methyl (5Z,8Z,10E)-12-oxododeca-5,8,10-trienoate

Details

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Internal ID e52cbd77-022e-4fa4-a123-97e4a4e18c2f
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Medium-chain aldehydes
IUPAC Name methyl (5Z,8Z,10E)-12-oxododeca-5,8,10-trienoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H18O3/c1-16-13(15)11-9-7-5-3-2-4-6-8-10-12-14/h3-6,8,10,12H,2,7,9,11H2,1H3/b5-3-,6-4-,10-8+
InChI Key LVOLVIHDJLHIGG-MARZPFHASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H18O3
Molecular Weight 222.28 g/mol
Exact Mass 222.125594432 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.59
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of methyl (5Z,8Z,10E)-12-oxododeca-5,8,10-trienoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9866 98.66%
Caco-2 + 0.8669 86.69%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6972 69.72%
OATP2B1 inhibitior - 0.8601 86.01%
OATP1B1 inhibitior - 0.3209 32.09%
OATP1B3 inhibitior + 0.9315 93.15%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.5641 56.41%
P-glycoprotein inhibitior - 0.9695 96.95%
P-glycoprotein substrate - 0.8826 88.26%
CYP3A4 substrate - 0.5161 51.61%
CYP2C9 substrate - 0.8021 80.21%
CYP2D6 substrate - 0.8781 87.81%
CYP3A4 inhibition - 0.9745 97.45%
CYP2C9 inhibition - 0.9357 93.57%
CYP2C19 inhibition - 0.9471 94.71%
CYP2D6 inhibition - 0.9669 96.69%
CYP1A2 inhibition - 0.7709 77.09%
CYP2C8 inhibition - 0.8557 85.57%
CYP inhibitory promiscuity - 0.9294 92.94%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6642 66.42%
Carcinogenicity (trinary) Non-required 0.7524 75.24%
Eye corrosion + 0.9114 91.14%
Eye irritation + 0.7674 76.74%
Skin irritation - 0.5341 53.41%
Skin corrosion - 0.9754 97.54%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5059 50.59%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.6690 66.90%
skin sensitisation - 0.6377 63.77%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.9397 93.97%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.4703 47.03%
Acute Oral Toxicity (c) III 0.5660 56.60%
Estrogen receptor binding - 0.6918 69.18%
Androgen receptor binding - 0.7920 79.20%
Thyroid receptor binding - 0.6416 64.16%
Glucocorticoid receptor binding + 0.6818 68.18%
Aromatase binding + 0.5418 54.18%
PPAR gamma + 0.6519 65.19%
Honey bee toxicity - 0.9560 95.60%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9357 93.57%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 95.00% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.87% 96.09%
CHEMBL239 Q07869 Peroxisome proliferator-activated receptor alpha 89.07% 90.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.90% 91.11%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 86.73% 94.33%
CHEMBL2581 P07339 Cathepsin D 85.21% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.47% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 80.33% 94.73%

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 14384185
LOTUS LTS0267445
wikiData Q105157954