BDBM50039947 2-(5-Nonyloxy-1H-indol-3-yl)-ethylamine::CHEMBL97450

SMILES: CCCCCCCCCOc1ccc2[nH]cc(CCN)c2c1

InChI Key: InChIKey=YHSMSRREJYOGQJ-UHFFFAOYSA-N

Data: 7 KI  1 EC50

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 8 hits for monomerid = 50039947   

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 1B (Homo sapiens (Human))	BDBM50039947 (2-(5-Nonyloxy-1H-indol-3-yl)-ethylamine | CHEMBL97...) Show SMILES CCCCCCCCCOc1ccc2[nH]cc(CCN)c2c1 Show InChI InChI=1S/C19H30N2O/c1-2-3-4-5-6-7-8-13-22-17-9-10-19-18(14-17)16(11-12-20)15-21-19/h9-10,14-15,21H,2-8,11-13,20H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	1.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Medical College of Virginia/Virginia Commonwealth University Curated by ChEMBL					Assay Description Binding affinity was measured on 5-hydroxytryptamine 1D receptor beta in CHO cells transfected with human 5-HT1D beta gene labeled with [3H]-5-HT				J Med Chem 37: 2828-30 (1994) BindingDB Entry DOI: 10.7270/Q2GH9H0R
					More data for this Ligand-Target Pair
Serotonin 1B/1D receptor (Rattus norvegicus (Rat))	BDBM50039947 (2-(5-Nonyloxy-1H-indol-3-yl)-ethylamine | CHEMBL97...) Show SMILES CCCCCCCCCOc1ccc2[nH]cc(CCN)c2c1 Show InChI InChI=1S/C19H30N2O/c1-2-3-4-5-6-7-8-13-22-17-9-10-19-18(14-17)16(11-12-20)15-21-19/h9-10,14-15,21H,2-8,11-13,20H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	13	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Medical College of Virginia/Virginia Commonwealth University Curated by ChEMBL					Assay Description Binding affinity was measured on 5-hydroxytryptamine 1B receptor in rat striatum labeled with [3H]-5-HT				J Med Chem 37: 2828-30 (1994) BindingDB Entry DOI: 10.7270/Q2GH9H0R
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1D (Homo sapiens (Human))	BDBM50039947 (2-(5-Nonyloxy-1H-indol-3-yl)-ethylamine | CHEMBL97...) Show SMILES CCCCCCCCCOc1ccc2[nH]cc(CCN)c2c1 Show InChI InChI=1S/C19H30N2O/c1-2-3-4-5-6-7-8-13-22-17-9-10-19-18(14-17)16(11-12-20)15-21-19/h9-10,14-15,21H,2-8,11-13,20H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	16	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Medical College of Virginia/Virginia Commonwealth University Curated by ChEMBL					Assay Description Binding affinity was measured on 5-hydroxytryptamine 1D receptor alpha in COS cells transfected with human 5-HT1D alpha gene labeled with [3H]-5-HT				J Med Chem 37: 2828-30 (1994) BindingDB Entry DOI: 10.7270/Q2GH9H0R
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 2A (Homo sapiens (Human))	BDBM50039947 (2-(5-Nonyloxy-1H-indol-3-yl)-ethylamine | CHEMBL97...) Show SMILES CCCCCCCCCOc1ccc2[nH]cc(CCN)c2c1 Show InChI InChI=1S/C19H30N2O/c1-2-3-4-5-6-7-8-13-22-17-9-10-19-18(14-17)16(11-12-20)15-21-19/h9-10,14-15,21H,2-8,11-13,20H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	260	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Medical College of Virginia/Virginia Commonwealth University Curated by ChEMBL					Assay Description Binding affinity was measured on 5-hydroxytryptamine 2A receptor in GF6 cells transfected with human 5-HT2A gene labeled with [3H]-ketanserin				J Med Chem 37: 2828-30 (1994) BindingDB Entry DOI: 10.7270/Q2GH9H0R
