Compile Data Set for Download or QSAR

Found 77 hits with Last Name = 'fantegrossi' and Initial = 'we'   

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
Cannabinoid receptor 1 (Mus musculus (Mouse))	BDBM239073 (US9416103, CP-55,940) Show SMILES CCCCCCC(C)(C)c1ccc(C2CC(O)CC[C@H]2CCCO)c(O)c1 |r| Show InChI InChI=1S/C24H40O3/c1-4-5-6-7-14-24(2,3)19-11-13-21(23(27)16-19)22-17-20(26)12-10-18(22)9-8-15-25/h11,13,16,18,20,22,25-27H,4-10,12,14-15,17H2,1-3H3/t18-,20?,22?/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	US Patent	0.370	-53.8	n/a	n/a	n/a	n/a	n/a	n/a	25
The Board of Trustees of the University of Arkansas; The University of Kansas US Patent					Assay Description Competition receptor binding was performed as previously described [Shoemaker et al., J. Pharmacol. Exp. Ther., 314:868-75]. Briefly, 50 μg of mou...				US Patent US9416103 (2016) BindingDB Entry DOI: 10.7270/Q2HX1BKQ
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM239078 (US9416103, TV-5-157) Show SMILES CCCCn1cc(C(=O)c2cccc3ccccc23)c2cccc(OC)c12 Show InChI InChI=1S/C24H23NO2/c1-3-4-15-25-16-21(19-12-8-14-22(27-2)23(19)25)24(26)20-13-7-10-17-9-5-6-11-18(17)20/h5-14,16H,3-4,15H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	0.810	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Kansas Curated by ChEMBL					Assay Description Agonist activity at human CB2 receptor transfected in CHO cells assessed as inhibition of forskolin-stimulated adenylyl cyclase activity after 15 min...				J Med Chem 56: 4537-50 (2013) Article DOI: 10.1021/jm400268b BindingDB Entry DOI: 10.7270/Q25M68M1
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM239078 (US9416103, TV-5-157) Show SMILES CCCCn1cc(C(=O)c2cccc3ccccc23)c2cccc(OC)c12 Show InChI InChI=1S/C24H23NO2/c1-3-4-15-25-16-21(19-12-8-14-22(27-2)23(19)25)24(26)20-13-7-10-17-9-5-6-11-18(17)20/h5-14,16H,3-4,15H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	0.810	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Board of Trustees of the University of Arkansas; The University of Kansas US Patent					Assay Description A functional assay screen for the inhibition of adenylate cyclase (AC) activity was chosen as the subsequent assay. This screen would allow us to gai...				US Patent US9416103 (2016) BindingDB Entry DOI: 10.7270/Q2HX1BKQ
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Mus musculus (Mouse))	BDBM239078 (US9416103, TV-5-157) Show SMILES CCCCn1cc(C(=O)c2cccc3ccccc23)c2cccc(OC)c12 Show InChI InChI=1S/C24H23NO2/c1-3-4-15-25-16-21(19-12-8-14-22(27-2)23(19)25)24(26)20-13-7-10-17-9-5-6-11-18(17)20/h5-14,16H,3-4,15H2,1-2H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	1.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Board of Trustees of the University of Arkansas; The University of Kansas US Patent					Assay Description A functional assay screen for the inhibition of adenylate cyclase (AC) activity was chosen as the subsequent assay. This screen would allow us to gai...				US Patent US9416103 (2016) BindingDB Entry DOI: 10.7270/Q2HX1BKQ
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Mus musculus (Mouse))	BDBM239078 (US9416103, TV-5-157) Show SMILES CCCCn1cc(C(=O)c2cccc3ccccc23)c2cccc(OC)c12 Show InChI InChI=1S/C24H23NO2/c1-3-4-15-25-16-21(19-12-8-14-22(27-2)23(19)25)24(26)20-13-7-10-17-9-5-6-11-18(17)20/h5-14,16H,3-4,15H2,1-2H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Kansas Curated by ChEMBL					Assay Description Agonist activity at CB1 receptor in mouse Neuro2a cells assessed as inhibition of forskolin-stimulated adenylyl cyclase activity after 15 mins by liq...				J Med Chem 56: 4537-50 (2013) Article DOI: 10.1021/jm400268b BindingDB Entry DOI: 10.7270/Q25M68M1
					More data for this Ligand-Target Pair
Alpha-1A adrenergic receptor (Homo sapiens (Human))	BDBM50160160 ((S)-1,2-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-...) Show SMILES COc1cc2CCN(C)[C@H]3Cc4cc5OCOc5cc4-c(c1OC)c23 Show InChI InChI=1S/C20H21NO4/c1-21-5-4-11-7-17(22-2)20(23-3)19-13-9-16-15(24-10-25-16)8-12(13)6-14(21)18(11)19/h7-9,14H,4-6,10H2,1-3H3/t14-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	2	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Hunter College and the Graduate Center of the City University of New York Curated by ChEMBL					Assay Description Displacement of [3H]Prazosin from human adrenergic alpha1A receptor				Bioorg Med Chem Lett 20: 628-31 (2010) Article DOI: 10.1016/j.bmcl.2009.11.053 BindingDB Entry DOI: 10.7270/Q2C53MT3
