trans,trans-2,4-Nonadienal

Details

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Internal ID 67b4f359-3bc3-416a-9592-1e7673cd7de1
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Medium-chain aldehydes
IUPAC Name (2E,4E)-nona-2,4-dienal
SMILES (Canonical) CCCCC=CC=CC=O
SMILES (Isomeric) CCCC/C=C/C=C/C=O
InChI InChI=1S/C9H14O/c1-2-3-4-5-6-7-8-9-10/h5-9H,2-4H2,1H3/b6-5+,8-7+
InChI Key ZHHYXNZJDGDGPJ-BSWSSELBSA-N
Popularity 372 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 2.70
Atomic LogP (AlogP) 2.49
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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5910-87-2
2,4-Nonadienal, (2E,4E)-
Nonadienal
2,4-NONADIENAL
(2E,4E)-nona-2,4-dienal
6750-03-4
2,4-Nonadienal, (E,E)-
2,4-trans,trans-Nonadienal
trans,trans-2,4-Nonadien-1-al
Nona-2,4-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,trans-2,4-Nonadienal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9956 99.56%
Caco-2 + 0.9688 96.88%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Plasma membrane 0.4659 46.59%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8432 84.32%
OATP1B3 inhibitior + 0.9270 92.70%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9166 91.66%
P-glycoprotein inhibitior - 0.9891 98.91%
P-glycoprotein substrate - 0.9375 93.75%
CYP3A4 substrate - 0.6485 64.85%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8597 85.97%
CYP3A4 inhibition - 0.9891 98.91%
CYP2C9 inhibition - 0.9349 93.49%
CYP2C19 inhibition - 0.9232 92.32%
CYP2D6 inhibition - 0.9661 96.61%
CYP1A2 inhibition + 0.6283 62.83%
CYP2C8 inhibition - 0.9574 95.74%
CYP inhibitory promiscuity - 0.7877 78.77%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5100 51.00%
Carcinogenicity (trinary) Non-required 0.6411 64.11%
Eye corrosion + 0.9954 99.54%
Eye irritation + 0.9842 98.42%
Skin irritation + 0.9262 92.62%
Skin corrosion - 0.6116 61.16%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6860 68.60%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation + 0.9462 94.62%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity - 0.8333 83.33%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.7331 73.31%
Acute Oral Toxicity (c) III 0.8462 84.62%
Estrogen receptor binding - 0.9166 91.66%
Androgen receptor binding - 0.5832 58.32%
Thyroid receptor binding - 0.6540 65.40%
Glucocorticoid receptor binding - 0.6489 64.89%
Aromatase binding - 0.8585 85.85%
PPAR gamma - 0.7033 70.33%
Honey bee toxicity - 0.9801 98.01%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.8445 84.45%

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
CHEMBL2581 P07339 Cathepsin D 90.42% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 86.52% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.50% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.25% 96.09%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 82.60% 92.86%

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.
Bupleurum chinense
Bupleurum falcatum
Bupleurum scorzonerifolium
Codonopsis pilosula
Prunus persica

Cross-Links

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PubChem 5283339
NPASS NPC72024
LOTUS LTS0142459
wikiData Q27294239