2-(Methylazaniumyl)acetate

Details

Top
Internal ID 5cf865f0-0846-459f-8e34-93fb7c7d9598
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids
IUPAC Name 2-(methylazaniumyl)acetate
SMILES (Canonical) C[NH2+]CC(=O)[O-]
SMILES (Isomeric) C[NH2+]CC(=O)[O-]
InChI InChI=1S/C3H7NO2/c1-4-2-3(5)6/h4H,2H2,1H3,(H,5,6)
InChI Key FSYKKLYZXJSNPZ-UHFFFAOYSA-N
Popularity 126 references in papers

Physical and Chemical Properties

Top
Molecular Formula C3H7NO2
Molecular Weight 89.09 g/mol
Exact Mass 89.047678466 g/mol
Topological Polar Surface Area (TPSA) 56.70 Ų
XlogP -2.10
Atomic LogP (AlogP) -3.07
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

Top
68411-97-2
sarcosine zwitterion
methylammon ioacetate
(methylammonio)acetate
(methylazaniumyl)acetate
CHEBI:57433

2D Structure

Top
2D Structure of 2-(Methylazaniumyl)acetate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9393 93.93%
Caco-2 + 0.7496 74.96%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Lysosomes 0.7169 71.69%
OATP2B1 inhibitior - 0.8674 86.74%
OATP1B1 inhibitior + 0.9376 93.76%
OATP1B3 inhibitior + 0.9515 95.15%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9681 96.81%
P-glycoprotein inhibitior - 0.9847 98.47%
P-glycoprotein substrate - 0.9812 98.12%
CYP3A4 substrate - 0.7500 75.00%
CYP2C9 substrate - 0.6069 60.69%
CYP2D6 substrate - 0.8355 83.55%
CYP3A4 inhibition - 0.9742 97.42%
CYP2C9 inhibition - 0.9476 94.76%
CYP2C19 inhibition - 0.9423 94.23%
CYP2D6 inhibition - 0.9546 95.46%
CYP1A2 inhibition - 0.8343 83.43%
CYP2C8 inhibition - 0.9864 98.64%
CYP inhibitory promiscuity - 0.9839 98.39%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5054 50.54%
Carcinogenicity (trinary) Non-required 0.5729 57.29%
Eye corrosion + 0.9008 90.08%
Eye irritation + 0.9817 98.17%
Skin irritation + 0.4909 49.09%
Skin corrosion + 0.5545 55.45%
Ames mutagenesis - 0.6664 66.64%
Human Ether-a-go-go-Related Gene inhibition - 0.8628 86.28%
Micronuclear - 0.8241 82.41%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.9325 93.25%
Respiratory toxicity - 0.9000 90.00%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity + 0.6017 60.17%
Acute Oral Toxicity (c) III 0.5441 54.41%
Estrogen receptor binding - 0.9602 96.02%
Androgen receptor binding - 0.9266 92.66%
Thyroid receptor binding - 0.9111 91.11%
Glucocorticoid receptor binding - 0.9268 92.68%
Aromatase binding - 0.8981 89.81%
PPAR gamma - 0.9300 93.00%
Honey bee toxicity - 0.9583 95.83%
Biodegradation + 0.9250 92.50%
Crustacea aquatic toxicity - 0.8000 80.00%
Fish aquatic toxicity - 0.9762 97.62%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.80% 96.09%
CHEMBL2581 P07339 Cathepsin D 83.06% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.95% 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.
Allium sativum
Biancaea sappan
Hypericum japonicum

Cross-Links

Top
PubChem 7311726
NPASS NPC134570