2020
DOI: 10.1016/j.bioorg.2020.103878
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Design, synthesis, and pharmacological evaluation of novel and selective COX-2 inhibitors based on bumetanide scaffold

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Cited by 11 publications
(5 citation statements)
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“…These compounds are selective on COX-2 with SI = 61.13 ( 11a ), 71.93 ( 11b ), and 115.82 ( 11c ). Based on in vitro and in vivo experiment results, compounds 11b and 11c exhibited the highest anti-inflammatory activities and lowest incidence of pepticulcer 26 .…”
Section: Recent Development In Anti-inflammatory Agentsmentioning
confidence: 99%
“…These compounds are selective on COX-2 with SI = 61.13 ( 11a ), 71.93 ( 11b ), and 115.82 ( 11c ). Based on in vitro and in vivo experiment results, compounds 11b and 11c exhibited the highest anti-inflammatory activities and lowest incidence of pepticulcer 26 .…”
Section: Recent Development In Anti-inflammatory Agentsmentioning
confidence: 99%
“…Benzenesulfonamide derivatives ( 14) with a bumetanide main scaffold bearing pyrazole and triazole moieties were reported by Ibrahim et al 76 to be selective COX-2 inhibitors with IC 50 = 0.17-4.79 μM (SI = 4.84-115.82) (Fig. 15).…”
Section: Rsc Medicinal Chemistry Reviewmentioning
confidence: 99%
“…In 2020, Ibrahim et al. 63 have reported several novel benzenesulfonamide analogs which aim to developed as COX-2 inhibitors. Structurally, bumetanide was used as a precursor to synthesized new analogues.…”
Section: Chemistry and Pharmacology Of Structurally Modified Cox-2 In...mentioning
confidence: 99%