| Weight | 192.17 g/mol |
|---|---|
| Formula | C10H8O4 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
4-Methylesculetin (529-84-0)
6,7-dihydroxy-4-methylcoumarin · DHMC-6,7
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- Intestinal anti-inflammatory activity of esculetin and 4-methylesculetin in the trinitrobenzenesulphonic acid model of rat colitis (Chemico-Biological Interactions, 2010)
- Suppression of TNBS-induced colitis in rats by 4-methylesculetin, a natural coumarin: Comparison with prednisolone and sulphasalazine (Chemico-Biological Interactions, 2012)
- Electrochemical dimerization of 4-methylesculetin: Synthesis and kinetic study of a highly-oxygenated dimer (Journal of Electroanalytical Chemistry, 2011)
- Inhibitory effect of 4-methylesculetin on hyaluronan synthesis slows the development of human pancreatic cancer in vitro and in nude mice (International Journal of Cancer, 2007)
- Antiarthritic and antiinflammatory propensity of 4-methylesculetin, a coumarin derivative. (Biochimie, 2013)
- Absence of genotoxic effects of the coumarin derivative 4-methylesculetin in vivo and its potential chemoprevention against doxorubicin-induced DNA damage (Journal of Applied Toxicology, 2014)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 6,7-dihydroxy-4-methylcoumarin
- DHMC-6,7
-
SMILESCC1=CC(=O)OC2=CC(=C(C=C12)O)O
-
InChIKeyKVOJTUXGYQVLAJ-UHFFFAOYSA-N
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4-Methylesculetin
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