3-Bromo-4-hydroxybenzoic acid

Details

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Internal ID 1028b114-4041-4a88-9107-e5ea624dc580
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Hydroxybenzoic acid derivatives
IUPAC Name 3-bromo-4-hydroxybenzoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H5BrO3/c8-5-3-4(7(10)11)1-2-6(5)9/h1-3,9H,(H,10,11)
InChI Key XMEQDAIDOBVHEK-UHFFFAOYSA-N
Popularity 25 references in papers

Physical and Chemical Properties

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Molecular Formula C7H5BrO3
Molecular Weight 217.02 g/mol
Exact Mass 215.94221 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.85
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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14348-41-5
EINECS 238-299-7
CHEBI:140241
DTXSID90931899
RefChem:93166
DTXCID701360599
238-299-7
MFCD00017547
3-BROMO-4-HYDROXYBENZOIC ACID HYDRATE
3-bromo-4-hydroxy-benzoic acid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Bromo-4-hydroxybenzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9930 99.30%
Caco-2 + 0.6713 67.13%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.9079 90.79%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9689 96.89%
OATP1B3 inhibitior + 0.9505 95.05%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9744 97.44%
P-glycoprotein inhibitior - 0.9864 98.64%
P-glycoprotein substrate - 0.9938 99.38%
CYP3A4 substrate - 0.8083 80.83%
CYP2C9 substrate - 0.8120 81.20%
CYP2D6 substrate - 0.8684 86.84%
CYP3A4 inhibition - 0.9003 90.03%
CYP2C9 inhibition - 0.6453 64.53%
CYP2C19 inhibition - 0.8616 86.16%
CYP2D6 inhibition - 0.9650 96.50%
CYP1A2 inhibition - 0.8288 82.88%
CYP2C8 inhibition - 0.7760 77.60%
CYP inhibitory promiscuity - 0.8783 87.83%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.6062 60.62%
Carcinogenicity (trinary) Non-required 0.5273 52.73%
Eye corrosion + 0.7451 74.51%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.8792 87.92%
Skin corrosion - 0.9032 90.32%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9028 90.28%
Micronuclear + 0.6598 65.98%
Hepatotoxicity + 0.7452 74.52%
skin sensitisation + 0.8089 80.89%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.5997 59.97%
Acute Oral Toxicity (c) III 0.8035 80.35%
Estrogen receptor binding - 0.8266 82.66%
Androgen receptor binding - 0.5863 58.63%
Thyroid receptor binding - 0.8244 82.44%
Glucocorticoid receptor binding - 0.7237 72.37%
Aromatase binding - 0.7837 78.37%
PPAR gamma - 0.7400 74.00%
Honey bee toxicity - 0.9753 97.53%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.8700 87.00%
Fish aquatic toxicity + 0.9852 98.52%

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
CHEMBL3194 P02766 Transthyretin 94.51% 90.71%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.22% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.56% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.11% 86.33%
CHEMBL1811 P34995 Prostanoid EP1 receptor 85.42% 95.71%
CHEMBL4208 P20618 Proteasome component C5 85.17% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.49% 99.17%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 80.50% 81.11%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 80.47% 87.67%

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 84368
LOTUS LTS0271696
wikiData Q72456830