4-Octanone

Details

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Internal ID e7073b16-9ee1-4a21-bba9-089e5789d7e7
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name octan-4-one
SMILES (Canonical) CCCCC(=O)CCC
SMILES (Isomeric) CCCCC(=O)CCC
InChI InChI=1S/C8H16O/c1-3-5-7-8(9)6-4-2/h3-7H2,1-2H3
InChI Key YWXLSHOWXZUMSR-UHFFFAOYSA-N
Popularity 81 references in papers

Physical and Chemical Properties

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Molecular Formula C8H16O
Molecular Weight 128.21 g/mol
Exact Mass 128.120115130 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.55
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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Octan-4-one
589-63-9
Butyl propyl ketone
Propyl n-butyl ketone
EINECS 209-655-9
propyl butyl ketone
n-C4H9COCH2CH2CH3
SCHEMBL109288
DTXSID40207637
NSC43245
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-Octanone

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 + 0.9847 98.47%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.4585 45.85%
OATP2B1 inhibitior - 0.8229 82.29%
OATP1B1 inhibitior + 0.9149 91.49%
OATP1B3 inhibitior + 0.9431 94.31%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8973 89.73%
P-glycoprotein inhibitior - 0.9804 98.04%
P-glycoprotein substrate - 0.9489 94.89%
CYP3A4 substrate - 0.7108 71.08%
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 - 0.9657 96.57%
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 + 0.9913 99.13%
Skin irritation + 0.7185 71.85%
Skin corrosion - 0.9333 93.33%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6372 63.72%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5667 56.67%
skin sensitisation + 0.9027 90.27%
Respiratory toxicity - 0.9556 95.56%
Reproductive toxicity - 0.9578 95.78%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.4729 47.29%
Acute Oral Toxicity (c) III 0.8455 84.55%
Estrogen receptor binding - 0.9837 98.37%
Androgen receptor binding - 0.9383 93.83%
Thyroid receptor binding - 0.9100 91.00%
Glucocorticoid receptor binding - 0.9606 96.06%
Aromatase binding - 0.9165 91.65%
PPAR gamma - 0.8830 88.30%
Honey bee toxicity - 0.9933 99.33%
Biodegradation + 1.0000 100.00%
Crustacea aquatic toxicity - 0.5332 53.32%
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
CHEMBL2581 P07339 Cathepsin D 91.67% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.62% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.60% 96.09%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 84.65% 85.94%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.05% 96.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 80.36% 97.29%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 80.21% 92.08%

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.
Angelica acutiloba
Angelica gigas
Angelica sinensis

Cross-Links

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PubChem 11516
NPASS NPC83394