null

SMILES: C[C@@H](N)Cc1c2CCOc2c(CCC(O)=O)c2CCOc12

InChI Key: InChIKey=TZUQOPZXSVCNQP-SECBINFHSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50210082   

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 (Rattus norvegicus (rat))	BDBM50210082 (3-[8-((R)-2-amino-propyl)-2,3,6,7-tetrahydro-benzo...) Show SMILES C[C@@H](N)Cc1c2CCOc2c(CCC(O)=O)c2CCOc12 Show InChI InChI=1S/C16H21NO4/c1-9(17)8-13-12-5-7-20-15(12)10(2-3-14(18)19)11-4-6-21-16(11)13/h9H,2-8,17H2,1H3,(H,18,19)/t9-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	>1.00E+3	n/a	n/a	n/a	n/a
Alcon Research, Ltd Curated by ChEMBL					Assay Description Agonist activity at 5HT2A receptor in rat A7r5 cells assessed as intracellular calcium mobilization relative to 5HT				Bioorg Med Chem Lett 17: 2998-3002 (2007) Article DOI: 10.1016/j.bmcl.2007.03.073 BindingDB Entry DOI: 10.7270/Q2KS6R7B
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 2A (Rattus norvegicus (rat))	BDBM50210082 (3-[8-((R)-2-amino-propyl)-2,3,6,7-tetrahydro-benzo...) Show SMILES C[C@@H](N)Cc1c2CCOc2c(CCC(O)=O)c2CCOc12 Show InChI InChI=1S/C16H21NO4/c1-9(17)8-13-12-5-7-20-15(12)10(2-3-14(18)19)11-4-6-21-16(11)13/h9H,2-8,17H2,1H3,(H,18,19)/t9-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
Alcon Research, Ltd Curated by ChEMBL					Assay Description Displacement of [125I]DOI from 5HT2A receptor in rat cerebral cortex				Bioorg Med Chem Lett 17: 2998-3002 (2007) Article DOI: 10.1016/j.bmcl.2007.03.073 BindingDB Entry DOI: 10.7270/Q2KS6R7B
					More data for this Ligand-Target Pair