MOLECULE
α-Bisabolol
(+)-alpha-Bisabolol is a sesquiterpenoid.
Summary from ChEBI, via PubChem.
Identity
Chemistry
- Formula
- C15H26O
- Molecular weight
- 222.37 g/mol
- IUPAC name
- (2R)-6-methyl-2-[(1R)-4-methylcyclohex-3-en-1-yl]hept-5-en-2-ol
- InChIKey
- RGZSQWQPBWRIAQ-LSDHHAIUSA-N
- SMILES
- CC1=CCC(CC1)C(C)(CCC=C(C)C)O
- PubChem
- CID 1549992 ↗
Provenance
Contributing sources
- PubChem
- ChEBI
- LOTUS
Natural occurrence
Found in
- C. recutita 3
- Wild Chamomile 3
- Black pepper 3
- Khingan fir 2
- Siberian Cypress 2
- Orange jasmine 2
- Korean Pine 2
- Siberian Pine 2
- White Poplar 2
- Ontario Balsam Poplar 2
- P. candicans 2
- Ginger 2
- A. sachalinensis var. mayriana 1
- Siberian Fir 1
- Wild Celery 1
- A. adamsii 1
- Sweet wormwood 1
- A. chamaemelifolia 1
- Gmelin's wormwood 1
- A. santolinifolia 1
- A. stechmanniana 1
- A. xanthochroa 1
- Emory baccharis 1
- Roman Chamomile 1
- Wild Carrot 1
- Siberian ginseng 1
- E. erythropappus 1
- E. incanus 1
- Tall thoroughwort 1
- F. hermonis 1
- Fujian Cypress 1
- G. mucronata 1
- H. mimetes 1
- Common goldenbush 1
- Red-cedar 1
- L. morii 1
- L. ericoides 1
- O. dubium 1
- Sweet marjoram 1
- O. lanceolata 1
- O. quadripartita 1
- O. wightiana 1
- Korean ginseng 1
- P. epiphylla 1
- P. mucronata 1
- P. albus 1
- Common Butterbur 1
- P. tremellosa 1
- Dwarf Stone Pine 1
- P. fimbriulatum 1
- Guava 1
- P. incana 1
- R. officinalis 1
- Lanceleaf sage 1
- Sandalwood 1
- S. spicatum 1
- S. buchtormense 1
- S. transcaucasicum 1
- Taiwania 1
- T. camphoratus 1
- Common Valerian 1
61 organisms, ranked by how many independent papers report the compound in each. Occurrence data from LOTUS, across 57 references.
Pharmacology
Protein interactions
-
5-hydroxytryptamine (serotonin) receptor 2A activity 0 uM
-
Cytochrome P450 2C19 Potency 5.0119 uM
-
cytochrome P450, family 2, subfamily C, polypeptide 19 Potency 8.709 uM
-
cytochrome P450 3A7 Potency 13.8029 uM
-
cytochrome P450 family 2 subfamily C polypeptide 9 Potency 17.3768 uM
-
cytochrome P450 family 3 subfamily A polypeptide 4 Potency 27.5404 uM
-
pregnane X nuclear receptor Potency 29.8493 uM
Laboratory measurements of the compound at its own doses. They do not describe any product that contains it.
Human evidence in progress
Registered clinical trials
2 registered on ClinicalTrials.gov naming this molecule as an intervention. See all terpene trials.
Evidence