Compile Data Set for Download or QSAR

Found 27 hits with Last Name = 'france' and Initial = 'cp'   

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
Glutamate receptor ionotropic, NMDA 2C (Rattus norvegicus (Rat))	BDBM50015743 (Acetic acid 3-[1-(3,6-dihydro-2H-pyridin-1-yl)-cyc...) Show SMILES CC(=O)Oc1cccc(c1)C1(CCCCC1)N1CCC=CC1 |c:21| Show InChI InChI=1S/C19H25NO2/c1-16(21)22-18-10-8-9-17(15-18)19(11-4-2-5-12-19)20-13-6-3-7-14-20/h3,6,8-10,15H,2,4-5,7,11-14H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]- TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.				J Med Chem 33: 2211-5 (1990) BindingDB Entry DOI: 10.7270/Q2BZ6515
					More data for this Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C (Rattus norvegicus (Rat))	BDBM50015738 (3-[1-(3,6-Dihydro-2H-pyridin-1-yl)-cyclohexyl]-phe...) Show SMILES Oc1cccc(c1)C1(CCCCC1)N1CCC=CC1 |c:18| Show InChI InChI=1S/C17H23NO/c19-16-9-7-8-15(14-16)17(10-3-1-4-11-17)18-12-5-2-6-13-18/h2,5,7-9,14,19H,1,3-4,6,10-13H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	7	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]-TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.				J Med Chem 33: 2211-5 (1990) BindingDB Entry DOI: 10.7270/Q2BZ6515
					More data for this Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C (Rattus norvegicus (Rat))	BDBM50015734 (1-(1-Thiophen-2-yl-cyclohexyl)-1,2,3,6-tetrahydro-...) Show SMILES C1CCC(CC1)(N1CCC=CC1)c1cccs1 |c:10| Show InChI InChI=1S/C15H21NS/c1-3-9-15(10-4-1,14-8-7-13-17-14)16-11-5-2-6-12-16/h2,5,7-8,13H,1,3-4,6,9-12H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	12	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]-TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.				J Med Chem 33: 2211-5 (1990) BindingDB Entry DOI: 10.7270/Q2BZ6515
					More data for this Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C (Rattus norvegicus (Rat))	BDBM50015741 (1-[1-(3-Methoxy-phenyl)-cyclohexyl]-1,2,3,6-tetrah...) Show SMILES COc1cccc(c1)C1(CCCCC1)N1CCC=CC1 |c:19| Show InChI InChI=1S/C18H25NO/c1-20-17-10-8-9-16(15-17)18(11-4-2-5-12-18)19-13-6-3-7-14-19/h3,6,8-10,15H,2,4-5,7,11-14H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	33	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]-TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.				J Med Chem 33: 2211-5 (1990) BindingDB Entry DOI: 10.7270/Q2BZ6515
					More data for this Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C (Rattus norvegicus (Rat))	BDBM50015732 (1-(1-Phenyl-cyclohexyl)-1,2,3,6-tetrahydro-pyridin...) Show SMILES C1CCC(CC1)(N1CCC=CC1)c1ccccc1 |c:10| Show InChI InChI=1S/C17H23N/c1-4-10-16(11-5-1)17(12-6-2-7-13-17)18-14-8-3-9-15-18/h1,3-5,8,10-11H,2,6-7,9,12-15H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	37	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]- TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.				J Med Chem 33: 2211-5 (1990) BindingDB Entry DOI: 10.7270/Q2BZ6515
