Falcarindiol
Chemical compound
From Wikipedia, the free encyclopedia
Falcarindiol is a polyyne found in carrot roots which has antifungal activity.[1][2] Falcarindiol is the main compound responsible for bitterness in carrots.[3] Falcarindiol and other falcarindiol-type polyacetylenes are also found in many other plants of the family Apiaceae, including some commonly used seasonings such as dill and parsley.[4]
| Names | |
|---|---|
| Preferred IUPAC name
(3R,8S,9Z)-Heptadeca-1,9-diene-4,6-diyne-3,8-diol | |
| Other names
cis-Heptadeca-1,9-diene-4,6-diyne-3,8-diol | |
| Identifiers | |
3D model (JSmol) |
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| ChEMBL | |
| ChemSpider | |
PubChem CID |
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CompTox Dashboard (EPA) |
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| Properties | |
| C17H24O2 | |
| Molar mass | 260.377 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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A variety of bioactivities have been reported for falcarindiol and the falcarindiol-type polyacetylenes,[5][6][7] and because of potential health-promoting metabolic effects these compounds are studied as potential nutraceuticals.[8] Falcarindiol is the most-active among several polyynes found in Devil's club (Oplopanax horridus) that inhibit cell proliferation.[9]

