null

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

InChI Key InChIKey=ILPLXBQAXZPQTP-DPIDSQGUSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 6 hits for monomerid = 50104304   

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

Curated by ChEMBL
LigandPNGBDBM50104304(2-[((S)-1-Hydroxy-ethylamino)-methyl]-pyrrolidine-...)copy SMILEScopy InChI
Affinity DataKi:  5.90E+4nMAssay Description:Inhibitory activity towards Alpha-mannosidase from Jack beanMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2H70GBZPubMed
TargetAlpha-mannosidase 2(Homo sapiens (Human))
Universidade do Porto 687

Curated by ChEMBL
LigandPNGBDBM50104304(2-[((S)-1-Hydroxy-ethylamino)-methyl]-pyrrolidine-...)copy SMILEScopy InChI
Affinity DataKi:  4.50E+5nMAssay Description:Inhibition of human golgi alpha mannosidase 2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26T0NTCPubMed
TargetEndoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase(Homo sapiens (Human))
Universidade do Porto 687

Curated by ChEMBL
LigandPNGBDBM50104304(2-[((S)-1-Hydroxy-ethylamino)-methyl]-pyrrolidine-...)copy SMILEScopy InChI
Affinity DataKi:  9.18E+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-1,2-Mannosidase(Glycine max)
Section de Chimie de l'Universit£ de Lausanne

Curated by ChEMBL
LigandPNGBDBM50104304(2-[((S)-1-Hydroxy-ethylamino)-methyl]-pyrrolidine-...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+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
LigandPNGBDBM50104304(2-[((S)-1-Hydroxy-ethylamino)-methyl]-pyrrolidine-...)copy SMILEScopy InChI
Affinity DataIC50: 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
TargetBeta-glucosidase(Prunus avium)
Section de Chimie de l'Universit£ de Lausanne

Curated by ChEMBL
LigandPNGBDBM50104304(2-[((S)-1-Hydroxy-ethylamino)-methyl]-pyrrolidine-...)copy SMILEScopy InChI
Affinity DataIC50: 4.10E+5nMAssay Description:Inhibitory activity towards Beta-Glucosidase from AlmondMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2H70GBZPubMed