null

SMILES: CC(=O)c1ccc(OCCCN2CC[C@H](N)C2)cc1

InChI Key: InChIKey=PHNZBVSSQHIXIP-AWEZNQCLSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 6 hits for monomerid = 50119696   

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
Histamine H3 receptor (Rattus norvegicus (rat))	BDBM50119696 (1-{4-[3-((S)-3-Amino-pyrrolidin-1-yl)-propoxy]-phe...) Show SMILES CC(=O)c1ccc(OCCCN2CC[C@H](N)C2)cc1 Show InChI InChI=1S/C15H22N2O2/c1-12(18)13-3-5-15(6-4-13)19-10-2-8-17-9-7-14(16)11-17/h3-6,14H,2,7-11,16H2,1H3/t14-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	676	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Binding affinity of the compound towards rat Histamine H3 receptor (For compound 11)				Bioorg Med Chem Lett 12: 3055-8 (2002) BindingDB Entry DOI: 10.7270/Q2B56J3P
					More data for this Ligand-Target Pair
Histamine H3 receptor (Rattus norvegicus (rat))	BDBM50119696 (1-{4-[3-((S)-3-Amino-pyrrolidin-1-yl)-propoxy]-phe...) Show SMILES CC(=O)c1ccc(OCCCN2CC[C@H](N)C2)cc1 Show InChI InChI=1S/C15H22N2O2/c1-12(18)13-3-5-15(6-4-13)19-10-2-8-17-9-7-14(16)11-17/h3-6,14H,2,7-11,16H2,1H3/t14-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	1.72E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Binding affinity against rat histamine H3 receptor				Bioorg Med Chem Lett 12: 3055-8 (2002) BindingDB Entry DOI: 10.7270/Q2B56J3P
					More data for this Ligand-Target Pair
Histamine H2 receptor (Homo sapiens (Human))	BDBM50119696 (1-{4-[3-((S)-3-Amino-pyrrolidin-1-yl)-propoxy]-phe...) Show SMILES CC(=O)c1ccc(OCCCN2CC[C@H](N)C2)cc1 Show InChI InChI=1S/C15H22N2O2/c1-12(18)13-3-5-15(6-4-13)19-10-2-8-17-9-7-14(16)11-17/h3-6,14H,2,7-11,16H2,1H3/t14-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	3.10E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Binding affinity of the compound towards human Histamine H2 receptor (For compound 11)				Bioorg Med Chem Lett 12: 3055-8 (2002) BindingDB Entry DOI: 10.7270/Q2B56J3P
					More data for this Ligand-Target Pair
Histamine H2 receptor (Homo sapiens (Human))	BDBM50119696 (1-{4-[3-((S)-3-Amino-pyrrolidin-1-yl)-propoxy]-phe...) Show SMILES CC(=O)c1ccc(OCCCN2CC[C@H](N)C2)cc1 Show InChI InChI=1S/C15H22N2O2/c1-12(18)13-3-5-15(6-4-13)19-10-2-8-17-9-7-14(16)11-17/h3-6,14H,2,7-11,16H2,1H3/t14-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Binding affinity to the human Histamine H2 receptor				Bioorg Med Chem Lett 12: 3055-8 (2002) BindingDB Entry DOI: 10.7270/Q2B56J3P
					More data for this Ligand-Target Pair
Histamine H1 receptor (Homo sapiens (Human))	BDBM50119696 (1-{4-[3-((S)-3-Amino-pyrrolidin-1-yl)-propoxy]-phe...) Show SMILES CC(=O)c1ccc(OCCCN2CC[C@H](N)C2)cc1 Show InChI InChI=1S/C15H22N2O2/c1-12(18)13-3-5-15(6-4-13)19-10-2-8-17-9-7-14(16)11-17/h3-6,14H,2,7-11,16H2,1H3/t14-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	9.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Binding affinity to the human Histamine H1 receptor				Bioorg Med Chem Lett 12: 3055-8 (2002) BindingDB Entry DOI: 10.7270/Q2B56J3P
					More data for this Ligand-Target Pair
Histamine H1 receptor (Homo sapiens (Human))	BDBM50119696 (1-{4-[3-((S)-3-Amino-pyrrolidin-1-yl)-propoxy]-phe...) Show SMILES CC(=O)c1ccc(OCCCN2CC[C@H](N)C2)cc1 Show InChI InChI=1S/C15H22N2O2/c1-12(18)13-3-5-15(6-4-13)19-10-2-8-17-9-7-14(16)11-17/h3-6,14H,2,7-11,16H2,1H3/t14-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Binding affinity of the compound towards human Histamine H1 receptor (For compound 11)				Bioorg Med Chem Lett 12: 3055-8 (2002) BindingDB Entry DOI: 10.7270/Q2B56J3P
					More data for this Ligand-Target Pair