5,5'-(Ethane-1,2-diyl)bis(3-bromobenzene-1,2-diol)

Details

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Internal ID 560514b2-d129-423c-83f0-59186bab3aca
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name 3-bromo-5-[2-(3-bromo-4,5-dihydroxyphenyl)ethyl]benzene-1,2-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H12Br2O4/c15-9-3-7(5-11(17)13(9)19)1-2-8-4-10(16)14(20)12(18)6-8/h3-6,17-20H,1-2H2
InChI Key IFYFPCNWTZBOEQ-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C14H12Br2O4
Molecular Weight 404.05 g/mol
Exact Mass 403.90818 g/mol
Topological Polar Surface Area (TPSA) 80.90 Ų
XlogP 4.10
Atomic LogP (AlogP) 3.82
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 3

Synonyms

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5,5'-(ethane-1,2-diyl)bis(3-bromobenzene-1,2-diol)
CHEMBL241792
Q27137765

2D Structure

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2D Structure of 5,5'-(Ethane-1,2-diyl)bis(3-bromobenzene-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 + 0.8736 87.36%
Caco-2 - 0.6507 65.07%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.8414 84.14%
OATP2B1 inhibitior - 0.5558 55.58%
OATP1B1 inhibitior + 0.8948 89.48%
OATP1B3 inhibitior + 0.9286 92.86%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.4872 48.72%
P-glycoprotein inhibitior - 0.9340 93.40%
P-glycoprotein substrate - 0.9609 96.09%
CYP3A4 substrate - 0.7102 71.02%
CYP2C9 substrate - 0.8012 80.12%
CYP2D6 substrate + 0.3716 37.16%
CYP3A4 inhibition - 0.6500 65.00%
CYP2C9 inhibition + 0.8732 87.32%
CYP2C19 inhibition + 0.6819 68.19%
CYP2D6 inhibition - 0.8467 84.67%
CYP1A2 inhibition + 0.7680 76.80%
CYP2C8 inhibition - 0.7523 75.23%
CYP inhibitory promiscuity + 0.6706 67.06%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6263 62.63%
Carcinogenicity (trinary) Non-required 0.4674 46.74%
Eye corrosion - 0.9097 90.97%
Eye irritation + 0.9661 96.61%
Skin irritation - 0.6078 60.78%
Skin corrosion - 0.9044 90.44%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4453 44.53%
Micronuclear - 0.5341 53.41%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation + 0.5554 55.54%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.9180 91.80%
Acute Oral Toxicity (c) III 0.6929 69.29%
Estrogen receptor binding + 0.7148 71.48%
Androgen receptor binding + 0.8389 83.89%
Thyroid receptor binding + 0.6930 69.30%
Glucocorticoid receptor binding + 0.7155 71.55%
Aromatase binding + 0.7205 72.05%
PPAR gamma + 0.8539 85.39%
Honey bee toxicity - 0.9488 94.88%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9875 98.75%

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 98.32% 91.11%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 89.55% 95.17%
CHEMBL2581 P07339 Cathepsin D 83.55% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.51% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.51% 99.15%
CHEMBL4208 P20618 Proteasome component C5 81.86% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.34% 96.09%
CHEMBL3194 P02766 Transthyretin 81.13% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.08% 86.33%

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 44437166
LOTUS LTS0183815
wikiData Q27137765