Methyl 5-(2,6-dimethylocta-1,5,7-trienyl)furan-3-carboxylate

Details

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Internal ID 4051adfe-9538-470b-81aa-2d4a0c048eb6
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Aromatic monoterpenoids
IUPAC Name methyl 5-(2,6-dimethylocta-1,5,7-trienyl)furan-3-carboxylate
SMILES (Canonical) CC(=CC1=CC(=CO1)C(=O)OC)CCC=C(C)C=C
SMILES (Isomeric) CC(=CC1=CC(=CO1)C(=O)OC)CCC=C(C)C=C
InChI InChI=1S/C16H20O3/c1-5-12(2)7-6-8-13(3)9-15-10-14(11-19-15)16(17)18-4/h5,7,9-11H,1,6,8H2,2-4H3
InChI Key SOGGMEVKELOHJA-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H20O3
Molecular Weight 260.33 g/mol
Exact Mass 260.14124450 g/mol
Topological Polar Surface Area (TPSA) 39.40 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.38
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl 5-(2,6-dimethylocta-1,5,7-trienyl)furan-3-carboxylate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9902 99.02%
Caco-2 + 0.7585 75.85%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.4460 44.60%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8459 84.59%
OATP1B3 inhibitior + 0.9074 90.74%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.5500 55.00%
P-glycoprotein inhibitior - 0.8249 82.49%
P-glycoprotein substrate - 0.7588 75.88%
CYP3A4 substrate + 0.5532 55.32%
CYP2C9 substrate - 0.8054 80.54%
CYP2D6 substrate - 0.8482 84.82%
CYP3A4 inhibition - 0.7747 77.47%
CYP2C9 inhibition - 0.7545 75.45%
CYP2C19 inhibition - 0.5835 58.35%
CYP2D6 inhibition - 0.9096 90.96%
CYP1A2 inhibition + 0.5991 59.91%
CYP2C8 inhibition + 0.5621 56.21%
CYP inhibitory promiscuity + 0.5947 59.47%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7528 75.28%
Carcinogenicity (trinary) Non-required 0.5629 56.29%
Eye corrosion - 0.8899 88.99%
Eye irritation - 0.6246 62.46%
Skin irritation - 0.5555 55.55%
Skin corrosion - 0.9637 96.37%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7627 76.27%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.5649 56.49%
skin sensitisation - 0.5458 54.58%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.4718 47.18%
Acute Oral Toxicity (c) III 0.5708 57.08%
Estrogen receptor binding + 0.5914 59.14%
Androgen receptor binding - 0.6788 67.88%
Thyroid receptor binding - 0.6879 68.79%
Glucocorticoid receptor binding + 0.8011 80.11%
Aromatase binding + 0.6883 68.83%
PPAR gamma + 0.7700 77.00%
Honey bee toxicity - 0.8414 84.14%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9653 96.53%

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 97.10% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 94.53% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.10% 99.17%
CHEMBL4208 P20618 Proteasome component C5 90.02% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.10% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.79% 96.09%
CHEMBL2581 P07339 Cathepsin D 85.37% 98.95%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.08% 91.07%

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 73194668
LOTUS LTS0163871
wikiData Q105256929