| Weight | 298.382 g/mol |
|---|---|
| Formula | C19H22O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 6 |
Auraptene (495-02-3)
Score:
#936 in Neuroscience
,
#1933 in Biochemistry
,
#4108 in Biology
,
#5174 in Chemistry
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- Sigma-Aldrich - Auraptene87.10 - 341.50 USD
- Fisher Scientific - Search for Auraptene
- TCI - Search for Auraptene
- Citrus Auraptene Exerts Dose-dependent Chemopreventive Activity in Rat Large Bowel Tumorigenesis: The Inhibition Correlates with Suppression of Cell Proliferation and Lipid Peroxidation and with Induction of Phase II Drug-metabolizing Enzymes (Cancer Research, 1998)
- Auraptene, a Citrus Coumarin, Inhibits 12-O-Tetradecanoylphorbol-13-acetate-induced Tumor Promotion in ICR Mouse Skin, Possibly through Suppression of Superoxide Generation in Leukocytes (Japanese Journal of Cancer Research, 1997)
- Citrus auraptene inhibits chemically induced colonic aberrant crypt foci in male F344 rats (Carcinogenesis, 1997)
- Suppression by citrus auraptene of phorbol ester- and endotoxin-induced inflammatory responses: role of attenuation of leukocyte activation (Carcinogenesis, 2000)
- Chemoprevention of 4-nitroquinoline 1-oxide-induced oral carcinogenesis by citrus auraptene in rats. (Carcinogenesis, 1998)
- Dietary administration with prenyloxycoumarins, auraptene and collinin, inhibits colitis-related colon carcinogenesis in mice (International Journal of Cancer, 2006)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C
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InChIKeyRSDDHGSKLOSQFK-UHFFFAOYSA-N
- Pubchem - Auraptene
- Wikipedia - auraptene
Auraptene is a natural bioactive monoterpene coumarin ether. It was first isolated from members of the genus Citrus. Auraptene has shown a remarkable effect in the prevention of degenerative diseases.
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