(4E,7E)-1,11-bis(furan-3-yl)-4,8-dimethylundeca-4,7-dien-6-one

Details

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Internal ID f0a99032-7002-47c0-9345-7d1add827351
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Aromatic monoterpenoids
IUPAC Name (4E,7E)-1,11-bis(furan-3-yl)-4,8-dimethylundeca-4,7-dien-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H26O3/c1-17(5-3-7-19-9-11-23-15-19)13-21(22)14-18(2)6-4-8-20-10-12-24-16-20/h9-16H,3-8H2,1-2H3/b17-13+,18-14+
InChI Key LMNQNJRZKZYBMX-HBKJEHTGSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H26O3
Molecular Weight 326.40 g/mol
Exact Mass 326.18819469 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 5.80
Atomic LogP (AlogP) 5.68
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4E,7E)-1,11-bis(furan-3-yl)-4,8-dimethylundeca-4,7-dien-6-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9935 99.35%
Caco-2 + 0.7218 72.18%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.4725 47.25%
OATP2B1 inhibitior - 0.8560 85.60%
OATP1B1 inhibitior + 0.7484 74.84%
OATP1B3 inhibitior + 0.9386 93.86%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.7976 79.76%
P-glycoprotein inhibitior + 0.6964 69.64%
P-glycoprotein substrate - 0.8738 87.38%
CYP3A4 substrate - 0.5412 54.12%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8551 85.51%
CYP3A4 inhibition - 0.8979 89.79%
CYP2C9 inhibition - 0.7419 74.19%
CYP2C19 inhibition - 0.6904 69.04%
CYP2D6 inhibition - 0.8648 86.48%
CYP1A2 inhibition + 0.6913 69.13%
CYP2C8 inhibition - 0.7664 76.64%
CYP inhibitory promiscuity + 0.6260 62.60%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.4525 45.25%
Eye corrosion - 0.9034 90.34%
Eye irritation - 0.7399 73.99%
Skin irritation + 0.5702 57.02%
Skin corrosion - 0.8689 86.89%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8355 83.55%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.5916 59.16%
skin sensitisation + 0.6420 64.20%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity - 0.5750 57.50%
Acute Oral Toxicity (c) III 0.7762 77.62%
Estrogen receptor binding + 0.6433 64.33%
Androgen receptor binding + 0.5463 54.63%
Thyroid receptor binding - 0.5150 51.50%
Glucocorticoid receptor binding - 0.4711 47.11%
Aromatase binding - 0.5607 56.07%
PPAR gamma + 0.7138 71.38%
Honey bee toxicity - 0.9582 95.82%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9449 94.49%

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
CHEMBL2581 P07339 Cathepsin D 93.51% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.35% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.00% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.90% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.72% 99.17%
CHEMBL2039 P27338 Monoamine oxidase B 90.92% 92.51%
CHEMBL3401 O75469 Pregnane X receptor 89.16% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.76% 86.33%

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 15625483
LOTUS LTS0031457
wikiData Q105154072