6-Undecanone

Details

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Internal ID 0d40f578-02db-4e7c-82a4-8725b4be2ba0
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Ketones
IUPAC Name undecan-6-one
SMILES (Canonical) CCCCCC(=O)CCCCC
SMILES (Isomeric) CCCCCC(=O)CCCCC
InChI InChI=1S/C11H22O/c1-3-5-7-9-11(12)10-8-6-4-2/h3-10H2,1-2H3
InChI Key ZPQAKYPOZRXKFA-UHFFFAOYSA-N
Popularity 88 references in papers

Physical and Chemical Properties

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Molecular Formula C11H22O
Molecular Weight 170.29 g/mol
Exact Mass 170.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.72
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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Undecan-6-one
927-49-1
Dipentyl ketone
Diamyl ketone
Amyl ketone
6-Oxoundecane
Pentyl ketone
Di-N-amyl ketone
Undecanone-(6)
EINECS 213-150-9
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 6-Undecanone

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 + 0.9742 97.42%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.4585 45.85%
OATP2B1 inhibitior - 0.8379 83.79%
OATP1B1 inhibitior + 0.9229 92.29%
OATP1B3 inhibitior + 0.9431 94.31%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.7609 76.09%
P-glycoprotein inhibitior - 0.9577 95.77%
P-glycoprotein substrate - 0.9524 95.24%
CYP3A4 substrate - 0.7518 75.18%
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 - 0.9782 97.82%
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 + 0.9872 98.72%
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 - 0.6788 67.88%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.7065 70.65%
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 + 0.5433 54.33%
Acute Oral Toxicity (c) III 0.8455 84.55%
Estrogen receptor binding - 0.9607 96.07%
Androgen receptor binding - 0.9091 90.91%
Thyroid receptor binding - 0.8178 81.78%
Glucocorticoid receptor binding - 0.9273 92.73%
Aromatase binding - 0.9094 90.94%
PPAR gamma - 0.8384 83.84%
Honey bee toxicity - 0.9950 99.50%
Biodegradation + 0.9750 97.50%
Crustacea aquatic toxicity + 0.5744 57.44%
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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.78% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.41% 99.17%
CHEMBL2581 P07339 Cathepsin D 91.86% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 89.18% 89.63%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 88.63% 85.94%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.47% 97.25%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 86.88% 92.08%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.27% 97.29%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.93% 96.95%

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 13561
NPASS NPC96988