Ethyl pyruvate-d3

Details

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Internal ID a34d1ff6-e749-4d73-ae2e-6ad49d0941d7
Taxonomy Organic acids and derivatives > Keto acids and derivatives > Alpha-keto acids and derivatives
IUPAC Name ethyl 3,3,3-trideuterio-2-oxopropanoate
SMILES (Canonical) CCOC(=O)C(=O)C
SMILES (Isomeric) [2H]C([2H])([2H])C(=O)C(=O)OCC
InChI InChI=1S/C5H8O3/c1-3-8-5(7)4(2)6/h3H2,1-2H3/i2D3
InChI Key XXRCUYVCPSWGCC-BMSJAHLVSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C5H8O3
Molecular Weight 119.13 g/mol
Exact Mass 119.066174351 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 3

Synonyms

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Ethyl pyruvate-d3
Ethyl 3,3,3-trideuterio-2-oxopropanoate
ethyl 2-oxo(?H?)propanoate
Ethyl pyruvate(3,3,3-d3)
HY-Y1362S
CS-0608546
D99744

2D Structure

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2D Structure of Ethyl pyruvate-d3

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9741 97.41%
Caco-2 + 0.5375 53.75%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8887 88.87%
OATP2B1 inhibitior - 0.8518 85.18%
OATP1B1 inhibitior + 0.9621 96.21%
OATP1B3 inhibitior + 0.9580 95.80%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9038 90.38%
P-glycoprotein inhibitior - 0.9600 96.00%
P-glycoprotein substrate - 0.9823 98.23%
CYP3A4 substrate - 0.5788 57.88%
CYP2C9 substrate - 0.8024 80.24%
CYP2D6 substrate - 0.8849 88.49%
CYP3A4 inhibition - 0.9504 95.04%
CYP2C9 inhibition - 0.8678 86.78%
CYP2C19 inhibition - 0.9130 91.30%
CYP2D6 inhibition - 0.9495 94.95%
CYP1A2 inhibition - 0.8165 81.65%
CYP2C8 inhibition - 0.9776 97.76%
CYP inhibitory promiscuity - 0.8133 81.33%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5466 54.66%
Carcinogenicity (trinary) Non-required 0.6350 63.50%
Eye corrosion + 0.9370 93.70%
Eye irritation + 0.8375 83.75%
Skin irritation + 0.5767 57.67%
Skin corrosion - 0.8418 84.18%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8053 80.53%
Micronuclear - 0.8126 81.26%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation + 0.8045 80.45%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.5450 54.50%
Acute Oral Toxicity (c) IV 0.5011 50.11%
Estrogen receptor binding - 0.8114 81.14%
Androgen receptor binding - 0.8667 86.67%
Thyroid receptor binding - 0.8239 82.39%
Glucocorticoid receptor binding - 0.9522 95.22%
Aromatase binding - 0.7772 77.72%
PPAR gamma - 0.8421 84.21%
Honey bee toxicity - 0.9137 91.37%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity - 0.3759 37.59%

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 12247697
NPASS NPC127162