3-Methoxy-5-methylbenzene-1,2-diol

Details

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Internal ID 49f5aea3-8f62-4f8e-a696-bd28e9af2239
Taxonomy Benzenoids > Phenols > Methoxyphenols
IUPAC Name 3-methoxy-5-methylbenzene-1,2-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H10O3/c1-5-3-6(9)8(10)7(4-5)11-2/h3-4,9-10H,1-2H3
InChI Key FALWUVSXNUUXQA-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C8H10O3
Molecular Weight 154.16 g/mol
Exact Mass 154.062994177 g/mol
Topological Polar Surface Area (TPSA) 49.70 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.41
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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1125-67-3
3-Methoxy-5-methylbenzene-1,2-diol
SCHEMBL10053939
DTXSID40503621
3-Methoxy-5-methylbenyene-1,2-diol
EN300-1599501

2D Structure

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2D Structure of 3-Methoxy-5-methylbenzene-1,2-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9801 98.01%
Caco-2 - 0.5562 55.62%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.8590 85.90%
OATP2B1 inhibitior - 0.8646 86.46%
OATP1B1 inhibitior + 0.9177 91.77%
OATP1B3 inhibitior + 0.9843 98.43%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9354 93.54%
P-glycoprotein inhibitior - 0.9665 96.65%
P-glycoprotein substrate - 0.9774 97.74%
CYP3A4 substrate - 0.6982 69.82%
CYP2C9 substrate - 0.7664 76.64%
CYP2D6 substrate + 0.3565 35.65%
CYP3A4 inhibition - 0.9564 95.64%
CYP2C9 inhibition - 0.9441 94.41%
CYP2C19 inhibition - 0.8355 83.55%
CYP2D6 inhibition - 0.9450 94.50%
CYP1A2 inhibition - 0.6528 65.28%
CYP2C8 inhibition - 0.7333 73.33%
CYP inhibitory promiscuity - 0.8049 80.49%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7690 76.90%
Carcinogenicity (trinary) Non-required 0.4813 48.13%
Eye corrosion + 0.7335 73.35%
Eye irritation + 0.9879 98.79%
Skin irritation + 0.8028 80.28%
Skin corrosion + 0.5338 53.38%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6810 68.10%
Micronuclear + 0.6100 61.00%
Hepatotoxicity + 0.5781 57.81%
skin sensitisation + 0.7217 72.17%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity - 0.6519 65.19%
Acute Oral Toxicity (c) III 0.8477 84.77%
Estrogen receptor binding - 0.5542 55.42%
Androgen receptor binding - 0.6693 66.93%
Thyroid receptor binding - 0.7331 73.31%
Glucocorticoid receptor binding - 0.8234 82.34%
Aromatase binding - 0.8294 82.94%
PPAR gamma - 0.7079 70.79%
Honey bee toxicity - 0.9663 96.63%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.7685 76.85%

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 96.31% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.59% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.32% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.66% 94.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 83.66% 92.94%
CHEMBL3194 P02766 Transthyretin 82.72% 90.71%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.27% 99.15%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 81.52% 98.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.36% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.68% 99.17%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 12591329
LOTUS LTS0265654
wikiData Q77569807