| Weight | 222.372 g/mol |
|---|---|
| Formula | C15H26O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 7 |
farnesol (4602-84-0)
Score:
#211 in Microbiology
,
#752 in Biochemistry
,
#2078 in Biology
,
#2548 in Chemistry
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- Identification of a nuclear receptor that is activated by farnesol metabolites. (Cell, 1995)
- Quorum sensing in the dimorphic fungus Candida albicans is mediated by farnesol (Applied and Environmental Microbiology, 2001)
- Inhibition of Candida albicans biofilm formation by farnesol, a quorum-sensing molecule. (Applied and Environmental Microbiology, 2002)
- Farnesol modification of Kirsten-ras exon 4B protein is essential for transformation. (Proceedings of the National Academy of Sciences of the United States of America, 1990)
- Farnesol and geranylgeraniol prevent activation of caspases by aminobisphosphonates: biochemical evidence for two distinct pharmacological classes of bisphosphonate drugs. (Molecular Pharmacology, 1999)
- New stereospecific synthesis of trisubstituted olefins. Stereospecific synthesis of farnesol (Journal of the American Chemical Society, 1967)
-
Predict GHS Hazards for Any Chemical in silico.
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SMILESCC(=CCCC(=CCCC(=CCO)C)C)C
-
InChIKeyCRDAMVZIKSXKFV-UHFFFAOYSA-N
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farnesol
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