2-(5-Oxohexyl)pent-2-enedioic acid

Details

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Internal ID f34aae1c-f815-496a-bdf8-b692df3cc66b
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Medium-chain fatty acids
IUPAC Name 2-(5-oxohexyl)pent-2-enedioic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H16O5/c1-8(12)4-2-3-5-9(11(15)16)6-7-10(13)14/h6H,2-5,7H2,1H3,(H,13,14)(H,15,16)
InChI Key ZVMSPBRNCJKZRT-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H16O5
Molecular Weight 228.24 g/mol
Exact Mass 228.09977361 g/mol
Topological Polar Surface Area (TPSA) 91.70 Ų
XlogP 0.50
Atomic LogP (AlogP) 1.62
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(5-Oxohexyl)pent-2-enedioic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9264 92.64%
Caco-2 - 0.5600 56.00%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8058 80.58%
OATP2B1 inhibitior - 0.8491 84.91%
OATP1B1 inhibitior + 0.9036 90.36%
OATP1B3 inhibitior + 0.9316 93.16%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9542 95.42%
P-glycoprotein inhibitior - 0.9792 97.92%
P-glycoprotein substrate - 0.9472 94.72%
CYP3A4 substrate - 0.6419 64.19%
CYP2C9 substrate - 0.7314 73.14%
CYP2D6 substrate - 0.9062 90.62%
CYP3A4 inhibition - 0.9097 90.97%
CYP2C9 inhibition - 0.9262 92.62%
CYP2C19 inhibition - 0.9453 94.53%
CYP2D6 inhibition - 0.9222 92.22%
CYP1A2 inhibition - 0.6615 66.15%
CYP2C8 inhibition - 0.9759 97.59%
CYP inhibitory promiscuity - 0.9527 95.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7735 77.35%
Carcinogenicity (trinary) Non-required 0.7290 72.90%
Eye corrosion - 0.8171 81.71%
Eye irritation + 0.9571 95.71%
Skin irritation - 0.6630 66.30%
Skin corrosion - 0.9583 95.83%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7632 76.32%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.7058 70.58%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.8648 86.48%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.6499 64.99%
Acute Oral Toxicity (c) III 0.6504 65.04%
Estrogen receptor binding - 0.7557 75.57%
Androgen receptor binding - 0.7832 78.32%
Thyroid receptor binding - 0.8259 82.59%
Glucocorticoid receptor binding - 0.6484 64.84%
Aromatase binding - 0.8335 83.35%
PPAR gamma - 0.6166 61.66%
Honey bee toxicity - 0.9645 96.45%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.8700 87.00%
Fish aquatic toxicity + 0.9746 97.46%

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 90.79% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.93% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.68% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.36% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.68% 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 163007003
LOTUS LTS0100562
wikiData Q104202837