Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C17H10F6N2O2S |
| Molecular Weight | 420.329 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
FC(F)C(F)(F)S(=O)(=O)C1=NC(=C(N1)C2=CC=C(F)C=C2)C3=CC=C(F)C=C3
InChI
InChIKey=XUOAKFNMJMYKBY-UHFFFAOYSA-N
InChI=1S/C17H10F6N2O2S/c18-11-5-1-9(2-6-11)13-14(10-3-7-12(19)8-4-10)25-16(24-13)28(26,27)17(22,23)15(20)21/h1-8,15H,(H,24,25)
Tiflamizole is a fluorinated diarylamidazole derivative patented by du Pont de Nemours, E. I., and Co. as an anti-inflammatory agent. Tiflamizole acts as a non-steroidal anti-inflammatory drug, that exerts potent inhibition of prostaglandin synthesis and exhibits anti-inflammatory, antipyretic, and analgesic activity in animal studies. Preliminary studies in animals and man have shown that Tiflamizole is rapidly absorbed from the gastrointestinal tract, is highly protein-bound, and is slowly excreted. Toxicity studies in animals focused on the gastrointestinal tract. Short-term toxicity studies in rats indicated that the margin of safety of Tiflamizole is greater than that for piroxicam, ibuprofen, or sulindac.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6734055
Loading dose 5mg (sinle dose at day 1)
Maintenance dose 0.25mg (day 2-14)
Total amount of tiflamizole 8.25mg
Route of Administration:
Oral
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C257
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ACTIVE MOIETY