| Weight | 225.191 g/mol |
|---|---|
| Formula | C7H6F3NO2S |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
3-(Trifluoromethyl)benzenesulfonamide (672-58-2)
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- Synthesis and in vivo evaluation of [18F]-4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide as a PET imaging probe for COX-2 expression (Bioorganic & Medicinal Chemistry, 2007)
- Discovery of a potent, orally bioavailable beta(3) adrenergic receptor agonist, (R)-N-[4-[2-[[2-hydroxy-2-(3-pyridinyl)ethyl]amino]ethyl]phenyl]-4-[4 -[4-(trifluoromethyl)phenyl]thiazol-2-yl]benzenesulfonamide. (Journal of Medicinal Chemistry, 2000)
- Enhancement of Doxorubicin Cytotoxicity on Human Esophageal Squamous Cell Carcinoma Cells by Indomethacin and 4-[5-(4-Chlorophenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide (SC236) via Inhibiting P-Glycoprotein Activity (Molecular Pharmacology, 2009)
- Cyclooxygenase-2 inhibitor SC-236 [4-[5-(4-chlorophenyl)-3-(trifluoromethyl)-1-pyrazol-1-l] benzenesulfonamide] suppresses nuclear factor-kappaB activation and phosphorylation of p38 mitogen-activated protein kinase, extracellular signal-regulated kinase, and c-Jun N-terminal kinase in human mast cell line cells. (Journal of Pharmacology and Experimental Therapeutics, 2005)
- 2-Hydroxymethyl-4-[5-(4-methoxyphenyl)-3-trifluoromethyl-1H-1-pyrazolyl]-1-benzenesulfonamide (DRF-4367): an orally active COX-2 inhibitor identified through pharmacophoric modulation (Organic and Biomolecular Chemistry, 2004)
- N-Acylated Sulfonamide Sodium Salt: A Prodrug of Choice for the Bifunctional 2-Hydroxymethyl-4-(5-phenyl-3-trifluoromethyl-pyrazol-1-yl) Benzenesulfonamide Class of COX-2 Inhibitors. (Bioorganic & Medicinal Chemistry Letters, 2006)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=CC(=C1)S(=O)(=O)N)C(F)(F)F
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InChIKeyZUTVRDMZQSHCID-UHFFFAOYSA-N
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Similar Compounds
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3-(Trifluoromethyl)benzenesulfonamide
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