| Weight | 222.372 g/mol |
|---|---|
| Formula | C15H26O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 4 |
Bisabolol (515-69-5, 72059-10-0)
bisabolol, (-)-isomer · levomenol · (+)-4-epi-alpha-bisabolol
Score:
#2076 in Biochemistry
,
#4315 in Biology
,
#5444 in Chemistry
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- Sensitization of Staphylococcus aureus and Escherichia coli to Antibiotics by the Sesquiterpenoids Nerolidol, Farnesol, Bisabolol, and Apritone (Antimicrobial Agents and Chemotherapy, 2003)
- A review of the application and pharmacological properties of -bisabolol and -bisabolol-rich oils. (Journal of the American Oil Chemists' Society, 2010)
- Microbiological transformations. 27. The first examples for preparative-scale enantioselective or diastereoselective epoxide hydrolyses using microorganisms. An unequivocal access to all four bisabolol stereoisomers (Journal of Organic Chemistry, 1993)
- Phase solubility studies of pure ()--bisabolol and camomile essential oil with -cyclodextrin (European Journal of Pharmaceutics and Biopharmaceutics, 2003)
- -Bisabolol, a nontoxic natural compound, strongly induces apoptosis in glioma cells (Biochemical and Biophysical Research Communications, 2004)
- Asymmetric Epoxidation of Homoallylic Alcohols and Application in a Concise Total Synthesis of ()--Bisabolol and ()-8-epi--Bisabolol (Angewandte Chemie, 2003)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - bisabolol, (-)-isomer
- levomenol
- (+)-4-epi-alpha-bisabolol
- bisabolol, (+)-isomer
-
SMILESCC1=CCC(CC1)C(C)(CCC=C(C)C)O
-
InChIKeyRGZSQWQPBWRIAQ-UHFFFAOYSA-N
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Bisabolol
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