Compile Data Set for Download or QSAR

Found 236 hits with Last Name = 'karmakar' and Initial = 's'   

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
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50365986 (CHEMBL1956427) Show SMILES CC(C)c1cc(cc(c1CO)-c1ccc(C)c(C)c1)C(C)(C)C Show InChI InChI=1S/C22H30O/c1-14(2)19-11-18(22(5,6)7)12-20(21(19)13-23)17-9-8-15(3)16(4)10-17/h8-12,14,23H,13H2,1-7H3	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	81	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50365985 (CHEMBL1956426) Show SMILES CC(C)c1cc(cc(-c2cccc(Cl)c2)c1CO)C(C)(C)C Show InChI InChI=1S/C20H25ClO/c1-13(2)17-10-15(20(3,4)5)11-18(19(17)12-22)14-7-6-8-16(21)9-14/h6-11,13,22H,12H2,1-5H3	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	100	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50366026 (CHEMBL1956425) Show SMILES CC(C)c1cc(cc(c1CO)-c1ccc2ccccc2c1)C(C)(C)C Show InChI InChI=1S/C24H28O/c1-16(2)21-13-20(24(3,4)5)14-22(23(21)15-25)19-11-10-17-8-6-7-9-18(17)12-19/h6-14,16,25H,15H2,1-5H3	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	120	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50366024 (CHEMBL1956413) Show SMILES CSc1cccc(c1)-c1cc(cc(C(C)C)c1CO)C(C)(C)C Show InChI InChI=1S/C21H28OS/c1-14(2)18-11-16(21(3,4)5)12-19(20(18)13-22)15-8-7-9-17(10-15)23-6/h7-12,14,22H,13H2,1-6H3	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	170	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50366025 (CHEMBL1956424) Show SMILES CC(C)c1cc(cc(c1CO)-c1cccc2ccccc12)C(C)(C)C Show InChI InChI=1S/C24H28O/c1-16(2)21-13-18(24(3,4)5)14-22(23(21)15-25)20-12-8-10-17-9-6-7-11-19(17)20/h6-14,16,25H,15H2,1-5H3	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	180	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50366023 (CHEMBL1956412) Show SMILES COc1cccc(c1)-c1cc(cc(C(C)C)c1CO)C(C)(C)C Show InChI InChI=1S/C21H28O2/c1-14(2)18-11-16(21(3,4)5)12-19(20(18)13-22)15-8-7-9-17(10-15)23-6/h7-12,14,22H,13H2,1-6H3	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	200	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50366022 (CHEMBL1956423) Show SMILES CC(C)c1cc(cc(c1CO)-c1cccc(c1)-c1ccccc1)C(C)(C)C Show InChI InChI=1S/C26H30O/c1-18(2)23-15-22(26(3,4)5)16-24(25(23)17-27)21-13-9-12-20(14-21)19-10-7-6-8-11-19/h6-16,18,27H,17H2,1-5H3	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	210	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50366021 (CHEMBL1956422) Show SMILES CC(C)c1cc(cc(c1CO)-c1cccc(C)c1)C(C)(C)C Show InChI InChI=1S/C21H28O/c1-14(2)18-11-17(21(4,5)6)12-19(20(18)13-22)16-9-7-8-15(3)10-16/h7-12,14,22H,13H2,1-6H3	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	240	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50366020 (CHEMBL1956421) Show SMILES CC(C)c1cc(cc(-c2ccc(Cl)cc2)c1CO)C(C)(C)C Show InChI InChI=1S/C20H25ClO/c1-13(2)17-10-15(20(3,4)5)11-18(19(17)12-22)14-6-8-16(21)9-7-14/h6-11,13,22H,12H2,1-5H3	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	290	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50365996 (CHEMBL1956433) Show SMILES O=C(CCc1ccccc1)Nc1sc2CCCCc2c1C#N Show InChI InChI=1S/C18H18N2OS/c19-12-15-14-8-4-5-9-16(14)22-18(15)20-17(21)11-10-13-6-2-1-3-7-13/h1-3,6-7H,4-5,8-11H2,(H,20,21)	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	290	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50366019 (CHEMBL1956420) Show SMILES CC(C)c1cc(cc(c1CO)-c1ccc(C)cc1)C(C)(C)C Show InChI InChI=1S/C21H28O/c1-14(2)18-11-17(21(4,5)6)12-19(20(18)13-22)16-9-7-15(3)8-10-16/h7-12,14,22H,13H2,1-6H3	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	300	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50366018 (CHEMBL1956419) Show SMILES CC(C)c1cc(cc(-c2cccc(c2)N(C)C)c1CO)C(C)(C)C Show InChI InChI=1S/C22H31NO/c1-15(2)19-12-17(22(3,4)5)13-20(21(19)14-24)16-9-8-10-18(11-16)23(6)7/h8-13,15,24H,14H2,1-7H3	