4-Bromophenacyl isobutanoate

Details

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Internal ID 0a67347e-3247-474e-82cf-72dcf337937f
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name [2-(4-bromophenyl)-2-oxoethyl] 2-methylpropanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H13BrO3/c1-8(2)12(15)16-7-11(14)9-3-5-10(13)6-4-9/h3-6,8H,7H2,1-2H3
InChI Key BDBPDPLJFCWUSK-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H13BrO3
Molecular Weight 285.13 g/mol
Exact Mass 284.00481 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 3.30
Atomic LogP (AlogP) 2.83
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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BDBPDPLJFCWUSK-UHFFFAOYSA-N
Isobutyric acid, 4-Br-phenacyl ester
2-(4-Bromophenyl)-2-oxoethyl 2-methylpropanoate #

2D Structure

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2D Structure of 4-Bromophenacyl isobutanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9888 98.88%
Caco-2 + 0.7887 78.87%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.8914 89.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9212 92.12%
OATP1B3 inhibitior + 0.9498 94.98%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8391 83.91%
P-glycoprotein inhibitior - 0.9686 96.86%
P-glycoprotein substrate - 0.9634 96.34%
CYP3A4 substrate - 0.6693 66.93%
CYP2C9 substrate - 0.6092 60.92%
CYP2D6 substrate - 0.8690 86.90%
CYP3A4 inhibition - 0.8840 88.40%
CYP2C9 inhibition - 0.5765 57.65%
CYP2C19 inhibition - 0.6883 68.83%
CYP2D6 inhibition - 0.9194 91.94%
CYP1A2 inhibition + 0.5811 58.11%
CYP2C8 inhibition - 0.8411 84.11%
CYP inhibitory promiscuity - 0.6085 60.85%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5397 53.97%
Carcinogenicity (trinary) Non-required 0.5694 56.94%
Eye corrosion - 0.6870 68.70%
Eye irritation + 0.6780 67.80%
Skin irritation - 0.7031 70.31%
Skin corrosion - 0.9497 94.97%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6723 67.23%
Micronuclear - 0.7282 72.82%
Hepatotoxicity + 0.6686 66.86%
skin sensitisation + 0.7283 72.83%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity - 0.5752 57.52%
Acute Oral Toxicity (c) III 0.6153 61.53%
Estrogen receptor binding - 0.6977 69.77%
Androgen receptor binding - 0.5400 54.00%
Thyroid receptor binding - 0.8256 82.56%
Glucocorticoid receptor binding - 0.5946 59.46%
Aromatase binding + 0.6783 67.83%
PPAR gamma - 0.7764 77.64%
Honey bee toxicity - 0.9382 93.82%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9643 96.43%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.01% 96.09%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 88.36% 100.00%
CHEMBL2581 P07339 Cathepsin D 87.79% 98.95%
CHEMBL4208 P20618 Proteasome component C5 86.55% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.15% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.44% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.16% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.03% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.11% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 80.23% 94.73%

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.
Ipomoea capillacea

Cross-Links

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PubChem 603110
LOTUS LTS0131465
wikiData Q104923782