2-Ethyl-5-(4-methyl-2,5-dioxofuran-3-yl)penta-2,4-dienoic acid

Details

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Internal ID a5895400-fc1f-4209-96db-9f8e9aca3860
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Monocyclic monoterpenoids
IUPAC Name 2-ethyl-5-(4-methyl-2,5-dioxofuran-3-yl)penta-2,4-dienoic acid
SMILES (Canonical) CCC(=CC=CC1=C(C(=O)OC1=O)C)C(=O)O
SMILES (Isomeric) CCC(=CC=CC1=C(C(=O)OC1=O)C)C(=O)O
InChI InChI=1S/C12H12O5/c1-3-8(10(13)14)5-4-6-9-7(2)11(15)17-12(9)16/h4-6H,3H2,1-2H3,(H,13,14)
InChI Key CEZITUXGGUVZCK-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C12H12O5
Molecular Weight 236.22 g/mol
Exact Mass 236.06847348 g/mol
Topological Polar Surface Area (TPSA) 80.70 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.36
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Ethyl-5-(4-methyl-2,5-dioxofuran-3-yl)penta-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 + 0.9797 97.97%
Caco-2 + 0.8058 80.58%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7337 73.37%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8453 84.53%
OATP1B3 inhibitior + 0.9537 95.37%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8012 80.12%
P-glycoprotein inhibitior - 0.9787 97.87%
P-glycoprotein substrate - 0.9361 93.61%
CYP3A4 substrate - 0.5822 58.22%
CYP2C9 substrate + 0.6092 60.92%
CYP2D6 substrate - 0.8964 89.64%
CYP3A4 inhibition - 0.9432 94.32%
CYP2C9 inhibition - 0.7850 78.50%
CYP2C19 inhibition - 0.7717 77.17%
CYP2D6 inhibition - 0.9395 93.95%
CYP1A2 inhibition - 0.8351 83.51%
CYP2C8 inhibition - 0.8403 84.03%
CYP inhibitory promiscuity - 0.8834 88.34%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8368 83.68%
Carcinogenicity (trinary) Non-required 0.4834 48.34%
Eye corrosion - 0.7909 79.09%
Eye irritation + 0.7710 77.10%
Skin irritation + 0.5208 52.08%
Skin corrosion - 0.6431 64.31%
Ames mutagenesis + 0.5763 57.63%
Human Ether-a-go-go-Related Gene inhibition - 0.6361 63.61%
Micronuclear - 0.5800 58.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.6255 62.55%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.6193 61.93%
Acute Oral Toxicity (c) III 0.6808 68.08%
Estrogen receptor binding - 0.6220 62.20%
Androgen receptor binding - 0.6793 67.93%
Thyroid receptor binding - 0.7080 70.80%
Glucocorticoid receptor binding - 0.8663 86.63%
Aromatase binding - 0.6233 62.33%
PPAR gamma - 0.5726 57.26%
Honey bee toxicity - 0.9701 97.01%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity + 0.9527 95.27%

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 90.92% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.96% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.08% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 84.73% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.24% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.57% 91.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.56% 96.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.42% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.32% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.27% 99.17%

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 162992996
LOTUS LTS0163625
wikiData Q103817669