BDBM50201702 (1R,2S)-2-phenoxy-7-oxa-5-aza-bicyclo[3.2.1]octane-6-thione::CHEMBL390643

SMILES: S=C1O[C@@H]2CN1CC[C@@H]2Oc1ccccc1

InChI Key: InChIKey=BMIOGAIQRVIVKQ-WDEREUQCSA-N

Data: 9 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 = 50201702   

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
Dipeptidyl peptidase I (Homo sapiens (Human))	BDBM50201702 ((1R,2S)-2-phenoxy-7-oxa-5-aza-bicyclo[3.2.1]octane...) Show SMILES S=C1O[C@@H]2CN1CC[C@@H]2Oc1ccccc1 Show InChI InChI=1S/C12H13NO2S/c16-12-13-7-6-10(11(8-13)15-12)14-9-4-2-1-3-5-9/h1-5,10-11H,6-8H2/t10-,11+/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	606	n/a	n/a	n/a	n/a	n/a	n/a
The Genomics Institute of the Novartis Research Foundation Curated by ChEMBL					Assay Description Inhibition of human recombinant cathepsin C				Bioorg Med Chem Lett 17: 1254-9 (2007) Article DOI: 10.1016/j.bmcl.2006.12.014 BindingDB Entry DOI: 10.7270/Q2QN66DT
					More data for this Ligand-Target Pair
Cathepsin K (Homo sapiens (Human))	BDBM50201702 ((1R,2S)-2-phenoxy-7-oxa-5-aza-bicyclo[3.2.1]octane...) Show SMILES S=C1O[C@@H]2CN1CC[C@@H]2Oc1ccccc1 Show InChI InChI=1S/C12H13NO2S/c16-12-13-7-6-10(11(8-13)15-12)14-9-4-2-1-3-5-9/h1-5,10-11H,6-8H2/t10-,11+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.83E+3	n/a	n/a	n/a	n/a	n/a	n/a
The Genomics Institute of the Novartis Research Foundation Curated by ChEMBL					Assay Description Inhibition of human recombinant cathepsin K				Bioorg Med Chem Lett 17: 1254-9 (2007) Article DOI: 10.1016/j.bmcl.2006.12.014 BindingDB Entry DOI: 10.7270/Q2QN66DT
					More data for this Ligand-Target Pair
Pro-cathepsin H (Homo sapiens (Human))	BDBM50201702 ((1R,2S)-2-phenoxy-7-oxa-5-aza-bicyclo[3.2.1]octane...) Show SMILES S=C1O[C@@H]2CN1CC[C@@H]2Oc1ccccc1 Show InChI InChI=1S/C12H13NO2S/c16-12-13-7-6-10(11(8-13)15-12)14-9-4-2-1-3-5-9/h1-5,10-11H,6-8H2/t10-,11+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
The Genomics Institute of the Novartis Research Foundation Curated by ChEMBL					Assay Description Inhibition of human recombinant cathepsin H				Bioorg Med Chem Lett 17: 1254-9 (2007) Article DOI: 10.1016/j.bmcl.2006.12.014 BindingDB Entry DOI: 10.7270/Q2QN66DT
					More data for this Ligand-Target Pair
Procathepsin L (Homo sapiens (Human))	BDBM50201702 ((1R,2S)-2-phenoxy-7-oxa-5-aza-bicyclo[3.2.1]octane...) Show SMILES S=C1O[C@@H]2CN1CC[C@@H]2Oc1ccccc1 Show InChI InChI=1S/C12H13NO2S/c16-12-13-7-6-10(11(8-13)15-12)14-9-4-2-1-3-5-9/h1-5,10-11H,6-8H2/t10-,11+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	994	n/a	n/a	n/a	n/a	n/a	n/a
The Genomics Institute of the Novartis Research Foundation Curated by ChEMBL					Assay Description Inhibition of human recombinant cathepsin L				Bioorg Med Chem Lett 17: 1254-9 (2007) Article DOI: 10.1016/j.bmcl.2006.12.014 BindingDB Entry DOI: 10.7270/Q2QN66DT
					More data for this Ligand-Target Pair
