Urethane

Details

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Internal ID eb7b4795-354c-4543-97b2-885877c92cea
Taxonomy Organic acids and derivatives > Carboximidic acids and derivatives
IUPAC Name ethyl carbamate
SMILES (Canonical) CCOC(=O)N
SMILES (Isomeric) CCOC(=O)N
InChI InChI=1S/C3H7NO2/c1-2-6-3(4)5/h2H2,1H3,(H2,4,5)
InChI Key JOYRKODLDBILNP-UHFFFAOYSA-N
Popularity 26,228 references in papers

Physical and Chemical Properties

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Molecular Formula C3H7NO2
Molecular Weight 89.09 g/mol
Exact Mass 89.047678466 g/mol
Topological Polar Surface Area (TPSA) 52.30 Ų
XlogP -0.20
Atomic LogP (AlogP) 0.10
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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ETHYL CARBAMATE
51-79-6
Carbamic acid, ethyl ester
Carbamic acid ethyl ester
Ethylurethane
Pracarbamine
Leucethane
Ethylcarbamate
Ethyl urethane
O-Ethylurethane
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Urethane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.7279 72.79%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.5079 50.79%
OATP2B1 inhibitior - 0.8630 86.30%
OATP1B1 inhibitior + 0.9774 97.74%
OATP1B3 inhibitior + 0.9435 94.35%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8978 89.78%
P-glycoprotein inhibitior - 0.9877 98.77%
P-glycoprotein substrate - 0.9917 99.17%
CYP3A4 substrate - 0.7144 71.44%
CYP2C9 substrate - 0.8134 81.34%
CYP2D6 substrate - 0.7984 79.84%
CYP3A4 inhibition - 0.9765 97.65%
CYP2C9 inhibition - 0.9306 93.06%
CYP2C19 inhibition - 0.9537 95.37%
CYP2D6 inhibition - 0.9168 91.68%
CYP1A2 inhibition - 0.5553 55.53%
CYP2C8 inhibition - 0.9876 98.76%
CYP inhibitory promiscuity - 0.9452 94.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6026 60.26%
Carcinogenicity (trinary) Warning 0.5901 59.01%
Eye corrosion - 0.7835 78.35%
Eye irritation + 0.9927 99.27%
Skin irritation - 0.5764 57.64%
Skin corrosion - 0.8069 80.69%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8401 84.01%
Micronuclear + 0.9400 94.00%
Hepatotoxicity - 0.5241 52.41%
skin sensitisation - 0.9376 93.76%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.4767 47.67%
Acute Oral Toxicity (c) III 0.7994 79.94%
Estrogen receptor binding - 0.9335 93.35%
Androgen receptor binding - 0.9485 94.85%
Thyroid receptor binding - 0.8922 89.22%
Glucocorticoid receptor binding - 0.9286 92.86%
Aromatase binding - 0.8421 84.21%
PPAR gamma - 0.8988 89.88%
Honey bee toxicity - 0.9715 97.15%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity - 0.8300 83.00%
Fish aquatic toxicity - 0.5355 53.55%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL2903 P16050 Arachidonate 15-lipoxygenase 39810.7 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 95.09% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 91.40% 96.95%
CHEMBL4040 P28482 MAP kinase ERK2 88.08% 83.82%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 83.87% 97.21%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.66% 99.17%

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.
Cornus officinalis

Cross-Links

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PubChem 5641
NPASS NPC51414
ChEMBL CHEMBL462547
LOTUS LTS0084870
wikiData Q422884