11-Copaen-4-ol

Details

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Internal ID 63ce272a-a6e9-4824-a436-f2a02ef24617
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 1,3-dimethyl-8-prop-1-en-2-yltricyclo[4.4.0.02,7]decan-3-ol
SMILES (Canonical) CC(=C)C1CCC2(C3C1C2C(CC3)(C)O)C
SMILES (Isomeric) CC(=C)C1CCC2(C3C1C2C(CC3)(C)O)C
InChI InChI=1S/C15H24O/c1-9(2)10-5-7-14(3)11-6-8-15(4,16)13(14)12(10)11/h10-13,16H,1,5-8H2,2-4H3
InChI Key DGXZNOOUXAHVAE-UHFFFAOYSA-N
Popularity 4 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 3.90
Atomic LogP (AlogP) 3.39
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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11-Copen-3-ol
CHEBI:195988
1,3-dimethyl-8-prop-1-en-2-yltricyclo[4.4.0.02,7]decan-3-ol

2D Structure

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2D Structure of 11-Copaen-4-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9962 99.62%
Caco-2 + 0.7243 72.43%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Lysosomes 0.6042 60.42%
OATP2B1 inhibitior - 0.8475 84.75%
OATP1B1 inhibitior + 0.9413 94.13%
OATP1B3 inhibitior + 0.8879 88.79%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior - 0.9016 90.16%
P-glycoprotein inhibitior - 0.9402 94.02%
P-glycoprotein substrate - 0.8647 86.47%
CYP3A4 substrate + 0.5964 59.64%
CYP2C9 substrate + 0.5024 50.24%
CYP2D6 substrate - 0.7533 75.33%
CYP3A4 inhibition - 0.6409 64.09%
CYP2C9 inhibition - 0.6007 60.07%
CYP2C19 inhibition - 0.5384 53.84%
CYP2D6 inhibition - 0.9312 93.12%
CYP1A2 inhibition - 0.7396 73.96%
CYP2C8 inhibition - 0.8673 86.73%
CYP inhibitory promiscuity - 0.8792 87.92%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.5436 54.36%
Eye corrosion - 0.9771 97.71%
Eye irritation + 0.6640 66.40%
Skin irritation + 0.6034 60.34%
Skin corrosion - 0.9364 93.64%
Ames mutagenesis - 0.7753 77.53%
Human Ether-a-go-go-Related Gene inhibition - 0.4819 48.19%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.5411 54.11%
skin sensitisation + 0.5914 59.14%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.5992 59.92%
Acute Oral Toxicity (c) III 0.8512 85.12%
Estrogen receptor binding - 0.5149 51.49%
Androgen receptor binding + 0.5445 54.45%
Thyroid receptor binding - 0.5429 54.29%
Glucocorticoid receptor binding - 0.6097 60.97%
Aromatase binding - 0.7363 73.63%
PPAR gamma - 0.7012 70.12%
Honey bee toxicity - 0.8492 84.92%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9831 98.31%

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 97.18% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.22% 96.09%
CHEMBL218 P21554 Cannabinoid CB1 receptor 89.65% 96.61%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.53% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.24% 91.11%
CHEMBL1871 P10275 Androgen Receptor 87.14% 96.43%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 85.84% 93.04%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.81% 92.94%
CHEMBL226 P30542 Adenosine A1 receptor 83.67% 95.93%
CHEMBL233 P35372 Mu opioid receptor 83.31% 97.93%
CHEMBL221 P23219 Cyclooxygenase-1 81.62% 90.17%
CHEMBL206 P03372 Estrogen receptor alpha 81.14% 97.64%

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.
Ocimum americanum

Cross-Links

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PubChem 14807653
LOTUS LTS0200569
wikiData Q104979544