(2S)-2-amino-3-(5-methyl-3-oxo-1,2-oxazolidin-2-yl)propanoic acid

Details

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Internal ID b7b02a6e-6b21-4684-ab0c-c17031c364f6
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids > L-alpha-amino acids
IUPAC Name (2S)-2-amino-3-(5-methyl-3-oxo-1,2-oxazolidin-2-yl)propanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H12N2O4/c1-4-2-6(10)9(13-4)3-5(8)7(11)12/h4-5H,2-3,8H2,1H3,(H,11,12)/t4?,5-/m0/s1
InChI Key WUYBVXKJPCCIDP-AKGZTFGVSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C7H12N2O4
Molecular Weight 188.18 g/mol
Exact Mass 188.07970687 g/mol
Topological Polar Surface Area (TPSA) 92.90 Ų
XlogP -3.70
Atomic LogP (AlogP) -1.05
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S)-2-amino-3-(5-methyl-3-oxo-1,2-oxazolidin-2-yl)propanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6785 67.85%
Caco-2 - 0.6914 69.14%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.4438 44.38%
OATP2B1 inhibitior - 0.8547 85.47%
OATP1B1 inhibitior + 0.9426 94.26%
OATP1B3 inhibitior + 0.9324 93.24%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9516 95.16%
P-glycoprotein inhibitior - 0.9817 98.17%
P-glycoprotein substrate - 0.9036 90.36%
CYP3A4 substrate - 0.6569 65.69%
CYP2C9 substrate + 0.6054 60.54%
CYP2D6 substrate - 0.8028 80.28%
CYP3A4 inhibition - 0.8910 89.10%
CYP2C9 inhibition - 0.8880 88.80%
CYP2C19 inhibition - 0.8808 88.08%
CYP2D6 inhibition - 0.9241 92.41%
CYP1A2 inhibition - 0.8944 89.44%
CYP2C8 inhibition - 0.9857 98.57%
CYP inhibitory promiscuity - 0.9908 99.08%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7100 71.00%
Carcinogenicity (trinary) Non-required 0.4810 48.10%
Eye corrosion - 0.9822 98.22%
Eye irritation - 0.8649 86.49%
Skin irritation - 0.7608 76.08%
Skin corrosion - 0.9277 92.77%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8188 81.88%
Micronuclear + 0.7700 77.00%
Hepatotoxicity + 0.5839 58.39%
skin sensitisation - 0.8659 86.59%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.7487 74.87%
Acute Oral Toxicity (c) III 0.6168 61.68%
Estrogen receptor binding - 0.8632 86.32%
Androgen receptor binding - 0.6515 65.15%
Thyroid receptor binding - 0.8416 84.16%
Glucocorticoid receptor binding - 0.6147 61.47%
Aromatase binding - 0.8070 80.70%
PPAR gamma - 0.8377 83.77%
Honey bee toxicity - 0.9755 97.55%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity - 0.5277 52.77%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.41% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.33% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.52% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 86.51% 90.17%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.24% 90.71%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.05% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.85% 99.17%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.63% 93.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.46% 93.04%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.32% 97.09%

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.
Coix lacryma-jobi

Cross-Links

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PubChem 163188551
LOTUS LTS0070271
wikiData Q105313382