Ethyl 3-acetyloxy-5-(4-hydroxyphenyl)pentanoate

Details

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Internal ID 1aa6d853-fd9e-434b-8d89-2abea7d998c7
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name ethyl 3-acetyloxy-5-(4-hydroxyphenyl)pentanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H20O5/c1-3-19-15(18)10-14(20-11(2)16)9-6-12-4-7-13(17)8-5-12/h4-5,7-8,14,17H,3,6,9-10H2,1-2H3
InChI Key KIHREBPBKASOMN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O5
Molecular Weight 280.32 g/mol
Exact Mass 280.13107373 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.21
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Ethyl 3-acetyloxy-5-(4-hydroxyphenyl)pentanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9882 98.82%
Caco-2 + 0.7533 75.33%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.8143 81.43%
Subcellular localzation Mitochondria 0.9410 94.10%
OATP2B1 inhibitior - 0.8584 85.84%
OATP1B1 inhibitior + 0.9131 91.31%
OATP1B3 inhibitior + 0.9435 94.35%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.5586 55.86%
P-glycoprotein inhibitior - 0.8165 81.65%
P-glycoprotein substrate - 0.7491 74.91%
CYP3A4 substrate + 0.5558 55.58%
CYP2C9 substrate - 0.6092 60.92%
CYP2D6 substrate - 0.8168 81.68%
CYP3A4 inhibition - 0.7702 77.02%
CYP2C9 inhibition - 0.6761 67.61%
CYP2C19 inhibition - 0.5772 57.72%
CYP2D6 inhibition - 0.8572 85.72%
CYP1A2 inhibition - 0.7706 77.06%
CYP2C8 inhibition - 0.5653 56.53%
CYP inhibitory promiscuity - 0.8221 82.21%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7466 74.66%
Carcinogenicity (trinary) Non-required 0.6847 68.47%
Eye corrosion - 0.9656 96.56%
Eye irritation - 0.6014 60.14%
Skin irritation - 0.8883 88.83%
Skin corrosion - 0.9818 98.18%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4724 47.24%
Micronuclear - 0.8482 84.82%
Hepatotoxicity - 0.5675 56.75%
skin sensitisation - 0.8835 88.35%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.7830 78.30%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.8017 80.17%
Estrogen receptor binding + 0.8196 81.96%
Androgen receptor binding + 0.6087 60.87%
Thyroid receptor binding + 0.5650 56.50%
Glucocorticoid receptor binding + 0.5716 57.16%
Aromatase binding + 0.5807 58.07%
PPAR gamma - 0.7729 77.29%
Honey bee toxicity - 0.7839 78.39%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9447 94.47%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.07% 96.09%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 95.59% 97.21%
CHEMBL2581 P07339 Cathepsin D 95.49% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.92% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.87% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 91.41% 94.73%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 89.05% 96.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.03% 86.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 89.01% 95.50%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 86.36% 100.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.95% 95.89%
CHEMBL3437 Q16853 Amine oxidase, copper containing 82.99% 94.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.86% 93.56%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.04% 95.56%

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.
Haplopteris anguste-elongata

Cross-Links

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PubChem 21593984
LOTUS LTS0109634
wikiData Q105141520