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM85804 (1-Naphthyl(1-butyl-1H-indole-3-yl)methanone | JWH-...) Show SMILES CCCCn1cc(C(=O)c2cccc3ccccc23)c2ccccc12 Show InChI InChI=1S/C23H21NO/c1-2-3-15-24-16-21(19-12-6-7-14-22(19)24)23(25)20-13-8-10-17-9-4-5-11-18(17)20/h4-14,16H,2-3,15H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	9.80	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Kansas Curated by ChEMBL					Assay Description Agonist activity at human CB2 receptor transfected in CHO cells assessed as inhibition of forskolin-stimulated adenylyl cyclase activity after 15 min...				J Med Chem 56: 4537-50 (2013) Article DOI: 10.1021/jm400268b BindingDB Entry DOI: 10.7270/Q25M68M1
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM85804 (1-Naphthyl(1-butyl-1H-indole-3-yl)methanone | JWH-...) Show SMILES CCCCn1cc(C(=O)c2cccc3ccccc23)c2ccccc12 Show InChI InChI=1S/C23H21NO/c1-2-3-15-24-16-21(19-12-6-7-14-22(19)24)23(25)20-13-8-10-17-9-4-5-11-18(17)20/h4-14,16H,2-3,15H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	US Patent	9.80	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Board of Trustees of the University of Arkansas; The University of Kansas US Patent					Assay Description A functional assay screen for the inhibition of adenylate cyclase (AC) activity was chosen as the subsequent assay. This screen would allow us to gai...				US Patent US9416103 (2016) BindingDB Entry DOI: 10.7270/Q2HX1BKQ
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM239077 (US9416103, TV-5-249) Show SMILES CCCCn1cc(Cc2cccc3ccccc23)c2cccc(OC)c12 Show InChI InChI=1S/C24H25NO/c1-3-4-15-25-17-20(22-13-8-14-23(26-2)24(22)25)16-19-11-7-10-18-9-5-6-12-21(18)19/h5-14,17H,3-4,15-16H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	10.9	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Board of Trustees of the University of Arkansas; The University of Kansas US Patent					Assay Description A functional assay screen for the inhibition of adenylate cyclase (AC) activity was chosen as the subsequent assay. This screen would allow us to gai...				US Patent US9416103 (2016) BindingDB Entry DOI: 10.7270/Q2HX1BKQ
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM239077 (US9416103, TV-5-249) Show SMILES CCCCn1cc(Cc2cccc3ccccc23)c2cccc(OC)c12 Show InChI InChI=1S/C24H25NO/c1-3-4-15-25-17-20(22-13-8-14-23(26-2)24(22)25)16-19-11-7-10-18-9-5-6-12-21(18)19/h5-14,17H,3-4,15-16H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	11	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Kansas Curated by ChEMBL					Assay Description Agonist activity at human CB2 receptor transfected in CHO cells assessed as inhibition of forskolin-stimulated adenylyl cyclase activity after 15 min...				J Med Chem 56: 4537-50 (2013) Article DOI: 10.1021/jm400268b BindingDB Entry DOI: 10.7270/Q25M68M1
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Mus musculus (Mouse))	BDBM85804 (1-Naphthyl(1-butyl-1H-indole-3-yl)methanone | JWH-...) Show SMILES CCCCn1cc(C(=O)c2cccc3ccccc23)c2ccccc12 Show InChI InChI=1S/C23H21NO/c1-2-3-15-24-16-21(19-12-6-7-14-22(19)24)23(25)20-13-8-10-17-9-4-5-11-18(17)20/h4-14,16H,2-3,15H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	US Patent	12.9	-45.0	n/a	n/a	n/a	n/a	n/a	n/a	25
The Board of Trustees of the University of Arkansas; The University of Kansas US Patent					Assay Description Competition receptor binding was performed as previously described [Shoemaker et al., J. Pharmacol. Exp. Ther., 314:868-75]. Briefly, 50 μg of mou...				US Patent US9416103 (2016) BindingDB Entry DOI: 10.7270/Q2HX1BKQ
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Mus musculus (Mouse))	BDBM85804 (1-Naphthyl(1-butyl-1H-indole-3-yl)methanone | JWH-...) Show SMILES CCCCn1cc(C(=O)c2cccc3ccccc23)c2ccccc12 Show InChI InChI=1S/C23H21NO/c1-2-3-15-24-16-21(19-12-6-7-14-22(19)24)23(25)20-13-8-10-17-9-4-5-11-18(17)20/h4-14,16H,2-3,15H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	US Patent	12.9	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Board of Trustees of the University of Arkansas; The University of Kansas US Patent					Assay Description A functional assay screen for the inhibition of adenylate cyclase (AC) activity was chosen as the subsequent assay. This screen would allow us to gai...				US Patent US9416103 (2016) BindingDB Entry DOI: 10.7270/Q2HX1BKQ
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Mus musculus (Mouse))	BDBM85804 (1-Naphthyl(1-butyl-1H-indole-3-yl)methanone | JWH-...) Show SMILES CCCCn1cc(C(=O)c2cccc3ccccc23)c2ccccc12 Show InChI InChI=1S/C23H21NO/c1-2-3-15-24-16-21(19-12-6-7-14-22(19)24)23(25)20-13-8-10-17-9-4-5-11-18(17)20/h4-14,16H,2-3,15H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	13	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Kansas Curated by ChEMBL					Assay Description Agonist activity at CB1 receptor in mouse Neuro2a cells assessed as inhibition of forskolin-stimulated adenylyl cyclase activity after 15 mins by liq...				J Med Chem 56: 4537-50 (2013) Article DOI: 10.1021/jm400268b BindingDB Entry DOI: 10.7270/Q25M68M1
