beta-Cuprenene

Details

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Internal ID 1673221e-083d-457a-b387-d4d3445413ff
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 3-methylidene-6-[(1S)-1,2,2-trimethylcyclopentyl]cyclohexene
SMILES (Canonical) CC1(CCCC1(C)C2CCC(=C)C=C2)C
SMILES (Isomeric) C[C@]1(CCCC1(C)C)C2CCC(=C)C=C2
InChI InChI=1S/C15H24/c1-12-6-8-13(9-7-12)15(4)11-5-10-14(15,2)3/h6,8,13H,1,5,7,9-11H2,2-4H3/t13?,15-/m0/s1
InChI Key QPXHUMFBJLASJO-WUJWULDRSA-N
Popularity 0 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 5.40
Atomic LogP (AlogP) 4.73
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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QPXHUMFBJLASJO-WUJWULDRSA-N

2D Structure

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2D Structure of beta-Cuprenene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9905 99.05%
Caco-2 + 0.9261 92.61%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.8714 87.14%
Subcellular localzation Lysosomes 0.5673 56.73%
OATP2B1 inhibitior - 0.8501 85.01%
OATP1B1 inhibitior + 0.8899 88.99%
OATP1B3 inhibitior - 0.2866 28.66%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.8828 88.28%
P-glycoprotein inhibitior - 0.9755 97.55%
P-glycoprotein substrate - 0.8952 89.52%
CYP3A4 substrate + 0.5173 51.73%
CYP2C9 substrate - 0.8111 81.11%
CYP2D6 substrate - 0.7951 79.51%
CYP3A4 inhibition - 0.9373 93.73%
CYP2C9 inhibition - 0.8606 86.06%
CYP2C19 inhibition - 0.8238 82.38%
CYP2D6 inhibition - 0.9566 95.66%
CYP1A2 inhibition - 0.8271 82.71%
CYP2C8 inhibition - 0.8862 88.62%
CYP inhibitory promiscuity - 0.5843 58.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Warning 0.4624 46.24%
Eye corrosion - 0.8972 89.72%
Eye irritation - 0.7157 71.57%
Skin irritation - 0.5355 53.55%
Skin corrosion - 0.9886 98.86%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6806 68.06%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6607 66.07%
skin sensitisation + 0.8069 80.69%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.7794 77.94%
Acute Oral Toxicity (c) III 0.7540 75.40%
Estrogen receptor binding - 0.8469 84.69%
Androgen receptor binding - 0.7041 70.41%
Thyroid receptor binding - 0.6411 64.11%
Glucocorticoid receptor binding - 0.7643 76.43%
Aromatase binding - 0.6832 68.32%
PPAR gamma - 0.7980 79.80%
Honey bee toxicity - 0.8886 88.86%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 1.0000 100.00%

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 92.47% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.72% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.30% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.27% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.89% 100.00%
CHEMBL2581 P07339 Cathepsin D 85.01% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 83.79% 91.49%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.68% 95.89%
CHEMBL1937 Q92769 Histone deacetylase 2 82.51% 94.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.52% 97.09%

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.
Angelica acutiloba
Angelica gigas
Angelica sinensis

Cross-Links

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PubChem 91748715
NPASS NPC224057