Non-2-en-4-one

Details

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Internal ID e686441c-9ce9-464e-921f-de11c80f6a3d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha,beta-unsaturated ketones > Enones
IUPAC Name (E)-non-2-en-4-one
SMILES (Canonical) CCCCCC(=O)C=CC
SMILES (Isomeric) CCCCCC(=O)/C=C/C
InChI InChI=1S/C9H16O/c1-3-5-6-8-9(10)7-4-2/h4,7H,3,5-6,8H2,1-2H3/b7-4+
InChI Key WTAYWTBOEQYGOG-QPJJXVBHSA-N
Popularity 5 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 2.70
Atomic LogP (AlogP) 2.71
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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2-Nonen-4-one
non-2-en-4-one
2-Nonenone-4
2-Nonen-4-one, (2E)-
(E)-non-2-en-4-one
trans-2-Nonen-4-one
27743-70-0
32064-72-5
2-Nonen-4-one, (E)-
FEMA No. 4301
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Non-2-en-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9945 99.45%
Caco-2 + 0.9851 98.51%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Plasma membrane 0.4338 43.38%
OATP2B1 inhibitior - 0.8518 85.18%
OATP1B1 inhibitior + 0.9036 90.36%
OATP1B3 inhibitior + 0.9316 93.16%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9081 90.81%
P-glycoprotein inhibitior - 0.9891 98.91%
P-glycoprotein substrate - 0.9498 94.98%
CYP3A4 substrate - 0.6902 69.02%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8620 86.20%
CYP3A4 inhibition - 0.9734 97.34%
CYP2C9 inhibition - 0.9463 94.63%
CYP2C19 inhibition - 0.9385 93.85%
CYP2D6 inhibition - 0.9472 94.72%
CYP1A2 inhibition + 0.7749 77.49%
CYP2C8 inhibition - 0.9457 94.57%
CYP inhibitory promiscuity - 0.7417 74.17%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.6952 69.52%
Eye corrosion + 0.9386 93.86%
Eye irritation + 0.9697 96.97%
Skin irritation + 0.8586 85.86%
Skin corrosion - 0.9478 94.78%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6558 65.58%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6351 63.51%
skin sensitisation + 0.9422 94.22%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.4794 47.94%
Acute Oral Toxicity (c) III 0.7232 72.32%
Estrogen receptor binding - 0.9500 95.00%
Androgen receptor binding - 0.8959 89.59%
Thyroid receptor binding - 0.8684 86.84%
Glucocorticoid receptor binding - 0.7689 76.89%
Aromatase binding - 0.8681 86.81%
PPAR gamma - 0.8512 85.12%
Honey bee toxicity - 0.9847 98.47%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity + 0.5813 58.13%
Fish aquatic toxicity + 0.8228 82.28%

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 96.21% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.28% 99.17%
CHEMBL2581 P07339 Cathepsin D 89.14% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 87.26% 97.29%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 87.04% 92.08%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.88% 96.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.48% 96.09%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 85.11% 91.81%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.83% 91.11%

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.
Oplopanax elatus

Cross-Links

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PubChem 448996
NPASS NPC146543