null

SMILES: C1CC(CN1)c1ccccc1

InChI Key: InChIKey=PRRFFTYUBPGHLE-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50144660   

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
5-hydroxytryptamine receptor 2A (Homo sapiens (Human))	BDBM50144660 (3-Phenyl-pyrrolidine | CHEMBL75207) Show SMILES C1CC(CN1)c1ccccc1 Show InChI InChI=1S/C10H13N/c1-2-4-9(5-3-1)10-6-7-11-8-10/h1-5,10-11H,6-8H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Virginia Commonwealth University Curated by ChEMBL					Assay Description Binding affinity towards 5-hydroxytryptamine 2A receptor using [3H]-ketanserin				Bioorg Med Chem Lett 14: 2279-83 (2004) Article DOI: 10.1016/j.bmcl.2004.02.014 BindingDB Entry DOI: 10.7270/Q23B5ZK3
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 2A/2B/2C (Rattus norvegicus (rat)-RAT-Rattus norvegicus (Rat...)	BDBM50144660 (3-Phenyl-pyrrolidine | CHEMBL75207) Show SMILES C1CC(CN1)c1ccccc1 Show InChI InChI=1S/C10H13N/c1-2-4-9(5-3-1)10-6-7-11-8-10/h1-5,10-11H,6-8H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory concentration against [3H]ketanserin binding to 5-hydroxytryptamine 2 receptor expressed in CHO-K1 cells				Bioorg Med Chem Lett 7: 241-246 (1997) Article DOI: 10.1016/S0960-894X(96)00618-X BindingDB Entry DOI: 10.7270/Q200023S
					More data for this Ligand-Target Pair
D(2) dopamine receptor (Rattus norvegicus (rat))	BDBM50144660 (3-Phenyl-pyrrolidine | CHEMBL75207) Show SMILES C1CC(CN1)c1ccccc1 Show InChI InChI=1S/C10H13N/c1-2-4-9(5-3-1)10-6-7-11-8-10/h1-5,10-11H,6-8H2	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	486	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory concentration against [3H]-U-86,170 binding to Dopamine receptor D2 expressed in CHO-K1 cells				Bioorg Med Chem Lett 7: 241-246 (1997) Article DOI: 10.1016/S0960-894X(96)00618-X BindingDB Entry DOI: 10.7270/Q200023S
					More data for this Ligand-Target Pair
D(3) dopamine receptor (Rattus norvegicus (Rat))	BDBM50144660 (3-Phenyl-pyrrolidine | CHEMBL75207) Show SMILES C1CC(CN1)c1ccccc1 Show InChI InChI=1S/C10H13N/c1-2-4-9(5-3-1)10-6-7-11-8-10/h1-5,10-11H,6-8H2	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	>2.44E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory concentration against [3H]-spiperone binding to Dopamine receptor D3 expressed in CHO-K1 cells				Bioorg Med Chem Lett 7: 241-246 (1997) Article DOI: 10.1016/S0960-894X(96)00618-X BindingDB Entry DOI: 10.7270/Q200023S
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Rattus norvegicus (rat))	BDBM50144660 (3-Phenyl-pyrrolidine | CHEMBL75207) Show SMILES C1CC(CN1)c1ccccc1 Show InChI InChI=1S/C10H13N/c1-2-4-9(5-3-1)10-6-7-11-8-10/h1-5,10-11H,6-8H2	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibitory concentration against [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor expressed in CHO-K1 cells				Bioorg Med Chem Lett 7: 241-246 (1997) Article DOI: 10.1016/S0960-894X(96)00618-X BindingDB Entry DOI: 10.7270/Q200023S
					More data for this Ligand-Target Pair