1-(4-Ethylphenyl)propan-1-one

Details

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Internal ID f8db3888-a46b-44a9-a85d-4458b382210f
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 1-(4-ethylphenyl)propan-1-one
SMILES (Canonical) CCC1=CC=C(C=C1)C(=O)CC
SMILES (Isomeric) CCC1=CC=C(C=C1)C(=O)CC
InChI InChI=1S/C11H14O/c1-3-9-5-7-10(8-6-9)11(12)4-2/h5-8H,3-4H2,1-2H3
InChI Key VGQRIILEZYZAOE-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C11H14O
Molecular Weight 162.23 g/mol
Exact Mass 162.104465066 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.84
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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4'-Ethylpropiophenone
27465-51-6
4-Ethylpropiophenone
1-(4-Ethylphenyl)-1-propanone
MFCD00191646
p-Ethylpropiophenone
1-Propanone, 1-(4-ethylphenyl)-
Ethyl 4-Ethylphenyl Ketone
4-Athylpropiophenon
p-Aethylpropiophenon
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1-(4-Ethylphenyl)propan-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9973 99.73%
Caco-2 + 0.9795 97.95%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Mitochondria 0.7000 70.00%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9482 94.82%
OATP1B3 inhibitior + 0.9637 96.37%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8886 88.86%
P-glycoprotein inhibitior - 0.9811 98.11%
P-glycoprotein substrate - 0.9477 94.77%
CYP3A4 substrate - 0.7411 74.11%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.7338 73.38%
CYP3A4 inhibition - 0.9282 92.82%
CYP2C9 inhibition - 0.9094 90.94%
CYP2C19 inhibition - 0.8101 81.01%
CYP2D6 inhibition - 0.9207 92.07%
CYP1A2 inhibition + 0.7139 71.39%
CYP2C8 inhibition - 0.6679 66.79%
CYP inhibitory promiscuity - 0.6752 67.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5181 51.81%
Carcinogenicity (trinary) Non-required 0.6849 68.49%
Eye corrosion + 0.9275 92.75%
Eye irritation + 0.9879 98.79%
Skin irritation + 0.8549 85.49%
Skin corrosion - 0.9547 95.47%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7483 74.83%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.5426 54.26%
skin sensitisation + 0.9615 96.15%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity - 0.8260 82.60%
Acute Oral Toxicity (c) III 0.8981 89.81%
Estrogen receptor binding - 0.8323 83.23%
Androgen receptor binding - 0.6171 61.71%
Thyroid receptor binding - 0.7687 76.87%
Glucocorticoid receptor binding - 0.8025 80.25%
Aromatase binding - 0.6723 67.23%
PPAR gamma - 0.8074 80.74%
Honey bee toxicity - 0.9688 96.88%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity - 0.4505 45.05%

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 91.21% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.64% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 89.24% 90.17%
CHEMBL4208 P20618 Proteasome component C5 85.38% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.33% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.35% 86.33%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 82.51% 100.00%

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.
Camellia sinensis

Cross-Links

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PubChem 583750
LOTUS LTS0199857
wikiData Q27461321