1-Octen-3-one, (E)-

Details

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Internal ID a9a83ff2-0347-4515-a2c7-bcf1fd57939d
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives
IUPAC Name (E)-4-methyl-1-phenyloct-1-en-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H20O/c1-3-4-8-13(2)15(16)12-11-14-9-6-5-7-10-14/h5-7,9-13H,3-4,8H2,1-2H3/b12-11+
InChI Key FSBZDSXGWFRMCO-VAWYXSNFSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O
Molecular Weight 216.32 g/mol
Exact Mass 216.151415257 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.10
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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74975-54-5
1-Octen-3-one, (E)-
DTXSID80421714
NSC-298202

2D Structure

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2D Structure of 1-Octen-3-one, (E)-

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 + 0.9496 94.96%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Plasma membrane 0.4486 44.86%
OATP2B1 inhibitior - 0.8626 86.26%
OATP1B1 inhibitior + 0.8849 88.49%
OATP1B3 inhibitior + 0.9411 94.11%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.6916 69.16%
P-glycoprotein inhibitior - 0.9749 97.49%
P-glycoprotein substrate - 0.8669 86.69%
CYP3A4 substrate - 0.6874 68.74%
CYP2C9 substrate - 0.8001 80.01%
CYP2D6 substrate - 0.8273 82.73%
CYP3A4 inhibition - 0.9646 96.46%
CYP2C9 inhibition - 0.9135 91.35%
CYP2C19 inhibition - 0.8230 82.30%
CYP2D6 inhibition - 0.9161 91.61%
CYP1A2 inhibition + 0.7782 77.82%
CYP2C8 inhibition - 0.8464 84.64%
CYP inhibitory promiscuity + 0.5082 50.82%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.6499 64.99%
Eye corrosion + 0.6612 66.12%
Eye irritation + 0.6347 63.47%
Skin irritation + 0.8554 85.54%
Skin corrosion - 0.9086 90.86%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8580 85.80%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation + 0.9688 96.88%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.7164 71.64%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity - 0.6458 64.58%
Acute Oral Toxicity (c) III 0.7914 79.14%
Estrogen receptor binding - 0.7732 77.32%
Androgen receptor binding + 0.7349 73.49%
Thyroid receptor binding - 0.6598 65.98%
Glucocorticoid receptor binding - 0.8883 88.83%
Aromatase binding + 0.6988 69.88%
PPAR gamma - 0.8282 82.82%
Honey bee toxicity - 0.9914 99.14%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9659 96.59%

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 97.92% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 94.23% 96.00%
CHEMBL221 P23219 Cyclooxygenase-1 94.20% 90.17%
CHEMBL3359 P21462 Formyl peptide receptor 1 94.19% 93.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.15% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.05% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.96% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.68% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.64% 91.11%
CHEMBL4227 P25090 Lipoxin A4 receptor 86.07% 100.00%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 85.52% 100.00%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 85.29% 94.08%
CHEMBL3401 O75469 Pregnane X receptor 84.94% 94.73%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 83.93% 85.94%
CHEMBL1907 P15144 Aminopeptidase N 83.92% 93.31%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.07% 95.50%

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.
Perilla frutescens
Scutellaria barbata

Cross-Links

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PubChem 5995948
NPASS NPC187679