| Weight | 281.311 g/mol |
|---|---|
| Formula | C17H15NO3 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
indoprofen (53022-60-9, 31842-01-0)
Dexindoprofen
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- Indoprofen Upregulates the Survival Motor Neuron Protein through a Cyclooxygenase-Independent Mechanism (Chemistry & Biology, 2004)
- Double-Blind Trial of the New Analgesic and Anti-Inflammatory Drug Indoprofen in Post-Episiotomic Pain (Journal of International Medical Research, 1975)
- High-pressure liquid chromatographic determination of acetylsalicylic acid, salicylic acid, diflunisal, indomethacin, indoprofen and indobufen. (European Journal of Clinical Pharmacology, 1981)
- Indoprofen, a new analgesic and anti-inflammatory drug in cancer pain. (Clinical Pharmacology & Therapeutics, 1975)
- Biological activity of indoprofen and its optical isomers (Journal of Pharmacy and Pharmacology, 1983)
- Pharmacokinetics of the enantiomers of indoprofen in man. (International Journal of Clinical Pharmacology Research, 1984)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Dexindoprofen
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- Pubchem - indoprofen
- Wikipedia - indoprofen
Indoprofen is a nonsteroidal anti-inflammatory drug (NSAID). It was withdrawn worldwide in the 1980s after postmarketing reports of severe gastrointestinal bleeding. A 2004 study using high-throughput screening found indoprofen to increase production of the survival of motor neuron protein, suggesting it may provide insight into treatments for spinal muscular atrophies.
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