4-oxo-(E)-2-hexenal

Details

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Internal ID dc0dce59-e3f4-4588-85a4-5bde7e547683
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Medium-chain aldehydes
IUPAC Name (E)-4-oxohex-2-enal
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H8O2/c1-2-6(8)4-3-5-7/h3-5H,2H2,1H3/b4-3+
InChI Key GVKYFODEMNCLGS-ONEGZZNKSA-N
Popularity 99 references in papers

Physical and Chemical Properties

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Molecular Formula C6H8O2
Molecular Weight 112.13 g/mol
Exact Mass 112.052429494 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 0.10
Atomic LogP (AlogP) 0.72
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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(E)-4-Oxo-2-hexenal
2492-43-5
4-OXO-2-HEXENAL
4-oxo-2E-Hexenal
2-Hexenal, 4-oxo-, (E)-
2-Hexenal, 4-oxo-, (2E)-
(2E)-4-oxohex-2-enal
(E)-4-Oxo-2-hexen-1-al
4-Oxo-E-2-hexenal
4-oxo-trans-2-hexenal
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-(E)-2-hexenal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9941 99.41%
Caco-2 + 0.8421 84.21%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.6173 61.73%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9086 90.86%
OATP1B3 inhibitior + 0.9570 95.70%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9236 92.36%
P-glycoprotein inhibitior - 0.9891 98.91%
P-glycoprotein substrate - 0.9688 96.88%
CYP3A4 substrate - 0.6931 69.31%
CYP2C9 substrate - 0.8119 81.19%
CYP2D6 substrate - 0.8494 84.94%
CYP3A4 inhibition - 0.9468 94.68%
CYP2C9 inhibition - 0.8415 84.15%
CYP2C19 inhibition - 0.8288 82.88%
CYP2D6 inhibition - 0.9472 94.72%
CYP1A2 inhibition - 0.7238 72.38%
CYP2C8 inhibition - 0.9337 93.37%
CYP inhibitory promiscuity - 0.8117 81.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5946 59.46%
Carcinogenicity (trinary) Non-required 0.6518 65.18%
Eye corrosion + 0.9867 98.67%
Eye irritation + 0.9859 98.59%
Skin irritation + 0.9131 91.31%
Skin corrosion + 0.9083 90.83%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7809 78.09%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.5926 59.26%
skin sensitisation + 0.8919 89.19%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.6458 64.58%
Acute Oral Toxicity (c) III 0.8187 81.87%
Estrogen receptor binding - 0.9525 95.25%
Androgen receptor binding - 0.9127 91.27%
Thyroid receptor binding - 0.8970 89.70%
Glucocorticoid receptor binding - 0.8458 84.58%
Aromatase binding - 0.8816 88.16%
PPAR gamma - 0.9014 90.14%
Honey bee toxicity - 0.9790 97.90%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity - 0.6977 69.77%

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 91.17% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 86.82% 89.34%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.83% 96.95%

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 6365145
LOTUS LTS0001564
wikiData Q27146302