3-Oxoadipic acid

Details

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Internal ID 8052ac22-fe6a-4be0-9521-19506a78a435
Taxonomy Organic acids and derivatives > Keto acids and derivatives > Medium-chain keto acids and derivatives
IUPAC Name 3-oxohexanedioic acid
SMILES (Canonical) C(CC(=O)O)C(=O)CC(=O)O
SMILES (Isomeric) C(CC(=O)O)C(=O)CC(=O)O
InChI InChI=1S/C6H8O5/c7-4(3-6(10)11)1-2-5(8)9/h1-3H2,(H,8,9)(H,10,11)
InChI Key RTGHRDFWYQHVFW-UHFFFAOYSA-N
Popularity 251 references in papers

Physical and Chemical Properties

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Molecular Formula C6H8O5
Molecular Weight 160.12 g/mol
Exact Mass 160.03717335 g/mol
Topological Polar Surface Area (TPSA) 91.70 Ų
XlogP -0.90
Atomic LogP (AlogP) -0.11
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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3-oxohexanedioic acid
689-31-6
BETA-KETOADIPIC ACID
beta-ketoadipate
beta-Oxoadipic acid
Hexanedioic acid, 3-oxo-
3-Ketoadipic acid
3-oxo-adipic acid
3-ketoadipate
3-keto-adipate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Oxoadipic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6365 63.65%
Caco-2 - 0.6565 65.65%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.8889 88.89%
OATP2B1 inhibitior - 0.8506 85.06%
OATP1B1 inhibitior + 0.9532 95.32%
OATP1B3 inhibitior + 0.9651 96.51%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9650 96.50%
P-glycoprotein inhibitior - 0.9858 98.58%
P-glycoprotein substrate - 0.9796 97.96%
CYP3A4 substrate - 0.7687 76.87%
CYP2C9 substrate - 0.5862 58.62%
CYP2D6 substrate - 0.8476 84.76%
CYP3A4 inhibition - 0.9238 92.38%
CYP2C9 inhibition - 0.9462 94.62%
CYP2C19 inhibition - 0.9483 94.83%
CYP2D6 inhibition - 0.9602 96.02%
CYP1A2 inhibition - 0.9007 90.07%
CYP2C8 inhibition - 0.9917 99.17%
CYP inhibitory promiscuity - 0.9847 98.47%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7446 74.46%
Carcinogenicity (trinary) Non-required 0.7046 70.46%
Eye corrosion + 0.8236 82.36%
Eye irritation + 0.9888 98.88%
Skin irritation - 0.7532 75.32%
Skin corrosion - 0.5753 57.53%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7450 74.50%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation - 0.9651 96.51%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.8853 88.53%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.5519 55.19%
Acute Oral Toxicity (c) III 0.5915 59.15%
Estrogen receptor binding - 0.9403 94.03%
Androgen receptor binding - 0.9464 94.64%
Thyroid receptor binding - 0.8604 86.04%
Glucocorticoid receptor binding - 0.8986 89.86%
Aromatase binding - 0.8833 88.33%
PPAR gamma - 0.6390 63.90%
Honey bee toxicity - 0.9676 96.76%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.9800 98.00%
Fish aquatic toxicity - 0.6151 61.51%

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
CHEMBL4040 P28482 MAP kinase ERK2 96.78% 83.82%
CHEMBL221 P23219 Cyclooxygenase-1 92.01% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.48% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.72% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.29% 91.11%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
There are no matching plants.

Cross-Links

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PubChem 93
LOTUS LTS0002940
wikiData Q27117141