| Weight | 314.362 g/mol |
|---|---|
| Formula | C17H14O4S |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
rofecoxib (162011-90-7)
Score:
#54 in Neurology
,
#270 in Neuroscience
,
#1243 in Biology
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#1430 in Chemistry
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- COMPARISON OF UPPER GASTROINTESTINAL TOXICITY OF ROFECOXIB AND NAPROXEN IN PATIENTS WITH RHEUMATOID ARTHRITIS (The New England Journal of Medicine, 2000)
- Cardiovascular Events Associated with Rofecoxib in a Colorectal Adenoma Chemoprevention Trial (The New England Journal of Medicine, 2005)
- Risk of cardiovascular events and rofecoxib: cumulative meta-analysis (The Lancet, 2004)
- Effects of rofecoxib or naproxen vs placebo on Alzheimer disease progression: a randomized controlled trial. (JAMA, 2003)
- Adverse upper gastrointestinal effects of rofecoxib compared with NSAIDs. (JAMA, 1999)
- Failing the public health--rofecoxib, Merck, and the FDA. (The New England Journal of Medicine, 2004)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCS(=O)(=O)C1=CC=C(C=C1)C2=C(C(=O)OC2)C3=CC=CC=C3
-
InChIKeyRZJQGNCSTQAWON-UHFFFAOYSA-N
- Pubchem - rofecoxib
- Wikipedia - rofecoxib
Rofecoxib is a nonsteroidal anti-inflammatory drug (NSAID) that has now been withdrawn over safety concerns. It was marketed by Merck & Co. to treat osteoarthritis, acute pain conditions, and dysmenorrhea.
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Reactant
+
4-Chlorophenyl methyl sulfone
(Stille)
Reactant
+
4-Chlorophenyl methyl sulfone
(Heck non-terminal vinyl)
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