gamma-Bisabolene, (Z)-

Details

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Internal ID 1df2f547-2893-4cd9-bfbe-fb99109d2bf7
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (4Z)-1-methyl-4-(6-methylhept-5-en-2-ylidene)cyclohexene
SMILES (Canonical) CC1=CCC(=C(C)CCC=C(C)C)CC1
SMILES (Isomeric) CC1=CC/C(=C(/C)\CCC=C(C)C)/CC1
InChI InChI=1S/C15H24/c1-12(2)6-5-7-14(4)15-10-8-13(3)9-11-15/h6,8H,5,7,9-11H2,1-4H3/b15-14+
InChI Key XBGUIVFBMBVUEG-CCEZHUSRSA-N
Popularity 19 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24
Molecular Weight 204.35 g/mol
Exact Mass 204.187800766 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.70
Atomic LogP (AlogP) 5.18
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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Bisabolene
gamma-Bisabolene
cis-gamma-Bisabolene
Limene
13062-00-5
gamma-Bisabolene, (Z)-
gamma-Bisabolene, (4Z)-
495-62-5
UNII-E452K502K0
(Z)-.gamma.-Bisabolene
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of gamma-Bisabolene, (Z)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 + 0.9714 97.14%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.3565 35.65%
OATP2B1 inhibitior - 0.8524 85.24%
OATP1B1 inhibitior + 0.9331 93.31%
OATP1B3 inhibitior + 0.8986 89.86%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.6555 65.55%
P-glycoprotein inhibitior - 0.9679 96.79%
P-glycoprotein substrate - 0.9367 93.67%
CYP3A4 substrate - 0.5652 56.52%
CYP2C9 substrate - 0.8315 83.15%
CYP2D6 substrate - 0.7358 73.58%
CYP3A4 inhibition - 0.9377 93.77%
CYP2C9 inhibition - 0.8952 89.52%
CYP2C19 inhibition - 0.9033 90.33%
CYP2D6 inhibition - 0.9423 94.23%
CYP1A2 inhibition - 0.7359 73.59%
CYP2C8 inhibition - 0.9222 92.22%
CYP inhibitory promiscuity - 0.6099 60.99%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Warning 0.5088 50.88%
Eye corrosion + 0.5218 52.18%
Eye irritation + 0.9619 96.19%
Skin irritation + 0.7772 77.72%
Skin corrosion - 0.9609 96.09%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3617 36.17%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6324 63.24%
skin sensitisation + 0.9552 95.52%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.4652 46.52%
Acute Oral Toxicity (c) III 0.8619 86.19%
Estrogen receptor binding - 0.9318 93.18%
Androgen receptor binding - 0.5962 59.62%
Thyroid receptor binding - 0.8113 81.13%
Glucocorticoid receptor binding - 0.7137 71.37%
Aromatase binding - 0.7947 79.47%
PPAR gamma - 0.5113 51.13%
Honey bee toxicity - 0.9382 93.82%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9968 99.68%

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 93.43% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 89.28% 94.73%
CHEMBL2581 P07339 Cathepsin D 88.47% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.73% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.12% 96.09%
CHEMBL4208 P20618 Proteasome component C5 80.44% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.40% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 80.39% 90.17%

Plants that contains it

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Cross-Links

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PubChem 3033866
NPASS NPC26111
LOTUS LTS0143321
wikiData Q4039091