4'-Ethylacetophenone

Details

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Internal ID 2375227c-9c73-4e0d-936c-663005ad2153
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 1-(4-ethylphenyl)ethanone
SMILES (Canonical) CCC1=CC=C(C=C1)C(=O)C
SMILES (Isomeric) CCC1=CC=C(C=C1)C(=O)C
InChI InChI=1S/C10H12O/c1-3-9-4-6-10(7-5-9)8(2)11/h4-7H,3H2,1-2H3
InChI Key NODGRWCMFMEGJH-UHFFFAOYSA-N
Popularity 57 references in papers

Physical and Chemical Properties

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Molecular Formula C10H12O
Molecular Weight 148.20 g/mol
Exact Mass 148.088815002 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.45
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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937-30-4
1-(4-Ethylphenyl)ethanone
4-ETHYLACETOPHENONE
p-Ethylacetophenone
Ethanone, 1-(4-ethylphenyl)-
Acetophenone, 4'-ethyl-
p-Acetylethylbenzene
p-Ethylphenyl methyl ketone
MFCD00009262
LSA7B53YDO
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4'-Ethylacetophenone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9972 99.72%
Caco-2 + 0.9814 98.14%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.6941 69.41%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9500 95.00%
OATP1B3 inhibitior + 0.9627 96.27%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8868 88.68%
P-glycoprotein inhibitior - 0.9834 98.34%
P-glycoprotein substrate - 0.9386 93.86%
CYP3A4 substrate - 0.7583 75.83%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.7338 73.38%
CYP3A4 inhibition - 0.9555 95.55%
CYP2C9 inhibition - 0.9228 92.28%
CYP2C19 inhibition - 0.8532 85.32%
CYP2D6 inhibition - 0.9295 92.95%
CYP1A2 inhibition + 0.6566 65.66%
CYP2C8 inhibition - 0.8155 81.55%
CYP inhibitory promiscuity - 0.6383 63.83%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5481 54.81%
Carcinogenicity (trinary) Non-required 0.6739 67.39%
Eye corrosion + 0.9515 95.15%
Eye irritation + 0.9928 99.28%
Skin irritation + 0.8723 87.23%
Skin corrosion - 0.9541 95.41%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7298 72.98%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.6199 61.99%
skin sensitisation + 0.9744 97.44%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity - 0.7840 78.40%
Acute Oral Toxicity (c) III 0.9017 90.17%
Estrogen receptor binding - 0.9261 92.61%
Androgen receptor binding - 0.7922 79.22%
Thyroid receptor binding - 0.7911 79.11%
Glucocorticoid receptor binding - 0.8662 86.62%
Aromatase binding - 0.5417 54.17%
PPAR gamma - 0.8884 88.84%
Honey bee toxicity - 0.9690 96.90%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.7303 73.03%

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
CHEMBL2581 P07339 Cathepsin D 93.61% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.08% 96.09%
CHEMBL4208 P20618 Proteasome component C5 84.81% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.63% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.18% 99.17%

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
Gossypium hirsutum

Cross-Links

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PubChem 13642
LOTUS LTS0016861
wikiData Q63398062