11-Methyl-11-hydroxyldodecanoic acid amide

Details

Top
Internal ID cf962baa-bd94-47e6-8ff4-3ee87211abb8
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Tertiary alcohols
IUPAC Name 11-hydroxy-11-methyldodecanamide
SMILES (Canonical) CC(C)(CCCCCCCCCC(=O)N)O
SMILES (Isomeric) CC(C)(CCCCCCCCCC(=O)N)O
InChI InChI=1S/C13H27NO2/c1-13(2,16)11-9-7-5-3-4-6-8-10-12(14)15/h16H,3-11H2,1-2H3,(H2,14,15)
InChI Key ZVJUMMBZQZQUAS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C13H27NO2
Molecular Weight 229.36 g/mol
Exact Mass 229.204179104 g/mol
Topological Polar Surface Area (TPSA) 63.30 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.75
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 10

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 11-Methyl-11-hydroxyldodecanoic acid amide

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9915 99.15%
Caco-2 + 0.7631 76.31%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.5939 59.39%
OATP2B1 inhibitior - 0.8502 85.02%
OATP1B1 inhibitior + 0.9629 96.29%
OATP1B3 inhibitior + 0.9493 94.93%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.6837 68.37%
P-glycoprotein inhibitior - 0.9395 93.95%
P-glycoprotein substrate - 0.9033 90.33%
CYP3A4 substrate - 0.6536 65.36%
CYP2C9 substrate - 0.6090 60.90%
CYP2D6 substrate - 0.8568 85.68%
CYP3A4 inhibition - 0.9526 95.26%
CYP2C9 inhibition - 0.8698 86.98%
CYP2C19 inhibition - 0.8691 86.91%
CYP2D6 inhibition - 0.9284 92.84%
CYP1A2 inhibition - 0.7496 74.96%
CYP2C8 inhibition - 0.9805 98.05%
CYP inhibitory promiscuity - 0.8674 86.74%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.6483 64.83%
Eye corrosion - 0.9330 93.30%
Eye irritation + 0.5595 55.95%
Skin irritation - 0.7554 75.54%
Skin corrosion - 0.9260 92.60%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6339 63.39%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.5348 53.48%
skin sensitisation - 0.8711 87.11%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.5447 54.47%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.6711 67.11%
Acute Oral Toxicity (c) III 0.7882 78.82%
Estrogen receptor binding - 0.8019 80.19%
Androgen receptor binding - 0.9230 92.30%
Thyroid receptor binding - 0.5453 54.53%
Glucocorticoid receptor binding - 0.5625 56.25%
Aromatase binding - 0.8600 86.00%
PPAR gamma - 0.5339 53.39%
Honey bee toxicity - 0.9780 97.80%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.5476 54.76%
Fish aquatic toxicity - 0.6157 61.57%

Targets

Top

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
CHEMBL4040 P28482 MAP kinase ERK2 95.81% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.72% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.21% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.74% 96.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.74% 91.11%
CHEMBL2581 P07339 Cathepsin D 82.66% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 82.51% 94.73%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.23% 97.25%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 81.76% 100.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.57% 89.34%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 80.53% 95.17%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 139590552
LOTUS LTS0196307
wikiData Q104202833