3-(N-methylamino)glutaric acid

Details

Top
Internal ID 928e6f53-7c7c-4e92-a576-166be90d0209
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Amino fatty acids
IUPAC Name 3-(methylamino)pentanedioic acid
SMILES (Canonical) CNC(CC(=O)O)CC(=O)O
SMILES (Isomeric) CNC(CC(=O)O)CC(=O)O
InChI InChI=1S/C6H11NO4/c1-7-4(2-5(8)9)3-6(10)11/h4,7H,2-3H2,1H3,(H,8,9)(H,10,11)
InChI Key YVOZJYCBBUKBLG-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C6H11NO4
Molecular Weight 161.16 g/mol
Exact Mass 161.06880783 g/mol
Topological Polar Surface Area (TPSA) 86.60 Ų
XlogP -3.40
Atomic LogP (AlogP) -0.48
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

Top
3-(N-methylamino)glutaric acid

2D Structure

Top
2D Structure of 3-(N-methylamino)glutaric acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6954 69.54%
Caco-2 - 0.5957 59.57%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.5351 53.51%
OATP2B1 inhibitior - 0.8413 84.13%
OATP1B1 inhibitior + 0.9546 95.46%
OATP1B3 inhibitior + 0.9491 94.91%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9792 97.92%
P-glycoprotein inhibitior - 0.9746 97.46%
P-glycoprotein substrate - 0.9713 97.13%
CYP3A4 substrate - 0.7556 75.56%
CYP2C9 substrate + 0.6180 61.80%
CYP2D6 substrate - 0.7188 71.88%
CYP3A4 inhibition - 0.9801 98.01%
CYP2C9 inhibition - 0.9517 95.17%
CYP2C19 inhibition - 0.9679 96.79%
CYP2D6 inhibition - 0.9484 94.84%
CYP1A2 inhibition - 0.9245 92.45%
CYP2C8 inhibition - 0.9931 99.31%
CYP inhibitory promiscuity - 0.9936 99.36%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.7979 79.79%
Eye corrosion - 0.9355 93.55%
Eye irritation + 0.9747 97.47%
Skin irritation - 0.7881 78.81%
Skin corrosion - 0.7360 73.60%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7382 73.82%
Micronuclear - 0.5400 54.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.9559 95.59%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.6344 63.44%
Acute Oral Toxicity (c) III 0.6841 68.41%
Estrogen receptor binding - 0.8990 89.90%
Androgen receptor binding - 0.8043 80.43%
Thyroid receptor binding - 0.9077 90.77%
Glucocorticoid receptor binding - 0.7687 76.87%
Aromatase binding - 0.7868 78.68%
PPAR gamma - 0.9015 90.15%
Honey bee toxicity - 0.9514 95.14%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.9000 90.00%
Fish aquatic toxicity - 0.8415 84.15%

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 94.40% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.25% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.85% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 86.53% 90.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.41% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.42% 99.17%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 80.81% 100.00%

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 17903761
LOTUS LTS0230607
wikiData Q105365766