Compile Data Set for Download or QSAR

Found 94 hits with Last Name = 'rhodes' and Initial = 'di'   

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
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321697 (1-allyl-1-(1-(((3S,4R)-1-(cyclopentanecarbonyl)-4-...) Show SMILES O[C@@]1(CN(C[C@@H]1CN1CCC(CC1)N(CC=C)C(=O)NCc1ccc(cc1)C(F)(F)F)C(=O)C1CCCC1)c1ccccc1 |r| Show InChI InChI=1S/C34H43F3N4O3/c1-2-18-41(32(43)38-21-25-12-14-28(15-13-25)34(35,36)37)30-16-19-39(20-17-30)22-29-23-40(31(42)26-8-6-7-9-26)24-33(29,44)27-10-4-3-5-11-27/h2-5,10-15,26,29-30,44H,1,6-9,16-24H2,(H,38,43)/t29-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.10	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321683 (4-chlorobenzyl allyl(1-(((3S,4R)-1-(cyclopentaneca...) Show SMILES O[C@@]1(CN(C[C@@H]1CN1CCC(CC1)N(CC=C)C(=O)OCc1ccc(Cl)cc1)C(=O)C1CCCC1)c1ccccc1 |r| Show InChI InChI=1S/C33H42ClN3O4/c1-2-18-37(32(39)41-23-25-12-14-29(34)15-13-25)30-16-19-35(20-17-30)21-28-22-36(31(38)26-8-6-7-9-26)24-33(28,40)27-10-4-3-5-11-27/h2-5,10-15,26,28,30,40H,1,6-9,16-24H2/t28-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.10	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50325319 (1-allyl-1-(1-(((3S,4R)-1-(cyclopentanecarbonyl)-4-...) Show SMILES O[C@@]1(CN(C[C@@H]1CN1CCC(CC1)N(CC=C)C(=O)NCc1ccc(cc1)C(F)(F)F)C(=O)C1CCCC1)c1cccc(F)c1 |r| Show InChI InChI=1S/C34H42F4N4O3/c1-2-16-42(32(44)39-20-24-10-12-26(13-11-24)34(36,37)38)30-14-17-40(18-15-30)21-28-22-41(31(43)25-6-3-4-7-25)23-33(28,45)27-8-5-9-29(35)19-27/h2,5,8-13,19,25,28,30,45H,1,3-4,6-7,14-18,20-23H2,(H,39,44)/t28-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.38	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibition of human CCR5 expressed in CHO cells assessed as inhibition of RANTES-stimulated [35S]GTPgammaS binding				Bioorg Med Chem Lett 20: 5334-6 (2010) Article DOI: 10.1016/j.bmcl.2010.05.046 BindingDB Entry DOI: 10.7270/Q2J67H49
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321712 (CHEMBL1172625 | N-allyl-N-(1-(((3S,4R)-1-(cyclopen...) Show SMILES CNS(=O)(=O)c1ccc(CC(=O)N(CC=C)C2CCN(C[C@H]3CN(C[C@]3(O)c3ccccc3)C(=O)C3CCCC3)CC2)cc1 |r| Show InChI InChI=1S/C34H46N4O5S/c1-3-19-38(32(39)22-26-13-15-31(16-14-26)44(42,43)35-2)30-17-20-36(21-18-30)23-29-24-37(33(40)27-9-7-8-10-27)25-34(29,41)28-11-5-4-6-12-28/h3-6,11-16,27,29-30,35,41H,1,7-10,17-25H2,2H3/t29-,34-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.5	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321699 (1-allyl-1-(1-(((3S,4R)-1-(cyclopentanecarbonyl)-4-...) Show SMILES O[C@@]1(CN(C[C@@H]1CN1CCC(CC1)N(CC=C)C(=O)NCc1ccc(F)cc1F)C(=O)C1CCCC1)c1ccccc1 |r| Show InChI