					More data for this Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C (Rattus norvegicus (Rat))	BDBM50015733 (3-[1-(3,6-Dihydro-2H-pyridin-1-yl)-cyclohexyl]-ben...) Show SMILES O=NCc1cccc(c1)C1(CCCCC1)N1CCC=CC1 |c:20| Show InChI InChI=1S/C18H24N2O/c21-19-15-16-8-7-9-17(14-16)18(10-3-1-4-11-18)20-12-5-2-6-13-20/h2,5,7-9,14H,1,3-4,6,10-13,15H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	56	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]-TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.				J Med Chem 33: 2211-5 (1990) BindingDB Entry DOI: 10.7270/Q2BZ6515
					More data for this Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C (Rattus norvegicus (Rat))	BDBM50015735 (1-(1-m-Tolyl-cyclohexyl)-1,2,3,6-tetrahydro-pyridi...) Show SMILES Cc1cccc(c1)C1(CCCCC1)N1CCC=CC1 |c:18| Show InChI InChI=1S/C18H25N/c1-16-9-8-10-17(15-16)18(11-4-2-5-12-18)19-13-6-3-7-14-19/h3,6,8-10,15H,2,4-5,7,11-14H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	81	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]- TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.				J Med Chem 33: 2211-5 (1990) BindingDB Entry DOI: 10.7270/Q2BZ6515
					More data for this Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C (Rattus norvegicus (Rat))	BDBM50015744 (1-[1-(3-Methoxymethoxy-phenyl)-cyclohexyl]-1,2,3,6...) Show SMILES COCOc1cccc(c1)C1(CCCCC1)N1CCC=CC1 |c:21| Show InChI InChI=1S/C19H27NO2/c1-21-16-22-18-10-8-9-17(15-18)19(11-4-2-5-12-19)20-13-6-3-7-14-20/h3,6,8-10,15H,2,4-5,7,11-14,16H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	92	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]- TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.				J Med Chem 33: 2211-5 (1990) BindingDB Entry DOI: 10.7270/Q2BZ6515
					More data for this Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C (Rattus norvegicus (Rat))	BDBM50015740 (1-[1-(3-Vinyl-phenyl)-cyclohexyl]-1,2,3,6-tetrahyd...) Show SMILES C=Cc1cccc(c1)C1(CCCCC1)N1CCC=CC1 |c:19| Show InChI InChI=1S/C19H25N/c1-2-17-10-9-11-18(16-17)19(12-5-3-6-13-19)20-14-7-4-8-15-20/h2,4,7,9-11,16H,1,3,5-6,8,12-15H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	114	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]- TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.				J Med Chem 33: 2211-5 (1990) BindingDB Entry DOI: 10.7270/Q2BZ6515
					More data for this Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C (Rattus norvegicus (Rat))	BDBM50015731 (1-[1-(3-Methylsulfanyl-phenyl)-cyclohexyl]-1,2,3,6...) Show SMILES CSc1cccc(c1)C1(CCCCC1)N1CCC=CC1 |c:19| Show InChI InChI=1S/C18H25NS/c1-20-17-10-8-9-16(15-17)18(11-4-2-5-12-18)19-13-6-3-7-14-19/h3,6,8-10,15H,2,4-5,7,11-14H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	231	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]- TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.				J Med Chem 33: 2211-5 (1990) BindingDB Entry DOI: 10.7270/Q2BZ6515
					More data for this Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C (Rattus norvegicus (Rat))	BDBM50015736 (1-[1-(3-Fluoro-phenyl)-cyclohexyl]-1,2,3,6-tetrahy...) Show SMILES Fc1cccc(c1)C1(CCCCC1)N1CCC=CC1 |c:18| Show InChI InChI=1S/C17H22FN/c18-16-9-7-8-15(14-16)17(10-3-1-4-11-17)19-12-5-2-6-13-19/h2,5,7-9,14H,1,3-4,6,10-13H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	281	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]- TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.				J Med Chem 33: 2211-5 (1990) BindingDB Entry DOI: 10.7270/Q2BZ6515
