(Z)-Bisabol-11-ol

Details

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Internal ID e66f195e-8ca7-46ae-833c-98f95ee0ec36
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (Z)-2-methyl-6-(4-methylcyclohex-3-en-1-yl)hept-5-en-2-ol
SMILES (Canonical) CC1=CCC(CC1)C(=CCCC(C)(C)O)C
SMILES (Isomeric) CC1=CCC(CC1)/C(=C\CCC(C)(C)O)/C
InChI InChI=1S/C15H26O/c1-12-7-9-14(10-8-12)13(2)6-5-11-15(3,4)16/h6-7,14,16H,5,8-11H2,1-4H3/b13-6-
InChI Key AXLLSNSRONSXGV-MLPAPPSSSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O
Molecular Weight 222.37 g/mol
Exact Mass 222.198365449 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.23
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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AXLLSNSRONSXGV-MLPAPPSSSA-N

2D Structure

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2D Structure of (Z)-Bisabol-11-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 + 0.8172 81.72%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.4250 42.50%
OATP2B1 inhibitior - 0.8500 85.00%
OATP1B1 inhibitior + 0.9326 93.26%
OATP1B3 inhibitior + 0.9428 94.28%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.9592 95.92%
P-glycoprotein substrate - 0.8558 85.58%
CYP3A4 substrate - 0.5498 54.98%
CYP2C9 substrate - 0.5790 57.90%
CYP2D6 substrate - 0.7630 76.30%
CYP3A4 inhibition - 0.8202 82.02%
CYP2C9 inhibition - 0.8045 80.45%
CYP2C19 inhibition - 0.8687 86.87%
CYP2D6 inhibition - 0.9378 93.78%
CYP1A2 inhibition - 0.8121 81.21%
CYP2C8 inhibition - 0.7806 78.06%
CYP inhibitory promiscuity - 0.8039 80.39%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7328 73.28%
Carcinogenicity (trinary) Non-required 0.6275 62.75%
Eye corrosion - 0.9155 91.55%
Eye irritation + 0.6556 65.56%
Skin irritation + 0.6439 64.39%
Skin corrosion - 0.9806 98.06%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4198 41.98%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation + 0.9382 93.82%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity - 0.6718 67.18%
Acute Oral Toxicity (c) III 0.9039 90.39%
Estrogen receptor binding - 0.7719 77.19%
Androgen receptor binding - 0.8637 86.37%
Thyroid receptor binding - 0.7358 73.58%
Glucocorticoid receptor binding - 0.6695 66.95%
Aromatase binding - 0.7657 76.57%
PPAR gamma - 0.5771 57.71%
Honey bee toxicity - 0.9327 93.27%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9441 94.41%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.28% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.00% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.43% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.81% 96.09%
CHEMBL2581 P07339 Cathepsin D 85.64% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 84.63% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.44% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.96% 100.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.17% 95.89%

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.
Daucus carota

Cross-Links

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PubChem 91750291
NPASS NPC58947