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Mus musculus (Mouse))	BDBM239074 (US9416103, JWH-073-M1) Show SMILES CCCCn1cc(C(=O)c2cccc3ccccc23)c2c(O)cccc12 Show InChI InChI=1S/C23H21NO2/c1-2-3-14-24-15-19(22-20(24)12-7-13-21(22)25)23(26)18-11-6-9-16-8-4-5-10-17(16)18/h4-13,15,25H,2-3,14H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem	US Patent	14.1	-44.8	n/a	n/a	n/a	n/a	n/a	n/a	25
The Board of Trustees of the University of Arkansas; The University of Kansas US Patent					Assay Description Competition receptor binding was performed as previously described [Shoemaker et al., J. Pharmacol. Exp. Ther., 314:868-75]. Briefly, 50 μg of mou...				US Patent US9416103 (2016) BindingDB Entry DOI: 10.7270/Q2HX1BKQ
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Mus musculus (Mouse))	BDBM239077 (US9416103, TV-5-249) Show SMILES CCCCn1cc(Cc2cccc3ccccc23)c2cccc(OC)c12 Show InChI InChI=1S/C24H25NO/c1-3-4-15-25-17-20(22-13-8-14-23(26-2)24(22)25)16-19-11-7-10-18-9-5-6-12-21(18)19/h5-14,17H,3-4,15-16H2,1-2H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	15	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Kansas Curated by ChEMBL					Assay Description Agonist activity at CB1 receptor in mouse Neuro2a cells assessed as inhibition of forskolin-stimulated adenylyl cyclase activity after 15 mins by liq...				J Med Chem 56: 4537-50 (2013) Article DOI: 10.1021/jm400268b BindingDB Entry DOI: 10.7270/Q25M68M1
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Mus musculus (Mouse))	BDBM239077 (US9416103, TV-5-249) Show SMILES CCCCn1cc(Cc2cccc3ccccc23)c2cccc(OC)c12 Show InChI InChI=1S/C24H25NO/c1-3-4-15-25-17-20(22-13-8-14-23(26-2)24(22)25)16-19-11-7-10-18-9-5-6-12-21(18)19/h5-14,17H,3-4,15-16H2,1-2H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	15.4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Board of Trustees of the University of Arkansas; The University of Kansas US Patent					Assay Description A functional assay screen for the inhibition of adenylate cyclase (AC) activity was chosen as the subsequent assay. This screen would allow us to gai...				US Patent US9416103 (2016) BindingDB Entry DOI: 10.7270/Q2HX1BKQ
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Mus musculus (Mouse))	BDBM239075 (US9416103, JWH-073-M4) Show SMILES CCCCn1cc(C(=O)c2cccc3ccccc23)c2cccc(O)c12 Show InChI InChI=1S/C23H21NO2/c1-2-3-14-24-15-20(18-11-7-13-21(25)22(18)24)23(26)19-12-6-9-16-8-4-5-10-17(16)19/h4-13,15,25H,2-3,14H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem	Article PubMed	24	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Kansas Curated by ChEMBL					Assay Description Agonist activity at CB1 receptor in mouse Neuro2a cells assessed as inhibition of forskolin-stimulated adenylyl cyclase activity after 15 mins by liq...				J Med Chem 56: 4537-50 (2013) Article DOI: 10.1021/jm400268b BindingDB Entry DOI: 10.7270/Q25M68M1
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Mus musculus (Mouse))	BDBM239075 (US9416103, JWH-073-M4) Show SMILES CCCCn1cc(C(=O)c2cccc3ccccc23)c2cccc(O)c12 Show InChI InChI=1S/C23H21NO2/c1-2-3-14-24-15-20(18-11-7-13-21(25)22(18)24)23(26)19-12-6-9-16-8-4-5-10-17(16)19/h4-13,15,25H,2-3,14H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem	US Patent	24.2	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Board of Trustees of the University of Arkansas; The University of Kansas US Patent					Assay Description A functional assay screen for the inhibition of adenylate cyclase (AC) activity was chosen as the subsequent assay. This screen would allow us to gai...				US Patent US9416103 (2016) BindingDB Entry DOI: 10.7270/Q2HX1BKQ
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM239079 (US9416103, TV-6-41) Show SMILES CCCCn1cc(-c2cccc3ccccc23)c2cccc(OC)c12 Show InChI InChI=1S/C23H23NO/c1-3-4-15-24-16-21(20-13-8-14-22(25-2)23(20)24)19-12-7-10-17-9-5-6-11-18(17)19/h5-14,16H,3-4,15H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	26.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Board of Trustees of the University of Arkansas; The University of Kansas US Patent					Assay Description A functional assay screen for the inhibition of adenylate cyclase (AC) activity was chosen as the subsequent assay. This screen would allow us to gai...				US Patent US9416103 (2016) BindingDB Entry DOI: 10.7270/Q2HX1BKQ
