BDBM50104301 2-[((R)-1-Hydroxy-ethylamino)-methyl]-pyrrolidine-3,4-diol::BDBM50402987::CHEMBL2206827::CHEMBL79763

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

InChI Key: InChIKey=ILPLXBQAXZPQTP-BJMCJPPVSA-N

Data: 5 KI  4 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 9 hits for monomerid = 50104301   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Alpha-mannosidase (Glycine max)	BDBM50104301 (2-[((R)-1-Hydroxy-ethylamino)-methyl]-pyrrolidine-...) Show SMILES C[C@H](O)NC[C@H]1NC[C@H](O)[C@@H]1O |r| Show InChI InChI=1S/C7H16N2O3/c1-4(10)8-2-5-7(12)6(11)3-9-5/h4-12H,2-3H2,1H3/t4-,5?,6?,7?/m1/s1	KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.20E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Section de Chimie de l'Universit£ de Lausanne Curated by ChEMBL					Assay Description Inhibitory activity towards Alpha-mannosidase from Jack bean				Bioorg Med Chem Lett 11: 2489-93 (2001) BindingDB Entry DOI: 10.7270/Q2H70GBZ
					More data for this Ligand-Target Pair
Beta-glucosidase A (Caldocellum saccharolyticum)	BDBM50104301 (2-[((R)-1-Hydroxy-ethylamino)-methyl]-pyrrolidine-...) Show SMILES C[C@H](O)NC[C@H]1NC[C@H](O)[C@@H]1O |r| Show InChI InChI=1S/C7H16N2O3/c1-4(10)8-2-5-7(12)6(11)3-9-5/h4-12H,2-3H2,1H3/t4-,5?,6?,7?/m1/s1	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.70E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Section de Chimie de l'Universit£ de Lausanne Curated by ChEMBL					Assay Description Inhibitory activity towards Beta-Glucosidase from Caldocellum saccharol.				Bioorg Med Chem Lett 11: 2489-93 (2001) BindingDB Entry DOI: 10.7270/Q2H70GBZ
					More data for this Ligand-Target Pair
Beta-glucosidase (Prunus avium)	BDBM50104301 (2-[((R)-1-Hydroxy-ethylamino)-methyl]-pyrrolidine-...) Show SMILES C[C@H](O)NC[C@H]1NC[C@H](O)[C@@H]1O |r| Show InChI InChI=1S/C7H16N2O3/c1-4(10)8-2-5-7(12)6(11)3-9-5/h4-12H,2-3H2,1H3/t4-,5?,6?,7?/m1/s1	UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	3.40E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Section de Chimie de l'Universit£ de Lausanne Curated by ChEMBL					Assay Description Inhibitory activity towards Beta-Glucosidase from Caldocellum saccharol.				Bioorg Med Chem Lett 11: 2489-93 (2001) BindingDB Entry DOI: 10.7270/Q2H70GBZ
					More data for this Ligand-Target Pair
Endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase (Homo sapiens (Human))	BDBM50104301 (2-[((R)-1-Hydroxy-ethylamino)-methyl]-pyrrolidine-...) Show SMILES C[C@H](O)NC[C@H]1NC[C@H](O)[C@@H]1O |r| Show InChI InChI=1S/C7H16N2O3/c1-4(10)8-2-5-7(12)6(11)3-9-5/h4-12H,2-3H2,1H3/t4-,5?,6?,7?/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.88E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universidade do Porto 687 Curated by ChEMBL					Assay Description Inhibition of human ER alpha mannosidase 1				Bioorg Med Chem 20: 6945-59 (2012) Article DOI: 10.1016/j.bmc.2012.10.011 BindingDB Entry DOI: 10.7270/Q26T0NTC
					More data for this Ligand-Target Pair
