Ethyl pyruvate

Details

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Internal ID fd2a4f54-9f50-432a-8575-15c3298d2c78
Taxonomy Organic acids and derivatives > Keto acids and derivatives > Alpha-keto acids and derivatives
IUPAC Name ethyl 2-oxopropanoate
SMILES (Canonical) CCOC(=O)C(=O)C
SMILES (Isomeric) CCOC(=O)C(=O)C
InChI InChI=1S/C5H8O3/c1-3-8-5(7)4(2)6/h3H2,1-2H3
InChI Key XXRCUYVCPSWGCC-UHFFFAOYSA-N
Popularity 1,118 references in papers

Physical and Chemical Properties

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Molecular Formula C5H8O3
Molecular Weight 116.11 g/mol
Exact Mass 116.047344113 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 0.40
Atomic LogP (AlogP) 0.14
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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617-35-6
Ethyl 2-oxopropanoate
Ethyl 2-oxopropionate
Pyruvic acid, ethyl ester
Propanoic acid, 2-oxo-, ethyl ester
PYRUVIC ACID ETHYL ESTER
Ethyl pyroracemate
Ethyl acetylformate
FEMA No. 2457
CTI-01
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Ethyl pyruvate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9872 98.72%
Caco-2 + 0.6106 61.06%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.8739 87.39%
OATP2B1 inhibitior - 0.8530 85.30%
OATP1B1 inhibitior + 0.9690 96.90%
OATP1B3 inhibitior + 0.9561 95.61%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8931 89.31%
P-glycoprotein inhibitior - 0.9800 98.00%
P-glycoprotein substrate - 0.9919 99.19%
CYP3A4 substrate - 0.6370 63.70%
CYP2C9 substrate - 0.8024 80.24%
CYP2D6 substrate - 0.8849 88.49%
CYP3A4 inhibition - 0.9652 96.52%
CYP2C9 inhibition - 0.8727 87.27%
CYP2C19 inhibition - 0.9276 92.76%
CYP2D6 inhibition - 0.9500 95.00%
CYP1A2 inhibition - 0.8008 80.08%
CYP2C8 inhibition - 0.9829 98.29%
CYP inhibitory promiscuity - 0.7997 79.97%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5466 54.66%
Carcinogenicity (trinary) Non-required 0.6478 64.78%
Eye corrosion + 0.9359 93.59%
Eye irritation + 0.9703 97.03%
Skin irritation + 0.6127 61.27%
Skin corrosion - 0.7713 77.13%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7506 75.06%
Micronuclear - 0.8026 80.26%
Hepatotoxicity + 0.5409 54.09%
skin sensitisation + 0.8262 82.62%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.7053 70.53%
Acute Oral Toxicity (c) IV 0.5377 53.77%
Estrogen receptor binding - 0.9456 94.56%
Androgen receptor binding - 0.9268 92.68%
Thyroid receptor binding - 0.9355 93.55%
Glucocorticoid receptor binding - 0.9798 97.98%
Aromatase binding - 0.8694 86.94%
PPAR gamma - 0.9614 96.14%
Honey bee toxicity - 0.9330 93.30%
Biodegradation + 0.9500 95.00%
Crustacea aquatic toxicity - 0.8255 82.55%
Fish aquatic toxicity - 0.3793 37.93%

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 92.65% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 89.06% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 87.56% 97.21%
CHEMBL3401 O75469 Pregnane X receptor 82.64% 94.73%

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.
Zanthoxylum bungeanum
Zanthoxylum schinifolium

Cross-Links

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PubChem 12041
NPASS NPC5934
LOTUS LTS0141523
wikiData Q15632706