InChI=1S/C33H42F2N4O3/c1-2-16-39(32(41)36-20-25-12-13-28(34)19-30(25)35)29-14-17-37(18-15-29)21-27-22-38(31(40)24-8-6-7-9-24)23-33(27,42)26-10-4-3-5-11-26/h2-5,10-13,19,24,27,29,42H,1,6-9,14-18,20-23H2,(H,36,41)/t27-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.60	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321694 (1-allyl-1-(1-(((3S,4R)-1-(cyclopentanecarbonyl)-4-...) Show SMILES O[C@@]1(CN(C[C@@H]1CN1CCC(CC1)N(CC=C)C(=O)NCc1ccc(F)cc1)C(=O)C1CCCC1)c1ccccc1 |r| Show InChI InChI=1S/C33H43FN4O3/c1-2-18-38(32(40)35-21-25-12-14-29(34)15-13-25)30-16-19-36(20-17-30)22-28-23-37(31(39)26-8-6-7-9-26)24-33(28,41)27-10-4-3-5-11-27/h2-5,10-15,26,28,30,41H,1,6-9,16-24H2,(H,35,40)/t28-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.70	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321700 (1-allyl-1-(1-(((3S,4R)-1-(cyclopentanecarbonyl)-4-...) Show SMILES O[C@@]1(CN(C[C@@H]1CN1CCC(CC1)N(CC=C)C(=O)NCc1ccc(F)c(F)c1)C(=O)C1CCCC1)c1ccccc1 |r| Show InChI InChI=1S/C33H42F2N4O3/c1-2-16-39(32(41)36-20-24-12-13-29(34)30(35)19-24)28-14-17-37(18-15-28)21-27-22-38(31(40)25-8-6-7-9-25)23-33(27,42)26-10-4-3-5-11-26/h2-5,10-13,19,25,27-28,42H,1,6-9,14-18,20-23H2,(H,36,41)/t27-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.70	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321711 (CHEMBL1172624 | N-allyl-N-(1-(((3S,4R)-1-(cyclopen...) Show SMILES NS(=O)(=O)c1ccc(CC(=O)N(CC=C)C2CCN(C[C@H]3CN(C[C@]3(O)c3ccccc3)C(=O)C3CCCC3)CC2)cc1 |r| Show InChI InChI=1S/C33H44N4O5S/c1-2-18-37(31(38)21-25-12-14-30(15-13-25)43(34,41)42)29-16-19-35(20-17-29)22-28-23-36(32(39)26-8-6-7-9-26)24-33(28,40)27-10-4-3-5-11-27/h2-5,10-15,26,28-29,40H,1,6-9,16-24H2,(H2,34,41,42)/t28-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.10	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321695 (1-allyl-3-(4-chlorobenzyl)-1-(1-(((3S,4R)-1-(cyclo...) Show SMILES O[C@@]1(CN(C[C@@H]1CN1CCC(CC1)N(CC=C)C(=O)NCc1ccc(Cl)cc1)C(=O)C1CCCC1)c1ccccc1 |r| Show InChI InChI=1S/C33H43ClN4O3/c1-2-18-38(32(40)35-21-25-12-14-29(34)15-13-25)30-16-19-36(20-17-30)22-28-23-37(31(39)26-8-6-7-9-26)24-33(28,41)27-10-4-3-5-11-27/h2-5,10-15,26,28,30,41H,1,6-9,16-24H2,(H,35,40)/t28-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.70	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321682 (CHEMBL1172035 | nifeviroc) Show SMILES O[C@@]1(CN(C[C@@H]1CN1CCC(CC1)N(CC=C)C(=O)OCc1ccc(cc1)[N+]([O-])=O)C(=O)C1CCCC1)c1ccccc1 |r| Show InChI InChI=1S/C33H42N4O6/c1-2-18-36(32(39)43-23-25-12-14-30(15-13-25)37(41)42)29-16-19-34(20-17-29)21-28-22-35(31(38)26-8-6-7-9-26)24-33(28,40)27-10-4-3-5-11-27/h2-5,10-15,26,28-29,40H,1,6-9,16-24H2/t28-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.90	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibition of human CCR5 expressed in CHO cells assessed as inhibition of RANTES-stimulated [35S]GTPgammaS binding				Bioorg Med Chem Lett 20: 5334-6 (2010) Article DOI: 10.1016/j.bmcl.2010.05.046 BindingDB Entry DOI: 10.7270/Q2J67H49