Golgi alpha-mannosidase II (Homo sapiens (Human))	BDBM50104301 (2-[((R)-1-Hydroxy-ethylamino)-methyl]-pyrrolidine-...) Show SMILES C[C@H](O)NC[C@H]1NC[C@H](O)[C@@H]1O |r| Show InChI InChI=1S/C7H16N2O3/c1-4(10)8-2-5-7(12)6(11)3-9-5/h4-12H,2-3H2,1H3/t4-,5?,6?,7?/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	6.83E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universidade do Porto 687 Curated by ChEMBL					Assay Description Inhibition of human golgi alpha mannosidase 2				Bioorg Med Chem 20: 6945-59 (2012) Article DOI: 10.1016/j.bmc.2012.10.011 BindingDB Entry DOI: 10.7270/Q26T0NTC
					More data for this Ligand-Target Pair
Beta-galactosidase (Aspergillus niger)	BDBM50104301 (2-[((R)-1-Hydroxy-ethylamino)-methyl]-pyrrolidine-...) Show SMILES C[C@H](O)NC[C@H]1NC[C@H](O)[C@@H]1O |r| Show InChI InChI=1S/C7H16N2O3/c1-4(10)8-2-5-7(12)6(11)3-9-5/h4-12H,2-3H2,1H3/t4-,5?,6?,7?/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	4.80E+5	n/a	n/a	n/a	n/a	n/a	n/a
Section de Chimie de l'Universit£ de Lausanne Curated by ChEMBL					Assay Description Inhibitory activity towards Beta-galactosidase from Aspergillus niger				Bioorg Med Chem Lett 11: 2489-93 (2001) BindingDB Entry DOI: 10.7270/Q2H70GBZ
					More data for this Ligand-Target Pair
Beta-glucosidase (Prunus avium)	BDBM50104301 (2-[((R)-1-Hydroxy-ethylamino)-methyl]-pyrrolidine-...) Show SMILES C[C@H](O)NC[C@H]1NC[C@H](O)[C@@H]1O |r| Show InChI InChI=1S/C7H16N2O3/c1-4(10)8-2-5-7(12)6(11)3-9-5/h4-12H,2-3H2,1H3/t4-,5?,6?,7?/m1/s1	UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.90E+5	n/a	n/a	n/a	n/a	n/a	n/a
Section de Chimie de l'Universit£ de Lausanne Curated by ChEMBL					Assay Description Inhibitory activity towards Beta-Glucosidase from Almond				Bioorg Med Chem Lett 11: 2489-93 (2001) BindingDB Entry DOI: 10.7270/Q2H70GBZ
					More data for this Ligand-Target Pair
Beta-glucosidase A (Caldocellum saccharolyticum)	BDBM50104301 (2-[((R)-1-Hydroxy-ethylamino)-methyl]-pyrrolidine-...) Show SMILES C[C@H](O)NC[C@H]1NC[C@H](O)[C@@H]1O |r| Show InChI InChI=1S/C7H16N2O3/c1-4(10)8-2-5-7(12)6(11)3-9-5/h4-12H,2-3H2,1H3/t4-,5?,6?,7?/m1/s1	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.80E+5	n/a	n/a	n/a	n/a	n/a	n/a
Section de Chimie de l'Universit£ de Lausanne Curated by ChEMBL					Assay Description Inhibitory activity towards Beta-Glucosidase from Caldocellum saccharol.				Bioorg Med Chem Lett 11: 2489-93 (2001) BindingDB Entry DOI: 10.7270/Q2H70GBZ
					More data for this Ligand-Target Pair
Alpha-mannosidase (Glycine max)	BDBM50104301 (2-[((R)-1-Hydroxy-ethylamino)-methyl]-pyrrolidine-...) Show SMILES C[C@H](O)NC[C@H]1NC[C@H](O)[C@@H]1O |r| Show InChI InChI=1S/C7H16N2O3/c1-4(10)8-2-5-7(12)6(11)3-9-5/h4-12H,2-3H2,1H3/t4-,5?,6?,7?/m1/s1	KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	4.90E+5	n/a	n/a	n/a	n/a	n/a	n/a
Section de Chimie de l'Universit£ de Lausanne Curated by ChEMBL					Assay Description Inhibitory activity towards Alpha-mannosidase from Jack bean				Bioorg Med Chem Lett 11: 2489-93 (2001) BindingDB Entry DOI: 10.7270/Q2H70GBZ
					More data for this Ligand-Target Pair