Bisabolenol

Details

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Internal ID 3374920e-6c9c-4f92-b1ed-f39dd039948f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name [(4S)-4-(6-methylhepta-1,5-dien-2-yl)cyclohexen-1-yl]methanol
SMILES (Canonical) CC(=CCCC(=C)C1CCC(=CC1)CO)C
SMILES (Isomeric) CC(=CCCC(=C)[C@H]1CCC(=CC1)CO)C
InChI InChI=1S/C15H24O/c1-12(2)5-4-6-13(3)15-9-7-14(11-16)8-10-15/h5,7,15-16H,3-4,6,8-11H2,1-2H3/t15-/m1/s1
InChI Key AWXTUFPUJSQYGO-OAHLLOKOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.00
Atomic LogP (AlogP) 4.01
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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AWXTUFPUJSQYGO-OAHLLOKOSA-N

2D Structure

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2D Structure of Bisabolenol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9896 98.96%
Caco-2 + 0.6828 68.28%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.6533 65.33%
OATP2B1 inhibitior - 0.8520 85.20%
OATP1B1 inhibitior + 0.9006 90.06%
OATP1B3 inhibitior + 0.9366 93.66%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.8170 81.70%
P-glycoprotein inhibitior - 0.9534 95.34%
P-glycoprotein substrate - 0.8686 86.86%
CYP3A4 substrate - 0.5309 53.09%
CYP2C9 substrate - 0.6591 65.91%
CYP2D6 substrate - 0.7543 75.43%
CYP3A4 inhibition - 0.8339 83.39%
CYP2C9 inhibition - 0.8131 81.31%
CYP2C19 inhibition - 0.8390 83.90%
CYP2D6 inhibition - 0.8809 88.09%
CYP1A2 inhibition - 0.8397 83.97%
CYP2C8 inhibition - 0.8130 81.30%
CYP inhibitory promiscuity - 0.7573 75.73%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8128 81.28%
Carcinogenicity (trinary) Non-required 0.6865 68.65%
Eye corrosion - 0.6281 62.81%
Eye irritation + 0.7999 79.99%
Skin irritation - 0.6026 60.26%
Skin corrosion - 0.9467 94.67%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4636 46.36%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.6950 69.50%
skin sensitisation + 0.9103 91.03%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity - 0.6205 62.05%
Acute Oral Toxicity (c) III 0.7715 77.15%
Estrogen receptor binding - 0.7183 71.83%
Androgen receptor binding - 0.7702 77.02%
Thyroid receptor binding - 0.6936 69.36%
Glucocorticoid receptor binding - 0.4671 46.71%
Aromatase binding - 0.7836 78.36%
PPAR gamma - 0.4839 48.39%
Honey bee toxicity - 0.9123 91.23%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9850 98.50%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.99% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 96.40% 83.82%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.10% 97.25%
CHEMBL2581 P07339 Cathepsin D 89.82% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.20% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.57% 100.00%
CHEMBL226 P30542 Adenosine A1 receptor 83.27% 95.93%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.28% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.28% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.18% 99.17%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Prangos heyniae

Cross-Links

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PubChem 91747530
LOTUS LTS0109259
wikiData Q104375951