BDBM141891 US8921410, Table 2 Compound 30

SMILES: O=C(N1CC2CNCC(C2)C1)c1ccc(o1)[N+]#[C-]

InChI Key: InChIKey=ILBHGBTWZRVMPE-UHFFFAOYSA-N

Data: 2 KI

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 = 141891   

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
Neuronal acetylcholine receptor subunit alpha-4 (Homo sapiens (Human))	BDBM141891 (US8921410, Table 2 Compound 30) Show SMILES O=C(N1CC2CNCC(C2)C1)c1ccc(o1)[N+]#[C-] Show InChI InChI=1S/C13H15N3O2/c1-14-12-3-2-11(18-12)13(17)16-7-9-4-10(8-16)6-15-5-9/h2-3,9-10,15H,4-8H2	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	8.70	-10.8	n/a	n/a	n/a	n/a	n/a	n/a	21
Targacept, Inc. US Patent					Assay Description The binding of [3H]MLA was measured using a modification of the methods of Davies et al., Neuropharmacol. 38: 679 (1999). [3H]MLA (Specific Activity=...				US Patent US8921410 (2014) BindingDB Entry DOI: 10.7270/Q2QZ28PT
					More data for this Ligand-Target Pair
Neuronal acetylcholine receptor (Rattus norvegicus (Rat))	BDBM141891 (US8921410, Table 2 Compound 30) Show SMILES O=C(N1CC2CNCC(C2)C1)c1ccc(o1)[N+]#[C-] Show InChI InChI=1S/C13H15N3O2/c1-14-12-3-2-11(18-12)13(17)16-7-9-4-10(8-16)6-15-5-9/h2-3,9-10,15H,4-8H2	PDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	US Patent	35	-10.0	n/a	n/a	n/a	n/a	n/a	n/a	21
Targacept, Inc. US Patent					Assay Description The binding of [3H]MLA was measured using a modification of the methods of Davies et al., Neuropharmacol. 38: 679 (1999). [3H]MLA (Specific Activity=...				US Patent US8921410 (2014) BindingDB Entry DOI: 10.7270/Q2QZ28PT
					More data for this Ligand-Target Pair