					More data for this Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C (Rattus norvegicus (Rat))	BDBM50015739 (3-[1-(3,6-Dihydro-2H-pyridin-1-yl)-cyclohexyl]-ben...) Show SMILES O=Cc1cccc(c1)C1(CCCCC1)N1CCC=CC1 |c:19| Show InChI InChI=1S/C18H23NO/c20-15-16-8-7-9-17(14-16)18(10-3-1-4-11-18)19-12-5-2-6-13-19/h2,5,7-9,14-15H,1,3-4,6,10-13H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	324	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]- TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.				J Med Chem 33: 2211-5 (1990) BindingDB Entry DOI: 10.7270/Q2BZ6515
					More data for this Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C (Rattus norvegicus (Rat))	BDBM50015730 (1-[1-(3-Trifluoromethyl-phenyl)-cyclohexyl]-1,2,3,...) Show SMILES FC(F)(F)c1cccc(c1)C1(CCCCC1)N1CCC=CC1 |c:21| Show InChI InChI=1S/C18H22F3N/c19-18(20,21)16-9-7-8-15(14-16)17(10-3-1-4-11-17)22-12-5-2-6-13-22/h2,5,7-9,14H,1,3-4,6,10-13H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	422	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]- TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.				J Med Chem 33: 2211-5 (1990) BindingDB Entry DOI: 10.7270/Q2BZ6515
					More data for this Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C (Rattus norvegicus (Rat))	BDBM50015742 (1-[1-(3-[1,3]Dioxolan-2-yl-phenyl)-cyclohexyl]-1,2...) Show SMILES C1COC(O1)c1cccc(c1)C1(CCCCC1)N1CCC=CC1 |c:23| Show InChI InChI=1S/C20H27NO2/c1-3-10-20(11-4-1,21-12-5-2-6-13-21)18-9-7-8-17(16-18)19-22-14-15-23-19/h2,5,7-9,16,19H,1,3-4,6,10-15H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	601	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]-TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.				J Med Chem 33: 2211-5 (1990) BindingDB Entry DOI: 10.7270/Q2BZ6515
					More data for this Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C (Rattus norvegicus (Rat))	BDBM50015745 (1-[1-(3-Benzyloxy-phenyl)-cyclohexyl]-1,2,3,6-tetr...) Show SMILES C(Oc1cccc(c1)C1(CCCCC1)N1CCC=CC1)c1ccccc1 |c:19| Show InChI InChI=1S/C24H29NO/c1-4-11-21(12-5-1)20-26-23-14-10-13-22(19-23)24(15-6-2-7-16-24)25-17-8-3-9-18-25/h1,3-5,8,10-14,19H,2,6-7,9,15-18,20H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	733	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]-TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.				J Med Chem 33: 2211-5 (1990) BindingDB Entry DOI: 10.7270/Q2BZ6515
					More data for this Ligand-Target Pair
Gamma-hydroxybutyrate receptor (RAT)	BDBM86149 (CAS_131413 | NCS-382 | NSC_131413) Show SMILES OC1c2ccccc2CCC\C1=C\C([O-])=O Show InChI InChI=1S/C13H14O3/c14-12(15)8-10-6-3-5-9-4-1-2-7-11(9)13(10)16/h1-2,4,7-8,13,16H,3,5-6H2,(H,14,15)/p-1/b10-8-	UniProtKB/TrEMBL GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	1.80E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by PDSP Ki Database									J Pharmacol Exp Ther 305: 675-9 (2003) Article DOI: 10.1124/jpet.102.046797 BindingDB Entry DOI: 10.7270/Q2S1812F
