1-Phenylhex-4-yn-1-one

Details

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Internal ID ca753803-ded0-4a29-8123-34bb5b05c64f
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 1-phenylhex-4-yn-1-one
SMILES (Canonical) CC#CCCC(=O)C1=CC=CC=C1
SMILES (Isomeric) CC#CCCC(=O)C1=CC=CC=C1
InChI InChI=1S/C12H12O/c1-2-3-5-10-12(13)11-8-6-4-7-9-11/h4,6-9H,5,10H2,1H3
InChI Key KDMUYVQXLBQBFM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H12O
Molecular Weight 172.22 g/mol
Exact Mass 172.088815002 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.67
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Phenylhex-4-yn-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 + 0.9958 99.58%
Caco-2 + 0.9479 94.79%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.6000 60.00%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9255 92.55%
OATP1B3 inhibitior + 0.9569 95.69%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9089 90.89%
P-glycoprotein inhibitior - 0.9891 98.91%
P-glycoprotein substrate - 0.9668 96.68%
CYP3A4 substrate - 0.7187 71.87%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.7535 75.35%
CYP3A4 inhibition - 0.9091 90.91%
CYP2C9 inhibition - 0.9080 90.80%
CYP2C19 inhibition - 0.8225 82.25%
CYP2D6 inhibition - 0.9538 95.38%
CYP1A2 inhibition + 0.7289 72.89%
CYP2C8 inhibition - 0.8067 80.67%
CYP inhibitory promiscuity - 0.6517 65.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.6061 60.61%
Eye corrosion + 0.8432 84.32%
Eye irritation + 0.9593 95.93%
Skin irritation + 0.9022 90.22%
Skin corrosion - 0.6994 69.94%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8160 81.60%
Micronuclear - 0.9415 94.15%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation + 0.7894 78.94%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.7701 77.01%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity - 0.5766 57.66%
Acute Oral Toxicity (c) III 0.7497 74.97%
Estrogen receptor binding - 0.7901 79.01%
Androgen receptor binding - 0.8069 80.69%
Thyroid receptor binding - 0.7626 76.26%
Glucocorticoid receptor binding - 0.8516 85.16%
Aromatase binding - 0.7415 74.15%
PPAR gamma - 0.7148 71.48%
Honey bee toxicity - 0.9736 97.36%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity - 0.3973 39.73%

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 97.69% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.41% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.22% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.08% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.22% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.59% 95.50%
CHEMBL2535 P11166 Glucose transporter 82.42% 98.75%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 82.42% 94.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.90% 99.17%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 80.86% 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.
Artemisia capillaris

Cross-Links

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PubChem 9793970
LOTUS LTS0218852
wikiData Q105139235