Octa-2,4,6-trienic acid

Details

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Internal ID fd05d579-8a20-4bb0-a801-218c57c69ed9
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Medium-chain fatty acids
IUPAC Name octa-2,4,6-trienoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H10O2/c1-2-3-4-5-6-7-8(9)10/h2-7H,1H3,(H,9,10)
InChI Key IAAPVNQZSBLWKH-UHFFFAOYSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C8H10O2
Molecular Weight 138.16 g/mol
Exact Mass 138.068079557 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.76
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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NCI60_001203

2D Structure

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2D Structure of Octa-2,4,6-trienic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9944 99.44%
Caco-2 + 0.8622 86.22%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.4810 48.10%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9368 93.68%
OATP1B3 inhibitior + 0.9572 95.72%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8868 88.68%
P-glycoprotein inhibitior - 0.9916 99.16%
P-glycoprotein substrate - 0.9883 98.83%
CYP3A4 substrate - 0.7222 72.22%
CYP2C9 substrate - 0.5839 58.39%
CYP2D6 substrate - 0.9152 91.52%
CYP3A4 inhibition - 0.9748 97.48%
CYP2C9 inhibition - 0.9526 95.26%
CYP2C19 inhibition - 0.9816 98.16%
CYP2D6 inhibition - 0.9707 97.07%
CYP1A2 inhibition - 0.9227 92.27%
CYP2C8 inhibition - 0.9829 98.29%
CYP inhibitory promiscuity - 0.9839 98.39%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.7122 71.22%
Carcinogenicity (trinary) Non-required 0.7084 70.84%
Eye corrosion + 1.0000 100.00%
Eye irritation + 0.9938 99.38%
Skin irritation + 0.9613 96.13%
Skin corrosion + 1.0000 100.00%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8467 84.67%
Micronuclear - 0.6900 69.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.5344 53.44%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity - 0.7889 78.89%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.5758 57.58%
Acute Oral Toxicity (c) III 0.8675 86.75%
Estrogen receptor binding - 0.9236 92.36%
Androgen receptor binding - 0.7917 79.17%
Thyroid receptor binding - 0.8252 82.52%
Glucocorticoid receptor binding - 0.6532 65.32%
Aromatase binding - 0.8354 83.54%
PPAR gamma - 0.8112 81.12%
Honey bee toxicity - 0.9625 96.25%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.8500 85.00%
Fish aquatic toxicity - 0.4067 40.67%

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
CHEMBL4040 P28482 MAP kinase ERK2 89.30% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.06% 96.09%

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.
Deschampsia antarctica

Cross-Links

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PubChem 95509
LOTUS LTS0096681
wikiData Q105035995