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321701 (4-((3-allyl-3-(1-(((3S,4R)-1-(cyclopentanecarbonyl...) Show SMILES CNS(=O)(=O)c1ccc(CNC(=O)N(CC=C)C2CCN(C[C@H]3CN(C[C@]3(O)c3ccccc3)C(=O)C3CCCC3)CC2)cc1 |r| Show InChI InChI=1S/C34H47N5O5S/c1-3-19-39(33(41)36-22-26-13-15-31(16-14-26)45(43,44)35-2)30-17-20-37(21-18-30)23-29-24-38(32(40)27-9-7-8-10-27)25-34(29,42)28-11-5-4-6-12-28/h3-6,11-16,27,29-30,35,42H,1,7-10,17-25H2,2H3,(H,36,41)/t29-,34-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.90	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321682 (CHEMBL1172035 | nifeviroc) Show SMILES O[C@@]1(CN(C[C@@H]1CN1CCC(CC1)N(CC=C)C(=O)OCc1ccc(cc1)[N+]([O-])=O)C(=O)C1CCCC1)c1ccccc1 |r| Show InChI InChI=1S/C33H42N4O6/c1-2-18-36(32(39)43-23-25-12-14-30(15-13-25)37(41)42)29-16-19-34(20-17-29)21-28-22-35(31(38)26-8-6-7-9-26)24-33(28,40)27-10-4-3-5-11-27/h2-5,10-15,26,28-29,40H,1,6-9,16-24H2/t28-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.90	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50325321 (CHEMBL1222771 | N-allyl-N-(1-(((3S,4R)-1-(cyclopen...) Show SMILES CNS(=O)(=O)c1ccc(CC(=O)N(CC=C)C2CCN(C[C@H]3CN(C[C@]3(O)c3cccc(F)c3)C(=O)C3CCCC3)CC2)cc1 |r| Show InChI InChI=1S/C34H45FN4O5S/c1-3-17-39(32(40)20-25-11-13-31(14-12-25)45(43,44)36-2)30-15-18-37(19-16-30)22-28-23-38(33(41)26-7-4-5-8-26)24-34(28,42)27-9-6-10-29(35)21-27/h3,6,9-14,21,26,28,30,36,42H,1,4-5,7-8,15-20,22-24H2,2H3/t28-,34-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.98	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibition of human CCR5 expressed in CHO cells assessed as inhibition of RANTES-stimulated [35S]GTPgammaS binding				Bioorg Med Chem Lett 20: 5334-6 (2010) Article DOI: 10.1016/j.bmcl.2010.05.046 BindingDB Entry DOI: 10.7270/Q2J67H49
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321696 (1-allyl-1-(1-(((3S,4R)-1-(cyclopentanecarbonyl)-4-...) Show SMILES O[C@@]1(CN(C[C@@H]1CN1CCC(CC1)N(CC=C)C(=O)NCc1ccc(cc1)[N+]([O-])=O)C(=O)C1CCCC1)c1ccccc1 |r| Show InChI InChI=1S/C33H43N5O5/c1-2-18-37(32(40)34-21-25-12-14-30(15-13-25)38(42)43)29-16-19-35(20-17-29)22-28-23-36(31(39)26-8-6-7-9-26)24-33(28,41)27-10-4-3-5-11-27/h2-5,10-15,26,28-29,41H,1,6-9,16-24H2,(H,34,40)/t28-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.20	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321713 (CHEMBL1172626 | N-allyl-N-(1-(((3S,4R)-1-(cyclopen...) Show SMILES CN(C)S(=O)(=O)c1ccc(CC(=O)N(CC=C)C2CCN(C[C@H]3CN(C[C@]3(O)c3ccccc3)C(=O)C3CCCC3)CC2)cc1 |r| Show InChI InChI=1S/C35H48N4O5S/c1-4-20-39(33(40)23-27-14-16-32(17-15-27)45(43,44)36(2)3)31-18-21-37(22-19-31)24-30-25-38(34(41)28-10-8-9-11-28)26-35(30,42)29-12-6-5-7-13-29/h4-7,12-17,28,30-31,42H,1,8-11,18-26H2,2-3H3/t30-,35-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.30	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321703 (CHEMBL1172157 | N-allyl-N-(1-(((3S,4R)-1-(cyclopen...) Show SMILES O[C@@]1(CN(C[C@@H]1CN1CCC(CC1)N(CC=C)C(=O)Cc1ccccc1)C(=O)C1CCCC1)c1ccccc1 |r| Show InChI InChI=1S/C33H43N3O3/c1-2-19-36(31(37)22-26-11-5-3-6-12-26)30-17-20-34(21-18-30)23-29-24-35(32(38)27-13-9-10-14-27)25-33(29,39)28-15-7-4-8-16-28/h2-8,11-12,15-16,27,29-30,39H,1,9-10,13-14,17-25H2/t29-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.5	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321682 (CHEMBL1172035 | nifeviroc) Show SMILES O[C@@]1(CN(C[C@@H]1CN1CCC(CC1)N(CC=C)C(=O)OCc1ccc(cc1)[N+]([O-])=O)C(=O)C1CCCC1)c1ccccc1 |r| Show InChI InChI=1S/C33H42N4O6/c1-2-18-36(32(39)43-23-25-12-14-30(15-13-25)37(41)42)29-16-19-34(20-17-29)21-28-22-35(31(38)26-8-6-7-9-26)24-33(28,40)27-10-4-3-5-11-27/h2-5,10-15,26,28-29,40H,1,6-9,16-24H2/t28-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.5	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced calcium elevation				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321707 (CHEMBL1171030 | N-allyl-2-(4-chlorophenyl)-N-(1-((...) Show SMILES O[C@@]1(CN(C[C@@H]1CN1CCC(CC1)N(CC=C)C(=O)Cc1ccc(Cl)cc1)C(=O)C1CCCC1)c1ccccc1 |r| Show InChI InChI=1S/C33H42ClN3O3/c1-2-18-37(31(38)21-25-12-14-29(34)15-13-25)30-16-19-35(20-17-30)22-28-23-36(32(39)26-8-6-7-9-26)24-33(28,40)27-10-4-3-5-11-27/h2-5,10-15,26,28,30,40H,1,6-9,16-24H2/t28-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.60	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50325325 (4-((3-allyl-3-((1R,3S,5S)-8-(((3S,4R)-1-(cyclopent...) Show SMILES CNS(=O)(=O)c1ccc(CNC(=O)N(CC=C)[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@H]2CN(C[C@]2(O)c2cccc(F)c2)C(=O)C2CCCC2)cc1 |r,THB:25:24:17.23.18:21.20| Show InChI InChI=1S/C36H48FN5O5S/c1-3-17-41(35(44)39-21-25-11-15-33(16-12-25)48(46,47)38-2)32-19-30-13-14-31(20-32)42(30)23-28-22-40(34(43)26-7-4-5-8-26)24-36(28,45)27-9-6-10-29(37)18-27/h3,6,9-12,15-16,18,26,28,30-32,38,45H,1,4-5,7-8,13-14,17,19-24H2,2H3,(H,39,44)/t28-,30-,31+,32+,36+/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.98	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibition of human CCR5 expressed in CHO cells assessed as inhibition of RANTES-stimulated [35S]GTPgammaS binding				Bioorg Med Chem Lett 20: 5334-6 (2010) Article DOI: 10.1016/j.bmcl.2010.05.046 BindingDB Entry DOI: 10.7270/Q2J67H49
