3,4,5-Trihydroxybenzyl methyl ether

Details

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Internal ID f70b0585-e339-4fda-ae27-dc125dc3edea
Taxonomy Benzenoids > Phenols > Benzenetriols and derivatives > Pyrogallols and derivatives
IUPAC Name 5-(methoxymethyl)benzene-1,2,3-triol
SMILES (Canonical) COCC1=CC(=C(C(=C1)O)O)O
SMILES (Isomeric) COCC1=CC(=C(C(=C1)O)O)O
InChI InChI=1S/C8H10O4/c1-12-4-5-2-6(9)8(11)7(10)3-5/h2-3,9-11H,4H2,1H3
InChI Key YAXUEWSAEFZPFJ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C8H10O4
Molecular Weight 170.16 g/mol
Exact Mass 170.05790880 g/mol
Topological Polar Surface Area (TPSA) 69.90 Ų
XlogP 0.50
Atomic LogP (AlogP) 0.95
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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SCHEMBL24614011
5-(Methoxymethyl)-1,2,3-benzenetriol
Q63396095

2D Structure

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2D Structure of 3,4,5-Trihydroxybenzyl methyl ether

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7815 78.15%
Caco-2 + 0.6882 68.82%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7683 76.83%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8821 88.21%
OATP1B3 inhibitior + 0.9691 96.91%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9377 93.77%
P-glycoprotein inhibitior - 0.9763 97.63%
P-glycoprotein substrate - 0.9668 96.68%
CYP3A4 substrate - 0.6813 68.13%
CYP2C9 substrate - 0.7945 79.45%
CYP2D6 substrate - 0.6819 68.19%
CYP3A4 inhibition - 0.7896 78.96%
CYP2C9 inhibition - 0.7595 75.95%
CYP2C19 inhibition - 0.8341 83.41%
CYP2D6 inhibition - 0.8363 83.63%
CYP1A2 inhibition + 0.5433 54.33%
CYP2C8 inhibition - 0.6388 63.88%
CYP inhibitory promiscuity - 0.7861 78.61%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8423 84.23%
Carcinogenicity (trinary) Non-required 0.6596 65.96%
Eye corrosion - 0.9387 93.87%
Eye irritation + 0.9687 96.87%
Skin irritation - 0.6432 64.32%
Skin corrosion - 0.8478 84.78%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5623 56.23%
Micronuclear - 0.6345 63.45%
Hepatotoxicity - 0.6875 68.75%
skin sensitisation + 0.5774 57.74%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.5359 53.59%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.7029 70.29%
Acute Oral Toxicity (c) III 0.7522 75.22%
Estrogen receptor binding + 0.6569 65.69%
Androgen receptor binding + 0.7946 79.46%
Thyroid receptor binding - 0.7126 71.26%
Glucocorticoid receptor binding - 0.6087 60.87%
Aromatase binding - 0.7357 73.57%
PPAR gamma - 0.5642 56.42%
Honey bee toxicity - 0.9605 96.05%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.7842 78.42%

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 97.31% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.30% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.22% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.97% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.10% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.15% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 85.66% 94.73%
CHEMBL4208 P20618 Proteasome component C5 85.51% 90.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.20% 99.15%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.45% 96.95%

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.
Glycyrrhiza glabra
Piper nigrum

Cross-Links

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PubChem 14261265
NPASS NPC170247
LOTUS LTS0114462
wikiData Q63396095