BDBM50038178 (+)-4-Amino-3-isoxazolidinone::(4R)-4-aminoisoxazolidin-3-one::(R)-4-AMINO-ISOXAZOLIDIN-3-ONE::CHEMBL771::D-CYCLOSERINE::alpha-Cycloserine::cycloserine

SMILES N[C@@H]1CON=C1O

InChI Key InChIKey=DYDCUQKUCUHJBH-UHFFFAOYSA-N

Data  1 KI  2 IC50  1 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50038178   

TargetGlutamate receptor ionotropic, NMDA 2C(Rat)
Merck Sharp & Dohme Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50038178((4R)-4-aminoisoxazolidin-3-one | cycloserine | (+)...)
Affinity DataEC50:  1.81E+4nMAssay Description:Compound was evaluated for in vitro inhibition of [3H]TCP at NMDA receptor.More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlutamate receptor ionotropic, NMDA 1(Rat)
Institut De Recherches Servier

Curated by ChEMBL
LigandPNGBDBM50038178((4R)-4-aminoisoxazolidin-3-one | cycloserine | (+)...)
Affinity DataIC50: 7.37E+3nMAssay Description:In vitro inhibitory activity to inhibit [3H]glycine binding to NMDA receptorMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetUDP-N-acetylmuramoyl-tripeptide--D-alanyl-D-alanine ligase(Staphylococcus epidermidis (strain ATCC 35984 / RP...)
Merck Sharp and Dohme Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50038178((4R)-4-aminoisoxazolidin-3-one | cycloserine | (+)...)
Affinity DataIC50: 3.00E+5nMAssay Description:Antibacterial activity against D-alanyl-D-alanine ligase from Streptococcus faecalis (ATCC 8043)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetProton-coupled amino acid transporter 1(Human)
Martin-Luther-University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50038178((4R)-4-aminoisoxazolidin-3-one | cycloserine | (+)...)
Affinity DataKi:  4.40E+6nMAssay Description:Inhibition of human PAT1-mediated L-[3H]proline uptake in human Caco2 cells after 10 mins by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed