Propiophenone

Details

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Internal ID 1b7684f3-5063-41f6-a974-3001aa6fcd1a
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 1-phenylpropan-1-one
SMILES (Canonical) CCC(=O)C1=CC=CC=C1
SMILES (Isomeric) CCC(=O)C1=CC=CC=C1
InChI InChI=1S/C9H10O/c1-2-9(10)8-6-4-3-5-7-8/h3-7H,2H2,1H3
InChI Key KRIOVPPHQSLHCZ-UHFFFAOYSA-N
Popularity 1,110 references in papers

Physical and Chemical Properties

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Molecular Formula C9H10O
Molecular Weight 134.17 g/mol
Exact Mass 134.073164938 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.28
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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93-55-0
1-phenylpropan-1-one
Ethyl phenyl ketone
Propionylbenzene
PHENYL ETHYL KETONE
1-Propanone, 1-phenyl-
1-Phenyl-1-propanone
Ketone, ethyl phenyl
Propionphenone
1-Phenyl-propan-1-one
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Propiophenone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9974 99.74%
Caco-2 + 0.9539 95.39%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.9143 91.43%
Subcellular localzation Mitochondria 0.6560 65.60%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9533 95.33%
OATP1B3 inhibitior + 0.9662 96.62%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8824 88.24%
P-glycoprotein inhibitior - 0.9935 99.35%
P-glycoprotein substrate - 0.9783 97.83%
CYP3A4 substrate - 0.8206 82.06%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.7338 73.38%
CYP3A4 inhibition - 0.9590 95.90%
CYP2C9 inhibition - 0.9050 90.50%
CYP2C19 inhibition - 0.7972 79.72%
CYP2D6 inhibition - 0.9527 95.27%
CYP1A2 inhibition + 0.7612 76.12%
CYP2C8 inhibition - 0.8181 81.81%
CYP inhibitory promiscuity - 0.6710 67.10%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5181 51.81%
Carcinogenicity (trinary) Non-required 0.6491 64.91%
Eye corrosion + 0.9669 96.69%
Eye irritation + 0.9946 99.46%
Skin irritation + 0.9083 90.83%
Skin corrosion - 0.8599 85.99%
Ames mutagenesis - 0.9600 96.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8241 82.41%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.5052 50.52%
skin sensitisation + 0.9522 95.22%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity - 0.6457 64.57%
Acute Oral Toxicity (c) III 0.8675 86.75%
Estrogen receptor binding - 0.9524 95.24%
Androgen receptor binding - 0.8610 86.10%
Thyroid receptor binding - 0.8920 89.20%
Glucocorticoid receptor binding - 0.9444 94.44%
Aromatase binding - 0.8512 85.12%
PPAR gamma - 0.8902 89.02%
Honey bee toxicity - 0.9921 99.21%
Biodegradation + 0.8750 87.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity - 0.4912 49.12%

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
CHEMBL221 P23219 Cyclooxygenase-1 96.58% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.48% 86.33%
CHEMBL2581 P07339 Cathepsin D 88.31% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.66% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.07% 96.09%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 82.36% 100.00%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 80.93% 87.67%

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.
Artemisia judaica
Manilkara zapota
Senna alexandrina

Cross-Links

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PubChem 7148
NPASS NPC285470
LOTUS LTS0028243
wikiData Q415446