4-Oxo-2-(E)-nonenal

Details

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Internal ID e0dbf2fc-3e07-4fff-8e9e-26921166108c
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Medium-chain aldehydes
IUPAC Name (E)-4-oxonon-2-enal
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H14O2/c1-2-3-4-6-9(11)7-5-8-10/h5,7-8H,2-4,6H2,1H3/b7-5+
InChI Key SEPPVOUBHWNCAW-FNORWQNLSA-N
Popularity 249 references in papers

Physical and Chemical Properties

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Molecular Formula C9H14O2
Molecular Weight 154.21 g/mol
Exact Mass 154.099379685 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.89
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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103560-62-9
4-oxo-2-(e)-nonenal
DTXSID701032845
RefChem:912757
DTXCID101517871
4-oxonon-2-enal
(E)-4-oxonon-2-enal
4-oxo-nonenal
4-one
4-oxo-2E-nonenal
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Oxo-2-(E)-nonenal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9931 99.31%
Caco-2 + 0.9568 95.68%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Plasma membrane 0.4668 46.68%
OATP2B1 inhibitior - 0.8588 85.88%
OATP1B1 inhibitior + 0.8794 87.94%
OATP1B3 inhibitior + 0.9225 92.25%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9294 92.94%
P-glycoprotein inhibitior - 0.9889 98.89%
P-glycoprotein substrate - 0.9325 93.25%
CYP3A4 substrate - 0.6436 64.36%
CYP2C9 substrate - 0.8119 81.19%
CYP2D6 substrate - 0.8494 84.94%
CYP3A4 inhibition - 0.9562 95.62%
CYP2C9 inhibition - 0.9159 91.59%
CYP2C19 inhibition - 0.8998 89.98%
CYP2D6 inhibition - 0.9397 93.97%
CYP1A2 inhibition + 0.7360 73.60%
CYP2C8 inhibition - 0.8937 89.37%
CYP inhibitory promiscuity - 0.7887 78.87%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6100 61.00%
Carcinogenicity (trinary) Non-required 0.6935 69.35%
Eye corrosion + 0.9565 95.65%
Eye irritation + 0.9681 96.81%
Skin irritation + 0.8904 89.04%
Skin corrosion - 0.7343 73.43%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7045 70.45%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5274 52.74%
skin sensitisation + 0.7245 72.45%
Respiratory toxicity - 0.9000 90.00%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.4671 46.71%
Acute Oral Toxicity (c) III 0.7630 76.30%
Estrogen receptor binding - 0.9393 93.93%
Androgen receptor binding - 0.8908 89.08%
Thyroid receptor binding - 0.8312 83.12%
Glucocorticoid receptor binding - 0.6679 66.79%
Aromatase binding - 0.8247 82.47%
PPAR gamma - 0.6352 63.52%
Honey bee toxicity - 0.9914 99.14%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.6213 62.13%
Fish aquatic toxicity + 0.8420 84.20%

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
CHEMBL230 P35354 Cyclooxygenase-2 96.26% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.82% 99.17%
CHEMBL2581 P07339 Cathepsin D 91.77% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.26% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 87.47% 97.29%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 86.30% 92.08%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.39% 96.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.86% 91.11%

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 6445537
LOTUS LTS0226682
wikiData Q21099662