7-(4,9-Dioxodeca-2,7-dienoyloxy)-4,9-dioxodec-2-enoic acid

Details

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Internal ID 0b1777e6-aacb-46c6-a4c2-5d238c67a135
Taxonomy Organic acids and derivatives > Keto acids and derivatives > Medium-chain keto acids and derivatives
IUPAC Name 7-(4,9-dioxodeca-2,7-dienoyloxy)-4,9-dioxodec-2-enoic acid
SMILES (Canonical) CC(=O)CC(CCC(=O)C=CC(=O)O)OC(=O)C=CC(=O)CCC=CC(=O)C
SMILES (Isomeric) CC(=O)CC(CCC(=O)C=CC(=O)O)OC(=O)C=CC(=O)CCC=CC(=O)C
InChI InChI=1S/C20H24O8/c1-14(21)5-3-4-6-16(23)9-12-20(27)28-18(13-15(2)22)10-7-17(24)8-11-19(25)26/h3,5,8-9,11-12,18H,4,6-7,10,13H2,1-2H3,(H,25,26)
InChI Key BXDWMBHVQJFBPQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H24O8
Molecular Weight 392.40 g/mol
Exact Mass 392.14711772 g/mol
Topological Polar Surface Area (TPSA) 132.00 Ų
XlogP -0.10
Atomic LogP (AlogP) 1.92
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-(4,9-Dioxodeca-2,7-dienoyloxy)-4,9-dioxodec-2-enoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9092 90.92%
Caco-2 - 0.7751 77.51%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.7836 78.36%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9112 91.12%
OATP1B3 inhibitior + 0.9470 94.70%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.8475 84.75%
P-glycoprotein inhibitior + 0.6138 61.38%
P-glycoprotein substrate - 0.7508 75.08%
CYP3A4 substrate + 0.5720 57.20%
CYP2C9 substrate - 0.5839 58.39%
CYP2D6 substrate - 0.9066 90.66%
CYP3A4 inhibition - 0.8126 81.26%
CYP2C9 inhibition - 0.9204 92.04%
CYP2C19 inhibition - 0.9238 92.38%
CYP2D6 inhibition - 0.9479 94.79%
CYP1A2 inhibition - 0.8754 87.54%
CYP2C8 inhibition - 0.8666 86.66%
CYP inhibitory promiscuity - 0.9288 92.88%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5881 58.81%
Carcinogenicity (trinary) Non-required 0.6690 66.90%
Eye corrosion + 0.6113 61.13%
Eye irritation - 0.9248 92.48%
Skin irritation - 0.5742 57.42%
Skin corrosion - 0.9494 94.94%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7332 73.32%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.5468 54.68%
skin sensitisation - 0.7140 71.40%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.8679 86.79%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.6492 64.92%
Acute Oral Toxicity (c) III 0.7268 72.68%
Estrogen receptor binding + 0.5887 58.87%
Androgen receptor binding - 0.5117 51.17%
Thyroid receptor binding - 0.5820 58.20%
Glucocorticoid receptor binding - 0.4687 46.87%
Aromatase binding - 0.5601 56.01%
PPAR gamma - 0.5303 53.03%
Honey bee toxicity - 0.7760 77.60%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6755 67.55%
Fish aquatic toxicity + 0.8716 87.16%

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 93.49% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.83% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.42% 91.11%
CHEMBL2581 P07339 Cathepsin D 86.19% 98.95%
CHEMBL340 P08684 Cytochrome P450 3A4 84.15% 91.19%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.11% 96.00%

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 376409
LOTUS LTS0272930
wikiData Q104947880