Selina-3,7-diene

Details

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Internal ID 0e6bb217-dafb-4f26-a0bb-194f08698391
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (8aR)-4,8a-dimethyl-6-propan-2-yl-2,4a,5,8-tetrahydro-1H-naphthalene
SMILES (Canonical) CC1=CCCC2(C1CC(=CC2)C(C)C)C
SMILES (Isomeric) CC1=CCC[C@]2(C1CC(=CC2)C(C)C)C
InChI InChI=1S/C15H24/c1-11(2)13-7-9-15(4)8-5-6-12(3)14(15)10-13/h6-7,11,14H,5,8-10H2,1-4H3/t14?,15-/m1/s1
InChI Key SWCOCRTVQQHGKB-YSSOQSIOSA-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 4.10
Atomic LogP (AlogP) 4.73
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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SWCOCRTVQQHGKB-YSSOQSIOSA-N

2D Structure

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2D Structure of Selina-3,7-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9941 99.41%
Caco-2 + 0.8537 85.37%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.6591 65.91%
OATP2B1 inhibitior - 0.8507 85.07%
OATP1B1 inhibitior + 0.9283 92.83%
OATP1B3 inhibitior + 0.9060 90.60%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.6625 66.25%
P-glycoprotein inhibitior - 0.9392 93.92%
P-glycoprotein substrate - 0.8360 83.60%
CYP3A4 substrate - 0.5303 53.03%
CYP2C9 substrate - 0.7731 77.31%
CYP2D6 substrate - 0.7252 72.52%
CYP3A4 inhibition - 0.8496 84.96%
CYP2C9 inhibition - 0.7310 73.10%
CYP2C19 inhibition - 0.5883 58.83%
CYP2D6 inhibition - 0.9247 92.47%
CYP1A2 inhibition - 0.8599 85.99%
CYP2C8 inhibition - 0.9093 90.93%
CYP inhibitory promiscuity - 0.6021 60.21%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.4653 46.53%
Eye corrosion - 0.9347 93.47%
Eye irritation - 0.5167 51.67%
Skin irritation - 0.5967 59.67%
Skin corrosion - 0.9487 94.87%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3928 39.28%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5596 55.96%
skin sensitisation + 0.8700 87.00%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.7313 73.13%
Estrogen receptor binding - 0.9700 97.00%
Androgen receptor binding - 0.8143 81.43%
Thyroid receptor binding - 0.6673 66.73%
Glucocorticoid receptor binding - 0.8113 81.13%
Aromatase binding - 0.8357 83.57%
PPAR gamma - 0.8203 82.03%
Honey bee toxicity - 0.8839 88.39%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5900 59.00%
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 94.68% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.59% 96.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.21% 93.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.65% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 87.16% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.86% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.67% 94.45%
CHEMBL2581 P07339 Cathepsin D 84.27% 98.95%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.33% 93.04%
CHEMBL2996 Q05655 Protein kinase C delta 82.28% 97.79%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 81.70% 86.00%
CHEMBL1937 Q92769 Histone deacetylase 2 80.01% 94.75%

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.
Humulus lupulus

Cross-Links

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PubChem 6429221
NPASS NPC266847