null

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

InChI Key InChIKey=QNAYBMKLOCPYGJ-UWTATZPHSA-N

PDB links: 394 PDB IDs match this monomer.

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50000109   

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

Curated by ChEMBL

LigandBDBM50000109((2R)-2-aminopropanoic acid | (R)-2-aminopropanoic ...)copy SMILEScopy InChI

Affinity DataKi:  1.90E+7nMAssay 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

Target InfoReactome pathwayKEGG
UniProtKB/SwissProt
DrugBankantibodypediaGoogleScholar

Ligand InfoPurchaseCHEMBLMCE
KEGGMMDBPC cidPC sidPDBPatentsSimilars

In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NZ882DPubMed

TargetGlutamate receptor ionotropic, NMDA 1(RAT)
Warner-Lambert Company

Curated by ChEMBL

LigandBDBM50000109((2R)-2-aminopropanoic acid | (R)-2-aminopropanoic ...)copy SMILEScopy InChI

Affinity DataIC50: 9.09E+4nMAssay Description:Inhibitory concentration of the compound required to inhibit [3H]-strychnine binding to N-methyl-D-aspartate glutamate receptor 1 of rat spinal cord ...More data for this Ligand-Target Pair

Target InfoPDB
UniProtKB/SwissProt
GoogleScholar

Ligand InfoPurchaseCHEMBLMCE
KEGGMMDBPC cidPC sidPDBPatentsSimilars

In DepthDetails
BindingDB Entry DOI: 10.7270/Q26W9911PubMed