BDBM50473889 CHEMBL332216

SMILES: [H][C@@]12Cc3cc(O)ccc3C(C)(CCN1CCc1ccccc1)C2(C)C

InChI Key: InChIKey=ATFJOLYMKGOWSP-BBQAJUCSSA-N

Data: 1 KI  1 IC50

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 2 hits for monomerid = 50473889   

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
Sodium channel protein type 1/2/3 subunit alpha (Rattus norvegicus)	BDBM50473889 (CHEMBL332216) Show SMILES [H][C@@]12Cc3cc(O)ccc3C(C)(CCN1CCc1ccccc1)C2(C)C |THB:8:9:23:14.12.13,15:14:23:9.3.2| Show InChI InChI=1S/C23H29NO/c1-22(2)21-16-18-15-19(25)9-10-20(18)23(22,3)12-14-24(21)13-11-17-7-5-4-6-8-17/h4-10,15,21,25H,11-14,16H2,1-3H3/t21-,23?/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.29E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Boehringer Ingelheim Pharma KG Curated by ChEMBL					Assay Description Displacement of [3H]BTX from sodium channel of rat cerebral cortex synaptosomes				J Med Chem 45: 3755-64 (2002) Article DOI: 10.1021/jm020875j BindingDB Entry DOI: 10.7270/Q2ZS308Z
					More data for this Ligand-Target Pair
Sodium channel protein type 1/2/3 subunit alpha (Rattus norvegicus)	BDBM50473889 (CHEMBL332216) Show SMILES [H][C@@]12Cc3cc(O)ccc3C(C)(CCN1CCc1ccccc1)C2(C)C |THB:8:9:23:14.12.13,15:14:23:9.3.2| Show InChI InChI=1S/C23H29NO/c1-22(2)21-16-18-15-19(25)9-10-20(18)23(22,3)12-14-24(21)13-11-17-7-5-4-6-8-17/h4-10,15,21,25H,11-14,16H2,1-3H3/t21-,23?/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.03E+3	n/a	n/a	n/a	n/a	n/a	n/a
Boehringer Ingelheim Pharma KG Curated by ChEMBL					Assay Description Inhibitory effect against veratridine-induced glutamate release from rat brain slices				J Med Chem 45: 3755-64 (2002) Article DOI: 10.1021/jm020875j BindingDB Entry DOI: 10.7270/Q2ZS308Z
					More data for this Ligand-Target Pair