| Weight | 244.378 g/mol |
|---|---|
| Formula | C17H24O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 8 |
Falcarinol (21852-80-2)
falcarinol, (Z)-isomer · panaxynol
Score:
#31 in Agricultural
,
#1792 in Biochemistry
,
#3917 in Biology
,
#4930 in Chemistry
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- Bioactivity of falcarinol and the influenceof processing and storage on its content in carrots (Daucus carota L) (Journal of the Science of Food and Agriculture, 2003)
- Cytotoxic Falcarinol Oxylipins from Dendropanax arboreus (Journal of Natural Products, 1996)
- Inhibitory Effects of Feeding with Carrots or ()-Falcarinol on Development of Azoxymethane-Induced Preneoplastic Lesions in the Rat Colon (Journal of Agricultural and Food Chemistry, 2005)
- Antiplatelet actions of panaxynol and ginsenosides isolated from ginseng (Biochimica et Biophysica Acta, 1989)
- Antiproliferative constituents in Umbelliferae plants II. Screening for polyacetylenes in some Umbelliferae plants, and isolation of panaxynol and falcarindiol from the root of Heracleum moellendorffii. (Biological & Pharmaceutical Bulletin, 1998)
- Chemoenzymatic Asymmetric Total Syntheses of Antitumor Agents (3R,9R,10R)- and (3S,9R,10R)-Panaxytriol and (R)- and (S)-Falcarinol from Panax ginseng Using an Enantioconvergent Enzyme-Triggered Cascade Reaction (Journal of Organic Chemistry, 2002)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - falcarinol, (Z)-isomer
- panaxynol
-
SMILESCCCCCCCC=CCC#CC#CC(C=C)O
-
InChIKeyUGJAEDFOKNAMQD-UHFFFAOYSA-N
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