					More data for this Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2C (Rattus norvegicus (Rat))	BDBM50015737 (1-[1-(3,5-Dimethoxy-phenyl)-cyclohexyl]-1,2,3,6-te...) Show SMILES COc1cc(OC)cc(c1)C1(CCCCC1)N1CCC=CC1 |c:21| Show InChI InChI=1S/C19H27NO2/c1-21-17-13-16(14-18(15-17)22-2)19(9-5-3-6-10-19)20-11-7-4-8-12-20/h4,7,13-15H,3,5-6,8-12H2,1-2H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	8.60E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute of Diabetes Curated by ChEMBL					Assay Description Ability to displace [3H]-TCP from PCP receptor in tissue homogenate preparation of fresh whole rat brain minus cerebellum.				J Med Chem 33: 2211-5 (1990) BindingDB Entry DOI: 10.7270/Q2BZ6515
					More data for this Ligand-Target Pair
Gamma-hydroxybutyrate receptor (RAT)	BDBM86151 (UMB68) Show SMILES CC(C)(O)CCC([O-])=O Show InChI InChI=1S/C6H12O3/c1-6(2,9)4-3-5(7)8/h9H,3-4H2,1-2H3,(H,7,8)/p-1	UniProtKB/TrEMBL GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by PDSP Ki Database									J Pharmacol Exp Ther 305: 675-9 (2003) Article DOI: 10.1124/jpet.102.046797 BindingDB Entry DOI: 10.7270/Q2S1812F
					More data for this Ligand-Target Pair
Gamma-hydroxybutyrate receptor (RAT)	BDBM86152 (UMB75) Show SMILES CC(C)(O)CCCC([O-])=O Show InChI InChI=1S/C7H14O3/c1-7(2,10)5-3-4-6(8)9/h10H,3-5H2,1-2H3,(H,8,9)/p-1	UniProtKB/TrEMBL GoogleScholar AffyNet	Purchase PC cid PC sid UniChem	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by PDSP Ki Database									J Pharmacol Exp Ther 305: 675-9 (2003) Article DOI: 10.1124/jpet.102.046797 BindingDB Entry DOI: 10.7270/Q2S1812F
					More data for this Ligand-Target Pair
Gamma-hydroxybutyrate receptor (RAT)	BDBM86150 (UMB58) Show SMILES OCCCCC([O-])=O Show InChI InChI=1S/C5H10O3/c6-4-2-1-3-5(7)8/h6H,1-4H2,(H,7,8)/p-1	UniProtKB/TrEMBL GoogleScholar AffyNet	Purchase MCE KEGG PC cid PC sid UniChem Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by PDSP Ki Database									J Pharmacol Exp Ther 305: 675-9 (2003) Article DOI: 10.1124/jpet.102.046797 BindingDB Entry DOI: 10.7270/Q2S1812F
					More data for this Ligand-Target Pair
Gamma-hydroxybutyrate receptor (RAT)	BDBM50168281 (CHEMBL189853 | [3-(3-Phenyl-propoxy)-phenyl]-aceti...) Show SMILES OC(=O)Cc1cccc(OCCCc2ccccc2)c1 Show InChI InChI=1S/C17H18O3/c18-17(19)13-15-8-4-10-16(12-15)20-11-5-9-14-6-2-1-3-7-14/h1-4,6-8,10,12H,5,9,11,13H2,(H,18,19)	UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Displacement of [3H]-NCS-382 (16 nM) from GHB receptor of rat cerebrocortical membranes				Bioorg Med Chem Lett 15: 3201-2 (2005) Article DOI: 10.1016/j.bmcl.2005.05.011 BindingDB Entry DOI: 10.7270/Q2MP52TK
					More data for this Ligand-Target Pair
Gamma-hydroxybutyrate receptor (RAT)	BDBM50168285 ((3-Phenethyloxy-phenyl)-acetic acid | CHEMBL190961) Show SMILES OC(=O)Cc1cccc(OCCc2ccccc2)c1 Show InChI InChI=1S/C16H16O3/c17-16(18)12-14-7-4-8-15(11-14)19-10-9-13-5-2-1-3-6-13/h1-8,11H,9-10,12H2,(H,17,18)	UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Displacement of [3H]-NCS-382 (16 nM) from GHB receptor of rat cerebrocortical membranes				Bioorg Med Chem Lett 15: 3201-2 (2005) Article DOI: 10.1016/j.bmcl.2005.05.011 BindingDB Entry DOI: 10.7270/Q2MP52TK
