1-Phenylpentan-2-one

Details

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Internal ID 669b2435-33cf-40e5-94c5-01937daf005d
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 1-phenylpentan-2-one
SMILES (Canonical) CCCC(=O)CC1=CC=CC=C1
SMILES (Isomeric) CCCC(=O)CC1=CC=CC=C1
InChI InChI=1S/C11H14O/c1-2-6-11(12)9-10-7-4-3-5-8-10/h3-5,7-8H,2,6,9H2,1H3
InChI Key NFKAWBGFIMBUMB-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 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-2-pentanone
2-Pentanone, 1-phenyl-
Benzyl propyl ketone
UNII-36VW7X5C4P
36VW7X5C4P
EINECS 229-726-8
AI3-24761
DTXSID70216954
RefChem:76948
DTXCID00139445
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-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9964 99.64%
Caco-2 + 0.9752 97.52%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Plasma membrane 0.4435 44.35%
OATP2B1 inhibitior - 0.8703 87.03%
OATP1B1 inhibitior + 0.9213 92.13%
OATP1B3 inhibitior + 0.9529 95.29%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8358 83.58%
P-glycoprotein inhibitior - 0.9947 99.47%
P-glycoprotein substrate - 0.9604 96.04%
CYP3A4 substrate - 0.7261 72.61%
CYP2C9 substrate - 0.8151 81.51%
CYP2D6 substrate - 0.6914 69.14%
CYP3A4 inhibition - 0.9622 96.22%
CYP2C9 inhibition - 0.8917 89.17%
CYP2C19 inhibition - 0.8451 84.51%
CYP2D6 inhibition - 0.9332 93.32%
CYP1A2 inhibition + 0.7330 73.30%
CYP2C8 inhibition - 0.7823 78.23%
CYP inhibitory promiscuity - 0.6335 63.35%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6800 68.00%
Carcinogenicity (trinary) Non-required 0.5935 59.35%
Eye corrosion + 0.8661 86.61%
Eye irritation + 0.9779 97.79%
Skin irritation + 0.7880 78.80%
Skin corrosion - 0.9702 97.02%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7268 72.68%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation + 0.7640 76.40%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.7918 79.18%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity - 0.6618 66.18%
Acute Oral Toxicity (c) III 0.8726 87.26%
Estrogen receptor binding - 0.9257 92.57%
Androgen receptor binding - 0.9303 93.03%
Thyroid receptor binding - 0.8869 88.69%
Glucocorticoid receptor binding - 0.8497 84.97%
Aromatase binding - 0.8301 83.01%
PPAR gamma - 0.6169 61.69%
Honey bee toxicity - 0.9936 99.36%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.8412 84.12%

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 97.86% 90.17%
CHEMBL2581 P07339 Cathepsin D 97.63% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.70% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.13% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.11% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 84.96% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 82.97% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.90% 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.
Vitis rotundifolia

Cross-Links

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PubChem 81188
LOTUS LTS0114438
wikiData Q27256592