10-(4-Hydroxyphenyl)deca-3,5,7-trienyl acetate

Details

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Internal ID 7a3662f6-defc-4035-a161-53566193f517
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohol esters
IUPAC Name 10-(4-hydroxyphenyl)deca-3,5,7-trienyl acetate
SMILES (Canonical) CC(=O)OCCC=CC=CC=CCCC1=CC=C(C=C1)O
SMILES (Isomeric) CC(=O)OCCC=CC=CC=CCCC1=CC=C(C=C1)O
InChI InChI=1S/C18H22O3/c1-16(19)21-15-9-7-5-3-2-4-6-8-10-17-11-13-18(20)14-12-17/h2-7,11-14,20H,8-10,15H2,1H3
InChI Key LNQPSXMEDGPERO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H22O3
Molecular Weight 286.40 g/mol
Exact Mass 286.15689456 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 4.20
Atomic LogP (AlogP) 3.95
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 10-(4-Hydroxyphenyl)deca-3,5,7-trienyl acetate

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 + 0.6416 64.16%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.8834 88.34%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8431 84.31%
OATP1B3 inhibitior + 0.9512 95.12%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7310 73.10%
P-glycoprotein inhibitior - 0.7336 73.36%
P-glycoprotein substrate - 0.8692 86.92%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.8027 80.27%
CYP2D6 substrate - 0.8420 84.20%
CYP3A4 inhibition - 0.8858 88.58%
CYP2C9 inhibition - 0.9367 93.67%
CYP2C19 inhibition - 0.6789 67.89%
CYP2D6 inhibition - 0.9234 92.34%
CYP1A2 inhibition + 0.6610 66.10%
CYP2C8 inhibition + 0.4902 49.02%
CYP inhibitory promiscuity - 0.7950 79.50%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7761 77.61%
Carcinogenicity (trinary) Non-required 0.6586 65.86%
Eye corrosion - 0.9379 93.79%
Eye irritation + 0.6968 69.68%
Skin irritation - 0.5834 58.34%
Skin corrosion - 0.9687 96.87%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4758 47.58%
Micronuclear - 0.9515 95.15%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.6987 69.87%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.8576 85.76%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.5553 55.53%
Acute Oral Toxicity (c) III 0.5574 55.74%
Estrogen receptor binding + 0.8520 85.20%
Androgen receptor binding + 0.8583 85.83%
Thyroid receptor binding + 0.5631 56.31%
Glucocorticoid receptor binding + 0.6733 67.33%
Aromatase binding + 0.7849 78.49%
PPAR gamma + 0.8409 84.09%
Honey bee toxicity - 0.8670 86.70%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9082 90.82%

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
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 97.77% 94.62%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.41% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.59% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.33% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.22% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.56% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.94% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.42% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 83.07% 94.73%

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 72957004
LOTUS LTS0026447
wikiData Q105154442