| Weight | 216.324 g/mol |
|---|---|
| Formula | C15H20O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 4 |
ar-Turmerone (532-65-0)
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LabBot
- Antivenom and biological effects of ar-turmerone isolated from Curcuma longa (Zingiberaceae) (Toxicon, 1992)
- Antiplatelet property of Curcuma longa L. rhizome-derived ar-turmerone. (Bioresource Technology, 2006)
- TerpenoidsLX : Absolute configuration of ar-turmerone (Tetrahedron, 1964)
- Synthesis of (R)-ar-turmerone and its conversion to (R)-ar-himachalene, a pheromone component of the flea beetle: (R)-ar-himachalene is dextrorotatory in hexane, while levorotatory in chloroform (Tetrahedron-asymmetry, 2005)
- Induction of apoptosis by ar-turmerone on various cell lines (International Journal of Molecular Medicine, 2004)
- Application of dithioester reactions with Grignard reagents to carbon-carbon bond formation; synthesis of egomaketone and ar-turmerone (Journal of Organic Chemistry, 1979)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=CC=C(C=C1)C(C)CC(=O)C=C(C)C
-
InChIKeyNAAJVHHFAXWBOK-UHFFFAOYSA-N
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