(2E,6E)-3,7,11-trimethyldodeca-2,6-dienedioic acid

Details

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Internal ID bf0e04b0-52b5-47b6-bc94-a9c1ce82c794
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (2E,6E)-3,7,11-trimethyldodeca-2,6-dienedioic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O4/c1-11(7-5-9-13(3)15(18)19)6-4-8-12(2)10-14(16)17/h6,10,13H,4-5,7-9H2,1-3H3,(H,16,17)(H,18,19)/b11-6+,12-10+
InChI Key ZCHKUAFPTUCNJS-BFPRWLMKSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O4
Molecular Weight 268.35 g/mol
Exact Mass 268.16745924 g/mol
Topological Polar Surface Area (TPSA) 74.60 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.63
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2E,6E)-3,7,11-trimethyldodeca-2,6-dienedioic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9311 93.11%
Caco-2 - 0.5244 52.44%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6686 66.86%
OATP2B1 inhibitior - 0.8536 85.36%
OATP1B1 inhibitior + 0.8973 89.73%
OATP1B3 inhibitior + 0.9010 90.10%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.5779 57.79%
P-glycoprotein inhibitior - 0.9352 93.52%
P-glycoprotein substrate - 0.8758 87.58%
CYP3A4 substrate - 0.5574 55.74%
CYP2C9 substrate + 0.8284 82.84%
CYP2D6 substrate - 0.9201 92.01%
CYP3A4 inhibition - 0.8721 87.21%
CYP2C9 inhibition - 0.8496 84.96%
CYP2C19 inhibition - 0.9142 91.42%
CYP2D6 inhibition - 0.9077 90.77%
CYP1A2 inhibition - 0.7660 76.60%
CYP2C8 inhibition - 0.9652 96.52%
CYP inhibitory promiscuity - 0.9260 92.60%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7038 70.38%
Carcinogenicity (trinary) Non-required 0.7035 70.35%
Eye corrosion - 0.8018 80.18%
Eye irritation - 0.7037 70.37%
Skin irritation - 0.7496 74.96%
Skin corrosion - 0.9880 98.80%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6672 66.72%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation + 0.4827 48.27%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.7187 71.87%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.6235 62.35%
Acute Oral Toxicity (c) III 0.5914 59.14%
Estrogen receptor binding - 0.5851 58.51%
Androgen receptor binding - 0.6146 61.46%
Thyroid receptor binding - 0.5549 55.49%
Glucocorticoid receptor binding - 0.4883 48.83%
Aromatase binding - 0.7680 76.80%
PPAR gamma + 0.6451 64.51%
Honey bee toxicity - 0.9182 91.82%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity + 0.9964 99.64%

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 92.29% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.34% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.78% 99.17%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 88.44% 96.47%
CHEMBL3359 P21462 Formyl peptide receptor 1 87.41% 93.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.87% 90.71%
CHEMBL2039 P27338 Monoamine oxidase B 85.69% 92.51%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 82.46% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.91% 96.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 80.71% 92.08%
CHEMBL3401 O75469 Pregnane X receptor 80.44% 94.73%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.03% 100.00%

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 139591354
LOTUS LTS0225147
wikiData Q105371111