methyl 3-O-beta-glucopyranosyl-gallate

Details

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Internal ID 14916147-5b72-4ce0-a2d4-995f675f010c
Taxonomy Phenylpropanoids and polyketides > Tannins > Hydrolyzable tannins
IUPAC Name methyl 3,4-dihydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoate
SMILES (Canonical) COC(=O)C1=CC(=C(C(=C1)OC2C(C(C(C(O2)CO)O)O)O)O)O
SMILES (Isomeric) COC(=O)C1=CC(=C(C(=C1)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)O)O
InChI InChI=1S/C14H18O10/c1-22-13(21)5-2-6(16)9(17)7(3-5)23-14-12(20)11(19)10(18)8(4-15)24-14/h2-3,8,10-12,14-20H,4H2,1H3/t8-,10-,11+,12-,14-/m1/s1
InChI Key HVFHEQBFSAYLMY-RRZLQCMWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C14H18O10
Molecular Weight 346.29 g/mol
Exact Mass 346.08999677 g/mol
Topological Polar Surface Area (TPSA) 166.00 Ų
XlogP -1.30
Atomic LogP (AlogP) -1.94
H-Bond Acceptor 10
H-Bond Donor 6
Rotatable Bonds 4

Synonyms

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methyl 3-O-beta-glucopyranosyl-gallate
3,4-Dihydroxy-5-(beta-D-glucopyranosyloxy)benzoic acid methyl ester

2D Structure

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2D Structure of methyl 3-O-beta-glucopyranosyl-gallate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7149 71.49%
Caco-2 - 0.9318 93.18%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6648 66.48%
OATP2B1 inhibitior - 0.8578 85.78%
OATP1B1 inhibitior + 0.6965 69.65%
OATP1B3 inhibitior + 0.9586 95.86%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9391 93.91%
P-glycoprotein inhibitior - 0.9402 94.02%
P-glycoprotein substrate - 0.9062 90.62%
CYP3A4 substrate + 0.5170 51.70%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8557 85.57%
CYP3A4 inhibition - 0.8632 86.32%
CYP2C9 inhibition - 0.8775 87.75%
CYP2C19 inhibition - 0.9154 91.54%
CYP2D6 inhibition - 0.9346 93.46%
CYP1A2 inhibition - 0.8980 89.80%
CYP2C8 inhibition - 0.5747 57.47%
CYP inhibitory promiscuity - 0.7229 72.29%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7412 74.12%
Eye corrosion - 0.9872 98.72%
Eye irritation - 0.7754 77.54%
Skin irritation - 0.8102 81.02%
Skin corrosion - 0.9609 96.09%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5615 56.15%
Micronuclear - 0.5067 50.67%
Hepatotoxicity - 0.7500 75.00%
skin sensitisation - 0.8743 87.43%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.7406 74.06%
Acute Oral Toxicity (c) III 0.7844 78.44%
Estrogen receptor binding - 0.5172 51.72%
Androgen receptor binding - 0.6943 69.43%
Thyroid receptor binding - 0.6230 62.30%
Glucocorticoid receptor binding - 0.4813 48.13%
Aromatase binding - 0.5643 56.43%
PPAR gamma - 0.6694 66.94%
Honey bee toxicity - 0.9075 90.75%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity - 0.5277 52.77%

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 99.15% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.11% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.48% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 90.42% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.84% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.93% 86.33%
CHEMBL3194 P02766 Transthyretin 84.21% 90.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.18% 96.00%
CHEMBL4208 P20618 Proteasome component C5 84.10% 90.00%
CHEMBL2581 P07339 Cathepsin D 82.43% 98.95%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.73% 94.33%
CHEMBL5255 O00206 Toll-like receptor 4 80.72% 92.50%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.08% 90.71%

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.
Carpinus cordata
Rosa davurica

Cross-Links

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PubChem 14425702
NPASS NPC105827
LOTUS LTS0035438
wikiData Q105034213