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SMILES C[C@H](N)C(O)=O

InChI Key InChIKey=QNAYBMKLOCPYGJ-REOHCLBHSA-N

PDB links: 79 PDB IDs match this monomer.

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50000099   

TargetProton-coupled amino acid transporter 1(Homo sapiens (Human))
Martin-Luther-University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50000099((2S)-2-aminopropanoic acid | (S)-2-aminopropanoic ...)copy SMILEScopy InChI
Affinity DataKi:  2.80E+6nMAssay Description:Inhibition of human PAT1-mediated L-[3H]proline uptake in human Caco2 cells after 10 mins by liquid scintillation countingChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ882DPubMedDrugBank
TargetXanthine dehydrogenase/oxidase(Homo sapiens (Human))
CHINA PHARMACEUTICAL UNIVERSITY

US Patent
LigandPNGBDBM50000099((2S)-2-aminopropanoic acid | (S)-2-aminopropanoic ...)copy SMILEScopy InChI
Affinity DataIC50: 6.00E+4nMAssay Description:11.1 Preparation of Reagents and Standard Solutions(1) 75 mM phosphate buffer (PB, pH 7.4): containing KH2PO4 0.0956 g, K2HPO4 0.6946 g, EDTA 1.862 m...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2959MQDUS Patent
TargetGlutamate receptor ionotropic, NMDA 1(RAT)
Warner-Lambert Company

Curated by ChEMBL
LigandPNGBDBM50000099((2S)-2-aminopropanoic acid | (S)-2-aminopropanoic ...)copy SMILEScopy InChI
Affinity DataIC50: 1.98E+5nMAssay Description:Inhibitory concentration of the compound required to inhibit [3H]-strychnine binding to N-methyl-D-aspartate glutamate receptor 1More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q26W9911PubMed