Ethyl 3,4,5-Trimethoxybenzoate

Details

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Internal ID 2895bd0c-90f1-481d-84e2-cd909b9f061f
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Hydroxybenzoic acid derivatives > Gallic acid and derivatives
IUPAC Name ethyl 3,4,5-trimethoxybenzoate
SMILES (Canonical) CCOC(=O)C1=CC(=C(C(=C1)OC)OC)OC
SMILES (Isomeric) CCOC(=O)C1=CC(=C(C(=C1)OC)OC)OC
InChI InChI=1S/C12H16O5/c1-5-17-12(13)8-6-9(14-2)11(16-4)10(7-8)15-3/h6-7H,5H2,1-4H3
InChI Key UEOFNBCUGJADBM-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C12H16O5
Molecular Weight 240.25 g/mol
Exact Mass 240.09977361 g/mol
Topological Polar Surface Area (TPSA) 54.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.89
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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6178-44-5
3,4,5-Trimethoxybenzoic Acid Ethyl Ester
NSC26825
ethyltrimethoxy benzoate
CHEMBL501163
SCHEMBL4410910
DTXSID50282612
CHEBI:165215
Ethyl 3,4,5-trimethoxybenzoate;
AMY32800
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 3,4,5-Trimethoxybenzoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9934 99.34%
Caco-2 + 0.8786 87.86%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.8847 88.47%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9405 94.05%
OATP1B3 inhibitior + 0.9755 97.55%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7264 72.64%
P-glycoprotein inhibitior - 0.9237 92.37%
P-glycoprotein substrate - 0.9648 96.48%
CYP3A4 substrate - 0.5984 59.84%
CYP2C9 substrate - 0.6643 66.43%
CYP2D6 substrate - 0.8096 80.96%
CYP3A4 inhibition - 0.8884 88.84%
CYP2C9 inhibition - 0.7998 79.98%
CYP2C19 inhibition - 0.6687 66.87%
CYP2D6 inhibition - 0.9548 95.48%
CYP1A2 inhibition + 0.5883 58.83%
CYP2C8 inhibition + 0.5437 54.37%
CYP inhibitory promiscuity - 0.5620 56.20%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7243 72.43%
Carcinogenicity (trinary) Non-required 0.6443 64.43%
Eye corrosion - 0.8675 86.75%
Eye irritation + 0.9701 97.01%
Skin irritation - 0.7715 77.15%
Skin corrosion - 0.9854 98.54%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5255 52.55%
Micronuclear - 0.6705 67.05%
Hepatotoxicity + 0.5090 50.90%
skin sensitisation - 0.7408 74.08%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity + 0.5836 58.36%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity - 0.7925 79.25%
Acute Oral Toxicity (c) III 0.7533 75.33%
Estrogen receptor binding + 0.5794 57.94%
Androgen receptor binding - 0.7961 79.61%
Thyroid receptor binding - 0.6345 63.45%
Glucocorticoid receptor binding - 0.7404 74.04%
Aromatase binding + 0.5598 55.98%
PPAR gamma - 0.8552 85.52%
Honey bee toxicity - 0.9596 95.96%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.7287 72.87%
Fish aquatic toxicity + 0.9418 94.18%

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 94.84% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.99% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.81% 86.33%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 89.33% 97.21%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.74% 96.95%
CHEMBL2535 P11166 Glucose transporter 87.24% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.35% 96.00%
CHEMBL4208 P20618 Proteasome component C5 84.36% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.52% 94.00%

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.
Aronia arbutifolia
Clibadium sodiroi
Discaria serratifolia
Pteris dactylina
Pyrostegia venusta
Rostellularia hayatae
Silene viscaria

Cross-Links

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PubChem 231162
NPASS NPC288743