(+)-8, 9-Epoxyselina-4,11-diene

Details

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Internal ID 4758666a-8061-42ec-a535-2d443d7a449d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 4,7a-dimethyl-2-prop-1-en-2-yl-2,3,5,6,7,7b-hexahydro-1aH-naphtho[1,2-b]oxirene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O/c1-9(2)11-8-12-10(3)6-5-7-15(12,4)14-13(11)16-14/h11,13-14H,1,5-8H2,2-4H3
InChI Key HPCVOEQSOLQFPZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O
Molecular Weight 218.33 g/mol
Exact Mass 218.167065321 g/mol
Topological Polar Surface Area (TPSA) 12.50 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.86
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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HPCVOEQSOLQFPZ-UHFFFAOYSA-N

2D Structure

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2D Structure of (+)-8, 9-Epoxyselina-4,11-diene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9933 99.33%
Caco-2 + 0.8163 81.63%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Lysosomes 0.5268 52.68%
OATP2B1 inhibitior - 0.8501 85.01%
OATP1B1 inhibitior + 0.8563 85.63%
OATP1B3 inhibitior + 0.9485 94.85%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.8588 85.88%
P-glycoprotein inhibitior - 0.8601 86.01%
P-glycoprotein substrate - 0.9139 91.39%
CYP3A4 substrate + 0.5260 52.60%
CYP2C9 substrate - 0.7939 79.39%
CYP2D6 substrate - 0.7300 73.00%
CYP3A4 inhibition - 0.8730 87.30%
CYP2C9 inhibition + 0.6387 63.87%
CYP2C19 inhibition + 0.7012 70.12%
CYP2D6 inhibition - 0.9082 90.82%
CYP1A2 inhibition + 0.6864 68.64%
CYP2C8 inhibition - 0.7959 79.59%
CYP inhibitory promiscuity - 0.6471 64.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8000 80.00%
Carcinogenicity (trinary) Non-required 0.5682 56.82%
Eye corrosion - 0.9599 95.99%
Eye irritation + 0.5608 56.08%
Skin irritation - 0.6063 60.63%
Skin corrosion - 0.9544 95.44%
Ames mutagenesis - 0.7554 75.54%
Human Ether-a-go-go-Related Gene inhibition - 0.6588 65.88%
Micronuclear - 0.8000 80.00%
Hepatotoxicity + 0.6303 63.03%
skin sensitisation + 0.5866 58.66%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.6104 61.04%
Acute Oral Toxicity (c) III 0.7627 76.27%
Estrogen receptor binding - 0.8009 80.09%
Androgen receptor binding - 0.6011 60.11%
Thyroid receptor binding - 0.6369 63.69%
Glucocorticoid receptor binding - 0.6945 69.45%
Aromatase binding - 0.6295 62.95%
PPAR gamma - 0.6627 66.27%
Honey bee toxicity - 0.8717 87.17%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9923 99.23%

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 92.85% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.62% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.78% 100.00%
CHEMBL1951 P21397 Monoamine oxidase A 85.75% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.69% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.60% 97.25%
CHEMBL233 P35372 Mu opioid receptor 83.82% 97.93%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.57% 86.33%
CHEMBL2581 P07339 Cathepsin D 81.67% 98.95%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 81.65% 95.50%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.11% 93.04%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.29% 95.56%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 6431135
LOTUS LTS0014483
wikiData Q105031638