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321710 (CHEMBL1172623 | N-allyl-N-(1-(((3S,4R)-1-(cyclopen...) Show SMILES CS(=O)(=O)c1ccc(CC(=O)N(CC=C)C2CCN(C[C@H]3CN(C[C@]3(O)c3ccccc3)C(=O)C3CCCC3)CC2)cc1 |r| Show InChI InChI=1S/C34H45N3O5S/c1-3-19-37(32(38)22-26-13-15-31(16-14-26)43(2,41)42)30-17-20-35(21-18-30)23-29-24-36(33(39)27-9-7-8-10-27)25-34(29,40)28-11-5-4-6-12-28/h3-6,11-16,27,29-30,40H,1,7-10,17-25H2,2H3/t29-,34-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321702 (4-((3-allyl-3-(1-(((3S,4R)-1-(cyclopentanecarbonyl...) Show SMILES CN(C)S(=O)(=O)c1ccc(CNC(=O)N(CC=C)C2CCN(C[C@H]3CN(C[C@]3(O)c3ccccc3)C(=O)C3CCCC3)CC2)cc1 |r| Show InChI InChI=1S/C35H49N5O5S/c1-4-20-40(34(42)36-23-27-14-16-32(17-15-27)46(44,45)37(2)3)31-18-21-38(22-19-31)24-30-25-39(33(41)28-10-8-9-11-28)26-35(30,43)29-12-6-5-7-13-29/h4-7,12-17,28,30-31,43H,1,8-11,18-26H2,2-3H3,(H,36,42)/t30-,35-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321705 (CHEMBL1172439 | N-allyl-N-(1-(((3S,4R)-1-(cyclopen...) Show SMILES O[C@@]1(CN(C[C@@H]1CN1CCC(CC1)N(CC=C)C(=O)Cc1ccc(cc1)[N+]([O-])=O)C(=O)C1CCCC1)c1ccccc1 |r| Show InChI InChI=1S/C33H42N4O5/c1-2-18-36(31(38)21-25-12-14-30(15-13-25)37(41)42)29-16-19-34(20-17-29)22-28-23-35(32(39)26-8-6-7-9-26)24-33(28,40)27-10-4-3-5-11-27/h2-5,10-15,26,28-29,40H,1,6-9,16-24H2/t28-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.30	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321691 (4-methoxybenzyl allyl(1-(((3S,4R)-1-(cyclopentanec...) Show SMILES COc1ccc(COC(=O)N(CC=C)C2CCN(C[C@H]3CN(C[C@]3(O)c3ccccc3)C(=O)C3CCCC3)CC2)cc1 |r| Show InChI InChI=1S/C34H45N3O5/c1-3-19-37(33(39)42-24-26-13-15-31(41-2)16-14-26)30-17-20-35(21-18-30)22-29-23-36(32(38)27-9-7-8-10-27)25-34(29,40)28-11-5-4-6-12-28/h3-6,11-16,27,29-30,40H,1,7-10,17-25H2,2H3/t29-,34-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.20	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321685 (4-(trifluoromethoxy)benzyl allyl(1-(((3S,4R)-1-(cy...) Show SMILES O[C@@]1(CN(C[C@@H]1CN1CCC(CC1)N(CC=C)C(=O)OCc1ccc(OC(F)(F)F)cc1)C(=O)C1CCCC1)c1ccccc1 |r| Show InChI InChI=1S/C34H42F3N3O5/c1-2-18-40(32(42)44-23-25-12-14-30(15-13-25)45-34(35,36)37)29-16-19-38(20-17-29)21-28-22-39(31(41)26-8-6-7-9-26)24-33(28,43)27-10-4-3-5-11-27/h2-5,10-15,26,28-29,43H,1,6-9,16-24H2/t28-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.20	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321698 (1-allyl-1-(1-(((3S,4R)-1-(cyclopentanecarbonyl)-4-...) Show