4-(2-methoxyethyl)-N,N-dimethylaniline

Details

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Internal ID fdc06691-a6fa-4457-a0ec-9905bd3dd491
Taxonomy Organic nitrogen compounds > Organonitrogen compounds > Amines > Tertiary amines > Tertiary alkylarylamines > Dialkylarylamines
IUPAC Name 4-(2-methoxyethyl)-N,N-dimethylaniline
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H17NO/c1-12(2)11-6-4-10(5-7-11)8-9-13-3/h4-7H,8-9H2,1-3H3
InChI Key XHLATKPATPEGFC-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C11H17NO
Molecular Weight 179.26 g/mol
Exact Mass 179.131014166 g/mol
Topological Polar Surface Area (TPSA) 12.50 Ų
XlogP 2.20
Atomic LogP (AlogP) 1.94
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(2-methoxyethyl)-N,N-dimethylaniline

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9715 97.15%
Caco-2 + 0.9335 93.35%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.5954 59.54%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9260 92.60%
OATP1B3 inhibitior + 0.9418 94.18%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior - 0.8001 80.01%
P-glycoprotein inhibitior - 0.9744 97.44%
P-glycoprotein substrate - 0.8355 83.55%
CYP3A4 substrate - 0.5879 58.79%
CYP2C9 substrate - 0.8117 81.17%
CYP2D6 substrate + 0.5921 59.21%
CYP3A4 inhibition - 0.9286 92.86%
CYP2C9 inhibition - 0.9163 91.63%
CYP2C19 inhibition - 0.7840 78.40%
CYP2D6 inhibition - 0.8476 84.76%
CYP1A2 inhibition - 0.5080 50.80%
CYP2C8 inhibition - 0.8034 80.34%
CYP inhibitory promiscuity - 0.8651 86.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7220 72.20%
Carcinogenicity (trinary) Non-required 0.5044 50.44%
Eye corrosion - 0.8799 87.99%
Eye irritation + 0.9731 97.31%
Skin irritation + 0.5258 52.58%
Skin corrosion - 0.5172 51.72%
Ames mutagenesis + 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4904 49.04%
Micronuclear + 0.5900 59.00%
Hepatotoxicity - 0.5307 53.07%
skin sensitisation - 0.5878 58.78%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.6952 69.52%
Acute Oral Toxicity (c) III 0.7831 78.31%
Estrogen receptor binding - 0.5714 57.14%
Androgen receptor binding + 0.5348 53.48%
Thyroid receptor binding - 0.7185 71.85%
Glucocorticoid receptor binding - 0.6901 69.01%
Aromatase binding - 0.7109 71.09%
PPAR gamma - 0.8633 86.33%
Honey bee toxicity - 0.6781 67.81%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.6887 68.87%

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 96.64% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.74% 98.95%
CHEMBL2487 P05067 Beta amyloid A4 protein 89.51% 96.74%
CHEMBL3401 O75469 Pregnane X receptor 87.57% 94.73%
CHEMBL3492 P49721 Proteasome Macropain subunit 86.05% 90.24%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.32% 97.25%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 85.30% 95.17%
CHEMBL3230 O95977 Sphingosine 1-phosphate receptor Edg-6 84.82% 94.01%
CHEMBL2039 P27338 Monoamine oxidase B 81.07% 92.51%

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.
Zanthoxylum nitidum

Cross-Links

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PubChem 68899768
LOTUS LTS0263262
wikiData Q105328165