3-Decanone

Details

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Internal ID 9b4393e4-da16-44fe-a93d-828114ab4802
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name decan-3-one
SMILES (Canonical) CCCCCCCC(=O)CC
SMILES (Isomeric) CCCCCCCC(=O)CC
InChI InChI=1S/C10H20O/c1-3-5-6-7-8-9-10(11)4-2/h3-9H2,1-2H3
InChI Key XJLDYKIEURAVBW-UHFFFAOYSA-N
Popularity 49 references in papers

Physical and Chemical Properties

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Molecular Formula C10H20O
Molecular Weight 156.26 g/mol
Exact Mass 156.151415257 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.33
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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decan-3-one
928-80-3
Ethyl heptyl ketone
Ethyl n-heptyl ketone
UNII-CBT4991PRJ
CBT4991PRJ
EINECS 213-183-9
3-Decanone, 98%
3-Decanone, >=97%
3-DECANONE [FHFI]
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-Decanone

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 + 0.9619 96.19%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.4585 45.85%
OATP2B1 inhibitior - 0.8410 84.10%
OATP1B1 inhibitior + 0.9287 92.87%
OATP1B3 inhibitior + 0.9431 94.31%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8390 83.90%
P-glycoprotein inhibitior - 0.9766 97.66%
P-glycoprotein substrate - 0.9269 92.69%
CYP3A4 substrate - 0.7059 70.59%
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 - 0.9467 94.67%
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 + 0.9921 99.21%
Skin irritation + 0.7185 71.85%
Skin corrosion - 0.9333 93.33%
Ames mutagenesis - 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7254 72.54%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6424 64.24%
skin sensitisation + 0.9027 90.27%
Respiratory toxicity - 1.0000 100.00%
Reproductive toxicity - 0.9578 95.78%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.5177 51.77%
Acute Oral Toxicity (c) III 0.8455 84.55%
Estrogen receptor binding - 0.9503 95.03%
Androgen receptor binding - 0.8934 89.34%
Thyroid receptor binding - 0.8731 87.31%
Glucocorticoid receptor binding - 0.9081 90.81%
Aromatase binding - 0.8833 88.33%
PPAR gamma - 0.7895 78.95%
Honey bee toxicity - 0.9927 99.27%
Biodegradation + 0.9500 95.00%
Crustacea aquatic toxicity + 0.8323 83.23%
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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.09% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.62% 99.17%
CHEMBL2581 P07339 Cathepsin D 92.31% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.85% 92.08%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 90.19% 85.94%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 90.18% 97.29%
CHEMBL230 P35354 Cyclooxygenase-2 90.12% 89.63%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.97% 96.95%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 83.47% 91.81%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 82.98% 92.86%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 82.93% 95.17%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.49% 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.
Acorus calamus var. angustatus
Acorus gramineus
Pimenta racemosa

Cross-Links

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PubChem 13576
NPASS NPC131642
LOTUS LTS0150335
wikiData Q27159516