2-Oxobutanoic acid

Details

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Internal ID 49a81de3-21d8-47c9-a603-9e836a4311e5
Taxonomy Organic acids and derivatives > Keto acids and derivatives > Short-chain keto acids and derivatives
IUPAC Name 2-oxobutanoic acid
SMILES (Canonical) CCC(=O)C(=O)O
SMILES (Isomeric) CCC(=O)C(=O)O
InChI InChI=1S/C4H6O3/c1-2-3(5)4(6)7/h2H2,1H3,(H,6,7)
InChI Key TYEYBOSBBBHJIV-UHFFFAOYSA-N
Popularity 1,054 references in papers

Physical and Chemical Properties

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Molecular Formula C4H6O3
Molecular Weight 102.09 g/mol
Exact Mass 102.031694049 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 0.10
Atomic LogP (AlogP) 0.05
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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2-ketobutyric acid
2-oxobutyric acid
600-18-0
alpha-ketobutyric acid
BUTANOIC ACID, 2-OXO-
2-oxobutyrate
3-Methylpyruvic acid
Ketobutyrate
Propionylformic acid
Butyric acid, 2-oxo-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Oxobutanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9724 97.24%
Caco-2 + 0.5563 55.63%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.8750 87.50%
OATP2B1 inhibitior - 0.8609 86.09%
OATP1B1 inhibitior + 0.9436 94.36%
OATP1B3 inhibitior + 0.9536 95.36%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9323 93.23%
P-glycoprotein inhibitior - 0.9850 98.50%
P-glycoprotein substrate - 0.9902 99.02%
CYP3A4 substrate - 0.8127 81.27%
CYP2C9 substrate - 0.5862 58.62%
CYP2D6 substrate - 0.8822 88.22%
CYP3A4 inhibition - 0.9805 98.05%
CYP2C9 inhibition - 0.9075 90.75%
CYP2C19 inhibition - 0.9475 94.75%
CYP2D6 inhibition - 0.9664 96.64%
CYP1A2 inhibition - 0.9532 95.32%
CYP2C8 inhibition - 0.9835 98.35%
CYP inhibitory promiscuity - 0.9876 98.76%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5811 58.11%
Carcinogenicity (trinary) Non-required 0.6940 69.40%
Eye corrosion + 0.9854 98.54%
Eye irritation + 0.9932 99.32%
Skin irritation + 0.8622 86.22%
Skin corrosion + 0.9468 94.68%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8121 81.21%
Micronuclear - 0.7200 72.00%
Hepatotoxicity + 0.5199 51.99%
skin sensitisation + 0.5238 52.38%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity - 0.7333 73.33%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.5667 56.67%
Acute Oral Toxicity (c) III 0.8213 82.13%
Estrogen receptor binding - 0.9543 95.43%
Androgen receptor binding - 0.8708 87.08%
Thyroid receptor binding - 0.9070 90.70%
Glucocorticoid receptor binding - 0.9412 94.12%
Aromatase binding - 0.9035 90.35%
PPAR gamma - 0.9385 93.85%
Honey bee toxicity - 0.9902 99.02%
Biodegradation + 0.9250 92.50%
Crustacea aquatic toxicity - 0.8600 86.00%
Fish aquatic toxicity - 0.7011 70.11%

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 90.50% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 90.04% 83.82%
CHEMBL2581 P07339 Cathepsin D 85.32% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.80% 96.95%

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.
Solanum lycopersicum

Cross-Links

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PubChem 58
LOTUS LTS0020159
wikiData Q209457