Trigallic Acid

Details

Top
Internal ID f852cfee-bb6a-45e8-8fb4-52edd14e7927
Taxonomy Phenylpropanoids and polyketides > Depsides and depsidones
IUPAC Name 3-[3,4-dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxybenzoyl]oxy-4,5-dihydroxybenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H14O13/c22-10-2-8(3-11(23)16(10)26)20(31)34-15-6-9(4-13(25)18(15)28)21(32)33-14-5-7(19(29)30)1-12(24)17(14)27/h1-6,22-28H,(H,29,30)
InChI Key QUXNYZHQBWMPNX-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C21H14O13
Molecular Weight 474.30 g/mol
Exact Mass 474.04344050 g/mol
Topological Polar Surface Area (TPSA) 232.00 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.76
H-Bond Acceptor 12
H-Bond Donor 8
Rotatable Bonds 5

Synonyms

Top
m-Trigallic acid
2131-66-0
3-[3,4-dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxybenzoyl]oxy-4,5-dihydroxybenzoic acid
Metatrigallic acid
6HV67CW76G
SCHEMBL21584439
CHEBI:184664
DTXSID501317275
Gallic acid, 3-gallate, 3-gallate
Gallic acid, 3-ester with gallic acid, 3-gallate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Trigallic Acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8395 83.95%
Caco-2 - 0.9004 90.04%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7505 75.05%
OATP2B1 inhibitior + 0.7094 70.94%
OATP1B1 inhibitior + 0.9039 90.39%
OATP1B3 inhibitior + 0.8776 87.76%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6188 61.88%
P-glycoprotein inhibitior - 0.4508 45.08%
P-glycoprotein substrate - 0.9735 97.35%
CYP3A4 substrate - 0.7128 71.28%
CYP2C9 substrate - 0.7828 78.28%
CYP2D6 substrate - 0.8795 87.95%
CYP3A4 inhibition - 0.8888 88.88%
CYP2C9 inhibition - 0.7862 78.62%
CYP2C19 inhibition - 0.9570 95.70%
CYP2D6 inhibition - 0.9534 95.34%
CYP1A2 inhibition - 0.8010 80.10%
CYP2C8 inhibition - 0.5607 56.07%
CYP inhibitory promiscuity - 0.8663 86.63%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7997 79.97%
Carcinogenicity (trinary) Non-required 0.6780 67.80%
Eye corrosion - 0.9930 99.30%
Eye irritation + 0.5461 54.61%
Skin irritation - 0.5441 54.41%
Skin corrosion - 0.9097 90.97%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4113 41.13%
Micronuclear + 0.8100 81.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation - 0.5438 54.38%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.7730 77.30%
Acute Oral Toxicity (c) III 0.8285 82.85%
Estrogen receptor binding + 0.8130 81.30%
Androgen receptor binding + 0.7205 72.05%
Thyroid receptor binding + 0.5388 53.88%
Glucocorticoid receptor binding + 0.6275 62.75%
Aromatase binding - 0.6429 64.29%
PPAR gamma + 0.6590 65.90%
Honey bee toxicity - 0.8304 83.04%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7650 76.50%
Fish aquatic toxicity + 0.9902 99.02%

Targets

Top

Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL1828 P09884 DNA polymerase alpha subunit 830 nM
Ki
via Super-PRED
CHEMBL2392 P06746 DNA polymerase beta 390 nM
Ki
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3194 P02766 Transthyretin 97.32% 90.71%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.64% 91.11%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 88.22% 94.42%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.71% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.48% 99.17%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 83.45% 81.11%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.83% 95.50%
CHEMBL1255126 O15151 Protein Mdm4 82.81% 90.20%
CHEMBL1811 P34995 Prostanoid EP1 receptor 82.79% 95.71%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.41% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.26% 97.21%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 80.65% 87.67%

Plants that contains it

Top
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.
Quercus infectoria

Cross-Links

Top
PubChem 90470472
LOTUS LTS0131145
wikiData Q104393629