BDBM50402979 CHEMBL2207395

SMILES: CC(=O)N(CNC[C@H]1NC[C@H](O)[C@@H]1O)Cc1ccccc1

InChI Key: InChIKey=YXRLSAPWCWOKTL-QLFBSQMISA-N

Data: 2 KI

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 2 hits for monomerid = 50402979   

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
Endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase (Homo sapiens (Human))	BDBM50402979 (CHEMBL2207395) Show SMILES CC(=O)N(CNC[C@H]1NC[C@H](O)[C@@H]1O)Cc1ccccc1 |r| Show InChI InChI=1S/C15H23N3O3/c1-11(19)18(9-12-5-3-2-4-6-12)10-16-7-13-15(21)14(20)8-17-13/h2-6,13-17,20-21H,7-10H2,1H3/t13-,14+,15-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	4.48E+4	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))	BDBM50402979 (CHEMBL2207395) Show SMILES CC(=O)N(CNC[C@H]1NC[C@H](O)[C@@H]1O)Cc1ccccc1 |r| Show InChI InChI=1S/C15H23N3O3/c1-11(19)18(9-12-5-3-2-4-6-12)10-16-7-13-15(21)14(20)8-17-13/h2-6,13-17,20-21H,7-10H2,1H3/t13-,14+,15-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	6.49E+4	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