Ethyl gallic acid

Details

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Internal ID 52e86d0d-2038-470b-b9c5-2a33c2a07840
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Hydroxybenzoic acid derivatives > Gallic acid and derivatives > Gallic acids
IUPAC Name 2-ethyl-3,4,5-trihydroxybenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H10O5/c1-2-4-5(9(13)14)3-6(10)8(12)7(4)11/h3,10-12H,2H2,1H3,(H,13,14)
InChI Key CBQRQDRSNAPJKD-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C9H10O5
Molecular Weight 198.17 g/mol
Exact Mass 198.05282342 g/mol
Topological Polar Surface Area (TPSA) 98.00 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.06
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 2

Synonyms

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SCHEMBL39598

2D Structure

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2D Structure of Ethyl gallic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8425 84.25%
Caco-2 - 0.6894 68.94%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.7973 79.73%
OATP2B1 inhibitior - 0.8483 84.83%
OATP1B1 inhibitior + 0.8284 82.84%
OATP1B3 inhibitior + 0.9715 97.15%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9714 97.14%
P-glycoprotein inhibitior - 0.9678 96.78%
P-glycoprotein substrate - 0.9698 96.98%
CYP3A4 substrate - 0.8095 80.95%
CYP2C9 substrate - 0.8074 80.74%
CYP2D6 substrate - 0.8898 88.98%
CYP3A4 inhibition - 0.8417 84.17%
CYP2C9 inhibition - 0.8507 85.07%
CYP2C19 inhibition - 0.9227 92.27%
CYP2D6 inhibition - 0.9405 94.05%
CYP1A2 inhibition - 0.8770 87.70%
CYP2C8 inhibition - 0.8588 85.88%
CYP inhibitory promiscuity - 0.8730 87.30%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7823 78.23%
Carcinogenicity (trinary) Non-required 0.7344 73.44%
Eye corrosion - 0.9368 93.68%
Eye irritation + 0.8594 85.94%
Skin irritation + 0.6458 64.58%
Skin corrosion - 0.6647 66.47%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6826 68.26%
Micronuclear + 0.6359 63.59%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation + 0.6489 64.89%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.7859 78.59%
Acute Oral Toxicity (c) III 0.7269 72.69%
Estrogen receptor binding - 0.6652 66.52%
Androgen receptor binding + 0.6008 60.08%
Thyroid receptor binding - 0.8572 85.72%
Glucocorticoid receptor binding + 0.5531 55.31%
Aromatase binding - 0.7935 79.35%
PPAR gamma - 0.7001 70.01%
Honey bee toxicity - 0.9933 99.33%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.8800 88.00%
Fish aquatic toxicity + 0.9567 95.67%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.33% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.37% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.90% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.49% 99.17%
CHEMBL1811 P34995 Prostanoid EP1 receptor 83.85% 95.71%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 83.75% 94.42%
CHEMBL3194 P02766 Transthyretin 83.71% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.02% 95.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.86% 96.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.02% 89.34%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.24% 86.33%

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.
Dimocarpus longan

Cross-Links

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PubChem 21617649
LOTUS LTS0101718
wikiData Q104952650