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	310	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50366017 (CHEMBL1956418) Show SMILES CC(C)c1cc(cc(c1CO)-c1ccccc1)C(C)(C)C Show InChI InChI=1S/C20H26O/c1-14(2)17-11-16(20(3,4)5)12-18(19(17)13-21)15-9-7-6-8-10-15/h6-12,14,21H,13H2,1-5H3	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	390	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50366001 (CHEMBL1956438) Show SMILES COc1ccc(CCC(=O)Nc2sc3CCCCc3c2C#N)cc1 Show InChI InChI=1S/C19H20N2O2S/c1-23-14-9-6-13(7-10-14)8-11-18(22)21-19-16(12-20)15-4-2-3-5-17(15)24-19/h6-7,9-10H,2-5,8,11H2,1H3,(H,21,22)	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	410	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50365994 (CHEMBL396627) Show SMILES O=C(Nc1sc2CCCCc2c1C#N)C1CCCCC1 Show InChI InChI=1S/C16H20N2OS/c17-10-13-12-8-4-5-9-14(12)20-16(13)18-15(19)11-6-2-1-3-7-11/h11H,1-9H2,(H,18,19)	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	470	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50365993 (CHEMBL1956432) Show SMILES O=C(Nc1sc2CCCCc2c1C#N)C1CCCC1 Show InChI InChI=1S/C15H18N2OS/c16-9-12-11-7-3-4-8-13(11)19-15(12)17-14(18)10-5-1-2-6-10/h10H,1-8H2,(H,17,18)	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	470	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50365999 (CHEMBL1956436) Show SMILES Cc1ccc(CCC(=O)Nc2sc3CCCCc3c2C#N)cc1 Show InChI InChI=1S/C19H20N2OS/c1-13-6-8-14(9-7-13)10-11-18(22)21-19-16(12-20)15-4-2-3-5-17(15)23-19/h6-9H,2-5,10-11H2,1H3,(H,21,22)	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	480	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50366000 (CHEMBL1956437) Show SMILES COc1cccc(CCC(=O)Nc2sc3CCCCc3c2C#N)c1 Show InChI InChI=1S/C19H20N2O2S/c1-23-14-6-4-5-13(11-14)9-10-18(22)21-19-16(12-20)15-7-2-3-8-17(15)24-19/h4-6,11H,2-3,7-10H2,1H3,(H,21,22)	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	610	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50366016 (CHEMBL1956417) Show SMILES CC(C)c1cc(cc(c1CO)-c1ccc(cc1)-c1ccccc1)C(C)(C)C Show InChI InChI=1S/C26H30O/c1-18(2)23-15-22(26(3,4)5)16-24(25(23)17-27)21-13-11-20(12-14-21)19-9-7-6-8-10-19/h6-16,18,27H,17H2,1-5H3	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	680	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50366015 (CHEMBL1956416) Show SMILES CC(C)c1cc(cc(-c2ccc(F)cc2)c1CO)C(C)(C)C Show InChI InChI=1S/C20H25FO/c1-13(2)17-10-15(20(3,4)5)11-18(19(17)12-22)14-6-8-16(21)9-7-14/h6-11,13,22H,12H2,1-5H3	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	740	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50365998 (CHEMBL1956435) Show SMILES Cc1cccc(CCC(=O)Nc2sc3CCCCc3c2C#N)c1 Show InChI InChI=1S/C19H20N2OS/c1-13-5-4-6-14(11-13)9-10-18(22)21-19-16(12-20)15-7-2-3-8-17(15)23-19/h4-6,11H,2-3,7-10H2,1H3,(H,21,22)	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	750	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50366014 (CHEMBL1956415) Show SMILES COc1ccccc1-c1cc(cc(C(C)C)c1CO)C(C)(C)C Show InChI InChI=1S/C21H28O2/c1-14(2)17-11-15(21(3,4)5)12-18(19(17)13-22)16-9-7-8-10-20(16)23-6/h7-12,14,22H,13H2,1-6H3	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	820	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50366002 (CHEMBL1956439) Show SMILES Clc1ccc(CCC(=O)Nc2sc3CCCCc3c2C#N)cc1 Show InChI InChI=1S/C18H17ClN2OS/c19-13-8-5-12(6-9-13)7-10-17(22)21-18-15(11-20)14-3-1-2-4-16(14)23-18/h5-6,8-9H,1-4,7,10H2,(H,21,22)	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50366013 (CHEMBL1956414) Show SMILES COc1ccc(cc1)-c1cc(cc(C(C)C)c1CO)C(C)(C)C Show InChI InChI=1S/C21H28O2/c1-14(2)18-11-16(21(3,4)5)12-19(20(18)13-22)15-7-9-17(23-6)10-8-15/h7-12,14,22H,13H2,1-6H3	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50365995 (CHEMBL397167) Show SMILES O=C(Cc1ccccc1)Nc1sc2CCCCc2c1C#N Show InChI