carbonic anhydrase inhibitors: A pathway to novel research in medicinal chemistry review;Archiv der Pharmazie;2024-04-29

4. Synthesis, bioactivity assessment, molecular docking and ADMET studies of new chromone congeners exhibiting potent anticancer activity;Scientific Reports;2024-04-26

5. Novel thiazolidin-4-one benzenesulfonamide hybrids as PPARγ agonists: Design, synthesis and in vivo anti-diabetic evaluation;European Journal of Medicinal Chemistry;2024-04

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