4,6,8-Trimethyldeca-2,4-dienoic acid

Details

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Internal ID 85a16e09-5b8e-4c20-8e7c-8b7b281d267b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name 4,6,8-trimethyldeca-2,4-dienoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H22O2/c1-5-10(2)8-12(4)9-11(3)6-7-13(14)15/h6-7,9-10,12H,5,8H2,1-4H3,(H,14,15)
InChI Key OILLDIIQDQVGSY-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C13H22O2
Molecular Weight 210.31 g/mol
Exact Mass 210.161979940 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 4.50
Atomic LogP (AlogP) 3.65
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,6,8-Trimethyldeca-2,4-dienoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9959 99.59%
Caco-2 + 0.9617 96.17%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.3495 34.95%
OATP2B1 inhibitior - 0.8585 85.85%
OATP1B1 inhibitior + 0.9101 91.01%
OATP1B3 inhibitior + 0.9027 90.27%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.7541 75.41%
P-glycoprotein inhibitior - 0.9782 97.82%
P-glycoprotein substrate - 0.8830 88.30%
CYP3A4 substrate - 0.6385 63.85%
CYP2C9 substrate + 0.6200 62.00%
CYP2D6 substrate - 0.9036 90.36%
CYP3A4 inhibition - 0.9503 95.03%
CYP2C9 inhibition - 0.8954 89.54%
CYP2C19 inhibition - 0.9379 93.79%
CYP2D6 inhibition - 0.9233 92.33%
CYP1A2 inhibition - 0.8856 88.56%
CYP2C8 inhibition - 0.9505 95.05%
CYP inhibitory promiscuity - 0.8755 87.55%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6158 61.58%
Carcinogenicity (trinary) Non-required 0.6212 62.12%
Eye corrosion + 0.7591 75.91%
Eye irritation - 0.7014 70.14%
Skin irritation + 0.8477 84.77%
Skin corrosion + 0.6413 64.13%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5314 53.14%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation + 0.8034 80.34%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.8333 83.33%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.6925 69.25%
Acute Oral Toxicity (c) III 0.8805 88.05%
Estrogen receptor binding - 0.8569 85.69%
Androgen receptor binding - 0.7040 70.40%
Thyroid receptor binding - 0.7207 72.07%
Glucocorticoid receptor binding - 0.8593 85.93%
Aromatase binding - 0.7272 72.72%
PPAR gamma - 0.5672 56.72%
Honey bee toxicity - 0.9469 94.69%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.8600 86.00%
Fish aquatic toxicity + 0.9534 95.34%

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 91.03% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.43% 98.95%
CHEMBL206 P03372 Estrogen receptor alpha 88.63% 97.64%
CHEMBL221 P23219 Cyclooxygenase-1 87.90% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.84% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.80% 96.95%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 82.69% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.11% 93.56%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.33% 97.21%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 90911676
LOTUS LTS0128989
wikiData Q104193397