InChI=1S/C17H16N2OS/c18-11-14-13-8-4-5-9-15(13)21-17(14)19-16(20)10-12-6-2-1-3-7-12/h1-3,6-7H,4-5,8-10H2,(H,19,20)	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50365992 (CHEMBL1956431) Show SMILES O=C(Nc1sc2CCCCc2c1C#N)C1CCC1 Show InChI InChI=1S/C14H16N2OS/c15-8-11-10-6-1-2-7-12(10)18-14(11)16-13(17)9-4-3-5-9/h9H,1-7H2,(H,16,17)	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50365990 (CHEMBL1956429) Show SMILES CC(C)CC(=O)Nc1sc2CCCCc2c1C#N Show InChI InChI=1S/C14H18N2OS/c1-9(2)7-13(17)16-14-11(8-15)10-5-3-4-6-12(10)18-14/h9H,3-7H2,1-2H3,(H,16,17)	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50366003 (CHEMBL1956440) Show SMILES O=C(Cc1cc2ccccc2s1)Nc1sc2CCCCc2c1C#N Show InChI InChI=1S/C19H16N2OS2/c20-11-15-14-6-2-4-8-17(14)24-19(15)21-18(22)10-13-9-12-5-1-3-7-16(12)23-13/h1,3,5,7,9H,2,4,6,8,10H2,(H,21,22)	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50365991 (CHEMBL1956430) Show SMILES O=C(Nc1sc2CCCCc2c1C#N)C1CC1 Show InChI InChI=1S/C13H14N2OS/c14-7-10-9-3-1-2-4-11(9)17-13(10)15-12(16)8-5-6-8/h8H,1-6H2,(H,15,16)	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50366012 (CHEMBL1956259) Show SMILES CC(C)c1cc(cc(c1CO)-c1ccccc1-c1ccccc1)C(C)(C)C Show InChI InChI=1S/C26H30O/c1-18(2)23-15-20(26(3,4)5)16-24(25(23)17-27)22-14-10-9-13-21(22)19-11-7-6-8-12-19/h6-16,18,27H,17H2,1-5H3	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50365989 (CHEMBL1632048) Show SMILES CC(C)C(=O)Nc1sc2CCCCc2c1C#N Show InChI InChI=1S/C13H16N2OS/c1-8(2)12(16)15-13-10(7-14)9-5-3-4-6-11(9)17-13/h8H,3-6H2,1-2H3,(H,15,16)	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50366004 (CHEMBL1956441) Show SMILES O=C(CC1Cc2ccccc2O1)Nc1sc2CCCCc2c1C#N Show InChI InChI=1S/C19H18N2O2S/c20-11-15-14-6-2-4-8-17(14)24-19(15)21-18(22)10-13-9-12-5-1-3-7-16(12)23-13/h1,3,5,7,13H,2,4,6,8-10H2,(H,21,22)	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Vasoactive intestinal polypeptide receptor 1 (Rattus norvegicus)	BDBM50366008 (CHEMBL1956445) Show SMILES O=C(COc1ccccc1)Nc1sc2CCCCc2c1C#N Show InChI InChI=1S/C17H16N2O2S/c18-10-14-13-8-4-5-9-15(13)22-17(14)19-16(20)11-21-12-6-2-1-3-7-12/h1-3,6-7H,4-5,8-9,11H2,(H,19,20)	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Co. Curated by ChEMBL					Assay Description Antagonist activity at vasoactive intestinal peptide receptor 1 in rat RKE cells assessed as inhibition of VIP-induced intracellular cAMP accumulatio...				Bioorg Med Chem Lett 22: 2287-90 (2012) Article DOI: 10.1016/j.bmcl.2012.01.082 BindingDB Entry DOI: 10.7270/Q2Q240QR
					More data for this Ligand-Target Pair
Nuclear receptor ROR-beta (Homo sapiens (Human))	BDBM50509327 (CHEMBL4464711) Show SMILES [H][C@@]12CNc3cc(ccc3[C@@]1(CCN2C(=O)[C@H]1CC[C@@H](CC1)C(O)=O)S(=O)(=O)c1ccc(F)cc1)C(F)(C(F)(F)F)C(F)(F)F |r,wU:16.18,wD:19.25,1.0,10.28,(14.49,-6.66,;13.16,-7.44,;13.16,-5.88,;11.82,-5.1,;10.48,-5.88,;9.14,-5.12,;7.81,-5.89,;7.81,-7.43,;9.15,-8.2,;10.48,-7.44,;11.81,-8.21,;12.13,-9.73,;13.67,-9.9,;14.31,-8.49,;15.82,-8.17,;16.3,-6.71,;16.84,-9.32,;18.34,-9.01,;19.36,-10.15,;18.88,-11.62,;17.37,-11.93,;16.35,-10.79,;19.91,-12.77,;19.42,-14.24,;21.41,-12.46,;10.71,-9.29,;9.61,-10.38,;9.22,-8.89,;11.1,-10.78,;10,-11.86,;10.38,-13.35,;11.87,-13.76,;12.26,-15.25,;12.97,-12.67,;12.58,-11.19,;6.48,-5.12,;5.14,-4.35,;5.15,-5.89,;3.81,-5.12,;5.15,-7.43,;3.8,-6.65,;6.48,-3.58,;7.81,-2.81,;5.15,-2.81,;6.47,-2.04,)| Show InChI InChI=1S/C28H26F8N2O5S/c29-18-6-8-19(9-7-18)44(42,43)25-11-12-38(23(39)15-1-3-16(4-2-15)24(40)41)22(25)14-37-21-13-17(5-10-20(21)25)26(30,27(31,32)33)28(34,35)36/h5-10,13,15-16,22,37H,1-4,11-12,14H2,(H,40,41)/t15-,16-,22-,25-/m1/s1	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia 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
Bristol-Myers Squibb Curated by ChEMBL					Assay Description Activity at RORbeta (unknown origin)				J Med Chem 62: 9931-9946 (2019) Article DOI: 10.1021/acs.jmedchem.9b01369 BindingDB Entry DOI: 10.7270/Q2G44TKD
