Dodec-6-enal

Details

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Internal ID 5fdfaba1-afd2-4dbb-9647-5db4bfc38f9b
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Medium-chain aldehydes
IUPAC Name dodec-6-enal
SMILES (Canonical) CCCCCC=CCCCCC=O
SMILES (Isomeric) CCCCCC=CCCCCC=O
InChI InChI=1S/C12H22O/c1-2-3-4-5-6-7-8-9-10-11-12-13/h6-7,12H,2-5,8-11H2,1H3
InChI Key RKSXBPZEKYUCII-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C12H22O
Molecular Weight 182.30 g/mol
Exact Mass 182.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.88
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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76261-02-4
DTXSID70997594

2D Structure

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2D Structure of Dodec-6-enal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.8096 80.96%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Plasma membrane 0.6168 61.68%
OATP2B1 inhibitior - 0.8548 85.48%
OATP1B1 inhibitior + 0.7846 78.46%
OATP1B3 inhibitior + 0.8896 88.96%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6275 62.75%
P-glycoprotein inhibitior - 0.9750 97.50%
P-glycoprotein substrate - 0.9250 92.50%
CYP3A4 substrate - 0.6682 66.82%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7983 79.83%
CYP3A4 inhibition - 0.9832 98.32%
CYP2C9 inhibition - 0.9391 93.91%
CYP2C19 inhibition - 0.9524 95.24%
CYP2D6 inhibition - 0.9654 96.54%
CYP1A2 inhibition + 0.8016 80.16%
CYP2C8 inhibition - 0.9675 96.75%
CYP inhibitory promiscuity - 0.8166 81.66%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.7077 70.77%
Eye corrosion + 0.9897 98.97%
Eye irritation + 0.9877 98.77%
Skin irritation + 0.9083 90.83%
Skin corrosion - 0.8898 88.98%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5542 55.42%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.7551 75.51%
skin sensitisation + 0.9219 92.19%
Respiratory toxicity - 0.9889 98.89%
Reproductive toxicity - 0.9954 99.54%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.6151 61.51%
Acute Oral Toxicity (c) III 0.6225 62.25%
Estrogen receptor binding - 0.9003 90.03%
Androgen receptor binding - 0.8005 80.05%
Thyroid receptor binding - 0.5803 58.03%
Glucocorticoid receptor binding - 0.6634 66.34%
Aromatase binding - 0.8389 83.89%
PPAR gamma - 0.5252 52.52%
Honey bee toxicity - 0.9835 98.35%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.7053 70.53%
Fish aquatic toxicity + 0.9569 95.69%

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 95.72% 89.63%
CHEMBL2581 P07339 Cathepsin D 92.81% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.71% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.70% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.51% 97.29%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 88.07% 85.94%
CHEMBL1781 P11387 DNA topoisomerase I 85.05% 97.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.61% 96.09%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 83.97% 92.86%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.47% 89.34%
CHEMBL2664 P23526 Adenosylhomocysteinase 82.42% 86.67%
CHEMBL3401 O75469 Pregnane X receptor 81.76% 94.73%

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.
Angelica gigas

Cross-Links

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PubChem 53427725
LOTUS LTS0005305
wikiData Q82989784