trans-2,cis-6-Nonadienal

Details

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Internal ID b76fa810-18e8-4854-b45f-0a47872779dd
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Medium-chain aldehydes
IUPAC Name (2E,6Z)-nona-2,6-dienal
SMILES (Canonical) CCC=CCCC=CC=O
SMILES (Isomeric) CC/C=C\CC/C=C/C=O
InChI InChI=1S/C9H14O/c1-2-3-4-5-6-7-8-9-10/h3-4,7-9H,2,5-6H2,1H3/b4-3-,8-7+
InChI Key HZYHMHHBBBSGHB-ODYTWBPASA-N
Popularity 70 references in papers

Physical and Chemical Properties

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Molecular Formula C9H14O
Molecular Weight 138.21 g/mol
Exact Mass 138.104465066 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.49
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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557-48-2
(2E,6Z)-nona-2,6-dienal
Violet leaf aldehyde
trans,cis-2,6-Nonadienal
Cucumber aldehyde
2,6-Nonadienal, (2E,6Z)-
(E,Z)-2,6-nonadienal
(2E,6Z)-Nonadienal
2-trans-6-cis-Nonadienal
(2E,6Z)-Nona-2,6-dien-1-al
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of trans-2,cis-6-Nonadienal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9943 99.43%
Caco-2 + 0.8822 88.22%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Plasma membrane 0.5003 50.03%
OATP2B1 inhibitior - 0.8639 86.39%
OATP1B1 inhibitior + 0.8649 86.49%
OATP1B3 inhibitior + 0.9260 92.60%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8776 87.76%
P-glycoprotein inhibitior - 0.9868 98.68%
P-glycoprotein substrate - 0.9623 96.23%
CYP3A4 substrate - 0.6913 69.13%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8597 85.97%
CYP3A4 inhibition - 0.9894 98.94%
CYP2C9 inhibition - 0.9150 91.50%
CYP2C19 inhibition - 0.9557 95.57%
CYP2D6 inhibition - 0.9691 96.91%
CYP1A2 inhibition + 0.5172 51.72%
CYP2C8 inhibition - 0.9783 97.83%
CYP inhibitory promiscuity - 0.7097 70.97%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5000 50.00%
Carcinogenicity (trinary) Non-required 0.5703 57.03%
Eye corrosion + 0.9938 99.38%
Eye irritation + 0.9886 98.86%
Skin irritation + 0.8115 81.15%
Skin corrosion - 0.9557 95.57%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6019 60.19%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation + 0.9627 96.27%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.9177 91.77%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.4576 45.76%
Acute Oral Toxicity (c) III 0.9087 90.87%
Estrogen receptor binding - 0.8874 88.74%
Androgen receptor binding - 0.8868 88.68%
Thyroid receptor binding - 0.7174 71.74%
Glucocorticoid receptor binding - 0.6403 64.03%
Aromatase binding - 0.8748 87.48%
PPAR gamma - 0.6656 66.56%
Honey bee toxicity - 0.9421 94.21%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.8903 89.03%

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 82.33% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.22% 95.56%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.57% 89.34%
CHEMBL2581 P07339 Cathepsin D 80.54% 98.95%

Cross-Links

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PubChem 643731
NPASS NPC91504
LOTUS LTS0001161
wikiData Q158544