					More data for this Ligand-Target Pair
Oxysterols receptor LXR-alpha (Homo sapiens (Human))	BDBM382173 ((1R,4r)-4-((3aR,9bR)-9b-((4-fluorophenyl)sulfonyl)...) Show SMILES OC(=O)[C@H]1CC[C@@H](CC1)C(=O)N1CC[C@@]2([C@H]1CCc1cc(ccc21)C(F)(C(F)(F)F)C(F)(F)F)S(=O)(=O)c1ccc(F)cc1 |r,wU:15.16,3.2,wD:6.9,14.37,(-10.01,1.35,;-9.74,-.16,;-10.91,-1.16,;-8.29,-.68,;-7.11,.31,;-5.66,-.21,;-5.39,-1.73,;-6.57,-2.72,;-8.01,-2.2,;-3.94,-2.25,;-3.67,-3.76,;-2.76,-1.25,;-2.88,.28,;-1.45,.87,;-.46,-.31,;-1.27,-1.62,;-.54,-2.98,;1,-3.02,;1.81,-1.72,;3.35,-1.76,;4.16,-.46,;3.43,.9,;1.89,.95,;1.08,-.36,;5.7,-.5,;5.75,1.04,;7.24,-.55,;8.78,-.6,;7.19,-2.09,;7.29,.99,;5.65,-2.04,;4.29,-2.77,;6.96,-2.85,;5.6,-3.58,;.21,1.08,;1.74,1.24,;.84,2.48,;-.65,2.35,;-2.19,2.24,;-3.05,3.51,;-2.38,4.9,;-3.25,6.17,;-.85,5.01,;.02,3.74,)| Show InChI InChI=1S/C29H27F8NO5S/c30-20-7-9-21(10-8-20)44(42,43)26-13-14-38(24(39)16-1-3-17(4-2-16)25(40)41)23(26)12-5-18-15-19(6-11-22(18)26)27(31,28(32,33)34)29(35,36)37/h6-11,15-17,23H,1-5,12-14H2,(H,40,41)/t16-,17-,23-,26-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid PDB UniChem	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Curated by ChEMBL					Assay Description Activity at LXRalpha (unknown origin)				J Med Chem 62: 9931-9946 (2019) Article DOI: 10.1021/acs.jmedchem.9b01369 BindingDB Entry DOI: 10.7270/Q2G44TKD
					More data for this Ligand-Target Pair
Oxysterols receptor LXR-alpha (Homo sapiens (Human))	BDBM382198 (US10273259, Example 12 | US10711020, Example 12) Show SMILES OC(=O)C12CCC(CC1)(CC2)C(=O)N1CC[C@@]2([C@H]1CCc1cc(ccc21)C(F)(C(F)(F)F)C(F)(F)F)S(=O)(=O)c1ccc(F)cc1 |r| Show InChI InChI=1S/C31H29F8NO5S/c32-20-3-5-21(6-4-20)46(44,45)28-15-16-40(24(41)26-9-12-27(13-10-26,14-11-26)25(42)43)23(28)8-1-18-17-19(2-7-22(18)28)29(33,30(34,35)36)31(37,38)39/h2-7,17,23H,1,8-16H2,(H,42,43)/t23-,26?,27?,28-/m1/s1	PDB UniProtKB/SwissProt antibodypedia 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
Bristol-Myers Squibb Curated by ChEMBL					Assay Description Activity at LXRalpha (unknown origin)				J Med Chem 62: 9931-9946 (2019) Article DOI: 10.1021/acs.jmedchem.9b01369 BindingDB Entry DOI: 10.7270/Q2G44TKD
					More data for this Ligand-Target Pair
Nuclear receptor ROR-beta (Homo sapiens (Human))	BDBM50509330 (CHEMBL4525527) Show SMILES [H][C@@]12CCc3cc(ccc3[C@@]1(CCN2C(=O)[C@H]1CC[C@@H](CC1)C(O)=O)S(=O)(=O)c1ccc(Cl)cc1)C(F)(C(F)(F)F)C(F)(F)F |r,wU:16.18,wD:19.25,1.0,10.28,(39.12,-6.49,;37.79,-7.27,;37.79,-5.71,;36.45,-4.93,;35.11,-5.71,;33.77,-4.95,;32.44,-5.72,;32.44,-7.26,;33.78,-8.03,;35.11,-7.26,;36.44,-8.04,;36.76,-9.56,;38.3,-9.73,;38.94,-8.31,;40.45,-8,;40.93,-6.54,;41.47,-9.15,;42.97,-8.84,;43.99,-9.98,;43.51,-11.45,;42,-11.76,;40.98,-10.61,;44.54,-12.6,;44.05,-14.06,;46.04,-12.29,;35.34,-9.12,;34.24,-10.21,;33.85,-8.72,;35.73,-10.61,;34.63,-11.69,;35.01,-13.18,;36.5,-13.59,;36.89,-15.08,;37.6,-12.5,;37.21,-11.02,;31.11,-4.95,;29.77,-4.18,;29.78,-5.72,;28.44,-4.95,;29.78,-7.26,;28.43,-6.48,;31.11,-3.41,;32.44,-2.64,;29.78,-2.64,;31.1,-1.87,)| Show InChI InChI=1S/C29H27ClF7NO5S/c30-20-7-9-21(10-8-20)44(42,43)26-13-14-38(24(39)16-1-3-17(4-2-16)25(40)41)23(26)12-5-18-15-19(6-11-22(18)26)27(31,28(32,33)34)29(35,36)37/h6-11,15-17,23H,1-5,12-14H2,(H,40,41)/t16-,17-,23-,26-/m1/s1	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia 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
Bristol-Myers Squibb Curated by ChEMBL					Assay Description Activity at RORbeta (unknown origin)				J Med Chem 62: 9931-9946 (2019) Article DOI: 10.1021/acs.jmedchem.9b01369 BindingDB Entry DOI: 10.7270/Q2G44TKD
					More data for this Ligand-Target Pair
