1-Phenylpentan-3-one

Details

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Internal ID 6135f1a1-c9f6-49e4-81e0-ae23cc274260
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 1-phenylpentan-3-one
SMILES (Canonical) CCC(=O)CCC1=CC=CC=C1
SMILES (Isomeric) CCC(=O)CCC1=CC=CC=C1
InChI InChI=1S/C11H14O/c1-2-11(12)9-8-10-6-4-3-5-7-10/h3-7H,2,8-9H2,1H3
InChI Key GLVAUXMKXKUEEA-UHFFFAOYSA-N
Popularity 14 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 2.30
Atomic LogP (AlogP) 2.60
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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1-Phenyl-3-pentanone
20795-51-1
1-Phenyl-pentan-3-one
3-Pentanone, 1-phenyl-
AI3-21915
VEP8CR4F7Z
EINECS 244-045-6
5phenylpentan-3-one
UNII-VEP8CR4F7Z
SCHEMBL1874
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-Phenylpentan-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.9674 96.74%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.5087 50.87%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9145 91.45%
OATP1B3 inhibitior + 0.9534 95.34%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7135 71.35%
P-glycoprotein inhibitior - 0.9948 99.48%
P-glycoprotein substrate - 0.9011 90.11%
CYP3A4 substrate - 0.7141 71.41%
CYP2C9 substrate - 0.8151 81.51%
CYP2D6 substrate - 0.6914 69.14%
CYP3A4 inhibition - 0.9642 96.42%
CYP2C9 inhibition - 0.8908 89.08%
CYP2C19 inhibition - 0.8311 83.11%
CYP2D6 inhibition - 0.9300 93.00%
CYP1A2 inhibition + 0.7797 77.97%
CYP2C8 inhibition - 0.6490 64.90%
CYP inhibitory promiscuity - 0.6220 62.20%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.6637 66.37%
Eye corrosion + 0.8988 89.88%
Eye irritation + 0.9585 95.85%
Skin irritation + 0.8676 86.76%
Skin corrosion - 0.9340 93.40%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5390 53.90%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5786 57.86%
skin sensitisation + 0.7161 71.61%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.8081 80.81%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity - 0.7757 77.57%
Acute Oral Toxicity (c) III 0.7506 75.06%
Estrogen receptor binding - 0.9052 90.52%
Androgen receptor binding - 0.8231 82.31%
Thyroid receptor binding - 0.8839 88.39%
Glucocorticoid receptor binding - 0.7947 79.47%
Aromatase binding - 0.7820 78.20%
PPAR gamma - 0.6927 69.27%
Honey bee toxicity - 0.9756 97.56%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.8344 83.44%

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 96.83% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.49% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 88.46% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.74% 95.56%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 85.01% 94.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.06% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 82.81% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.08% 86.33%

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.
Amomyrtus luma

Cross-Links

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PubChem 88701
LOTUS LTS0122047
wikiData Q72498091