2,4,6-Tribromoanisole

Details

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Internal ID 2a4cb452-74ba-424b-a86d-fc9bd266da16
Taxonomy Benzenoids > Phenol ethers > Anisoles
IUPAC Name 1,3,5-tribromo-2-methoxybenzene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H5Br3O/c1-11-7-5(9)2-4(8)3-6(7)10/h2-3H,1H3
InChI Key YXTRCOAFNXQTKL-UHFFFAOYSA-N
Popularity 157 references in papers

Physical and Chemical Properties

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Molecular Formula C7H5Br3O
Molecular Weight 344.83 g/mol
Exact Mass 343.78700 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.98
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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607-99-8
1,3,5-Tribromo-2-methoxybenzene
Anisole, 2,4,6-tribromo-
Benzene, 1,3,5-tribromo-2-methoxy-
1,3,5-tribromo-2-methoxy-benzene
Methyl 2,4,6-tribromophenyl ether
DO7M3M4LX5
NSC-2218
MFCD00192510
1219795-33-1
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,4,6-Tribromoanisole

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9970 99.70%
Caco-2 + 0.7528 75.28%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.8714 87.14%
Subcellular localzation Mitochondria 0.7777 77.77%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9630 96.30%
OATP1B3 inhibitior + 0.9756 97.56%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8470 84.70%
P-glycoprotein inhibitior - 0.9827 98.27%
P-glycoprotein substrate - 0.9860 98.60%
CYP3A4 substrate - 0.7253 72.53%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3969 39.69%
CYP3A4 inhibition - 0.9048 90.48%
CYP2C9 inhibition - 0.6305 63.05%
CYP2C19 inhibition + 0.7231 72.31%
CYP2D6 inhibition - 0.9035 90.35%
CYP1A2 inhibition + 0.8999 89.99%
CYP2C8 inhibition - 0.9125 91.25%
CYP inhibitory promiscuity + 0.5326 53.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5466 54.66%
Carcinogenicity (trinary) Warning 0.5534 55.34%
Eye corrosion + 0.9165 91.65%
Eye irritation + 0.9706 97.06%
Skin irritation + 0.5050 50.50%
Skin corrosion - 0.6269 62.69%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6301 63.01%
Micronuclear - 0.7610 76.10%
Hepatotoxicity + 0.6034 60.34%
skin sensitisation + 0.6022 60.22%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity - 0.8227 82.27%
Acute Oral Toxicity (c) III 0.7963 79.63%
Estrogen receptor binding + 0.5351 53.51%
Androgen receptor binding - 0.8486 84.86%
Thyroid receptor binding - 0.6524 65.24%
Glucocorticoid receptor binding - 0.7771 77.71%
Aromatase binding - 0.8591 85.91%
PPAR gamma - 0.6263 62.63%
Honey bee toxicity - 0.9353 93.53%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.8300 83.00%
Fish aquatic toxicity + 0.9449 94.49%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.75% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.72% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.58% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.94% 94.00%
CHEMBL2487 P05067 Beta amyloid A4 protein 80.74% 96.74%
CHEMBL4208 P20618 Proteasome component C5 80.24% 90.00%

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 11839
LOTUS LTS0087101
wikiData Q4596770