N,N,N-trimethyl-2-phenoxyethanaminium

Details

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Internal ID 1a223416-4148-4eda-8dbb-0eaa46b5044a
Taxonomy Benzenoids > Phenol ethers
IUPAC Name trimethyl(2-phenoxyethyl)azanium
SMILES (Canonical) C[N+](C)(C)CCOC1=CC=CC=C1
SMILES (Isomeric) C[N+](C)(C)CCOC1=CC=CC=C1
InChI InChI=1S/C11H18NO/c1-12(2,3)9-10-13-11-7-5-4-6-8-11/h4-8H,9-10H2,1-3H3/q+1
InChI Key VCXBSHBJVUIQHJ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H18NO+
Molecular Weight 180.27 g/mol
Exact Mass 180.138839198 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.77
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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N,N,N-trimethyl-2-phenoxyethanaminium
trimethyl(2-phenoxyethyl)azanium
6779-86-8
SCHEMBL9182123
DTXSID40274501
BDBM50188956
AKOS040824765
n,n,n-trimethyl-2-phenoxyethanaminium bromide

2D Structure

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2D Structure of N,N,N-trimethyl-2-phenoxyethanaminium

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.8275 82.75%
Caco-2 + 0.9620 96.20%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.5737 57.37%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9712 97.12%
OATP1B3 inhibitior + 0.9470 94.70%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.8748 87.48%
P-glycoprotein inhibitior - 0.9818 98.18%
P-glycoprotein substrate - 0.9619 96.19%
CYP3A4 substrate - 0.6415 64.15%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate + 0.4006 40.06%
CYP3A4 inhibition - 0.9825 98.25%
CYP2C9 inhibition - 0.9579 95.79%
CYP2C19 inhibition - 0.9623 96.23%
CYP2D6 inhibition + 0.6685 66.85%
CYP1A2 inhibition - 0.5690 56.90%
CYP2C8 inhibition + 0.5300 53.00%
CYP inhibitory promiscuity - 0.9561 95.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.6520 65.20%
Eye corrosion - 0.9512 95.12%
Eye irritation + 0.9817 98.17%
Skin irritation - 0.6133 61.33%
Skin corrosion - 0.5264 52.64%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5899 58.99%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.7875 78.75%
skin sensitisation - 0.7174 71.74%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity - 0.6092 60.92%
Acute Oral Toxicity (c) III 0.6848 68.48%
Estrogen receptor binding - 0.8149 81.49%
Androgen receptor binding - 0.5993 59.93%
Thyroid receptor binding - 0.8090 80.90%
Glucocorticoid receptor binding - 0.8532 85.32%
Aromatase binding - 0.7626 76.26%
PPAR gamma - 0.8374 83.74%
Honey bee toxicity - 0.9835 98.35%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.8100 81.00%
Fish aquatic toxicity - 0.7815 78.15%

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
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 97.17% 94.62%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.32% 96.09%
CHEMBL2039 P27338 Monoamine oxidase B 89.00% 92.51%
CHEMBL3401 O75469 Pregnane X receptor 87.21% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.94% 86.33%
CHEMBL2581 P07339 Cathepsin D 84.93% 98.95%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 84.58% 92.67%
CHEMBL221 P23219 Cyclooxygenase-1 83.90% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.83% 95.56%
CHEMBL4208 P20618 Proteasome component C5 83.77% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.16% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.68% 96.00%

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.
Artemisia annua
Chimonanthus praecox
Paederia foetida
Syzygium aromaticum

Cross-Links

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PubChem 9725
NPASS NPC313918
ChEMBL CHEMBL209891