2-(2,3-Dibromo-4,5-dihydroxyphenyl)ethyl hydrogen sulfate

Details

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Internal ID 28b41273-11a7-4678-bba4-02fafd34937f
Taxonomy Benzenoids > Phenols > Tyrosols and derivatives
IUPAC Name 2-(2,3-dibromo-4,5-dihydroxyphenyl)ethyl hydrogen sulfate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H8Br2O6S/c9-6-4(1-2-16-17(13,14)15)3-5(11)8(12)7(6)10/h3,11-12H,1-2H2,(H,13,14,15)
InChI Key IVDRMONUQOVGSF-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C8H8Br2O6S
Molecular Weight 392.02 g/mol
Exact Mass 391.83878 g/mol
Topological Polar Surface Area (TPSA) 112.00 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.98
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(2,3-Dibromo-4,5-dihydroxyphenyl)ethyl hydrogen sulfate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7678 76.78%
Caco-2 - 0.5771 57.71%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.7498 74.98%
OATP2B1 inhibitior - 0.8515 85.15%
OATP1B1 inhibitior + 0.9114 91.14%
OATP1B3 inhibitior + 0.9406 94.06%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8619 86.19%
P-glycoprotein inhibitior - 0.9670 96.70%
P-glycoprotein substrate - 0.9475 94.75%
CYP3A4 substrate - 0.5615 56.15%
CYP2C9 substrate - 0.8054 80.54%
CYP2D6 substrate - 0.7341 73.41%
CYP3A4 inhibition - 0.9799 97.99%
CYP2C9 inhibition - 0.7369 73.69%
CYP2C19 inhibition - 0.7275 72.75%
CYP2D6 inhibition - 0.8930 89.30%
CYP1A2 inhibition - 0.6288 62.88%
CYP2C8 inhibition - 0.7364 73.64%
CYP inhibitory promiscuity - 0.8177 81.77%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) + 0.5504 55.04%
Carcinogenicity (trinary) Non-required 0.5574 55.74%
Eye corrosion - 0.9205 92.05%
Eye irritation + 0.8319 83.19%
Skin irritation - 0.7379 73.79%
Skin corrosion - 0.7576 75.76%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7039 70.39%
Micronuclear + 0.7318 73.18%
Hepatotoxicity + 0.6231 62.31%
skin sensitisation - 0.7462 74.62%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.7311 73.11%
Acute Oral Toxicity (c) III 0.6384 63.84%
Estrogen receptor binding + 0.7168 71.68%
Androgen receptor binding + 0.6030 60.30%
Thyroid receptor binding - 0.6489 64.89%
Glucocorticoid receptor binding - 0.6035 60.35%
Aromatase binding - 0.7793 77.93%
PPAR gamma + 0.5547 55.47%
Honey bee toxicity - 0.8161 81.61%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9802 98.02%

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 98.36% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 91.25% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.86% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.42% 95.56%
CHEMBL2581 P07339 Cathepsin D 86.03% 98.95%
CHEMBL3194 P02766 Transthyretin 84.24% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.12% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.76% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.30% 99.15%

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 11502039
LOTUS LTS0009387
wikiData Q105120982