3-Decen-5-one

Details

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Internal ID d5fa4363-93e1-4583-bf05-e98d6afb5320
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha,beta-unsaturated ketones > Enones
IUPAC Name (E)-dec-3-en-5-one
SMILES (Canonical) CCCCCC(=O)C=CCC
SMILES (Isomeric) CCCCCC(=O)/C=C/CC
InChI InChI=1S/C10H18O/c1-3-5-7-9-10(11)8-6-4-2/h6,8H,3-5,7,9H2,1-2H3/b8-6+
InChI Key IWQQYVVAYYANSF-SOFGYWHQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18O
Molecular Weight 154.25 g/mol
Exact Mass 154.135765193 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.10
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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32064-73-6
(3E)-3-Decen-5-one #
SCHEMBL7849547
IWQQYVVAYYANSF-SOFGYWHQSA-N

2D Structure

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2D Structure of 3-Decen-5-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.9879 98.79%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Plasma membrane 0.5009 50.09%
OATP2B1 inhibitior - 0.8449 84.49%
OATP1B1 inhibitior + 0.9052 90.52%
OATP1B3 inhibitior + 0.9266 92.66%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.7313 73.13%
P-glycoprotein inhibitior - 0.9804 98.04%
P-glycoprotein substrate - 0.9447 94.47%
CYP3A4 substrate - 0.6710 67.10%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8620 86.20%
CYP3A4 inhibition - 0.9750 97.50%
CYP2C9 inhibition - 0.9462 94.62%
CYP2C19 inhibition - 0.9536 95.36%
CYP2D6 inhibition - 0.9533 95.33%
CYP1A2 inhibition + 0.7766 77.66%
CYP2C8 inhibition - 0.9418 94.18%
CYP inhibitory promiscuity - 0.7751 77.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.7313 73.13%
Eye corrosion + 0.9484 94.84%
Eye irritation + 0.9761 97.61%
Skin irritation + 0.7936 79.36%
Skin corrosion - 0.9580 95.80%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7285 72.85%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6176 61.76%
skin sensitisation + 0.9555 95.55%
Respiratory toxicity - 0.9000 90.00%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity - 0.5982 59.82%
Acute Oral Toxicity (c) III 0.7050 70.50%
Estrogen receptor binding - 0.9283 92.83%
Androgen receptor binding - 0.8859 88.59%
Thyroid receptor binding - 0.8662 86.62%
Glucocorticoid receptor binding - 0.8294 82.94%
Aromatase binding - 0.9086 90.86%
PPAR gamma - 0.7260 72.60%
Honey bee toxicity - 0.9912 99.12%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity + 0.6060 60.60%
Fish aquatic toxicity + 0.9185 91.85%

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
CHEMBL230 P35354 Cyclooxygenase-2 97.95% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.21% 99.17%
CHEMBL2581 P07339 Cathepsin D 90.79% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.66% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.41% 97.29%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 86.30% 92.08%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.36% 96.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.66% 91.11%
CHEMBL218 P21554 Cannabinoid CB1 receptor 80.69% 96.61%

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.
Nelumbo nucifera

Cross-Links

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PubChem 5367760
NPASS NPC11278