| Weight | 222.372 g/mol |
|---|---|
| Formula | C15H26O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 7 |
NEROLIDOL
peruviol · nerolidol, (S-(E))-isomer · nerolidol, (Z)-isomer
1119-38-6, 7212-44-4, 142-50-7
Score:
#2057 in Biochemistry
,
#4284 in Biology
,
#5403 in Chemistry
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- The Maize Gene terpene synthase 1 Encodes a Sesquiterpene Synthase Catalyzing the Formation of ( E )--Farnesene, ( E )-Nerolidol, and ( E , E )-Farnesol after Herbivore Damage (Plant Physiology, 2002)
- Sensitization of Staphylococcus aureus and Escherichia coli to Antibiotics by the Sesquiterpenoids Nerolidol, Farnesol, Bisabolol, and Apritone (Antimicrobial Agents and Chemotherapy, 2003)
- Antileishmanial Activity of the Terpene Nerolidol (Antimicrobial Agents and Chemotherapy, 2005)
- Biosynthesis of acyclic homoterpenes: Enzyme selectivity and absolute configuration of the nerolidol precursor (Phytochemistry, 1995)
- Two nearly identical terpene synthases catalyze the formation of nerolidol and linalool in snapdragon flowers (Plant Journal, 2008)
- Demonstration and characterization of (E)-nerolidol synthase from maize: a herbivore-inducible terpene synthase participating in (3E)-4,8-dimethyl-1,3,7-nonatriene biosynthesis (Planta, 2000)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - peruviol
- nerolidol, (S-(E))-isomer
- nerolidol, (Z)-isomer
- nerolidol, (S-(Z))-isomer
- nerolidol, (E)-isomer
- 3,7,11-trimethyl-1,6,10-dodecatrien-3-ol
-
SMILESCC(=CCCC(=CCCC(C)(C=C)O)C)C
-
InChIKeyFQTLCLSUCSAZDY-UHFFFAOYSA-N
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NEROLIDOL
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