2-Amino-3-(5-oxooxolan-2-yl)propanoic acid

Details

Top
Internal ID 41cbe700-d374-409e-88d9-0f7f018921a8
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-amino-3-(5-oxooxolan-2-yl)propanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H11NO4/c8-5(7(10)11)3-4-1-2-6(9)12-4/h4-5H,1-3,8H2,(H,10,11)
InChI Key COZVJQVSNYNVIL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C7H11NO4
Molecular Weight 173.17 g/mol
Exact Mass 173.06880783 g/mol
Topological Polar Surface Area (TPSA) 89.60 Ų
XlogP -3.00
Atomic LogP (AlogP) -0.51
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 2-Amino-3-(5-oxooxolan-2-yl)propanoic acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7960 79.60%
Caco-2 - 0.9242 92.42%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.5681 56.81%
OATP2B1 inhibitior - 0.8510 85.10%
OATP1B1 inhibitior + 0.9555 95.55%
OATP1B3 inhibitior + 0.9462 94.62%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9389 93.89%
P-glycoprotein inhibitior - 0.9918 99.18%
P-glycoprotein substrate - 0.9783 97.83%
CYP3A4 substrate - 0.6896 68.96%
CYP2C9 substrate - 0.6054 60.54%
CYP2D6 substrate - 0.7827 78.27%
CYP3A4 inhibition - 0.9742 97.42%
CYP2C9 inhibition - 0.9560 95.60%
CYP2C19 inhibition - 0.9433 94.33%
CYP2D6 inhibition - 0.9564 95.64%
CYP1A2 inhibition - 0.9220 92.20%
CYP2C8 inhibition - 0.9526 95.26%
CYP inhibitory promiscuity - 0.9939 99.39%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6728 67.28%
Eye corrosion - 0.9741 97.41%
Eye irritation - 0.8541 85.41%
Skin irritation - 0.8194 81.94%
Skin corrosion - 0.8219 82.19%
Ames mutagenesis - 0.6828 68.28%
Human Ether-a-go-go-Related Gene inhibition - 0.7957 79.57%
Micronuclear - 0.5100 51.00%
Hepatotoxicity + 0.7806 78.06%
skin sensitisation - 0.9131 91.31%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.8599 85.99%
Acute Oral Toxicity (c) III 0.6245 62.45%
Estrogen receptor binding - 0.8907 89.07%
Androgen receptor binding - 0.8641 86.41%
Thyroid receptor binding - 0.8375 83.75%
Glucocorticoid receptor binding - 0.6072 60.72%
Aromatase binding - 0.9442 94.42%
PPAR gamma - 0.7347 73.47%
Honey bee toxicity - 0.9773 97.73%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity - 0.8329 83.29%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.39% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.94% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.25% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.17% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.53% 99.17%
CHEMBL2581 P07339 Cathepsin D 81.73% 98.95%

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.
Asplenium prolongatum

Cross-Links

Top
PubChem 101411018
LOTUS LTS0061831
wikiData Q104967395