Nuclear receptor ROR-beta (Homo sapiens (Human))	BDBM382198 (US10273259, Example 12 | US10711020, Example 12) Show SMILES OC(=O)C12CCC(CC1)(CC2)C(=O)N1CC[C@@]2([C@H]1CCc1cc(ccc21)C(F)(C(F)(F)F)C(F)(F)F)S(=O)(=O)c1ccc(F)cc1 |r| Show InChI InChI=1S/C31H29F8NO5S/c32-20-3-5-21(6-4-20)46(44,45)28-15-16-40(24(41)26-9-12-27(13-10-26,14-11-26)25(42)43)23(28)8-1-18-17-19(2-7-22(18)28)29(33,30(34,35)36)31(37,38)39/h2-7,17,23H,1,8-16H2,(H,42,43)/t23-,26?,27?,28-/m1/s1	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia 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
Bristol-Myers Squibb Curated by ChEMBL					Assay Description Activity at RORbeta (unknown origin)				J Med Chem 62: 9931-9946 (2019) Article DOI: 10.1021/acs.jmedchem.9b01369 BindingDB Entry DOI: 10.7270/Q2G44TKD
					More data for this Ligand-Target Pair
Oxysterols receptor LXR-beta (Homo sapiens (Human))	BDBM50509331 (CHEMBL4527625) Show SMILES [H][C@@]12COc3cc(ccc3[C@@]1(CCN2C(=O)[C@H]1CC[C@@H](CC1)C(O)=O)S(=O)(=O)c1ccc(F)cc1)C(F)(C(F)(F)F)C(F)(F)F |r,wU:16.18,wD:19.25,1.0,10.28,(38.73,-26.8,;37.4,-27.58,;37.4,-26.03,;36.05,-25.25,;34.71,-26.03,;33.38,-25.26,;32.05,-26.03,;32.05,-27.58,;33.38,-28.35,;34.71,-27.58,;36.05,-28.35,;36.36,-29.88,;37.91,-30.05,;38.55,-28.63,;40.06,-28.32,;40.54,-26.86,;41.08,-29.47,;42.57,-29.15,;43.6,-30.3,;43.12,-31.77,;41.61,-32.08,;40.58,-30.93,;44.14,-32.92,;43.66,-34.38,;45.65,-32.6,;34.95,-29.44,;33.85,-30.53,;33.45,-29.03,;35.33,-30.93,;34.23,-32.01,;34.62,-33.49,;36.11,-33.91,;36.49,-35.4,;37.21,-32.82,;36.81,-31.33,;30.72,-25.26,;29.38,-24.49,;29.38,-26.03,;28.05,-25.26,;29.38,-27.57,;28.04,-26.79,;30.72,-23.72,;32.05,-22.95,;29.38,-22.95,;30.71,-22.18,)| Show InChI InChI=1S/C28H25F8NO6S/c29-18-6-8-19(9-7-18)44(41,42)25-11-12-37(23(38)15-1-3-16(4-2-15)24(39)40)22(25)14-43-21-13-17(5-10-20(21)25)26(30,27(31,32)33)28(34,35)36/h5-10,13,15-16,22H,1-4,11-12,14H2,(H,39,40)/t15-,16-,22-,25-/m1/s1	PDB UniProtKB/SwissProt antibodypedia 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
Bristol-Myers Squibb Curated by ChEMBL					Assay Description Activity at LXRbeta (unknown origin)				J Med Chem 62: 9931-9946 (2019) Article DOI: 10.1021/acs.jmedchem.9b01369 BindingDB Entry DOI: 10.7270/Q2G44TKD
					More data for this Ligand-Target Pair
Oxysterols receptor LXR-alpha (Homo sapiens (Human))	BDBM50509327 (CHEMBL4464711) Show SMILES [H][C@@]12CNc3cc(ccc3[C@@]1(CCN2C(=O)[C@H]1CC[C@@H](CC1)C(O)=O)S(=O)(=O)c1ccc(F)cc1)C(F)(C(F)(F)F)C(F)(F)F |r,wU:16.18,wD:19.25,1.0,10.28,(14.49,-6.66,;13.16,-7.44,;13.16,-5.88,;11.82,-5.1,;10.48,-5.88,;9.14,-5.12,;7.81,-5.89,;7.81,-7.43,;9.15,-8.2,;10.48,-7.44,;11.81,-8.21,;12.13,-9.73,;13.67,-9.9,;14.31,-8.49,;15.82,-8.17,;16.3,-6.71,;16.84,-9.32,;18.34,-9.01,;19.36,-10.15,;18.88,-11.62,;17.37,-11.93,;16.35,-10.79,;19.91,-12.77,;19.42,-14.24,;21.41,-12.46,;10.71,-9.29,;9.61,-10.38,;9.22,-8.89,;11.1,-10.78,;10,-11.86,;10.38,-13.35,;11.87,-13.76,;12.26,-15.25,;12.97,-12.67,;12.58,-11.19,;6.48,-5.12,;5.14,-4.35,;5.15,-5.89,;3.81,-5.12,;5.15,-7.43,;3.8,-6.65,;6.48,-3.58,;7.81,-2.81,;5.15,-2.81,;6.47,-2.04,)| Show InChI InChI=1S/C28H26F8N2O5S/c29-18-6-8-19(9-7-18)44(42,43)25-11-12-38(23(39)15-1-3-16(4-2-15)24(40)41)22(25)14-37-21-13-17(5-10-20(21)25)26(30,27(31,32)33)28(34,35)36/h5-10,13,15-16,22,37H,1-4,11-12,14H2,(H,40,41)/t15-,16-,22-,25-/m1/s1	PDB UniProtKB/SwissProt antibodypedia 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
Bristol-Myers Squibb Curated by ChEMBL					Assay Description Activity at LXRalpha (unknown origin)				J Med Chem 62: 9931-9946 (2019) Article DOI: 10.1021/acs.jmedchem.9b01369 BindingDB Entry DOI: 10.7270/Q2G44TKD
					More data for this Ligand-Target Pair
