2,6-Nonadienal, (E,E)-

Details

Top
Internal ID 710f2806-7377-49fb-96b0-3c055981bad9
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Medium-chain aldehydes
IUPAC Name (2E,6E)-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-DYWGDJMRSA-N
Popularity 202 references in papers

Physical and Chemical Properties

Top
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

Top
2,6-Nonadienal, (E,E)-
2,6-Nonadienal, (2E,6E)-
FEMA No. 3766
(E,E)-2,6-nonadienal
XB6T1Z4FH7
RefChem:445832
241-557-1
trans,trans-2,6-Nonadienal
(2E,6E)-nona-2,6-dienal
(2E,6E)-2,6-Nonadienal
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 2,6-Nonadienal, (E,E)-

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
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

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
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%

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.
Rehmannia glutinosa

Cross-Links

Top
PubChem 636687
NPASS NPC295098