BDBM50185802 3-(1-(naphthalen-1-ylmethyl)piperidin-4-yl)-1H-pyrrolo[2,3-b]pyridine::CHEMBL377402

SMILES: C(N1CCC(CC1)c1c[nH]c2ncccc12)c1cccc2ccccc12

InChI Key: InChIKey=OIAARQYDFVPWDI-UHFFFAOYSA-N

Data: 4 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 4 hits for monomerid = 50185802   

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
Mu-type opioid receptor (Homo sapiens (Human))	BDBM50185802 (3-(1-(naphthalen-1-ylmethyl)piperidin-4-yl)-1H-pyr...) Show SMILES C(N1CCC(CC1)c1c[nH]c2ncccc12)c1cccc2ccccc12 Show InChI InChI=1S/C23H23N3/c1-2-8-20-17(5-1)6-3-7-19(20)16-26-13-10-18(11-14-26)22-15-25-23-21(22)9-4-12-24-23/h1-9,12,15,18H,10-11,13-14,16H2,(H,24,25)	PDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	340	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [3H]DAMGO from mu opioid receptor expressed in HEK293 cells				Bioorg Med Chem Lett 16: 3524-8 (2006) Article DOI: 10.1016/j.bmcl.2006.03.094 BindingDB Entry DOI: 10.7270/Q2VT1RQJ
					More data for this Ligand-Target Pair
Kappa-type opioid receptor (Homo sapiens (Human))	BDBM50185802 (3-(1-(naphthalen-1-ylmethyl)piperidin-4-yl)-1H-pyr...) Show SMILES C(N1CCC(CC1)c1c[nH]c2ncccc12)c1cccc2ccccc12 Show InChI InChI=1S/C23H23N3/c1-2-8-20-17(5-1)6-3-7-19(20)16-26-13-10-18(11-14-26)22-15-25-23-21(22)9-4-12-24-23/h1-9,12,15,18H,10-11,13-14,16H2,(H,24,25)	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	710	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [3H]U-69593 from kappa opioid receptor expressed in HEK293 cells				Bioorg Med Chem Lett 16: 3524-8 (2006) Article DOI: 10.1016/j.bmcl.2006.03.094 BindingDB Entry DOI: 10.7270/Q2VT1RQJ
					More data for this Ligand-Target Pair
Nociceptin receptor (Homo sapiens (Human))	BDBM50185802 (3-(1-(naphthalen-1-ylmethyl)piperidin-4-yl)-1H-pyr...) Show SMILES C(N1CCC(CC1)c1c[nH]c2ncccc12)c1cccc2ccccc12 Show InChI InChI=1S/C23H23N3/c1-2-8-20-17(5-1)6-3-7-19(20)16-26-13-10-18(11-14-26)22-15-25-23-21(22)9-4-12-24-23/h1-9,12,15,18H,10-11,13-14,16H2,(H,24,25)	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	820	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Agonist activity at ORL1 receptor expressed in HEK293 cells by calciun flux assay				Bioorg Med Chem Lett 16: 3524-8 (2006) Article DOI: 10.1016/j.bmcl.2006.03.094 BindingDB Entry DOI: 10.7270/Q2VT1RQJ
					More data for this Ligand-Target Pair
Delta-type opioid receptor (Homo sapiens (Human))	BDBM50185802 (3-(1-(naphthalen-1-ylmethyl)piperidin-4-yl)-1H-pyr...) Show SMILES C(N1CCC(CC1)c1c[nH]c2ncccc12)c1cccc2ccccc12 Show InChI InChI=1S/C23H23N3/c1-2-8-20-17(5-1)6-3-7-19(20)16-26-13-10-18(11-14-26)22-15-25-23-21(22)9-4-12-24-23/h1-9,12,15,18H,10-11,13-14,16H2,(H,24,25)	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	>5.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson & Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Displacement of [3H]DDPDE from delta opioid receptor expressed in HEK293 cells				Bioorg Med Chem Lett 16: 3524-8 (2006) Article DOI: 10.1016/j.bmcl.2006.03.094 BindingDB Entry DOI: 10.7270/Q2VT1RQJ
					More data for this Ligand-Target Pair