2,4-Octadienal

Details

Top
Internal ID 1ef490f6-b82c-45de-bb42-e0c7c09bd85d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Medium-chain aldehydes
IUPAC Name (2E,4E)-octa-2,4-dienal
SMILES (Canonical) CCCC=CC=CC=O
SMILES (Isomeric) CCC/C=C/C=C/C=O
InChI InChI=1S/C8H12O/c1-2-3-4-5-6-7-8-9/h4-8H,2-3H2,1H3/b5-4+,7-6+
InChI Key DVVATNQISMINCX-YTXTXJHMSA-N
Popularity 98 references in papers

Physical and Chemical Properties

Top
Molecular Formula C8H12O
Molecular Weight 124.18 g/mol
Exact Mass 124.088815002 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.10
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

Top
2,4-Octadienal
30361-28-5
(2E,4E)-2,4-Octadienal
5577-44-6
2,4-Octadienal, (2E,4E)-
Octadienal
(E,E)-2,4-Octadien-1-al
trans,trans-Octa-2,4-dienal
(E,E)-2,4-octadienal
Octa-2,4-dienal
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 2,4-Octadienal

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9940 99.40%
Caco-2 + 0.9489 94.89%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Plasma membrane 0.5310 53.10%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8858 88.58%
OATP1B3 inhibitior + 0.9367 93.67%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9225 92.25%
P-glycoprotein inhibitior - 0.9901 99.01%
P-glycoprotein substrate - 0.9670 96.70%
CYP3A4 substrate - 0.6926 69.26%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8597 85.97%
CYP3A4 inhibition - 0.9866 98.66%
CYP2C9 inhibition - 0.9367 93.67%
CYP2C19 inhibition - 0.9323 93.23%
CYP2D6 inhibition - 0.9683 96.83%
CYP1A2 inhibition + 0.5082 50.82%
CYP2C8 inhibition - 0.9755 97.55%
CYP inhibitory promiscuity - 0.7803 78.03%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5400 54.00%
Carcinogenicity (trinary) Non-required 0.5505 55.05%
Eye corrosion + 0.9958 99.58%
Eye irritation + 0.9760 97.60%
Skin irritation + 0.8751 87.51%
Skin corrosion - 0.8702 87.02%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7126 71.26%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation + 0.9493 94.93%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity + 0.6975 69.75%
Acute Oral Toxicity (c) III 0.8626 86.26%
Estrogen receptor binding - 0.8971 89.71%
Androgen receptor binding - 0.7328 73.28%
Thyroid receptor binding - 0.7138 71.38%
Glucocorticoid receptor binding - 0.7474 74.74%
Aromatase binding - 0.7951 79.51%
PPAR gamma - 0.7934 79.34%
Honey bee toxicity - 0.9431 94.31%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.6993 69.93%

Targets

Top

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
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.45% 89.34%
CHEMBL2581 P07339 Cathepsin D 81.89% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.84% 96.09%

Plants that contains it

Top
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.
Bupleurum chinense
Bupleurum falcatum
Bupleurum scorzonerifolium
Laennecia filaginoides

Cross-Links

Top
PubChem 5283329
NPASS NPC146244
LOTUS LTS0173449
wikiData Q27286719