Weight | 222.372 g/mol |
---|---|
Formula | C15H26O |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 4 |
LEVOMENOL (515-69-5, 23089-26-1)
bisabolol · bisabolol, (-)-isomer · (+)-4-epi-alpha-bisabolol
Score:
#1563 in Biochemistry
,
#3598 in Biology
,
#4514 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)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - bisabolol
- bisabolol, (-)-isomer
- (+)-4-epi-alpha-bisabolol
- bisabolol, (+)-isomer
-
SMILESCC1=CCC(CC1)C(C)(CCC=C(C)C)O
-
InChIKeyRGZSQWQPBWRIAQ-UHFFFAOYSA-N
- Pubchem - LEVOMENOL
- Wikipedia - levomenol
Bisabolol, or more formally -()-bisabolol or also known as levomenol, is a natural monocyclic sesquiterpene alcohol. It is a colorless viscous oil that is the primary constituent of the essential oil from German chamomile (Matricaria recutita) and Myoporum crassifolium. It is poorly soluble in water and glycerin, but soluble in ethanol.
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