9,17-Octadecadienal, (Z)-

Details

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Internal ID 35d93a52-52e4-4b5d-8338-b2d82b25e759
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty aldehydes
IUPAC Name (9Z)-octadeca-9,17-dienal
SMILES (Canonical) C=CCCCCCCC=CCCCCCCCC=O
SMILES (Isomeric) C=CCCCCCC/C=C\CCCCCCCC=O
InChI InChI=1S/C18H32O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h2,9-10,18H,1,3-8,11-17H2/b10-9-
InChI Key RXORHYFDDNAOQS-KTKRTIGZSA-N
Popularity 12 references in papers

Physical and Chemical Properties

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Molecular Formula C18H32O
Molecular Weight 264.40 g/mol
Exact Mass 264.245315640 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 6.70
Atomic LogP (AlogP) 6.00
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 15

Synonyms

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56554-35-9
(z)-9,17-octadecadienal
9,17-OCTADECADIENAL (Z)
SCHEMBL3966133
(9Z)-9,17-Octadecadienal #
RXORHYFDDNAOQS-KTKRTIGZSA-N
DTXSID501015908

2D Structure

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2D Structure of 9,17-Octadecadienal, (Z)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9874 98.74%
Caco-2 + 0.6185 61.85%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Plasma membrane 0.6052 60.52%
OATP2B1 inhibitior - 0.8571 85.71%
OATP1B1 inhibitior + 0.9088 90.88%
OATP1B3 inhibitior + 0.9379 93.79%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5716 57.16%
P-glycoprotein inhibitior - 0.8333 83.33%
P-glycoprotein substrate - 0.9546 95.46%
CYP3A4 substrate - 0.6246 62.46%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7636 76.36%
CYP3A4 inhibition - 0.9566 95.66%
CYP2C9 inhibition - 0.8837 88.37%
CYP2C19 inhibition - 0.9130 91.30%
CYP2D6 inhibition - 0.9722 97.22%
CYP1A2 inhibition - 0.5807 58.07%
CYP2C8 inhibition - 0.9586 95.86%
CYP inhibitory promiscuity - 0.8113 81.13%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5100 51.00%
Carcinogenicity (trinary) Non-required 0.6693 66.93%
Eye corrosion + 0.9965 99.65%
Eye irritation + 0.9735 97.35%
Skin irritation + 0.7532 75.32%
Skin corrosion - 0.8612 86.12%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7297 72.97%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation + 0.8778 87.78%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.6455 64.55%
Acute Oral Toxicity (c) III 0.8421 84.21%
Estrogen receptor binding - 0.5870 58.70%
Androgen receptor binding - 0.7726 77.26%
Thyroid receptor binding + 0.6518 65.18%
Glucocorticoid receptor binding - 0.6188 61.88%
Aromatase binding - 0.6640 66.40%
PPAR gamma + 0.7510 75.10%
Honey bee toxicity - 0.7692 76.92%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 0.7957 79.57%

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
CHEMBL1829 O15379 Histone deacetylase 3 93.25% 95.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.76% 99.17%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 86.88% 89.34%
CHEMBL1781 P11387 DNA topoisomerase I 80.77% 97.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.53% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 80.33% 97.29%

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.
Panax ginseng
Zanthoxylum armatum

Cross-Links

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PubChem 5365667
NPASS NPC57739