Bromobenzene

Details

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Internal ID dc47123b-acb6-4f7e-a7f8-0eab561b20ac
Taxonomy Benzenoids > Benzene and substituted derivatives > Halobenzenes > Bromobenzenes
IUPAC Name bromobenzene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H5Br/c7-6-4-2-1-3-5-6/h1-5H
InChI Key QARVLSVVCXYDNA-UHFFFAOYSA-N
Popularity 5,996 references in papers

Physical and Chemical Properties

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Molecular Formula C6H5Br
Molecular Weight 157.01 g/mol
Exact Mass 155.95746 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.45
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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108-86-1
Monobromobenzene
Phenyl bromide
Benzene, bromo-
C6H5Br
PhBr
NCI-C55492
BROMO-BENZENE
DTXSID5024637
CO4D5J547L
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Bromobenzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9874 98.74%
Caco-2 + 0.9143 91.43%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.8857 88.57%
Subcellular localzation Mitochondria 0.4849 48.49%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9690 96.90%
OATP1B3 inhibitior + 0.9626 96.26%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9096 90.96%
P-glycoprotein inhibitior - 0.9880 98.80%
P-glycoprotein substrate - 0.9964 99.64%
CYP3A4 substrate - 0.8455 84.55%
CYP2C9 substrate - 0.8036 80.36%
CYP2D6 substrate - 0.7277 72.77%
CYP3A4 inhibition - 0.9350 93.50%
CYP2C9 inhibition - 0.7239 72.39%
CYP2C19 inhibition - 0.6494 64.94%
CYP2D6 inhibition - 0.9492 94.92%
CYP1A2 inhibition + 0.6929 69.29%
CYP2C8 inhibition - 0.9331 93.31%
CYP inhibitory promiscuity - 0.7252 72.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5392 53.92%
Carcinogenicity (trinary) Warning 0.4875 48.75%
Eye corrosion + 0.9972 99.72%
Eye irritation + 0.9973 99.73%
Skin irritation + 0.9406 94.06%
Skin corrosion - 0.5369 53.69%
Ames mutagenesis - 0.9800 98.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8421 84.21%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.9875 98.75%
skin sensitisation + 0.8190 81.90%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.7889 78.89%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity - 0.5636 56.36%
Acute Oral Toxicity (c) III 0.8834 88.34%
Estrogen receptor binding - 0.8656 86.56%
Androgen receptor binding - 0.9235 92.35%
Thyroid receptor binding - 0.8484 84.84%
Glucocorticoid receptor binding - 0.8892 88.92%
Aromatase binding - 0.8680 86.80%
PPAR gamma - 0.8454 84.54%
Honey bee toxicity - 0.9457 94.57%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.9500 95.00%
Fish aquatic toxicity + 0.9688 96.88%

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
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 91.19% 94.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.59% 95.56%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 83.78% 94.23%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.65% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 81.75% 90.17%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 80.24% 94.08%

Plants that contains it

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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

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PubChem 7961
LOTUS LTS0091518
wikiData Q410597