					More data for this Ligand-Target Pair
Gamma-hydroxybutyrate receptor (RAT)	BDBM50168283 ((3-hydroxyphenyl)acetic acid | (m-hydroxyphenyl)ac...) Show SMILES OC(=O)Cc1cccc(O)c1 Show InChI InChI=1S/C8H8O3/c9-7-3-1-2-6(4-7)5-8(10)11/h1-4,9H,5H2,(H,10,11)	UniProtKB/TrEMBL GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	1.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Displacement of [3H]-NCS-382 (16 nM) from GHB receptor of rat cerebrocortical membranes				Bioorg Med Chem Lett 15: 3201-2 (2005) Article DOI: 10.1016/j.bmcl.2005.05.011 BindingDB Entry DOI: 10.7270/Q2MP52TK
					More data for this Ligand-Target Pair
Gamma-hydroxybutyrate receptor (RAT)	BDBM50060976 ((3-Phenoxy-phenyl)-acetic acid | CHEMBL107066) Show SMILES OC(=O)Cc1cccc(Oc2ccccc2)c1 Show InChI InChI=1S/C14H12O3/c15-14(16)10-11-5-4-8-13(9-11)17-12-6-2-1-3-7-12/h1-9H,10H2,(H,15,16)	UniProtKB/TrEMBL GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.63E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Displacement of [3H]-NCS-382 (16 nM) from GHB receptor of rat cerebrocortical membranes				Bioorg Med Chem Lett 15: 3201-2 (2005) Article DOI: 10.1016/j.bmcl.2005.05.011 BindingDB Entry DOI: 10.7270/Q2MP52TK
					More data for this Ligand-Target Pair
Gamma-hydroxybutyrate receptor (RAT)	BDBM50023575 (4-hydroxy-butyric acid | 4-hydroxybutanoic acid | ...) Show SMILES OCCCC(O)=O Show InChI InChI=1S/C4H8O3/c5-3-1-2-4(6)7/h5H,1-3H2,(H,6,7)	UniProtKB/TrEMBL GoogleScholar AffyNet	Purchase CHEMBL KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	2.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Displacement of [3H]-NCS-382 (16 nM) from GHB receptor of rat cerebrocortical membranes				Bioorg Med Chem Lett 15: 3201-2 (2005) Article DOI: 10.1016/j.bmcl.2005.05.011 BindingDB Entry DOI: 10.7270/Q2MP52TK
					More data for this Ligand-Target Pair
Gamma-hydroxybutyrate receptor (RAT)	BDBM50168282 ((3-Benzyloxy-phenyl)-acetic acid | CHEMBL190962) Show SMILES OC(=O)Cc1cccc(OCc2ccccc2)c1 Show InChI InChI=1S/C15H14O3/c16-15(17)10-13-7-4-8-14(9-13)18-11-12-5-2-1-3-6-12/h1-9H,10-11H2,(H,16,17)	UniProtKB/TrEMBL GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	4.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Displacement of [3H]-NCS-382 (16 nM) from GHB receptor of rat cerebrocortical membranes				Bioorg Med Chem Lett 15: 3201-2 (2005) Article DOI: 10.1016/j.bmcl.2005.05.011 BindingDB Entry DOI: 10.7270/Q2MP52TK
					More data for this Ligand-Target Pair
Gamma-hydroxybutyrate receptor (RAT)	BDBM50168284 (4-Phenoxy-butyric acid | CHEMBL190723) Show SMILES OC(=O)CCCOc1ccccc1 Show InChI InChI=1S/C10H12O3/c11-10(12)7-4-8-13-9-5-2-1-3-6-9/h1-3,5-6H,4,7-8H2,(H,11,12)	UniProtKB/TrEMBL GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	2.10E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Maryland Curated by ChEMBL					Assay Description Displacement of [3H]-NCS-382 (16 nM) from GHB receptor of rat cerebrocortical membranes				Bioorg Med Chem Lett 15: 3201-2 (2005) Article DOI: 10.1016/j.bmcl.2005.05.011 BindingDB Entry DOI: 10.7270/Q2MP52TK
					More data for this Ligand-Target Pair