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM50491525 (CHEMBL2380408) Show SMILES CCCCn1cc(-c2ccc3ccccc3c2)c2cccc(OC)c12 Show InChI InChI=1S/C23H23NO/c1-3-4-14-24-16-21(20-10-7-11-22(25-2)23(20)24)19-13-12-17-8-5-6-9-18(17)15-19/h5-13,15-16H,3-4,14H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	27	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Kansas Curated by ChEMBL					Assay Description Agonist activity at human CB2 receptor transfected in CHO cells assessed as inhibition of forskolin-stimulated adenylyl cyclase activity after 15 min...				J Med Chem 56: 4537-50 (2013) Article DOI: 10.1021/jm400268b BindingDB Entry DOI: 10.7270/Q25M68M1
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Mus musculus (Mouse))	BDBM50491525 (CHEMBL2380408) Show SMILES CCCCn1cc(-c2ccc3ccccc3c2)c2cccc(OC)c12 Show InChI InChI=1S/C23H23NO/c1-3-4-14-24-16-21(20-10-7-11-22(25-2)23(20)24)19-13-12-17-8-5-6-9-18(17)15-19/h5-13,15-16H,3-4,14H2,1-2H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	37	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Kansas Curated by ChEMBL					Assay Description Agonist activity at CB1 receptor in mouse Neuro2a cells assessed as inhibition of forskolin-stimulated adenylyl cyclase activity after 15 mins by liq...				J Med Chem 56: 4537-50 (2013) Article DOI: 10.1021/jm400268b BindingDB Entry DOI: 10.7270/Q25M68M1
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Mus musculus (Mouse))	BDBM239079 (US9416103, TV-6-41) Show SMILES CCCCn1cc(-c2cccc3ccccc23)c2cccc(OC)c12 Show InChI InChI=1S/C23H23NO/c1-3-4-15-24-16-21(20-13-8-14-22(25-2)23(20)24)19-12-7-10-17-9-5-6-11-18(17)19/h5-14,16H,3-4,15H2,1-2H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	37.3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Board of Trustees of the University of Arkansas; The University of Kansas US Patent					Assay Description A functional assay screen for the inhibition of adenylate cyclase (AC) activity was chosen as the subsequent assay. This screen would allow us to gai...				US Patent US9416103 (2016) BindingDB Entry DOI: 10.7270/Q2HX1BKQ
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1D (Homo sapiens (Human))	BDBM50160160 ((S)-1,2-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-...) Show SMILES COc1cc2CCN(C)[C@H]3Cc4cc5OCOc5cc4-c(c1OC)c23 Show InChI InChI=1S/C20H21NO4/c1-21-5-4-11-7-17(22-2)20(23-3)19-13-9-16-15(24-10-25-16)8-12(13)6-14(21)18(11)19/h7-9,14H,4-6,10H2,1-3H3/t14-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	49	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Hunter College and the Graduate Center of the City University of New York Curated by ChEMBL					Assay Description Displacement of [3H]GR127543 from human 5HT1D receptor				Bioorg Med Chem Lett 20: 628-31 (2010) Article DOI: 10.1016/j.bmcl.2009.11.053 BindingDB Entry DOI: 10.7270/Q2C53MT3
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 7 (Homo sapiens (Human))	BDBM50160160 ((S)-1,2-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-...) Show SMILES COc1cc2CCN(C)[C@H]3Cc4cc5OCOc5cc4-c(c1OC)c23 Show InChI InChI=1S/C20H21NO4/c1-21-5-4-11-7-17(22-2)20(23-3)19-13-9-16-15(24-10-25-16)8-12(13)6-14(21)18(11)19/h7-9,14H,4-6,10H2,1-3H3/t14-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	67	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Hunter College and the Graduate Center of the City University of New York Curated by ChEMBL					Assay Description Displacement of [3H]LSD from human 5HT7 receptor				Bioorg Med Chem Lett 20: 628-31 (2010) Article DOI: 10.1016/j.bmcl.2009.11.053 BindingDB Entry DOI: 10.7270/Q2C53MT3
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM239075 (US9416103, JWH-073-M4) Show SMILES CCCCn1cc(C(=O)c2cccc3ccccc23)c2cccc(O)c12 Show InChI InChI=1S/C23H21NO2/c1-2-3-14-24-15-20(18-11-7-13-21(25)22(18)24)23(26)19-12-6-9-16-8-4-5-10-17(16)19/h4-13,15,25H,2-3,14H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem	Article PubMed	78	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Kansas Curated by ChEMBL					Assay Description Agonist activity at human CB2 receptor transfected in CHO cells assessed as inhibition of forskolin-stimulated adenylyl cyclase activity after 15 min...				J Med Chem 56: 4537-50 (2013) Article DOI: 10.1021/jm400268b BindingDB Entry DOI: 10.7270/Q25M68M1
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM239075 (US9416103, JWH-073-M4) Show SMILES CCCCn1cc(C(=O)c2cccc3ccccc23)c2cccc(O)c12 Show InChI InChI=1S/C23H21NO2/c1-2-3-14-24-15-20(18-11-7-13-21(25)22(18)24)23(26)19-12-6-9-16-8-4-5-10-17(16)19/h4-13,15,25H,2-3,14H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem	US Patent	78.3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Board of Trustees of the University of Arkansas; The University of Kansas US Patent					Assay Description A functional assay screen for the inhibition of adenylate cyclase (AC) activity was chosen as the subsequent assay. This screen would allow us to gai...				US Patent US9416103 (2016) BindingDB Entry DOI: 10.7270/Q2HX1BKQ