					More data for this Ligand-Target Pair
Serotonin receptor 2a and 2c (5HT2A and 5HT2C) (Rattus norvegicus (Rat))	BDBM50039947 (2-(5-Nonyloxy-1H-indol-3-yl)-ethylamine | CHEMBL97...) Show SMILES CCCCCCCCCOc1ccc2[nH]cc(CCN)c2c1 Show InChI InChI=1S/C19H30N2O/c1-2-3-4-5-6-7-8-13-22-17-9-10-19-18(14-17)16(11-12-20)15-21-19/h9-10,14-15,21H,2-8,11-13,20H2,1H3	KEGG UniProtKB/SwissProt DrugBank GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	270	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Medical College of Virginia/Virginia Commonwealth University Curated by ChEMBL					Assay Description Binding affinity was measured on 5-hydroxytryptamine 2C receptor in J1 cells transfected with rat 5-HT2C gene labeled with [3H]-mesulergine				J Med Chem 37: 2828-30 (1994) BindingDB Entry DOI: 10.7270/Q2GH9H0R
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1A (Homo sapiens (Human))	BDBM50039947 (2-(5-Nonyloxy-1H-indol-3-yl)-ethylamine | CHEMBL97...) Show SMILES CCCCCCCCCOc1ccc2[nH]cc(CCN)c2c1 Show InChI InChI=1S/C19H30N2O/c1-2-3-4-5-6-7-8-13-22-17-9-10-19-18(14-17)16(11-12-20)15-21-19/h9-10,14-15,21H,2-8,11-13,20H2,1H3	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	315	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Medical College of Virginia/Virginia Commonwealth University Curated by ChEMBL					Assay Description Binding affinity was measured on 5-hydroxytryptamine 1A receptor in AK cells transfected with human 5-HT1A gene labeled with [3H]-8-OH-DPAT				J Med Chem 37: 2828-30 (1994) BindingDB Entry DOI: 10.7270/Q2GH9H0R
					More data for this Ligand-Target Pair
Serotonin 3a (5-HT3a)/3b (5-HT3b) receptor (Rattus norvegicus-RAT)	BDBM50039947 (2-(5-Nonyloxy-1H-indol-3-yl)-ethylamine | CHEMBL97...) Show SMILES CCCCCCCCCOc1ccc2[nH]cc(CCN)c2c1 Show InChI InChI=1S/C19H30N2O/c1-2-3-4-5-6-7-8-13-22-17-9-10-19-18(14-17)16(11-12-20)15-21-19/h9-10,14-15,21H,2-8,11-13,20H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Medical College of Virginia/Virginia Commonwealth University Curated by ChEMBL					Assay Description Binding affinity of the compound was measured on 5-hydroxytryptamine 3 receptor in NG-108 cells labeled with [3H]-GR-65,630				J Med Chem 37: 2828-30 (1994) BindingDB Entry DOI: 10.7270/Q2GH9H0R
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1D (Homo sapiens (Human))	BDBM50039947 (2-(5-Nonyloxy-1H-indol-3-yl)-ethylamine | CHEMBL97...) Show SMILES CCCCCCCCCOc1ccc2[nH]cc(CCN)c2c1 Show InChI InChI=1S/C19H30N2O/c1-2-3-4-5-6-7-8-13-22-17-9-10-19-18(14-17)16(11-12-20)15-21-19/h9-10,14-15,21H,2-8,11-13,20H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	n/a	n/a	68	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for its ability inhibit forskolin-stimulated activity of adenylate cyclase coupled to human 5-HT 1Dbeta receptor in CHO-K1 cells				Bioorg Med Chem Lett 5: 663-666 (1995) Article DOI: 10.1016/0960-894X(95)00091-7 BindingDB Entry DOI: 10.7270/Q2ZK5GMX
					More data for this Ligand-Target Pair