3,4-Dibromo-5-((methylsulfonyl)methyl)benzene-1,2-diol

Details

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Internal ID e7eb69d7-925b-434b-9abe-5a8db452cd57
Taxonomy Benzenoids > Phenols > Benzenediols > Catechols
IUPAC Name 3,4-dibromo-5-(methylsulfonylmethyl)benzene-1,2-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H8Br2O4S/c1-15(13,14)3-4-2-5(11)8(12)7(10)6(4)9/h2,11-12H,3H2,1H3
InChI Key BYDYQRLHNMDRJE-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C8H8Br2O4S
Molecular Weight 360.02 g/mol
Exact Mass 359.84896 g/mol
Topological Polar Surface Area (TPSA) 83.00 Ų
XlogP 1.80
Atomic LogP (AlogP) 2.17
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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SCHEMBL27746750
BDBM50589082
3,4-dibromo-5-((methylsulfonyl)methyl)benzene-1,2-diol

2D Structure

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2D Structure of 3,4-Dibromo-5-((methylsulfonyl)methyl)benzene-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 + 0.9037 90.37%
Caco-2 + 0.6005 60.05%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.6554 65.54%
OATP2B1 inhibitior - 0.8583 85.83%
OATP1B1 inhibitior + 0.8752 87.52%
OATP1B3 inhibitior + 0.9413 94.13%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8679 86.79%
P-glycoprotein inhibitior - 0.9658 96.58%
P-glycoprotein substrate - 0.9513 95.13%
CYP3A4 substrate - 0.6513 65.13%
CYP2C9 substrate - 0.6141 61.41%
CYP2D6 substrate - 0.7510 75.10%
CYP3A4 inhibition - 0.8666 86.66%
CYP2C9 inhibition - 0.6771 67.71%
CYP2C19 inhibition - 0.6456 64.56%
CYP2D6 inhibition - 0.8761 87.61%
CYP1A2 inhibition - 0.5836 58.36%
CYP2C8 inhibition - 0.9206 92.06%
CYP inhibitory promiscuity - 0.8258 82.58%
UGT catelyzed + 0.7362 73.62%
Carcinogenicity (binary) + 0.5242 52.42%
Carcinogenicity (trinary) Non-required 0.5989 59.89%
Eye corrosion - 0.9104 91.04%
Eye irritation + 0.8421 84.21%
Skin irritation - 0.7641 76.41%
Skin corrosion - 0.8512 85.12%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7136 71.36%
Micronuclear + 0.6681 66.81%
Hepatotoxicity + 0.6930 69.30%
skin sensitisation - 0.7692 76.92%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.5853 58.53%
Acute Oral Toxicity (c) III 0.5678 56.78%
Estrogen receptor binding - 0.6114 61.14%
Androgen receptor binding - 0.5774 57.74%
Thyroid receptor binding - 0.7638 76.38%
Glucocorticoid receptor binding - 0.5318 53.18%
Aromatase binding - 0.8890 88.90%
PPAR gamma - 0.5998 59.98%
Honey bee toxicity - 0.9141 91.41%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9788 97.88%

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 97.57% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.62% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 92.59% 94.73%
CHEMBL2581 P07339 Cathepsin D 89.78% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.87% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.22% 94.00%

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 54589802
LOTUS LTS0219462
wikiData Q104949168