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 1B (Homo sapiens (Human))	BDBM50160160 ((S)-1,2-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-...) Show SMILES COc1cc2CCN(C)[C@H]3Cc4cc5OCOc5cc4-c(c1OC)c23 Show InChI InChI=1S/C20H21NO4/c1-21-5-4-11-7-17(22-2)20(23-3)19-13-9-16-15(24-10-25-16)8-12(13)6-14(21)18(11)19/h7-9,14H,4-6,10H2,1-3H3/t14-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	100	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Hunter College and the Graduate Center of the City University of New York Curated by ChEMBL					Assay Description Displacement of [3H]GR127543 from human 5HT1B receptor				Bioorg Med Chem Lett 20: 628-31 (2010) Article DOI: 10.1016/j.bmcl.2009.11.053 BindingDB Entry DOI: 10.7270/Q2C53MT3
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Mus musculus (Mouse))	BDBM239075 (US9416103, JWH-073-M4) Show SMILES CCCCn1cc(C(=O)c2cccc3ccccc23)c2cccc(O)c12 Show InChI InChI=1S/C23H21NO2/c1-2-3-14-24-15-20(18-11-7-13-21(25)22(18)24)23(26)19-12-6-9-16-8-4-5-10-17(16)19/h4-13,15,25H,2-3,14H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem	US Patent	122	-39.5	n/a	n/a	n/a	n/a	n/a	n/a	25
The Board of Trustees of the University of Arkansas; The University of Kansas US Patent					Assay Description Competition receptor binding was performed as previously described [Shoemaker et al., J. Pharmacol. Exp. Ther., 314:868-75]. Briefly, 50 μg of mou...				US Patent US9416103 (2016) BindingDB Entry DOI: 10.7270/Q2HX1BKQ
					More data for this Ligand-Target Pair
Alpha-2C adrenergic receptor (Homo sapiens (Human))	BDBM50160160 ((S)-1,2-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-...) Show SMILES COc1cc2CCN(C)[C@H]3Cc4cc5OCOc5cc4-c(c1OC)c23 Show InChI InChI=1S/C20H21NO4/c1-21-5-4-11-7-17(22-2)20(23-3)19-13-9-16-15(24-10-25-16)8-12(13)6-14(21)18(11)19/h7-9,14H,4-6,10H2,1-3H3/t14-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	181	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Hunter College and the Graduate Center of the City University of New York Curated by ChEMBL					Assay Description Displacement of [3H]Clonidine from human adrenergic Alpha-2C receptor				Bioorg Med Chem Lett 20: 628-31 (2010) Article DOI: 10.1016/j.bmcl.2009.11.053 BindingDB Entry DOI: 10.7270/Q2C53MT3
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Mus musculus (Mouse))	BDBM60993 (US9416103, JWH-073-M5) Show SMILES OCCCCn1cc(C(=O)c2cccc3ccccc23)c2ccccc12 Show InChI InChI=1S/C23H21NO2/c25-15-6-5-14-24-16-21(19-11-3-4-13-22(19)24)23(26)20-12-7-9-17-8-1-2-10-18(17)20/h1-4,7-13,16,25H,5-6,14-15H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem Similars	US Patent	224	-38.0	n/a	n/a	n/a	n/a	n/a	n/a	25
The Board of Trustees of the University of Arkansas; The University of Kansas US Patent					Assay Description Competition receptor binding was performed as previously described [Shoemaker et al., J. Pharmacol. Exp. Ther., 314:868-75]. Briefly, 50 μg of mou...				US Patent US9416103 (2016) BindingDB Entry DOI: 10.7270/Q2HX1BKQ
					More data for this Ligand-Target Pair
Sodium-dependent serotonin transporter (Homo sapiens (Human))	BDBM50160160 ((S)-1,2-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-...) Show SMILES COc1cc2CCN(C)[C@H]3Cc4cc5OCOc5cc4-c(c1OC)c23 Show InChI InChI=1S/C20H21NO4/c1-21-5-4-11-7-17(22-2)20(23-3)19-13-9-16-15(24-10-25-16)8-12(13)6-14(21)18(11)19/h7-9,14H,4-6,10H2,1-3H3/t14-/m0/s1	PDB KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	244	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Hunter College and the Graduate Center of the City University of New York Curated by ChEMBL					Assay Description Displacement of [3H]Citalopram from human SERT				Bioorg Med Chem Lett 20: 628-31 (2010) Article DOI: 10.1016/j.bmcl.2009.11.053 BindingDB Entry DOI: 10.7270/Q2C53MT3
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM239075 (US9416103, JWH-073-M4) Show SMILES CCCCn1cc(C(=O)c2cccc3ccccc23)c2cccc(O)c12 Show InChI InChI=1S/C23H21NO2/c1-2-3-14-24-15-20(18-11-7-13-21(25)22(18)24)23(26)19-12-6-9-16-8-4-5-10-17(16)19/h4-13,15,25H,2-3,14H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem	US Patent	251	-37.7	n/a	n/a	n/a	n/a	n/a	n/a	25
The Board of Trustees of the University of Arkansas; The University of Kansas US Patent					Assay Description Competition receptor binding was performed as previously described [Shoemaker et al., J. Pharmacol. Exp. Ther., 314:868-75]. Briefly, 50 μg of mou...				US Patent US9416103 (2016) BindingDB Entry DOI: 10.7270/Q2HX1BKQ
