null

SMILES C[C@H](O)NC[C@H]1NC[C@H](O)[C@@H]1O

InChI Key InChIKey=ILPLXBQAXZPQTP-BJMCJPPVSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 9 hits for monomerid = 50104301   

Targetalpha-1,2-Mannosidase(Glycine max)
Section de Chimie de l'Universit£ de Lausanne

Curated by ChEMBL
LigandPNGBDBM50104301(2-[((R)-1-Hydroxy-ethylamino)-methyl]-pyrrolidine-...)copy SMILEScopy InChI
Affinity DataKi:  1.20E+5nMAssay Description:Inhibitory activity towards Alpha-mannosidase from Jack beanMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2H70GBZPubMed
TargetBeta-glucosidase A(Caldocellum saccharolyticum)
Section de Chimie de l'Universit£ de Lausanne

Curated by ChEMBL
LigandPNGBDBM50104301(2-[((R)-1-Hydroxy-ethylamino)-methyl]-pyrrolidine-...)copy SMILEScopy InChI
Affinity DataKi:  1.70E+5nMAssay Description:Inhibitory activity towards Beta-Glucosidase from Caldocellum saccharol.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2H70GBZPubMed
TargetBeta-glucosidase(Prunus avium)
Section de Chimie de l'Universit£ de Lausanne

Curated by ChEMBL
LigandPNGBDBM50104301(2-[((R)-1-Hydroxy-ethylamino)-methyl]-pyrrolidine-...)copy SMILEScopy InChI
Affinity DataKi:  3.40E+5nMAssay Description:Inhibitory activity towards Beta-Glucosidase from Caldocellum saccharol.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2H70GBZPubMed
TargetEndoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase(Homo sapiens (Human))
Universidade do Porto 687

Curated by ChEMBL
LigandPNGBDBM50104301(2-[((R)-1-Hydroxy-ethylamino)-methyl]-pyrrolidine-...)copy SMILEScopy InChI
Affinity DataKi:  4.88E+5nMAssay Description:Inhibition of human ER alpha mannosidase 1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26T0NTCPubMed
TargetAlpha-mannosidase 2(Homo sapiens (Human))
Universidade do Porto 687

Curated by ChEMBL
LigandPNGBDBM50104301(2-[((R)-1-Hydroxy-ethylamino)-methyl]-pyrrolidine-...)copy SMILEScopy InChI
Affinity DataKi:  6.83E+5nMAssay Description:Inhibition of human golgi alpha mannosidase 2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26T0NTCPubMed
TargetBeta-galactosidase(Aspergillus niger)
Section de Chimie de l'Universit£ de Lausanne

Curated by ChEMBL
LigandPNGBDBM50104301(2-[((R)-1-Hydroxy-ethylamino)-methyl]-pyrrolidine-...)copy SMILEScopy InChI
Affinity DataIC50: 4.80E+5nMAssay Description:Inhibitory activity towards Beta-galactosidase from Aspergillus nigerMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2H70GBZPubMed
TargetBeta-glucosidase(Prunus avium)
Section de Chimie de l'Universit£ de Lausanne

Curated by ChEMBL
LigandPNGBDBM50104301(2-[((R)-1-Hydroxy-ethylamino)-methyl]-pyrrolidine-...)copy SMILEScopy InChI
Affinity DataIC50: 2.90E+5nMAssay Description:Inhibitory activity towards Beta-Glucosidase from AlmondMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2H70GBZPubMed
TargetBeta-glucosidase A(Caldocellum saccharolyticum)
Section de Chimie de l'Universit£ de Lausanne

Curated by ChEMBL
LigandPNGBDBM50104301(2-[((R)-1-Hydroxy-ethylamino)-methyl]-pyrrolidine-...)copy SMILEScopy InChI
Affinity DataIC50: 1.80E+5nMAssay Description:Inhibitory activity towards Beta-Glucosidase from Caldocellum saccharol.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2H70GBZPubMed
Targetalpha-1,2-Mannosidase(Glycine max)
Section de Chimie de l'Universit£ de Lausanne

Curated by ChEMBL
LigandPNGBDBM50104301(2-[((R)-1-Hydroxy-ethylamino)-methyl]-pyrrolidine-...)copy SMILEScopy InChI
Affinity DataIC50: 4.90E+5nMAssay Description:Inhibitory activity towards Alpha-mannosidase from Jack beanMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2H70GBZPubMed