3-Nonen-2-one

Details

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Internal ID 25f34d8d-1790-42e8-8e13-921948a23abc
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha,beta-unsaturated ketones > Enones
IUPAC Name (E)-non-3-en-2-one
SMILES (Canonical) CCCCCC=CC(=O)C
SMILES (Isomeric) CCCCC/C=C/C(=O)C
InChI InChI=1S/C9H16O/c1-3-4-5-6-7-8-9(2)10/h7-8H,3-6H2,1-2H3/b8-7+
InChI Key HDKLIZDXVUCLHQ-BQYQJAHWSA-N
Popularity 126 references in papers

Physical and Chemical Properties

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Molecular Formula C9H16O
Molecular Weight 140.22 g/mol
Exact Mass 140.120115130 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.71
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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trans-3-Nonen-2-one
14309-57-0
(E)-Non-3-en-2-one
18402-83-0
(e)-3-nonen-2-one
3-Nonen-2-one, (3E)-
(3E)-NON-3-EN-2-ONE
3-Nonen-2-one [FHFI]
3-Nonen-2-one, (E)-
FEMA No. 3955
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Nonen-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 + 0.9946 99.46%
Caco-2 + 0.9534 95.34%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Plasma membrane 0.3533 35.33%
OATP2B1 inhibitior - 0.8546 85.46%
OATP1B1 inhibitior + 0.8372 83.72%
OATP1B3 inhibitior + 0.9344 93.44%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9147 91.47%
P-glycoprotein inhibitior - 0.9853 98.53%
P-glycoprotein substrate - 0.9460 94.60%
CYP3A4 substrate - 0.6589 65.89%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8620 86.20%
CYP3A4 inhibition - 0.9858 98.58%
CYP2C9 inhibition - 0.9359 93.59%
CYP2C19 inhibition - 0.9359 93.59%
CYP2D6 inhibition - 0.9451 94.51%
CYP1A2 inhibition + 0.7224 72.24%
CYP2C8 inhibition - 0.9502 95.02%
CYP inhibitory promiscuity - 0.6726 67.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.6448 64.48%
Eye corrosion + 0.9519 95.19%
Eye irritation + 0.9613 96.13%
Skin irritation + 0.8911 89.11%
Skin corrosion - 0.9101 91.01%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6474 64.74%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation + 0.9741 97.41%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.9375 93.75%
Nephrotoxicity + 0.5847 58.47%
Acute Oral Toxicity (c) III 0.6650 66.50%
Estrogen receptor binding - 0.9484 94.84%
Androgen receptor binding - 0.8508 85.08%
Thyroid receptor binding - 0.8518 85.18%
Glucocorticoid receptor binding - 0.7610 76.10%
Aromatase binding - 0.8708 87.08%
PPAR gamma - 0.8370 83.70%
Honey bee toxicity - 0.9906 99.06%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity + 0.6653 66.53%
Fish aquatic toxicity + 0.9131 91.31%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 92.20% 99.17%
CHEMBL2581 P07339 Cathepsin D 91.98% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.38% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 85.98% 97.29%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.10% 92.08%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.86% 96.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.76% 89.34%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.09% 94.33%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.74% 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.
Akebia trifoliata
Liquidambar formosana

Cross-Links

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PubChem 5317045
NPASS NPC78797
LOTUS LTS0223363
wikiData Q27278142