null

SMILES OC(=O)[C@@H]1CCCN1

InChI Key InChIKey=ONIBWKKTOPOVIA-BYPYZUCNSA-N

PDB links: 59 PDB IDs match this monomer.

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50000100   

TargetAngiotensin-converting enzyme(Homo sapiens (Human))
E£tv£s Lor£nd University

Curated by ChEMBL
LigandPNGBDBM50000100((-)-(S)-proline | (-)-2-pyrrolidinecarboxylic acid...)copy SMILEScopy InChI
Affinity DataKi:  8.60E+4nMAssay Description:Inhibition of ACE (unknown origin) assessed as 3-Hydroxybutyril-glycil-glycil-glycine conversion to 3-hydroxybutyric acid after 60 mins by WST assayMore data for this Ligand-Target Pair
TargetProton-coupled amino acid transporter 1(Homo sapiens (Human))
Martin-Luther-University Halle-Wittenberg

Curated by ChEMBL
LigandPNGBDBM50000100((-)-(S)-proline | (-)-2-pyrrolidinecarboxylic acid...)copy SMILEScopy InChI
Affinity DataKi:  1.60E+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/Q2NZ882DPubMed
TargetGlutamate receptor ionotropic, NMDA 1(RAT)
Warner-Lambert Company

Curated by ChEMBL
LigandPNGBDBM50000100((-)-(S)-proline | (-)-2-pyrrolidinecarboxylic acid...)copy SMILEScopy InChI
Affinity DataIC50: 4.14E+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