Oxysterols receptor LXR-beta (Homo sapiens (Human))	BDBM50509332 (CHEMBL4462790) Show SMILES [H][C@@]12CCc3cc(ccc3[C@@]1(CCN2C(=O)[C@H]1CC[C@@H](CC1)C(O)=O)S(=O)(=O)c1ccc(C)cc1)C(F)(C(F)(F)F)C(F)(F)F |r,wU:16.18,wD:19.25,1.0,10.28,(64.23,-6.6,;62.9,-7.39,;62.9,-5.83,;61.56,-5.05,;60.21,-5.83,;58.88,-5.06,;57.55,-5.83,;57.55,-7.38,;58.88,-8.15,;60.21,-7.38,;61.55,-8.15,;61.86,-9.68,;63.41,-9.85,;64.05,-8.43,;65.56,-8.12,;66.04,-6.66,;66.58,-9.27,;68.07,-8.96,;69.1,-10.1,;68.62,-11.57,;67.11,-11.88,;66.09,-10.73,;69.64,-12.72,;69.16,-14.18,;71.15,-12.41,;60.45,-9.24,;59.35,-10.33,;58.96,-8.83,;60.83,-10.73,;59.74,-11.81,;60.12,-13.3,;61.61,-13.71,;62,-15.2,;62.71,-12.62,;62.32,-11.13,;56.22,-5.06,;54.88,-4.29,;54.88,-5.83,;53.55,-5.06,;54.88,-7.37,;53.54,-6.6,;56.22,-3.52,;57.55,-2.75,;54.88,-2.75,;56.21,-1.98,)| Show InChI InChI=1S/C30H30F7NO5S/c1-17-2-10-22(11-3-17)44(42,43)27-14-15-38(25(39)18-4-6-19(7-5-18)26(40)41)24(27)13-8-20-16-21(9-12-23(20)27)28(31,29(32,33)34)30(35,36)37/h2-3,9-12,16,18-19,24H,4-8,13-15H2,1H3,(H,40,41)/t18-,19-,24-,27-/m1/s1	PDB UniProtKB/SwissProt antibodypedia 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
Bristol-Myers Squibb Curated by ChEMBL					Assay Description Activity at LXRbeta (unknown origin)				J Med Chem 62: 9931-9946 (2019) Article DOI: 10.1021/acs.jmedchem.9b01369 BindingDB Entry DOI: 10.7270/Q2G44TKD
					More data for this Ligand-Target Pair
Oxysterols receptor LXR-beta (Homo sapiens (Human))	BDBM382181 ((1S,4s)-4-fluoro-4-((3aR,9bR)-9b-((4-fluorophenyl)...) Show SMILES OC(=O)[C@H]1CC[C@@](F)(CC1)C(=O)N1CC[C@@]2([C@H]1CCc1cc(ccc21)C(F)(C(F)(F)F)C(F)(F)F)S(=O)(=O)c1ccc(F)cc1 |r,wU:16.17,3.2,6.6,wD:6.10,15.38,(-6.98,10.68,;-7.74,9.34,;-9.28,9.33,;-6.97,8.01,;-5.43,8.01,;-4.65,6.68,;-5.42,5.35,;-5.68,3.83,;-6.96,5.34,;-7.73,6.67,;-3.97,4.83,;-3.7,3.31,;-2.79,5.82,;-2.91,7.36,;-1.48,7.94,;-.49,6.76,;-1.3,5.45,;-.57,4.1,;.97,4.05,;1.78,5.36,;3.32,5.31,;4.13,6.62,;3.4,7.97,;1.86,8.02,;1.05,6.71,;5.67,6.57,;5.72,8.11,;7.21,6.52,;8.75,6.47,;7.16,4.98,;7.26,8.06,;5.62,5.03,;4.27,4.3,;6.93,4.22,;5.58,3.49,;.18,8.15,;1.65,8.62,;.66,9.61,;-.68,9.42,;-2.22,9.31,;-3.08,10.58,;-2.41,11.97,;-3.28,13.24,;-.88,12.08,;-.01,10.81,)| Show InChI InChI=1S/C29H26F9NO5S/c30-19-3-5-20(6-4-19)45(43,44)26-13-14-39(24(42)25(31)11-9-16(10-12-25)23(40)41)22(26)8-1-17-15-18(2-7-21(17)26)27(32,28(33,34)35)29(36,37)38/h2-7,15-16,22H,1,8-14H2,(H,40,41)/t16-,22-,25+,26-/m1/s1	PDB UniProtKB/SwissProt antibodypedia 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
Bristol-Myers Squibb Curated by ChEMBL					Assay Description Activity at LXRbeta (unknown origin)				J Med Chem 62: 9931-9946 (2019) Article DOI: 10.1021/acs.jmedchem.9b01369 BindingDB Entry DOI: 10.7270/Q2G44TKD
					More data for this Ligand-Target Pair
Cytochrome P450 2C9 (Homo sapiens (Human))	BDBM382356 (US10273259, Example 69 | US10711020, Example 69) Show SMILES OC1(CCS(=O)(=O)CC1)C(=O)N1CC[C@@]2([C@H]1CCc1cc(ccc21)C(F)(C(F)(F)F)C(F)(F)F)S(=O)(=O)c1ccc(F)cc1 |r| Show InChI InChI=1S/C27H25F8NO6S2/c28-18-3-5-19(6-4-18)44(41,42)24-9-12-36(22(37)23(38)10-13-43(39,40)14-11-23)21(24)8-1-16-15-17(2-7-20(16)24)25(29,26(30,31)32)27(33,34)35/h2-7,15,21,38H,1,8-14H2/t21-,24-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia 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
Bristol-Myers Squibb Curated by ChEMBL					Assay Description Inhibition of recombinant CYP2C9 (unknown origin)				J Med Chem 62: 9931-9946 (2019) Article DOI: 10.1021/acs.jmedchem.9b01369 BindingDB Entry DOI: 10.7270/Q2G44TKD
					More data for this Ligand-Target Pair
Nuclear receptor ROR-alpha (Homo sapiens (Human))	BDBM382356 (US10273259, Example 69 | US10711020, Example 69) Show SMILES OC1(CCS(=O)(=O)CC1)C(=O)N1CC[C@@]2([C@H]1CCc1cc(ccc21)C(F)(C(F)(F)F)C(F)(F)F)S(=O)(=O)c1ccc(F)cc1 |r| Show InChI InChI=1S/C27H25F8NO6S2/c28-18-3-5-19(6-4-18)44(41,42)24-9-12-36(22(37)23(38)10-13-43(39,40)14-11-23)21(24)8-1-16-15-17(2-7-20(16)24)25(29,26(30,31)32)27(33,34)35/h2-7,15,21,38H,1,8-14H2/t21-,24-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia 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
