2-Bromo-4,5-dihydroxybenzaldehyde

Details

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Internal ID 76f7104b-f829-4ab1-b224-30d2d6fca71d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Benzaldehydes > Hydroxybenzaldehydes
IUPAC Name 2-bromo-4,5-dihydroxybenzaldehyde
SMILES (Canonical) C1=C(C(=CC(=C1O)O)Br)C=O
SMILES (Isomeric) C1=C(C(=CC(=C1O)O)Br)C=O
InChI InChI=1S/C7H5BrO3/c8-5-2-7(11)6(10)1-4(5)3-9/h1-3,10-11H
InChI Key JXHKKMRNIFLPBR-UHFFFAOYSA-N
Popularity 3 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 1.40
Atomic LogP (AlogP) 1.67
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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4815-99-0
Benzaldehyde, 2-bromo-4,5-dihydroxy-
SCHEMBL2336761
DTXSID10462296
CS-0498421

2D Structure

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2D Structure of 2-Bromo-4,5-dihydroxybenzaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9887 98.87%
Caco-2 + 0.7933 79.33%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.8809 88.09%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8510 85.10%
OATP1B3 inhibitior + 0.9553 95.53%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9562 95.62%
P-glycoprotein inhibitior - 0.9813 98.13%
P-glycoprotein substrate - 0.9934 99.34%
CYP3A4 substrate - 0.7499 74.99%
CYP2C9 substrate - 0.8024 80.24%
CYP2D6 substrate - 0.7915 79.15%
CYP3A4 inhibition - 0.8305 83.05%
CYP2C9 inhibition - 0.6906 69.06%
CYP2C19 inhibition - 0.7842 78.42%
CYP2D6 inhibition - 0.9361 93.61%
CYP1A2 inhibition - 0.5394 53.94%
CYP2C8 inhibition - 0.9545 95.45%
CYP inhibitory promiscuity - 0.7747 77.47%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.6873 68.73%
Carcinogenicity (trinary) Warning 0.4748 47.48%
Eye corrosion + 0.9027 90.27%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.8210 82.10%
Skin corrosion - 0.6983 69.83%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8139 81.39%
Micronuclear + 0.8029 80.29%
Hepatotoxicity + 0.6053 60.53%
skin sensitisation + 0.9023 90.23%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.6042 60.42%
Acute Oral Toxicity (c) III 0.7882 78.82%
Estrogen receptor binding - 0.6427 64.27%
Androgen receptor binding - 0.6871 68.71%
Thyroid receptor binding - 0.6085 60.85%
Glucocorticoid receptor binding - 0.5579 55.79%
Aromatase binding - 0.6480 64.80%
PPAR gamma - 0.5712 57.12%
Honey bee toxicity - 0.8892 88.92%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9698 96.98%

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
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 99.08% 98.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.49% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.46% 91.11%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 87.43% 93.40%
CHEMBL3194 P02766 Transthyretin 85.20% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 83.84% 94.73%
CHEMBL4208 P20618 Proteasome component C5 80.28% 90.00%

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 11321900
LOTUS LTS0233563
wikiData Q82286806