					More data for this Ligand-Target Pair
Alpha-2B adrenergic receptor (Homo sapiens (Human))	BDBM50160160 ((S)-1,2-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-...) Show SMILES COc1cc2CCN(C)[C@H]3Cc4cc5OCOc5cc4-c(c1OC)c23 Show InChI InChI=1S/C20H21NO4/c1-21-5-4-11-7-17(22-2)20(23-3)19-13-9-16-15(24-10-25-16)8-12(13)6-14(21)18(11)19/h7-9,14H,4-6,10H2,1-3H3/t14-/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	252	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Hunter College and the Graduate Center of the City University of New York Curated by ChEMBL					Assay Description Displacement of [3H]Clonidine from human adrenergic alpha2B receptor				Bioorg Med Chem Lett 20: 628-31 (2010) Article DOI: 10.1016/j.bmcl.2009.11.053 BindingDB Entry DOI: 10.7270/Q2C53MT3
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 6 (Homo sapiens (Human))	BDBM50160160 ((S)-1,2-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-...) Show SMILES COc1cc2CCN(C)[C@H]3Cc4cc5OCOc5cc4-c(c1OC)c23 Show InChI InChI=1S/C20H21NO4/c1-21-5-4-11-7-17(22-2)20(23-3)19-13-9-16-15(24-10-25-16)8-12(13)6-14(21)18(11)19/h7-9,14H,4-6,10H2,1-3H3/t14-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	257	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Hunter College and the Graduate Center of the City University of New York Curated by ChEMBL					Assay Description Displacement of [3H]LSD from human 5HT6 receptor				Bioorg Med Chem Lett 20: 628-31 (2010) Article DOI: 10.1016/j.bmcl.2009.11.053 BindingDB Entry DOI: 10.7270/Q2C53MT3
					More data for this Ligand-Target Pair
D(4) dopamine receptor (Homo sapiens (Human))	BDBM50160160 ((S)-1,2-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-...) Show SMILES COc1cc2CCN(C)[C@H]3Cc4cc5OCOc5cc4-c(c1OC)c23 Show InChI InChI=1S/C20H21NO4/c1-21-5-4-11-7-17(22-2)20(23-3)19-13-9-16-15(24-10-25-16)8-12(13)6-14(21)18(11)19/h7-9,14H,4-6,10H2,1-3H3/t14-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	262	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Hunter College and the Graduate Center of the City University of New York Curated by ChEMBL					Assay Description Displacement of [3H]N-methylspiperone from human dopamine D4 receptor				Bioorg Med Chem Lett 20: 628-31 (2010) Article DOI: 10.1016/j.bmcl.2009.11.053 BindingDB Entry DOI: 10.7270/Q2C53MT3
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM239076 (US9416103, TV-5-129) Show SMILES CCCCn1cc(C(=O)Cc2ccc(F)cc2)c2cccc(OC)c12 Show InChI InChI=1S/C21H22FNO2/c1-3-4-12-23-14-18(17-6-5-7-20(25-2)21(17)23)19(24)13-15-8-10-16(22)11-9-15/h5-11,14H,3-4,12-13H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	281	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Kansas Curated by ChEMBL					Assay Description Agonist activity at human CB2 receptor transfected in CHO cells assessed as inhibition of forskolin-stimulated adenylyl cyclase activity after 15 min...				J Med Chem 56: 4537-50 (2013) Article DOI: 10.1021/jm400268b BindingDB Entry DOI: 10.7270/Q25M68M1
					More data for this Ligand-Target Pair
Cannabinoid receptor 2 (Homo sapiens (Human))	BDBM239076 (US9416103, TV-5-129) Show SMILES CCCCn1cc(C(=O)Cc2ccc(F)cc2)c2cccc(OC)c12 Show InChI InChI=1S/C21H22FNO2/c1-3-4-12-23-14-18(17-6-5-7-20(25-2)21(17)23)19(24)13-15-8-10-16(22)11-9-15/h5-11,14H,3-4,12-13H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	281	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Board of Trustees of the University of Arkansas; The University of Kansas US Patent					Assay Description A functional assay screen for the inhibition of adenylate cyclase (AC) activity was chosen as the subsequent assay. This screen would allow us to gai...				US Patent US9416103 (2016) BindingDB Entry DOI: 10.7270/Q2HX1BKQ
					More data for this Ligand-Target Pair
D(3) dopamine receptor (Homo sapiens (Human))	BDBM50160160 ((S)-1,2-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-...) Show SMILES COc1cc2CCN(C)[C@H]3Cc4cc5OCOc5cc4-c(c1OC)c23 Show InChI InChI=1S/C20H21NO4/c1-21-5-4-11-7-17(22-2)20(23-3)19-13-9-16-15(24-10-25-16)8-12(13)6-14(21)18(11)19/h7-9,14H,4-6,10H2,1-3H3/t14-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	309	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Hunter College and the Graduate Center of the City University of New York Curated by ChEMBL					Assay Description Displacement of [3H]N-methylspiperone from human dopamine D3 receptor				Bioorg Med Chem Lett 20: 628-31 (2010) Article DOI: 10.1016/j.bmcl.2009.11.053 BindingDB Entry DOI: 10.7270/Q2C53MT3
