2,4-Undecadienal

Details

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Internal ID 0fc1019f-ed05-49a9-90b9-1042108e391c
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Medium-chain aldehydes
IUPAC Name (2E,4E)-undeca-2,4-dienal
SMILES (Canonical) CCCCCCC=CC=CC=O
SMILES (Isomeric) CCCCCC/C=C/C=C/C=O
InChI InChI=1S/C11H18O/c1-2-3-4-5-6-7-8-9-10-11-12/h7-11H,2-6H2,1H3/b8-7+,10-9+
InChI Key UVIUIIFPIWRILL-XBLVEGMJSA-N
Popularity 18 references in papers

Physical and Chemical Properties

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Molecular Formula C11H18O
Molecular Weight 166.26 g/mol
Exact Mass 166.135765193 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.27
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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(2E,4E)-Undeca-2,4-dienal
30361-29-6
13162-46-4
trans,trans-2,4-Undecadienal
2,4-Undecadienal, (2E,4E)-
trans,trans-2,4-Undecadien-1-al
Undeca-2,4-dien-1-al
2,4-trans,trans-Undecadienal
FEMA No. 3422
2,4-Undecadienal, (E,E)-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,4-Undecadienal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 + 0.9716 97.16%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Plasma membrane 0.5260 52.60%
OATP2B1 inhibitior - 0.8598 85.98%
OATP1B1 inhibitior + 0.8399 83.99%
OATP1B3 inhibitior + 0.9016 90.16%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8943 89.43%
P-glycoprotein inhibitior - 0.9787 97.87%
P-glycoprotein substrate - 0.9338 93.38%
CYP3A4 substrate - 0.6245 62.45%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8597 85.97%
CYP3A4 inhibition - 0.9911 99.11%
CYP2C9 inhibition - 0.9285 92.85%
CYP2C19 inhibition - 0.9519 95.19%
CYP2D6 inhibition - 0.9653 96.53%
CYP1A2 inhibition + 0.7244 72.44%
CYP2C8 inhibition - 0.9204 92.04%
CYP inhibitory promiscuity - 0.7617 76.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.6467 64.67%
Eye corrosion + 0.9927 99.27%
Eye irritation + 0.9825 98.25%
Skin irritation + 0.9187 91.87%
Skin corrosion - 0.8516 85.16%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5977 59.77%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5701 57.01%
skin sensitisation + 0.9648 96.48%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity - 0.9954 99.54%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.6381 63.81%
Acute Oral Toxicity (c) III 0.8135 81.35%
Estrogen receptor binding - 0.8286 82.86%
Androgen receptor binding + 0.5307 53.07%
Thyroid receptor binding - 0.5068 50.68%
Glucocorticoid receptor binding - 0.5656 56.56%
Aromatase binding - 0.7223 72.23%
PPAR gamma + 0.5397 53.97%
Honey bee toxicity - 0.9804 98.04%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.9053 90.53%
Fish aquatic toxicity + 0.9804 98.04%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.99% 92.08%
CHEMBL230 P35354 Cyclooxygenase-2 94.12% 89.63%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 92.50% 92.86%
CHEMBL2581 P07339 Cathepsin D 92.26% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.38% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 89.80% 97.29%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 89.41% 85.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.53% 96.09%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 83.79% 91.81%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.38% 89.34%
CHEMBL3401 O75469 Pregnane X receptor 81.81% 94.73%
CHEMBL1781 P11387 DNA topoisomerase I 81.71% 97.00%

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.
Foeniculum vulgare

Cross-Links

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PubChem 5367531
NPASS NPC131555