(2R)-2-(methoxymethyl)-3-(trimethylazaniumyl)propanoate

Details

Top
Internal ID 3df0217f-11bb-47ba-867f-4e08b3a062c6
Taxonomy Organic nitrogen compounds > Organonitrogen compounds > Quaternary ammonium salts > Tetraalkylammonium salts
IUPAC Name (2R)-2-(methoxymethyl)-3-(trimethylazaniumyl)propanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H17NO3/c1-9(2,3)5-7(6-12-4)8(10)11/h7H,5-6H2,1-4H3/t7-/m1/s1
InChI Key PAJPPKOLTBGLSP-SSDOTTSWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C8H17NO3
Molecular Weight 175.23 g/mol
Exact Mass 175.12084340 g/mol
Topological Polar Surface Area (TPSA) 49.40 Ų
XlogP 0.30
Atomic LogP (AlogP) -1.29
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (2R)-2-(methoxymethyl)-3-(trimethylazaniumyl)propanoate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9658 96.58%
Caco-2 + 0.4921 49.21%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.7571 75.71%
Subcellular localzation Mitochondria 0.6003 60.03%
OATP2B1 inhibitior - 0.8155 81.55%
OATP1B1 inhibitior + 0.9600 96.00%
OATP1B3 inhibitior + 0.9460 94.60%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8872 88.72%
P-glycoprotein inhibitior - 0.9649 96.49%
P-glycoprotein substrate - 0.9295 92.95%
CYP3A4 substrate - 0.6107 61.07%
CYP2C9 substrate + 0.5915 59.15%
CYP2D6 substrate - 0.8471 84.71%
CYP3A4 inhibition - 0.9668 96.68%
CYP2C9 inhibition - 0.9306 93.06%
CYP2C19 inhibition - 0.9245 92.45%
CYP2D6 inhibition - 0.9359 93.59%
CYP1A2 inhibition - 0.9204 92.04%
CYP2C8 inhibition - 0.9450 94.50%
CYP inhibitory promiscuity - 0.9644 96.44%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5077 50.77%
Carcinogenicity (trinary) Non-required 0.5791 57.91%
Eye corrosion + 0.5156 51.56%
Eye irritation + 0.9424 94.24%
Skin irritation - 0.6000 60.00%
Skin corrosion - 0.7307 73.07%
Ames mutagenesis - 0.6054 60.54%
Human Ether-a-go-go-Related Gene inhibition - 0.8067 80.67%
Micronuclear - 0.8200 82.00%
Hepatotoxicity - 0.7716 77.16%
skin sensitisation - 0.8269 82.69%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.5421 54.21%
Acute Oral Toxicity (c) III 0.6336 63.36%
Estrogen receptor binding - 0.8269 82.69%
Androgen receptor binding - 0.7019 70.19%
Thyroid receptor binding - 0.8493 84.93%
Glucocorticoid receptor binding - 0.7861 78.61%
Aromatase binding - 0.7963 79.63%
PPAR gamma - 0.7437 74.37%
Honey bee toxicity - 0.9216 92.16%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.8300 83.00%
Fish aquatic toxicity - 0.6614 66.14%

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 98.46% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.90% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.35% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.77% 99.17%
CHEMBL2581 P07339 Cathepsin D 86.99% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.94% 94.45%

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 162806209
LOTUS LTS0146946
wikiData Q105204560