Bristol-Myers Squibb Curated by ChEMBL					Assay Description Activity at RORalpha (unknown origin)				J Med Chem 62: 9931-9946 (2019) Article DOI: 10.1021/acs.jmedchem.9b01369 BindingDB Entry DOI: 10.7270/Q2G44TKD
					More data for this Ligand-Target Pair
Nuclear receptor ROR-alpha (Homo sapiens (Human))	BDBM50509328 (CHEMBL4452650) Show SMILES [H][C@@]12CCc3cc(ccc3[C@@]1(CCN2C(=O)[C@H]1CC[C@@H](CC1)C(O)=O)S(=O)(=O)Cc1ccccc1)C(F)(C(F)(F)F)C(F)(F)F |r,wU:16.18,wD:19.25,1.0,10.28,(38.9,-47.28,;37.57,-48.06,;37.57,-46.51,;36.22,-45.72,;34.88,-46.5,;33.55,-45.74,;32.22,-46.51,;32.22,-48.05,;33.55,-48.82,;34.88,-48.06,;36.22,-48.83,;36.53,-50.35,;38.08,-50.52,;38.72,-49.11,;40.23,-48.8,;40.71,-47.34,;41.25,-49.95,;42.74,-49.63,;43.77,-50.78,;43.29,-52.25,;41.78,-52.56,;40.75,-51.41,;44.31,-53.4,;43.83,-54.86,;45.82,-53.08,;35.12,-49.92,;34.02,-51.01,;33.62,-49.51,;35.5,-51.41,;34.4,-52.49,;32.93,-52.07,;31.83,-53.15,;32.21,-54.64,;33.71,-55.05,;34.8,-53.97,;30.89,-45.74,;29.55,-44.97,;29.55,-46.51,;28.22,-45.74,;29.55,-48.05,;28.21,-47.27,;30.89,-44.2,;32.22,-43.43,;29.55,-43.43,;30.88,-42.66,)| Show InChI InChI=1S/C30H30F7NO5S/c31-28(29(32,33)34,30(35,36)37)22-11-12-23-21(16-22)10-13-24-27(23,44(42,43)17-18-4-2-1-3-5-18)14-15-38(24)25(39)19-6-8-20(9-7-19)26(40)41/h1-5,11-12,16,19-20,24H,6-10,13-15,17H2,(H,40,41)/t19-,20-,24-,27-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia 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
Bristol-Myers Squibb Curated by ChEMBL					Assay Description Activity at RORalpha (unknown origin)				J Med Chem 62: 9931-9946 (2019) Article DOI: 10.1021/acs.jmedchem.9b01369 BindingDB Entry DOI: 10.7270/Q2G44TKD
					More data for this Ligand-Target Pair
Nuclear receptor ROR-alpha (Homo sapiens (Human))	BDBM50509331 (CHEMBL4527625) Show SMILES [H][C@@]12COc3cc(ccc3[C@@]1(CCN2C(=O)[C@H]1CC[C@@H](CC1)C(O)=O)S(=O)(=O)c1ccc(F)cc1)C(F)(C(F)(F)F)C(F)(F)F |r,wU:16.18,wD:19.25,1.0,10.28,(38.73,-26.8,;37.4,-27.58,;37.4,-26.03,;36.05,-25.25,;34.71,-26.03,;33.38,-25.26,;32.05,-26.03,;32.05,-27.58,;33.38,-28.35,;34.71,-27.58,;36.05,-28.35,;36.36,-29.88,;37.91,-30.05,;38.55,-28.63,;40.06,-28.32,;40.54,-26.86,;41.08,-29.47,;42.57,-29.15,;43.6,-30.3,;43.12,-31.77,;41.61,-32.08,;40.58,-30.93,;44.14,-32.92,;43.66,-34.38,;45.65,-32.6,;34.95,-29.44,;33.85,-30.53,;33.45,-29.03,;35.33,-30.93,;34.23,-32.01,;34.62,-33.49,;36.11,-33.91,;36.49,-35.4,;37.21,-32.82,;36.81,-31.33,;30.72,-25.26,;29.38,-24.49,;29.38,-26.03,;28.05,-25.26,;29.38,-27.57,;28.04,-26.79,;30.72,-23.72,;32.05,-22.95,;29.38,-22.95,;30.71,-22.18,)| Show InChI InChI=1S/C28H25F8NO6S/c29-18-6-8-19(9-7-18)44(41,42)25-11-12-37(23(38)15-1-3-16(4-2-15)24(39)40)22(25)14-43-21-13-17(5-10-20(21)25)26(30,27(31,32)33)28(34,35)36/h5-10,13,15-16,22H,1-4,11-12,14H2,(H,39,40)/t15-,16-,22-,25-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia 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
Bristol-Myers Squibb Curated by ChEMBL					Assay Description Activity at RORalpha (unknown origin)				J Med Chem 62: 9931-9946 (2019) Article DOI: 10.1021/acs.jmedchem.9b01369 BindingDB Entry DOI: 10.7270/Q2G44TKD
					More data for this Ligand-Target Pair
Nuclear receptor ROR-alpha (Homo sapiens (Human))	BDBM50509329 (CHEMBL4578712) Show SMILES [H][C@@]12COc3cc(ccc3[C@@]1(CCN2C(=O)C1(O)CCS(=O)(=O)CC1)S(=O)(=O)c1ccc(F)cc1)C(F)(C(F)(F)F)C(F)(F)F |r| Show InChI InChI=1S/C26H23F8NO7S2/c27-16-2-4-17(5-3-16)44(40,41)23-7-10-35(21(36)22(37)8-11-43(38,39)12-9-22)20(23)14-42-19-13-15(1-6-18(19)23)24(28,25(29,30)31)26(32,33)34/h1-6,13,20,37H,7-12,14H2/t20-,23-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia 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
