3-Bromo-4-hydroxybenzyl methyl ether

Details

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Internal ID 585786cd-9a15-4ed4-ad97-198aeb33114b
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzylethers
IUPAC Name 2-bromo-4-(methoxymethyl)phenol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H9BrO2/c1-11-5-6-2-3-8(10)7(9)4-6/h2-4,10H,5H2,1H3
InChI Key ZRBQVZHDXOUSOX-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C8H9BrO2
Molecular Weight 217.06 g/mol
Exact Mass 215.97859 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.30
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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3-bromo-4-hydroxybenzyl methyl ether

2D Structure

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2D Structure of 3-Bromo-4-hydroxybenzyl 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 + 0.9954 99.54%
Caco-2 + 0.8566 85.66%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8519 85.19%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9380 93.80%
OATP1B3 inhibitior + 0.9489 94.89%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9231 92.31%
P-glycoprotein inhibitior - 0.9882 98.82%
P-glycoprotein substrate - 0.9576 95.76%
CYP3A4 substrate - 0.6524 65.24%
CYP2C9 substrate - 0.7945 79.45%
CYP2D6 substrate - 0.6690 66.90%
CYP3A4 inhibition - 0.8326 83.26%
CYP2C9 inhibition - 0.7815 78.15%
CYP2C19 inhibition + 0.5467 54.67%
CYP2D6 inhibition - 0.7941 79.41%
CYP1A2 inhibition + 0.7955 79.55%
CYP2C8 inhibition + 0.5136 51.36%
CYP inhibitory promiscuity - 0.6613 66.13%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.5949 59.49%
Carcinogenicity (trinary) Non-required 0.5115 51.15%
Eye corrosion - 0.6341 63.41%
Eye irritation + 0.9790 97.90%
Skin irritation - 0.6490 64.90%
Skin corrosion - 0.8555 85.55%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7149 71.49%
Micronuclear - 0.8035 80.35%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation + 0.6536 65.36%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity - 0.7026 70.26%
Acute Oral Toxicity (c) III 0.6490 64.90%
Estrogen receptor binding - 0.5101 51.01%
Androgen receptor binding + 0.7080 70.80%
Thyroid receptor binding - 0.7657 76.57%
Glucocorticoid receptor binding - 0.7815 78.15%
Aromatase binding - 0.7385 73.85%
PPAR gamma - 0.7358 73.58%
Honey bee toxicity - 0.9093 90.93%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9173 91.73%

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 96.52% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.17% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.90% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.83% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.76% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.17% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.00% 94.00%
CHEMBL4208 P20618 Proteasome component C5 86.88% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.95% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.52% 95.56%
CHEMBL3492 P49721 Proteasome Macropain subunit 80.08% 90.24%

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 13651772
LOTUS LTS0139163
wikiData Q105381874