4-Nonanone

Details

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Internal ID 4a9ef067-2867-4019-be9f-c6c018ee0a90
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name nonan-4-one
SMILES (Canonical) CCCCCC(=O)CCC
SMILES (Isomeric) CCCCCC(=O)CCC
InChI InChI=1S/C9H18O/c1-3-5-6-8-9(10)7-4-2/h3-8H2,1-2H3
InChI Key TYBCSQFBSWACAA-UHFFFAOYSA-N
Popularity 51 references in papers

Physical and Chemical Properties

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Molecular Formula C9H18O
Molecular Weight 142.24 g/mol
Exact Mass 142.135765193 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.94
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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Nonan-4-one
4485-09-0
Amyl Propyl Ketone
Propyl amyl ketone
Pentyl Propyl Ketone
n-Pentyl n-propyl ketone
EINECS 224-770-4
SCHEMBL129432
DTXSID5063493
CHEBI:179604
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-Nonanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9947 99.47%
Caco-2 + 0.9809 98.09%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.4585 45.85%
OATP2B1 inhibitior - 0.8361 83.61%
OATP1B1 inhibitior + 0.9199 91.99%
OATP1B3 inhibitior + 0.9431 94.31%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8906 89.06%
P-glycoprotein inhibitior - 0.9770 97.70%
P-glycoprotein substrate - 0.9315 93.15%
CYP3A4 substrate - 0.7101 71.01%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7622 76.22%
CYP3A4 inhibition - 0.9815 98.15%
CYP2C9 inhibition - 0.9433 94.33%
CYP2C19 inhibition - 0.9645 96.45%
CYP2D6 inhibition - 0.9502 95.02%
CYP1A2 inhibition + 0.6890 68.90%
CYP2C8 inhibition - 0.9625 96.25%
CYP inhibitory promiscuity - 0.8752 87.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.7622 76.22%
Eye corrosion + 0.9821 98.21%
Eye irritation + 0.9920 99.20%
Skin irritation + 0.7185 71.85%
Skin corrosion - 0.9333 93.33%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6910 69.10%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5991 59.91%
skin sensitisation + 0.9027 90.27%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.9578 95.78%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.4582 45.82%
Acute Oral Toxicity (c) III 0.8455 84.55%
Estrogen receptor binding - 0.9710 97.10%
Androgen receptor binding - 0.9243 92.43%
Thyroid receptor binding - 0.8743 87.43%
Glucocorticoid receptor binding - 0.9392 93.92%
Aromatase binding - 0.9287 92.87%
PPAR gamma - 0.9063 90.63%
Honey bee toxicity - 0.9931 99.31%
Biodegradation + 0.8750 87.50%
Crustacea aquatic toxicity + 0.5944 59.44%
Fish aquatic toxicity + 0.8149 81.49%

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 92.41% 99.17%
CHEMBL2581 P07339 Cathepsin D 91.72% 98.95%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 91.19% 85.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.77% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 88.11% 92.08%
CHEMBL230 P35354 Cyclooxygenase-2 86.44% 89.63%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 85.60% 97.29%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.44% 97.25%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 80.25% 91.81%

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.
Capillipedium parviflorum
Cymbopogon flexuosus

Cross-Links

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PubChem 78236
LOTUS LTS0040837
wikiData Q31838919