4-Oxohex-2-enedioate

Details

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Internal ID ddbcd132-99e4-4027-9cf7-41a3d7b6d15b
Taxonomy Organic acids and derivatives > Keto acids and derivatives > Medium-chain keto acids and derivatives
IUPAC Name (Z)-4-oxohex-2-enedioic acid
SMILES (Canonical) C(C(=O)C=CC(=O)O)C(=O)O
SMILES (Isomeric) C(C(=O)/C=C\C(=O)O)C(=O)O
InChI InChI=1S/C6H6O5/c7-4(3-6(10)11)1-2-5(8)9/h1-2H,3H2,(H,8,9)(H,10,11)/b2-1-
InChI Key SOXXPQLIZIPMIZ-UPHRSURJSA-N
Popularity 24 references in papers

Physical and Chemical Properties

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Molecular Formula C6H6O5
Molecular Weight 158.11 g/mol
Exact Mass 158.02152329 g/mol
Topological Polar Surface Area (TPSA) 91.70 Ų
XlogP -0.60
Atomic LogP (AlogP) -0.33
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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maleylacetic acid
2-maleylacetate
24740-88-3
4-oxohex-2-enedioate
(Z)-4-oxo-2-hexenedioic acid
(2Z)-4-oxohex-2-enedioic acid
(2Z)-4-Oxo-2-hexenedioic acid
Maleoylacetic acid
(Z)-4-oxohex-2-enedioic acid
JAD9FA3JG6
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Oxohex-2-enedioate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8746 87.46%
Caco-2 - 0.5187 51.87%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.7931 79.31%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9654 96.54%
OATP1B3 inhibitior + 0.9644 96.44%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9681 96.81%
P-glycoprotein inhibitior - 0.9895 98.95%
P-glycoprotein substrate - 0.9779 97.79%
CYP3A4 substrate - 0.7436 74.36%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8616 86.16%
CYP3A4 inhibition - 0.8829 88.29%
CYP2C9 inhibition - 0.9697 96.97%
CYP2C19 inhibition - 0.9573 95.73%
CYP2D6 inhibition - 0.9568 95.68%
CYP1A2 inhibition - 0.9597 95.97%
CYP2C8 inhibition - 0.9884 98.84%
CYP inhibitory promiscuity - 0.9791 97.91%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5046 50.46%
Carcinogenicity (trinary) Non-required 0.7032 70.32%
Eye corrosion + 0.9321 93.21%
Eye irritation + 0.9952 99.52%
Skin irritation + 0.6586 65.86%
Skin corrosion + 0.6477 64.77%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8876 88.76%
Micronuclear - 0.7300 73.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.8227 82.27%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity - 0.6391 63.91%
Acute Oral Toxicity (c) III 0.8244 82.44%
Estrogen receptor binding - 0.9661 96.61%
Androgen receptor binding - 0.8887 88.87%
Thyroid receptor binding - 0.8978 89.78%
Glucocorticoid receptor binding - 0.9153 91.53%
Aromatase binding - 0.9287 92.87%
PPAR gamma - 0.6538 65.38%
Honey bee toxicity - 0.9427 94.27%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.9400 94.00%
Fish aquatic toxicity - 0.5575 55.75%

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
CHEMBL221 P23219 Cyclooxygenase-1 90.41% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.95% 99.17%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.74% 89.34%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.18% 96.09%

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 5280500
LOTUS LTS0039244
wikiData Q76280924