Bristol-Myers Squibb Curated by ChEMBL					Assay Description Activity at RORalpha (unknown origin)				J Med Chem 62: 9931-9946 (2019) Article DOI: 10.1021/acs.jmedchem.9b01369 BindingDB Entry DOI: 10.7270/Q2G44TKD
					More data for this Ligand-Target Pair
Nuclear receptor ROR-alpha (Homo sapiens (Human))	BDBM50509334 (CHEMBL4436417) Show SMILES [H][C@@]12CNc3cc(ccc3[C@@]1(CCN2C(=O)C1(O)CCS(=O)(=O)CC1)S(=O)(=O)c1ccc(F)cc1)C(F)(C(F)(F)F)C(F)(F)F |r| Show InChI InChI=1S/C26H24F8N2O6S2/c27-16-2-4-17(5-3-16)44(41,42)23-7-10-36(21(37)22(38)8-11-43(39,40)12-9-22)20(23)14-35-19-13-15(1-6-18(19)23)24(28,25(29,30)31)26(32,33)34/h1-6,13,20,35,38H,7-12,14H2/t20-,23-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia 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
Bristol-Myers Squibb Curated by ChEMBL					Assay Description Activity at RORalpha (unknown origin)				J Med Chem 62: 9931-9946 (2019) Article DOI: 10.1021/acs.jmedchem.9b01369 BindingDB Entry DOI: 10.7270/Q2G44TKD
					More data for this Ligand-Target Pair
Nuclear receptor ROR-beta (Homo sapiens (Human))	BDBM382173 ((1R,4r)-4-((3aR,9bR)-9b-((4-fluorophenyl)sulfonyl)...) Show SMILES OC(=O)[C@H]1CC[C@@H](CC1)C(=O)N1CC[C@@]2([C@H]1CCc1cc(ccc21)C(F)(C(F)(F)F)C(F)(F)F)S(=O)(=O)c1ccc(F)cc1 |r,wU:15.16,3.2,wD:6.9,14.37,(-10.01,1.35,;-9.74,-.16,;-10.91,-1.16,;-8.29,-.68,;-7.11,.31,;-5.66,-.21,;-5.39,-1.73,;-6.57,-2.72,;-8.01,-2.2,;-3.94,-2.25,;-3.67,-3.76,;-2.76,-1.25,;-2.88,.28,;-1.45,.87,;-.46,-.31,;-1.27,-1.62,;-.54,-2.98,;1,-3.02,;1.81,-1.72,;3.35,-1.76,;4.16,-.46,;3.43,.9,;1.89,.95,;1.08,-.36,;5.7,-.5,;5.75,1.04,;7.24,-.55,;8.78,-.6,;7.19,-2.09,;7.29,.99,;5.65,-2.04,;4.29,-2.77,;6.96,-2.85,;5.6,-3.58,;.21,1.08,;1.74,1.24,;.84,2.48,;-.65,2.35,;-2.19,2.24,;-3.05,3.51,;-2.38,4.9,;-3.25,6.17,;-.85,5.01,;.02,3.74,)| Show InChI InChI=1S/C29H27F8NO5S/c30-20-7-9-21(10-8-20)44(42,43)26-13-14-38(24(39)16-1-3-17(4-2-16)25(40)41)23(26)12-5-18-15-19(6-11-22(18)26)27(31,28(32,33)34)29(35,36)37/h6-11,15-17,23H,1-5,12-14H2,(H,40,41)/t16-,17-,23-,26-/m1/s1	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid PDB UniChem	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Bristol-Myers Squibb Curated by ChEMBL					Assay Description Activity at RORbeta (unknown origin)				J Med Chem 62: 9931-9946 (2019) Article DOI: 10.1021/acs.jmedchem.9b01369 BindingDB Entry DOI: 10.7270/Q2G44TKD
					More data for this Ligand-Target Pair
Nuclear receptor ROR-beta (Homo sapiens (Human))	BDBM50509337 (CHEMBL4555822) Show SMILES [H][C@@]12CCc3cc(ccc3[C@@]1(CCN2C(=O)[C@H]1CC[C@@H](CC1)C(O)=O)S(=O)(=O)c1cccc(F)c1)C(F)(C(F)(F)F)C(F)(F)F |r,wU:16.18,wD:19.25,1.0,10.28,(15.64,-25.66,;14.31,-26.44,;14.32,-24.88,;12.97,-24.1,;11.63,-24.88,;10.29,-24.12,;8.96,-24.89,;8.96,-26.43,;10.3,-27.2,;11.63,-26.44,;12.96,-27.21,;13.28,-28.73,;14.82,-28.9,;15.46,-27.49,;16.97,-27.17,;17.45,-25.71,;17.99,-28.33,;19.49,-28.01,;20.51,-29.15,;20.03,-30.62,;18.52,-30.94,;17.5,-29.79,;21.06,-31.77,;20.57,-33.24,;22.56,-31.46,;11.86,-28.29,;10.76,-29.38,;10.37,-27.89,;12.25,-29.78,;11.15,-30.86,;11.54,-32.35,;13.02,-32.76,;14.12,-31.67,;15.61,-32.08,;13.73,-30.19,;7.63,-24.12,;6.29,-23.35,;6.3,-24.89,;4.96,-24.12,;6.3,-26.43,;4.95,-25.65,;7.63,-22.58,;8.96,-21.81,;6.3,-21.81,;7.62,-21.04,)| Show InChI InChI=1S/C29H27F8NO5S/c30-20-2-1-3-21(15-20)44(42,43)26-12-13-38(24(39)16-4-6-17(7-5-16)25(40)41)23(26)11-8-18-14-19(9-10-22(18)26)27(31,28(32,33)34)29(35,36)37/h1-3,9-10,14-17,23H,4-8,11-13H2,(H,40,41)/t16-,17-,23-,26-/m1/s1	PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD DrugBank antibodypedia 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
Bristol-Myers Squibb Curated by ChEMBL					Assay Description Activity at RORbeta (unknown origin)				J Med Chem 62: 9931-9946 (2019) Article DOI: 10.1021/acs.jmedchem.9b01369 BindingDB Entry DOI: 10.7270/Q2G44TKD
					More data for this Ligand-Target Pair

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