Benzenesulfonamide, 3-(butylamino)-5-(4,5-dihydro-4-phenyl-5-thioxo-1H-1,2,4-triazol-3-yl)-2-phenoxy- manufacturers
- COX-2-IN-23
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- $2500.00
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2026-04-21
- CAS:2417995-08-3
- Purity:
- Supply Ability: 10g
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| | Benzenesulfonamide, 3-(butylamino)-5-(4,5-dihydro-4-phenyl-5-thioxo-1H-1,2,4-triazol-3-yl)-2-phenoxy- Basic information |
| | Benzenesulfonamide, 3-(butylamino)-5-(4,5-dihydro-4-phenyl-5-thioxo-1H-1,2,4-triazol-3-yl)-2-phenoxy- Chemical Properties |
| Boiling point | 651.3±65.0 °C(Predicted) | | density | 1.37±0.1 g/cm3(Predicted) | | pka | 5.03±0.20(Predicted) |
| | Benzenesulfonamide, 3-(butylamino)-5-(4,5-dihydro-4-phenyl-5-thioxo-1H-1,2,4-triazol-3-yl)-2-phenoxy- Usage And Synthesis |
| Uses | COX-2-IN-23 (compound 9a) is a selective COX-2 inhibitor with IC50 values of 0.28 and 20.14 μM for COX-2 and COX-1. COX-2-IN-23 has anti-inflammatory activity and low ulcerogenic activity. | | in vivo | COX-2-IN-23 (compound 9a) (9 mg/kg; a single i.p.; 0-4 hours) exhibits anti-inflammatory activities and lowest incidence of pepticulcer[1]. | Animal Model: | Mature male albino rats[1] | | Dosage: | 9 mg/kg | | Administration: | Intraperitoneal injection; 0, 1, 2, 3 and 4 hours. | | Result: | Had similar ulcerogenic activity to celecoxib. |
| | IC 50 | COX-2: 0.28 μM (IC50); COX-1: 20.14 μM (IC50) | | References | [1] Ibrahim TS, et al. Design, synthesis, and pharmacological evaluation of novel and selective COX-2 inhibitors based on bumetanide scaffold. Bioorg Chem. 2020 Jul;100:103878. DOI:10.1016/j.bioorg.2020.103878 |
| | Benzenesulfonamide, 3-(butylamino)-5-(4,5-dihydro-4-phenyl-5-thioxo-1H-1,2,4-triazol-3-yl)-2-phenoxy- Preparation Products And Raw materials |
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