Oct-3-en-2-one

Details

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Internal ID 6dd247cc-f401-4ef5-96ff-29fba137ed08
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha,beta-unsaturated ketones > Enones
IUPAC Name oct-3-en-2-one
SMILES (Canonical) CCCCC=CC(=O)C
SMILES (Isomeric) CCCCC=CC(=O)C
InChI InChI=1S/C8H14O/c1-3-4-5-6-7-8(2)9/h6-7H,3-5H2,1-2H3
InChI Key ZCFOBLITZWHNNC-UHFFFAOYSA-N
Popularity 27 references in papers

Physical and Chemical Properties

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Molecular Formula C8H14O
Molecular Weight 126.20 g/mol
Exact Mass 126.104465066 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.32
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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Octenone
3-octen-2-ona
SCHEMBL230668
DTXSID1061867
FT-0616284
FT-0690383

2D Structure

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2D Structure of Oct-3-en-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 + 0.9951 99.51%
Caco-2 + 0.9585 95.85%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Plasma membrane 0.2941 29.41%
OATP2B1 inhibitior - 0.8576 85.76%
OATP1B1 inhibitior + 0.8720 87.20%
OATP1B3 inhibitior + 0.9328 93.28%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8966 89.66%
P-glycoprotein inhibitior - 0.9867 98.67%
P-glycoprotein substrate - 0.9434 94.34%
CYP3A4 substrate - 0.6653 66.53%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8620 86.20%
CYP3A4 inhibition - 0.9893 98.93%
CYP2C9 inhibition - 0.9478 94.78%
CYP2C19 inhibition - 0.9310 93.10%
CYP2D6 inhibition - 0.9501 95.01%
CYP1A2 inhibition + 0.6440 64.40%
CYP2C8 inhibition - 0.9709 97.09%
CYP inhibitory promiscuity - 0.7242 72.42%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5300 53.00%
Carcinogenicity (trinary) Non-required 0.6612 66.12%
Eye corrosion + 0.9610 96.10%
Eye irritation + 0.9706 97.06%
Skin irritation + 0.9063 90.63%
Skin corrosion - 0.8040 80.40%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6927 69.27%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation + 0.9722 97.22%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.6902 69.02%
Acute Oral Toxicity (c) III 0.7671 76.71%
Estrogen receptor binding - 0.9783 97.83%
Androgen receptor binding - 0.8843 88.43%
Thyroid receptor binding - 0.8506 85.06%
Glucocorticoid receptor binding - 0.8497 84.97%
Aromatase binding - 0.9081 90.81%
PPAR gamma - 0.8765 87.65%
Honey bee toxicity - 0.9906 99.06%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.7721 77.21%

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 90.15% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.48% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.23% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.08% 96.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 80.74% 97.29%

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.
Aspalathus linearis
Bellis perennis
Panax notoginseng
Polygala senega
Trigonella foenum-graecum

Cross-Links

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PubChem 15475
NPASS NPC217778
LOTUS LTS0270613
wikiData Q104253467