| Weight | 379.775 g/mol |
|---|---|
| Formula | C19H15ClNNaO4 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 4 |
INDOMETHACIN SODIUM (7681-54-1)
Indomethacin · Indocin · Indometacin
Score:
#32 in Neuroscience
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#172 in Biology
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#178 in Chemistry
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- Peroxisome Proliferator-activated Receptors and Are Activated by Indomethacin and Other Non-steroidal Anti-inflammatory Drugs (Journal of Biological Chemistry, 1997)
- Prostaglandin synthase 1 gene disruption in mice reduces arachidonic acid-induced inflammation and indomethacin-induced gastric ulceration (Cell, 1995)
- Clinical trial of indomethacin in Alzheimer's disease (Neurology, 1993)
- Spectroscopic characterization of interactions between PVP and indomethacin in amorphous molecular dispersions. (Pharmaceutical Research, 1997)
- Indomethacin and Aspirin abolish Prostaglandin Release from the Spleen (Nature, 1971)
- Long-term effects of indomethacin prophylaxis in extremely-low-birth-weight infants. (The New England Journal of Medicine, 2001)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Indomethacin
- Indocin
- Indometacin
- Indocid
- Amuno
- Osmosin
- Indomet 140
- Metindol
- Indomethacin Hydrochloride
-
SMILESCC1=C(C2=C(N1C(=O)C3=CC=C(C=C3)Cl)C=CC(=C2)OC)CC(=O)[O-].[Na+]
-
InChIKeyJMHRGKDWGWORNU-UHFFFAOYSA-M
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