Ethyl 4-deuteriobenzoate

Details

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Internal ID bcc05bca-4c20-45f5-8b6a-77bbc4473635
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Benzoic acid esters
IUPAC Name ethyl 4-deuteriobenzoate
SMILES (Canonical) CCOC(=O)C1=CC=CC=C1
SMILES (Isomeric) [2H]C1=CC=C(C=C1)C(=O)OCC
InChI InChI=1S/C9H10O2/c1-2-11-9(10)8-6-4-3-5-7-8/h3-7H,2H2,1H3/i3D
InChI Key MTZQAGJQAFMTAQ-WFVSFCRTSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H10O2
Molecular Weight 151.18 g/mol
Exact Mass 151.074356303 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 2.60
Atomic LogP (AlogP) 1.86
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Ethyl 4-deuteriobenzoate

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 + 0.8509 85.09%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.7797 77.97%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9371 93.71%
OATP1B3 inhibitior + 0.9674 96.74%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9079 90.79%
P-glycoprotein inhibitior - 0.9898 98.98%
P-glycoprotein substrate - 0.9770 97.70%
CYP3A4 substrate - 0.6465 64.65%
CYP2C9 substrate - 0.7945 79.45%
CYP2D6 substrate - 0.8429 84.29%
CYP3A4 inhibition - 0.9817 98.17%
CYP2C9 inhibition - 0.8860 88.60%
CYP2C19 inhibition - 0.8897 88.97%
CYP2D6 inhibition - 0.9525 95.25%
CYP1A2 inhibition + 0.7888 78.88%
CYP2C8 inhibition - 0.7605 76.05%
CYP inhibitory promiscuity - 0.7227 72.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5239 52.39%
Carcinogenicity (trinary) Non-required 0.6038 60.38%
Eye corrosion + 0.8185 81.85%
Eye irritation + 0.9716 97.16%
Skin irritation + 0.8823 88.23%
Skin corrosion - 0.8782 87.82%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8250 82.50%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.5021 50.21%
skin sensitisation + 0.7518 75.18%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.7889 78.89%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity - 0.6693 66.93%
Acute Oral Toxicity (c) III 0.9356 93.56%
Estrogen receptor binding + 0.6613 66.13%
Androgen receptor binding - 0.5590 55.90%
Thyroid receptor binding - 0.8649 86.49%
Glucocorticoid receptor binding - 0.8608 86.08%
Aromatase binding + 0.7299 72.99%
PPAR gamma - 0.8845 88.45%
Honey bee toxicity - 0.9659 96.59%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity - 0.7050 70.50%
Fish aquatic toxicity + 0.9145 91.45%

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
CHEMBL221 P23219 Cyclooxygenase-1 93.89% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.14% 86.33%
CHEMBL2581 P07339 Cathepsin D 89.89% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.44% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.00% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 86.41% 94.73%
CHEMBL4267 P37173 TGF-beta receptor type II 82.66% 88.18%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.57% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.08% 95.50%

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.
Hemerocallis fulva
Paederia foetida
Prunus persica
Syzygium aromaticum

Cross-Links

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PubChem 11240586
NPASS NPC56161