Compile Data Set for Download or QSAR

Found 4 hits Enz. Inhib. hit(s) with Target = 'Nicotinic acetylcholine receptor alpha1 subunit'   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Nicotinic acetylcholine receptor alpha1 subunit (Heliothis virescens)	BDBM50376053 (PROTOSTEMODIOL) Show SMILES COC1=C(OC(=O)C1C)C(=O)[C@@H](C)[C@@H]1[C@@H]2CC[C@@H]([C@@H]3C[C@H](C)C(=O)O3)N2CCC[C@@H]1O |t:2| Show InChI InChI=1S/C23H33NO7/c1-11-10-17(30-22(11)27)14-7-8-15-18(16(25)6-5-9-24(14)15)12(2)19(26)21-20(29-4)13(3)23(28)31-21/h11-18,25H,5-10H2,1-4H3/t11-,12-,13?,14-,15-,16-,17-,18+/m0/s1	UniProtKB/TrEMBL GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at nAChR in Heliothis virescens neuronal cells by voltage clamp technique				J Nat Prod 71: 112-6 (2008) Article DOI: 10.1021/np070427k BindingDB Entry DOI: 10.7270/Q21Z4596
					More data for this Ligand-Target Pair
Nicotinic acetylcholine receptor alpha1 subunit (Heliothis virescens)	BDBM50376055 (CHEMBL404139) Show SMILES CCCC[C@]12[C@@H]3C[C@H]4[C@H]5[C@H](C)C(O[C@]5(O3)[C@@H]1CCN24)C1OC(=O)C(CO)=C1OC |w:11.11,19.24,c:30,TLB:16:15:7.18.8:5.14,6:7:15:5.14,THB:17:18:15:5.14,17:18:5.6:15.13.8,6:5:15:7.18.8,9:8:15:5.14| Show InChI InChI=1S/C22H31NO6/c1-4-5-7-21-14-6-8-23(21)13-9-15(21)28-22(14)16(13)11(2)17(29-22)19-18(26-3)12(10-24)20(25)27-19/h11,13-17,19,24H,4-10H2,1-3H3/t11-,13-,14+,15-,16+,17?,19?,21?,22+/m0/s1	UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	12	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Agonist activity at nAChR in Heliothis virescens neuronal cells by voltage clamp technique				J Nat Prod 71: 112-6 (2008) Article DOI: 10.1021/np070427k BindingDB Entry DOI: 10.7270/Q21Z4596
					More data for this Ligand-Target Pair
Nicotinic acetylcholine receptor alpha1 subunit (Heliothis virescens)	BDBM50376054 (CHEMBL255667) Show SMILES CCCC[C@]12[C@H]3C[C@H]4[C@H]5[C@H](C)C(O[C@]5(O3)[C@@H]1[C@H](O)CN24)C1OC(=O)C(C)=C1OC |w:11.11,20.25,c:30,TLB:16:15:7.19.8:5.14,6:7:15:5.14,THB:18:19:15:5.14,18:19:5.6:15.13.8,6:5:15:7.19.8,9:8:15:5.14| Show InChI InChI=1S/C22H31NO6/c1-5-6-7-21-14-8-12-15-10(2)17(18-16(26-4)11(3)20(25)27-18)29-22(15,28-14)19(21)13(24)9-23(12)21/h10,12-15,17-19,24H,5-9H2,1-4H3/t10-,12-,13+,14+,15+,17?,18?,19+,21?,22-/m0/s1	UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	157	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Agonist activity at nAChR in Heliothis virescens neuronal cells by voltage clamp technique				J Nat Prod 71: 112-6 (2008) Article DOI: 10.1021/np070427k BindingDB Entry DOI: 10.7270/Q21Z4596
					More data for this Ligand-Target Pair
Nicotinic acetylcholine receptor alpha1 subunit (Heliothis virescens)	BDBM50376056 (STEMOFOLINE) Show SMILES CCCC[C@]12[C@H]3C[C@H]4[C@H]5[C@H](C)\C(O[C@]5(O3)C1CCN24)=C1\OC(=O)C(C)=C1OC |w:15.18,c:29,TLB:14:13:17.16:4,THB:17:18:5.6:15.13.8,6:7:17.16:4,9:8:17.16:4,12:13:17.16:4,TEB:16:15:7.18.8:5.14,16:15:18:5.6| Show InChI InChI=1S/C22H29NO5/c1-5-6-8-21-14-7-9-23(21)13-10-15(21)27-22(14)16(13)11(2)18(28-22)19-17(25-4)12(3)20(24)26-19/h11,13-16H,5-10H2,1-4H3/b19-18-/t11-,13-,14?,15+,16+,21?,22+/m0/s1	UniProtKB/TrEMBL GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	n/a	n/a	50	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Agonist activity at nAChR in Heliothis virescens neuronal cells by voltage clamp technique				J Nat Prod 71: 112-6 (2008) Article DOI: 10.1021/np070427k BindingDB Entry DOI: 10.7270/Q21Z4596
					More data for this Ligand-Target Pair