p-Bromophenacyl 2r-methyl-3r-hydroxybutyrate

Details

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Internal ID 269ecf3b-d776-43dc-98b3-096380e87bd1
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name [2-(4-bromophenyl)-2-oxoethyl] (2R,3R)-3-hydroxy-2-methylbutanoate
SMILES (Canonical) CC(C(C)O)C(=O)OCC(=O)C1=CC=C(C=C1)Br
SMILES (Isomeric) C[C@H]([C@@H](C)O)C(=O)OCC(=O)C1=CC=C(C=C1)Br
InChI InChI=1S/C13H15BrO4/c1-8(9(2)15)13(17)18-7-12(16)10-3-5-11(14)6-4-10/h3-6,8-9,15H,7H2,1-2H3/t8-,9-/m1/s1
InChI Key ZQBYIWXDRNSUCD-RKDXNWHRSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C13H15BrO4
Molecular Weight 315.16 g/mol
Exact Mass 314.01537 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.19
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of p-Bromophenacyl 2r-methyl-3r-hydroxybutyrate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9403 94.03%
Caco-2 + 0.8066 80.66%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.8574 85.74%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9226 92.26%
OATP1B3 inhibitior + 0.9353 93.53%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8244 82.44%
P-glycoprotein inhibitior - 0.9628 96.28%
P-glycoprotein substrate - 0.9397 93.97%
CYP3A4 substrate - 0.6420 64.20%
CYP2C9 substrate - 0.6062 60.62%
CYP2D6 substrate - 0.8505 85.05%
CYP3A4 inhibition - 0.8042 80.42%
CYP2C9 inhibition - 0.6765 67.65%
CYP2C19 inhibition - 0.6820 68.20%
CYP2D6 inhibition - 0.9226 92.26%
CYP1A2 inhibition - 0.6240 62.40%
CYP2C8 inhibition - 0.7864 78.64%
CYP inhibitory promiscuity - 0.8193 81.93%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6180 61.80%
Carcinogenicity (trinary) Non-required 0.6018 60.18%
Eye corrosion - 0.8458 84.58%
Eye irritation - 0.6477 64.77%
Skin irritation - 0.7026 70.26%
Skin corrosion - 0.9656 96.56%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7999 79.99%
Micronuclear - 0.6549 65.49%
Hepatotoxicity + 0.6186 61.86%
skin sensitisation + 0.4868 48.68%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity - 0.6333 63.33%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity - 0.6627 66.27%
Acute Oral Toxicity (c) III 0.7085 70.85%
Estrogen receptor binding - 0.6882 68.82%
Androgen receptor binding - 0.5994 59.94%
Thyroid receptor binding - 0.6919 69.19%
Glucocorticoid receptor binding + 0.5445 54.45%
Aromatase binding + 0.6078 60.78%
PPAR gamma - 0.6792 67.92%
Honey bee toxicity - 0.9406 94.06%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.8050 80.50%
Fish aquatic toxicity + 0.9350 93.50%

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 94.27% 96.09%
CHEMBL4208 P20618 Proteasome component C5 91.03% 90.00%
CHEMBL2581 P07339 Cathepsin D 89.97% 98.95%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 88.96% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.58% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.27% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.65% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.74% 96.00%

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.
Cuscuta australis
Ipomoea capillacea

Cross-Links

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PubChem 14033792
LOTUS LTS0228207
wikiData Q105381382