Cathepsin B (Homo sapiens (Human))	BDBM50201702 ((1R,2S)-2-phenoxy-7-oxa-5-aza-bicyclo[3.2.1]octane...) Show SMILES S=C1O[C@@H]2CN1CC[C@@H]2Oc1ccccc1 Show InChI InChI=1S/C12H13NO2S/c16-12-13-7-6-10(11(8-13)15-12)14-9-4-2-1-3-5-9/h1-5,10-11H,6-8H2/t10-,11+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	519	n/a	n/a	n/a	n/a	n/a	n/a
The Genomics Institute of the Novartis Research Foundation Curated by ChEMBL					Assay Description Inhibition of human recombinant cathepsin B				Bioorg Med Chem Lett 17: 1254-9 (2007) Article DOI: 10.1016/j.bmcl.2006.12.014 BindingDB Entry DOI: 10.7270/Q2QN66DT
					More data for this Ligand-Target Pair
Cathepsin F (Homo sapiens (Human))	BDBM50201702 ((1R,2S)-2-phenoxy-7-oxa-5-aza-bicyclo[3.2.1]octane...) Show SMILES S=C1O[C@@H]2CN1CC[C@@H]2Oc1ccccc1 Show InChI InChI=1S/C12H13NO2S/c16-12-13-7-6-10(11(8-13)15-12)14-9-4-2-1-3-5-9/h1-5,10-11H,6-8H2/t10-,11+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
The Genomics Institute of the Novartis Research Foundation Curated by ChEMBL					Assay Description Inhibition of human recombinant cathepsin F				Bioorg Med Chem Lett 17: 1254-9 (2007) Article DOI: 10.1016/j.bmcl.2006.12.014 BindingDB Entry DOI: 10.7270/Q2QN66DT
					More data for this Ligand-Target Pair
Cathepsin S (Homo sapiens (Human))	BDBM50201702 ((1R,2S)-2-phenoxy-7-oxa-5-aza-bicyclo[3.2.1]octane...) Show SMILES S=C1O[C@@H]2CN1CC[C@@H]2Oc1ccccc1 Show InChI InChI=1S/C12H13NO2S/c16-12-13-7-6-10(11(8-13)15-12)14-9-4-2-1-3-5-9/h1-5,10-11H,6-8H2/t10-,11+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	696	n/a	n/a	n/a	n/a	n/a	n/a
The Genomics Institute of the Novartis Research Foundation Curated by ChEMBL					Assay Description Inhibition of human recombinant cathepsin S				Bioorg Med Chem Lett 17: 1254-9 (2007) Article DOI: 10.1016/j.bmcl.2006.12.014 BindingDB Entry DOI: 10.7270/Q2QN66DT
					More data for this Ligand-Target Pair
Cathepsin K (Homo sapiens (Human))	BDBM50201702 ((1R,2S)-2-phenoxy-7-oxa-5-aza-bicyclo[3.2.1]octane...) Show SMILES S=C1O[C@@H]2CN1CC[C@@H]2Oc1ccccc1 Show InChI InChI=1S/C12H13NO2S/c16-12-13-7-6-10(11(8-13)15-12)14-9-4-2-1-3-5-9/h1-5,10-11H,6-8H2/t10-,11+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	7.15E+3	n/a	n/a	n/a	n/a	n/a	n/a
The Genomics Institute of the Novartis Research Foundation Curated by ChEMBL					Assay Description Inhibition of human recombinant cathepsin X				Bioorg Med Chem Lett 17: 1254-9 (2007) Article DOI: 10.1016/j.bmcl.2006.12.014 BindingDB Entry DOI: 10.7270/Q2QN66DT
					More data for this Ligand-Target Pair
Cathepsin L2 (Homo sapiens (Human))	BDBM50201702 ((1R,2S)-2-phenoxy-7-oxa-5-aza-bicyclo[3.2.1]octane...) Show SMILES S=C1O[C@@H]2CN1CC[C@@H]2Oc1ccccc1 Show InChI InChI=1S/C12H13NO2S/c16-12-13-7-6-10(11(8-13)15-12)14-9-4-2-1-3-5-9/h1-5,10-11H,6-8H2/t10-,11+/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.17E+3	n/a	n/a	n/a	n/a	n/a	n/a
The Genomics Institute of the Novartis Research Foundation Curated by ChEMBL					Assay Description Inhibition of human recombinant cathepsin V				Bioorg Med Chem Lett 17: 1254-9 (2007) Article DOI: 10.1016/j.bmcl.2006.12.014 BindingDB Entry DOI: 10.7270/Q2QN66DT
					More data for this Ligand-Target Pair