					More data for this Ligand-Target Pair
Alpha-1D adrenergic receptor (Homo sapiens (Human))	BDBM50160160 ((S)-1,2-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-...) Show SMILES COc1cc2CCN(C)[C@H]3Cc4cc5OCOc5cc4-c(c1OC)c23 Show InChI InChI=1S/C20H21NO4/c1-21-5-4-11-7-17(22-2)20(23-3)19-13-9-16-15(24-10-25-16)8-12(13)6-14(21)18(11)19/h7-9,14H,4-6,10H2,1-3H3/t14-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	340	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Hunter College and the Graduate Center of the City University of New York Curated by ChEMBL					Assay Description Binding affinity to human adrenergic Alpha-1D receptor				Bioorg Med Chem Lett 20: 628-31 (2010) Article DOI: 10.1016/j.bmcl.2009.11.053 BindingDB Entry DOI: 10.7270/Q2C53MT3
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Mus musculus (Mouse))	BDBM239076 (US9416103, TV-5-129) Show SMILES CCCCn1cc(C(=O)Cc2ccc(F)cc2)c2cccc(OC)c12 Show InChI InChI=1S/C21H22FNO2/c1-3-4-12-23-14-18(17-6-5-7-20(25-2)21(17)23)19(24)13-15-8-10-16(22)11-9-15/h5-11,14H,3-4,12-13H2,1-2H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	387	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Board of Trustees of the University of Arkansas; The University of Kansas US Patent					Assay Description A functional assay screen for the inhibition of adenylate cyclase (AC) activity was chosen as the subsequent assay. This screen would allow us to gai...				US Patent US9416103 (2016) BindingDB Entry DOI: 10.7270/Q2HX1BKQ
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Mus musculus (Mouse))	BDBM239076 (US9416103, TV-5-129) Show SMILES CCCCn1cc(C(=O)Cc2ccc(F)cc2)c2cccc(OC)c12 Show InChI InChI=1S/C21H22FNO2/c1-3-4-12-23-14-18(17-6-5-7-20(25-2)21(17)23)19(24)13-15-8-10-16(22)11-9-15/h5-11,14H,3-4,12-13H2,1-2H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	387	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The University of Kansas Curated by ChEMBL					Assay Description Agonist activity at CB1 receptor in mouse Neuro2a cells assessed as inhibition of forskolin-stimulated adenylyl cyclase activity after 15 mins by liq...				J Med Chem 56: 4537-50 (2013) Article DOI: 10.1021/jm400268b BindingDB Entry DOI: 10.7270/Q25M68M1
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 2B (Homo sapiens (Human))	BDBM50160160 ((S)-1,2-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-...) Show SMILES COc1cc2CCN(C)[C@H]3Cc4cc5OCOc5cc4-c(c1OC)c23 Show InChI InChI=1S/C20H21NO4/c1-21-5-4-11-7-17(22-2)20(23-3)19-13-9-16-15(24-10-25-16)8-12(13)6-14(21)18(11)19/h7-9,14H,4-6,10H2,1-3H3/t14-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	543	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Hunter College and the Graduate Center of the City University of New York Curated by ChEMBL					Assay Description Displacement of [3H]LSD from human 5HT2B receptor				Bioorg Med Chem Lett 20: 628-31 (2010) Article DOI: 10.1016/j.bmcl.2009.11.053 BindingDB Entry DOI: 10.7270/Q2C53MT3
					More data for this Ligand-Target Pair
Histamine H2 receptor (Homo sapiens (Human))	BDBM50160160 ((S)-1,2-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-...) Show SMILES COc1cc2CCN(C)[C@H]3Cc4cc5OCOc5cc4-c(c1OC)c23 Show InChI InChI=1S/C20H21NO4/c1-21-5-4-11-7-17(22-2)20(23-3)19-13-9-16-15(24-10-25-16)8-12(13)6-14(21)18(11)19/h7-9,14H,4-6,10H2,1-3H3/t14-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	672	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Hunter College and the Graduate Center of the City University of New York Curated by ChEMBL					Assay Description Displacement of [3H]Tiotidine from human histamine H2 receptor				Bioorg Med Chem Lett 20: 628-31 (2010) Article DOI: 10.1016/j.bmcl.2009.11.053 BindingDB Entry DOI: 10.7270/Q2C53MT3
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 2A (Homo sapiens (Human))	BDBM50160160 ((S)-1,2-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-...) Show SMILES COc1cc2CCN(C)[C@H]3Cc4cc5OCOc5cc4-c(c1OC)c23 Show InChI InChI=1S/C20H21NO4/c1-21-5-4-11-7-17(22-2)20(23-3)19-13-9-16-15(24-10-25-16)8-12(13)6-14(21)18(11)19/h7-9,14H,4-6,10H2,1-3H3/t14-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	832	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Hunter College and the Graduate Center of the City University of New York Curated by ChEMBL					Assay Description Displacement of [3H]Ketanserin from human 5HT2A receptor				Bioorg Med Chem Lett 20: 628-31 (2010) Article DOI: 10.1016/j.bmcl.2009.11.053 BindingDB Entry DOI: 10.7270/Q2C53MT3
					More data for this Ligand-Target Pair
