Diethyl carbonate

Details

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Internal ID 971fcf88-a56d-40fa-83a7-e138484f9277
Taxonomy Organic acids and derivatives > Organic carbonic acids and derivatives > Carbonic acid diesters
IUPAC Name diethyl carbonate
SMILES (Canonical) CCOC(=O)OCC
SMILES (Isomeric) CCOC(=O)OCC
InChI InChI=1S/C5H10O3/c1-3-7-5(6)8-4-2/h3-4H2,1-2H3
InChI Key OIFBSDVPJOWBCH-UHFFFAOYSA-N
Popularity 3,168 references in papers

Physical and Chemical Properties

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Molecular Formula C5H10O3
Molecular Weight 118.13 g/mol
Exact Mass 118.062994177 g/mol
Topological Polar Surface Area (TPSA) 35.50 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.18
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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105-58-8
Ethyl carbonate
Carbonic acid diethyl ester
Carbonic acid, diethyl ester
Eufin
Diatol
Diaethylcarbonat
Carbonic ether
Ethoxyformic anhydride
Diethylkarbonat
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Diethyl carbonate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9948 99.48%
Caco-2 + 0.7877 78.77%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.8266 82.66%
OATP2B1 inhibitior - 0.8370 83.70%
OATP1B1 inhibitior + 0.9615 96.15%
OATP1B3 inhibitior + 0.9567 95.67%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8962 89.62%
P-glycoprotein inhibitior - 0.9873 98.73%
P-glycoprotein substrate - 0.9975 99.75%
CYP3A4 substrate - 0.7033 70.33%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.7646 76.46%
CYP3A4 inhibition - 0.9718 97.18%
CYP2C9 inhibition - 0.9210 92.10%
CYP2C19 inhibition - 0.9101 91.01%
CYP2D6 inhibition - 0.9470 94.70%
CYP1A2 inhibition - 0.8183 81.83%
CYP2C8 inhibition - 0.9872 98.72%
CYP inhibitory promiscuity - 0.8229 82.29%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5077 50.77%
Carcinogenicity (trinary) Non-required 0.6562 65.62%
Eye corrosion + 0.9635 96.35%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.7421 74.21%
Skin corrosion - 0.8459 84.59%
Ames mutagenesis - 0.9800 98.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8390 83.90%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.6009 60.09%
skin sensitisation - 0.9393 93.93%
Respiratory toxicity - 0.9444 94.44%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.6515 65.15%
Acute Oral Toxicity (c) IV 0.5495 54.95%
Estrogen receptor binding - 0.9209 92.09%
Androgen receptor binding - 0.9471 94.71%
Thyroid receptor binding - 0.8853 88.53%
Glucocorticoid receptor binding - 0.9129 91.29%
Aromatase binding - 0.8666 86.66%
PPAR gamma - 0.9242 92.42%
Honey bee toxicity - 0.9601 96.01%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity - 0.8089 80.89%
Fish aquatic toxicity + 0.8486 84.86%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL3577 P00352 Aldehyde dehydrogenase 1A1 28183.8 nM
Potency
via CMAUP

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.20% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 91.38% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 87.91% 97.21%
CHEMBL3401 O75469 Pregnane X receptor 81.26% 94.73%
CHEMBL2581 P07339 Cathepsin D 81.02% 98.95%

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.
Ananas comosus
Citrus × aurantium
Opuntia ficus-indica
Vitis rotundifolia

Cross-Links

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PubChem 7766
NPASS NPC2419
ChEMBL CHEMBL1533495
LOTUS LTS0249178
wikiData Q420616