11-Aminoundecanoic acid

Details

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Internal ID 7afc50de-3793-4fb5-9c85-ee832a04d501
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Medium-chain fatty acids
IUPAC Name 11-aminoundecanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H23NO2/c12-10-8-6-4-2-1-3-5-7-9-11(13)14/h1-10,12H2,(H,13,14)
InChI Key GUOSQNAUYHMCRU-UHFFFAOYSA-N
Popularity 183 references in papers

Physical and Chemical Properties

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Molecular Formula C11H23NO2
Molecular Weight 201.31 g/mol
Exact Mass 201.172878976 g/mol
Topological Polar Surface Area (TPSA) 63.30 Ų
XlogP -1.00
Atomic LogP (AlogP) 2.54
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 10

Synonyms

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2432-99-7
Undecanoic acid, 11-amino-
11-Aminoundecylic acid
NCI-C50613
SFU34976HB
NSC-240503
NSC-662428
DTXSID5020077
RefChem:907971
DTXCID1077
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 11-Aminoundecanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9705 97.05%
Caco-2 - 0.6529 65.29%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.4827 48.27%
OATP2B1 inhibitior - 0.8534 85.34%
OATP1B1 inhibitior + 0.9671 96.71%
OATP1B3 inhibitior + 0.9479 94.79%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8267 82.67%
P-glycoprotein inhibitior - 0.9645 96.45%
P-glycoprotein substrate - 0.9714 97.14%
CYP3A4 substrate - 0.7824 78.24%
CYP2C9 substrate + 0.6180 61.80%
CYP2D6 substrate - 0.7526 75.26%
CYP3A4 inhibition - 0.9546 95.46%
CYP2C9 inhibition - 0.9540 95.40%
CYP2C19 inhibition - 0.9777 97.77%
CYP2D6 inhibition - 0.9711 97.11%
CYP1A2 inhibition - 0.9190 91.90%
CYP2C8 inhibition - 0.9838 98.38%
CYP inhibitory promiscuity - 0.9796 97.96%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6335 63.35%
Carcinogenicity (trinary) Non-required 0.5860 58.60%
Eye corrosion - 0.9679 96.79%
Eye irritation + 0.9162 91.62%
Skin irritation - 0.6564 65.64%
Skin corrosion - 0.6858 68.58%
Ames mutagenesis - 0.9800 98.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5923 59.23%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.8750 87.50%
skin sensitisation - 0.8931 89.31%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.6785 67.85%
Acute Oral Toxicity (c) IV 0.6342 63.42%
Estrogen receptor binding - 0.8287 82.87%
Androgen receptor binding - 0.9016 90.16%
Thyroid receptor binding - 0.7101 71.01%
Glucocorticoid receptor binding - 0.7352 73.52%
Aromatase binding - 0.7959 79.59%
PPAR gamma + 0.5368 53.68%
Honey bee toxicity - 0.9857 98.57%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity - 0.9205 92.05%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL2903 P16050 Arachidonate 15-lipoxygenase 5 nM
Potency
via Super-PRED
CHEMBL1947 P10828 Thyroid hormone receptor beta-1 398.1 nM
Potency
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.60% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.29% 99.17%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 89.95% 92.26%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.31% 91.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.57% 96.95%
CHEMBL4581 P52732 Kinesin-like protein 1 83.60% 93.18%
CHEMBL3492 P49721 Proteasome Macropain subunit 82.02% 90.24%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.28% 97.21%
CHEMBL1255126 O15151 Protein Mdm4 80.47% 90.20%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 17083
LOTUS LTS0047140
wikiData Q15632699