(-)-ALPHA-BISABOLOL OXIDE A
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Name
(-)-ALPHA-BISABOLOL OXIDE A
IUPAC name
(3R,6R)-2,2,6-trimethyl-6-(4-methylcyclohex-3-en-1-yl)tetrahydro-2H-pyran-3-ol
SMILES
CC1=CCC(CC1)[C@]2(CC[C@H](C(O2)(C)C)O)C
Molecular formula
C15H26O2
Molecular weight
238.37 g/mol
Monoisotopic mass
238.1933 Da
Chemical classification: NPClassifier (Kim et al., 2021)
| Plant | Plant part | Amount | Reference |
|---|---|---|---|
| Matricaria chamomilla L. | aerial parts | - |
Mericli, A.H. (1990). The lipophilic compounds of a turkish Matricaria chamomilla variety with no chamazulene in the volatile oil. Int J Crude Drug Res, 28(2), 145-147 doi:10.3109/13880209009082799
|
| Matricaria chamomilla L. | essential oil | - |
Repcak, M., Imrich, J., Garcar, J. (1999). Quantitative evaluation of the main sesquiterpenes and polyacetylenes of Chamomilla recutita essential oil by high-performance liquid chromatography. Phytochem Anal, 10(6), 335-338 doi:10.1002/(sici)1099-1565(199911/12)10:6
|
| Matricaria chamomilla L. | flower | - |
Reichling, J., Bisson, W., Becker, H. (1984). Comparative study on the production and accumulation of essential oil in the whole plant and in the callus culture of Matricaria chamomilla. Planta Med, 50(4), 334-337
|
| Matricaria chamomilla L. | flower | - |
Repcak, M., Halasova, J., Honcariv, R. (1984). Localization of essential oil in the Matricaria chamomilla L. inflorescence and its composition. Ukr Bot Zh, 41(1), 27-29,49
|
| Matricaria chamomilla L. | flower | - |
Zekovic, Z.P. (2000). Chamomile ligulate flowers in supercritical co-2-extraction. J Essent Oil Res, 12(1), 85-93 doi:10.1080/10412905.2000.9712049
|
| Matricaria chamomilla L. | flower, essential oil | - |
Salamon, I. (1992). Production of chamomile, Chamomilla recutita (L.) rauschert, in slovakia. J Herbs Spices Med Plants, 1(1/2), 37-45 doi:10.1300/j044v01n01_05
|