D(2) dopamine receptor (Homo sapiens (Human))	BDBM50160160 ((S)-1,2-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-...) Show SMILES COc1cc2CCN(C)[C@H]3Cc4cc5OCOc5cc4-c(c1OC)c23 Show InChI InChI=1S/C20H21NO4/c1-21-5-4-11-7-17(22-2)20(23-3)19-13-9-16-15(24-10-25-16)8-12(13)6-14(21)18(11)19/h7-9,14H,4-6,10H2,1-3H3/t14-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	858	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Hunter College and the Graduate Center of the City University of New York Curated by ChEMBL					Assay Description Displacement of [3H]N-methylspiperone from human dopamine D2 receptor				Bioorg Med Chem Lett 20: 628-31 (2010) Article DOI: 10.1016/j.bmcl.2009.11.053 BindingDB Entry DOI: 10.7270/Q2C53MT3
					More data for this Ligand-Target Pair
D(1A) dopamine receptor (Homo sapiens (Human))	BDBM50160160 ((S)-1,2-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-...) Show SMILES COc1cc2CCN(C)[C@H]3Cc4cc5OCOc5cc4-c(c1OC)c23 Show InChI InChI=1S/C20H21NO4/c1-21-5-4-11-7-17(22-2)20(23-3)19-13-9-16-15(24-10-25-16)8-12(13)6-14(21)18(11)19/h7-9,14H,4-6,10H2,1-3H3/t14-/m0/s1	PDB KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	895	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Hunter College and the Graduate Center of the City University of New York Curated by ChEMBL					Assay Description Displacement of [3H]SCH233930 from human dopamine D1 receptor				Bioorg Med Chem Lett 20: 628-31 (2010) Article DOI: 10.1016/j.bmcl.2009.11.053 BindingDB Entry DOI: 10.7270/Q2C53MT3
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 2C (Homo sapiens (Human))	BDBM50160160 ((S)-1,2-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-...) Show SMILES COc1cc2CCN(C)[C@H]3Cc4cc5OCOc5cc4-c(c1OC)c23 Show InChI InChI=1S/C20H21NO4/c1-21-5-4-11-7-17(22-2)20(23-3)19-13-9-16-15(24-10-25-16)8-12(13)6-14(21)18(11)19/h7-9,14H,4-6,10H2,1-3H3/t14-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	1.07E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Hunter College and the Graduate Center of the City University of New York Curated by ChEMBL					Assay Description Displacement of [3H]Mesulergine from human 5HT2C receptor				Bioorg Med Chem Lett 20: 628-31 (2010) Article DOI: 10.1016/j.bmcl.2009.11.053 BindingDB Entry DOI: 10.7270/Q2C53MT3
					More data for this Ligand-Target Pair
Alpha-1B adrenergic receptor (Homo sapiens (Human))	BDBM50160160 ((S)-1,2-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-...) Show SMILES COc1cc2CCN(C)[C@H]3Cc4cc5OCOc5cc4-c(c1OC)c23 Show InChI InChI=1S/C20H21NO4/c1-21-5-4-11-7-17(22-2)20(23-3)19-13-9-16-15(24-10-25-16)8-12(13)6-14(21)18(11)19/h7-9,14H,4-6,10H2,1-3H3/t14-/m0/s1	UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	1.19E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Hunter College and the Graduate Center of the City University of New York Curated by ChEMBL					Assay Description Displacement of [3H]Prazosin from human adrenergic Alpha-1B receptor				Bioorg Med Chem Lett 20: 628-31 (2010) Article DOI: 10.1016/j.bmcl.2009.11.053 BindingDB Entry DOI: 10.7270/Q2C53MT3
					More data for this Ligand-Target Pair
Cannabinoid receptor 1 (Mus musculus (Mouse))	BDBM60992 (US9416103, JWH-073-M3) Show SMILES CCCCn1cc(C(=O)c2cccc3ccccc23)c2ccc(O)cc12 Show InChI InChI=1S/C23H21NO2/c1-2-3-13-24-15-21(19-12-11-17(25)14-22(19)24)23(26)20-10-6-8-16-7-4-5-9-18(16)20/h4-12,14-15,25H,2-3,13H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem	US Patent	1.28E+3	-33.6	n/a	n/a	n/a	n/a	n/a	n/a	25
The Board of Trustees of the University of Arkansas; The University of Kansas US Patent					Assay Description Competition receptor binding was performed as previously described [Shoemaker et al., J. Pharmacol. Exp. Ther., 314:868-75]. Briefly, 50 μg of mou...				US Patent US9416103 (2016) BindingDB Entry DOI: 10.7270/Q2HX1BKQ
					More data for this Ligand-Target Pair
Alpha-2A adrenergic receptor (Homo sapiens (Human))	BDBM50160160 ((S)-1,2-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-...) Show SMILES COc1cc2CCN(C)[C@H]3Cc4cc5OCOc5cc4-c(c1OC)c23 Show InChI InChI=1S/C20H21NO4/c1-21-5-4-11-7-17(22-2)20(23-3)19-13-9-16-15(24-10-25-16)8-12(13)6-14(21)18(11)19/h7-9,14H,4-6,10H2,1-3H3/t14-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	1.29E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Hunter College and the Graduate Center of the City University of New York Curated by ChEMBL					Assay Description Displacement of [3H]Clonidine from human adrenergic alpha2A receptor				Bioorg Med Chem Lett 20: 628-31 (2010) Article DOI: 10.1016/j.bmcl.2009.11.053 BindingDB Entry DOI: 10.7270/Q2C53MT3
					More data for this Ligand-Target Pair

Displayed 1 to 50 (of 77 total )  |  Next  |  Last  >>

Jump to: