7-ethenyl-2-methoxy-7-methyl-6-prop-1-en-2-yl-6,8-dihydro-5H-naphthalene-1,4-dione

Details

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Internal ID c1df651a-910a-4543-876a-28f003ceef20
Taxonomy Organic acids and derivatives > Vinylogous esters
IUPAC Name 7-ethenyl-2-methoxy-7-methyl-6-prop-1-en-2-yl-6,8-dihydro-5H-naphthalene-1,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H20O3/c1-6-17(4)9-12-11(7-13(17)10(2)3)14(18)8-15(20-5)16(12)19/h6,8,13H,1-2,7,9H2,3-5H3
InChI Key JGQRGTHAFFLZCG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H20O3
Molecular Weight 272.34 g/mol
Exact Mass 272.14124450 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.14
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-ethenyl-2-methoxy-7-methyl-6-prop-1-en-2-yl-6,8-dihydro-5H-naphthalene-1,4-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.7786 77.86%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.6978 69.78%
OATP2B1 inhibitior - 0.8606 86.06%
OATP1B1 inhibitior + 0.9274 92.74%
OATP1B3 inhibitior + 0.9540 95.40%
MATE1 inhibitior - 0.6400 64.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7666 76.66%
P-glycoprotein inhibitior - 0.8919 89.19%
P-glycoprotein substrate - 0.7786 77.86%
CYP3A4 substrate + 0.5740 57.40%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8779 87.79%
CYP3A4 inhibition + 0.5402 54.02%
CYP2C9 inhibition - 0.7945 79.45%
CYP2C19 inhibition - 0.7192 71.92%
CYP2D6 inhibition - 0.9342 93.42%
CYP1A2 inhibition - 0.6185 61.85%
CYP2C8 inhibition - 0.8139 81.39%
CYP inhibitory promiscuity - 0.7251 72.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8963 89.63%
Carcinogenicity (trinary) Non-required 0.4821 48.21%
Eye corrosion - 0.9804 98.04%
Eye irritation - 0.7441 74.41%
Skin irritation - 0.6305 63.05%
Skin corrosion - 0.9661 96.61%
Ames mutagenesis - 0.6578 65.78%
Human Ether-a-go-go-Related Gene inhibition - 0.4214 42.14%
Micronuclear - 0.6000 60.00%
Hepatotoxicity + 0.7408 74.08%
skin sensitisation - 0.5983 59.83%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.8438 84.38%
Acute Oral Toxicity (c) III 0.5757 57.57%
Estrogen receptor binding - 0.5361 53.61%
Androgen receptor binding + 0.5758 57.58%
Thyroid receptor binding - 0.5583 55.83%
Glucocorticoid receptor binding + 0.5636 56.36%
Aromatase binding - 0.7548 75.48%
PPAR gamma - 0.4942 49.42%
Honey bee toxicity - 0.6570 65.70%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9966 99.66%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.53% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.97% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 96.79% 91.49%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.82% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.63% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.80% 95.56%
CHEMBL1902 P62942 FK506-binding protein 1A 91.74% 97.05%
CHEMBL2581 P07339 Cathepsin D 91.10% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.99% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.80% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.50% 95.89%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.18% 92.94%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.94% 97.14%

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.
Cordia millenii

Cross-Links

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PubChem 162911880
LOTUS LTS0127718
wikiData Q105127619