Ethyl 8-(3-formyloxiran-2-yl)octanoate

Details

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Internal ID 3c656f70-df87-482a-9bcf-ef6d08016491
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name ethyl 8-(3-formyloxiran-2-yl)octanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H22O4/c1-2-16-13(15)9-7-5-3-4-6-8-11-12(10-14)17-11/h10-12H,2-9H2,1H3
InChI Key VPBUIYXHUNIYKF-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H22O4
Molecular Weight 242.31 g/mol
Exact Mass 242.15180918 g/mol
Topological Polar Surface Area (TPSA) 55.90 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.25
H-Bond Acceptor 4
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 Ethyl 8-(3-formyloxiran-2-yl)octanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9361 93.61%
Caco-2 + 0.5915 59.15%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.8571 85.71%
Subcellular localzation Mitochondria 0.8465 84.65%
OATP2B1 inhibitior - 0.8491 84.91%
OATP1B1 inhibitior + 0.8964 89.64%
OATP1B3 inhibitior + 0.9573 95.73%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.6278 62.78%
P-glycoprotein inhibitior - 0.9263 92.63%
P-glycoprotein substrate - 0.9537 95.37%
CYP3A4 substrate + 0.5220 52.20%
CYP2C9 substrate - 0.7947 79.47%
CYP2D6 substrate - 0.8667 86.67%
CYP3A4 inhibition - 0.9255 92.55%
CYP2C9 inhibition - 0.7009 70.09%
CYP2C19 inhibition - 0.6068 60.68%
CYP2D6 inhibition - 0.9122 91.22%
CYP1A2 inhibition - 0.7081 70.81%
CYP2C8 inhibition - 0.8518 85.18%
CYP inhibitory promiscuity - 0.8083 80.83%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7543 75.43%
Carcinogenicity (trinary) Non-required 0.6761 67.61%
Eye corrosion - 0.8050 80.50%
Eye irritation - 0.6409 64.09%
Skin irritation - 0.5951 59.51%
Skin corrosion - 0.9024 90.24%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4853 48.53%
Micronuclear - 0.7300 73.00%
Hepatotoxicity - 0.5572 55.72%
skin sensitisation - 0.7058 70.58%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.8627 86.27%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.5417 54.17%
Acute Oral Toxicity (c) III 0.7659 76.59%
Estrogen receptor binding - 0.7054 70.54%
Androgen receptor binding - 0.9193 91.93%
Thyroid receptor binding - 0.5235 52.35%
Glucocorticoid receptor binding - 0.6102 61.02%
Aromatase binding - 0.6329 63.29%
PPAR gamma - 0.6370 63.70%
Honey bee toxicity - 0.9312 93.12%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.6024 60.24%
Fish aquatic toxicity + 0.8043 80.43%

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 95.48% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.84% 99.17%
CHEMBL4040 P28482 MAP kinase ERK2 92.10% 83.82%
CHEMBL3401 O75469 Pregnane X receptor 91.24% 94.73%
CHEMBL5255 O00206 Toll-like receptor 4 91.16% 92.50%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 87.52% 97.21%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.30% 96.95%
CHEMBL340 P08684 Cytochrome P450 3A4 81.27% 91.19%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.15% 96.47%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.88% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.52% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.23% 97.09%

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.
Phleum pratense

Cross-Links

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PubChem 14467738
LOTUS LTS0094125
wikiData Q105290633