2,3-Dibromophenol

Details

Top
Internal ID bf476dda-0799-4071-b4a1-deb10360f632
Taxonomy Benzenoids > Phenols > Halophenols > Bromophenols > O-bromophenols
IUPAC Name 2,3-dibromophenol
SMILES (Canonical) C1=CC(=C(C(=C1)Br)Br)O
SMILES (Isomeric) C1=CC(=C(C(=C1)Br)Br)O
InChI InChI=1S/C6H4Br2O/c7-4-2-1-3-5(9)6(4)8/h1-3,9H
InChI Key FNAKEOXYWBWIRT-UHFFFAOYSA-N
Popularity 101 references in papers

Physical and Chemical Properties

Top
Molecular Formula C6H4Br2O
Molecular Weight 251.90 g/mol
Exact Mass 251.86084 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.92
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

Top
57383-80-9
DIBROMOPHENOL
28514-45-6
dibromo-phenol
2,3-Dibromophenol, 95%
SCHEMBL386016
FNAKEOXYWBWIRT-UHFFFAOYSA-N
DTXSID501334116
MFCD08166474
AKOS024168482
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of 2,3-Dibromophenol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9953 99.53%
Caco-2 + 0.8558 85.58%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.7986 79.86%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9699 96.99%
OATP1B3 inhibitior + 0.9519 95.19%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9319 93.19%
P-glycoprotein inhibitior - 0.9865 98.65%
P-glycoprotein substrate - 0.9843 98.43%
CYP3A4 substrate - 0.7589 75.89%
CYP2C9 substrate - 0.6786 67.86%
CYP2D6 substrate - 0.6944 69.44%
CYP3A4 inhibition - 0.8567 85.67%
CYP2C9 inhibition + 0.5000 50.00%
CYP2C19 inhibition + 0.5634 56.34%
CYP2D6 inhibition - 0.9386 93.86%
CYP1A2 inhibition + 0.8452 84.52%
CYP2C8 inhibition - 0.7849 78.49%
CYP inhibitory promiscuity - 0.6483 64.83%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.5626 56.26%
Carcinogenicity (trinary) Non-required 0.5232 52.32%
Eye corrosion + 0.9873 98.73%
Eye irritation + 0.9957 99.57%
Skin irritation + 0.9251 92.51%
Skin corrosion + 0.9186 91.86%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8032 80.32%
Micronuclear - 0.6651 66.51%
Hepatotoxicity + 0.9250 92.50%
skin sensitisation + 0.9120 91.20%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity + 0.9392 93.92%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity - 0.6576 65.76%
Acute Oral Toxicity (c) III 0.5271 52.71%
Estrogen receptor binding - 0.6168 61.68%
Androgen receptor binding - 0.8426 84.26%
Thyroid receptor binding - 0.6976 69.76%
Glucocorticoid receptor binding - 0.7656 76.56%
Aromatase binding - 0.8806 88.06%
PPAR gamma - 0.7070 70.70%
Honey bee toxicity - 0.9766 97.66%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9565 95.65%

Targets

Top

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 95.03% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.07% 95.56%
CHEMBL3959 P16083 Quinone reductase 2 87.72% 89.49%
CHEMBL2581 P07339 Cathepsin D 85.97% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.54% 93.99%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.06% 99.15%
CHEMBL3401 O75469 Pregnane X receptor 80.97% 94.73%

Plants that contains it

Top
Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
There are no matching plants.

Cross-Links

Top
PubChem 34264
LOTUS LTS0013031
wikiData Q209166