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SMILES C[C@H](N)C(=O)N1CCC[C@H]1C(O)=O

InChI Key InChIKey=WPWUFUBLGADILS-WDSKDSINSA-N

  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 10 hits for monomerid = 50020390   

TargetSolute carrier family 15 member 2(Homo sapiens (Human))
Universit£ degli Studi di Milano

Curated by ChEMBL
LigandPNGBDBM50020390((2S)-1-[(2S)-2-aminopropanoyl]pyrrolidine-2-carbox...)copy SMILEScopy InChI
Affinity DataKi:  1.20E+4nMAssay Description:Binding affinity to human PepT2 in SKTP cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MP549PPubMed
TargetAngiotensin-converting enzyme(Oryctolagus cuniculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50020390((2S)-1-[(2S)-2-aminopropanoyl]pyrrolidine-2-carbox...)copy SMILEScopy InChI
Affinity DataKi:  3.00E+4nMpH: 8.3Assay Description:Inhibitory constant was evaluated against Angiotensin I converting enzyme from rabbit lungs at pH 8.3More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Z60N24PubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50020390((2S)-1-[(2S)-2-aminopropanoyl]pyrrolidine-2-carbox...)copy SMILEScopy InChI
Affinity DataKi:  5.00E+4nMAssay Description:Inhibitory activity of the compound against Angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1QZZ
TargetAngiotensin-converting enzyme(Oryctolagus cuniculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50020390((2S)-1-[(2S)-2-aminopropanoyl]pyrrolidine-2-carbox...)copy SMILEScopy InChI
Affinity DataKi:  5.00E+4nMpH: 7.5Assay Description:Inhibitory constant was evaluated against Angiotensin I converting enzyme from rabbit lungs at pH 8More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Z60N24PubMed
TargetTripeptidyl-peptidase 2(Rattus norvegicus)
University College London

Curated by ChEMBL
LigandPNGBDBM50020390((2S)-1-[(2S)-2-aminopropanoyl]pyrrolidine-2-carbox...)copy SMILEScopy InChI
Affinity DataKi:  1.40E+6nMAssay Description:Inhibition potency against Cholecystokinin-8-Inactivating Peptidase (Serine Peptidase).More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2RX9CTGPubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50020390((2S)-1-[(2S)-2-aminopropanoyl]pyrrolidine-2-carbox...)copy SMILEScopy InChI
Affinity DataIC50: 2.29E+5nMAssay Description:Inhibitory activity against angiotensin converting enzyme (ACE)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2Z320V9PubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50020390((2S)-1-[(2S)-2-aminopropanoyl]pyrrolidine-2-carbox...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+5nMAssay Description:Inhibition of Angiotensin I converting enzyme from pig renal cortex, hippuryl-histidyl-leucine as substrateMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2XP75JSPubMed
TargetAngiotensin-converting enzyme(Oryctolagus cuniculus)
TBA

Curated by ChEMBL
LigandPNGBDBM50020390((2S)-1-[(2S)-2-aminopropanoyl]pyrrolidine-2-carbox...)copy SMILEScopy InChI
Affinity DataIC50: 2.70E+5nMAssay Description:Inhibition of rabbit lung ACE preincubated for 5 mins by spectrophotometric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DR2VV7PubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50020390((2S)-1-[(2S)-2-aminopropanoyl]pyrrolidine-2-carbox...)copy SMILEScopy InChI
Affinity DataIC50: 2.69E+8nMAssay Description:Inhibition of ACE (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29025F2PubMed
TargetAngiotensin-converting enzyme(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50020390((2S)-1-[(2S)-2-aminopropanoyl]pyrrolidine-2-carbox...)copy SMILEScopy InChI
Affinity DataIC50: 4.20E+4nMAssay Description:Inhibitory concentration against Angiotensin I converting enzymeMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J67HH7PubMed