SMILES O[C@@]1(CN(C[C@@H]1CN1CCC(CC1)N(CC=C)C(=O)NCc1ccc(OC(F)(F)F)cc1)C(=O)C1CCCC1)c1ccccc1 |r| Show InChI InChI=1S/C34H43F3N4O4/c1-2-18-41(32(43)38-21-25-12-14-30(15-13-25)45-34(35,36)37)29-16-19-39(20-17-29)22-28-23-40(31(42)26-8-6-7-9-26)24-33(28,44)27-10-4-3-5-11-27/h2-5,10-15,26,28-29,44H,1,6-9,16-24H2,(H,38,43)/t28-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.20	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50325322 (1-allyl-1-((1R,3S,5S)-8-(((3S,4R)-1-(cyclopentanec...) Show SMILES O[C@@]1(CN(C[C@@H]1CN1[C@H]2CC[C@@H]1C[C@@H](C2)N(CC=C)C(=O)NCc1ccc(cc1)C(F)(F)F)C(=O)C1CCCC1)c1cccc(F)c1 |r,THB:6:7:13.12.14:10.9| Show InChI InChI=1S/C36H44F4N4O3/c1-2-16-43(34(46)41-20-24-10-12-26(13-11-24)36(38,39)40)32-18-30-14-15-31(19-32)44(30)22-28-21-42(33(45)25-6-3-4-7-25)23-35(28,47)27-8-5-9-29(37)17-27/h2,5,8-13,17,25,28,30-32,47H,1,3-4,6-7,14-16,18-23H2,(H,41,46)/t28-,30-,31+,32+,35+/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.77	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibition of human CCR5 expressed in CHO cells assessed as inhibition of RANTES-stimulated [35S]GTPgammaS binding				Bioorg Med Chem Lett 20: 5334-6 (2010) Article DOI: 10.1016/j.bmcl.2010.05.046 BindingDB Entry DOI: 10.7270/Q2J67H49
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321692 (CHEMBL1171965 | benzyl allyl(1-(((3S,4R)-1-(cyclop...) Show SMILES O[C@@]1(CN(C[C@@H]1CN1CCC(CC1)N(CC=C)C(=O)OCc1ccccc1)C(=O)C1CCCC1)c1ccccc1 |r| Show InChI InChI=1S/C33H43N3O4/c1-2-19-36(32(38)40-24-26-11-5-3-6-12-26)30-17-20-34(21-18-30)22-29-23-35(31(37)27-13-9-10-14-27)25-33(29,39)28-15-7-4-8-16-28/h2-8,11-12,15-16,27,29-30,39H,1,9-10,13-14,17-25H2/t29-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.80	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50325317 (4-nitrobenzyl allyl(1-(((3S,4R)-1-(cyclopentanecar...) Show SMILES O[C@@]1(CN(C[C@@H]1CN1CCC(CC1)N(CC=C)C(=O)OCc1ccc(cc1)[N+]([O-])=O)C(=O)C1CCCC1)c1cccc(F)c1 |r| Show InChI InChI=1S/C33H41FN4O6/c1-2-16-37(32(40)44-22-24-10-12-30(13-11-24)38(42)43)29-14-17-35(18-15-29)20-27-21-36(31(39)25-6-3-4-7-25)23-33(27,41)26-8-5-9-28(34)19-26/h2,5,8-13,19,25,27,29,41H,1,3-4,6-7,14-18,20-23H2/t27-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.85	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibition of human CCR5 expressed in CHO cells assessed as inhibition of RANTES-stimulated [35S]GTPgammaS binding				Bioorg Med Chem Lett 20: 5334-6 (2010) Article DOI: 10.1016/j.bmcl.2010.05.046 BindingDB Entry DOI: 10.7270/Q2J67H49
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321706 (CHEMBL1171029 | N-allyl-N-(1-(((3S,4R)-1-(cyclopen...) Show SMILES O[C@@]1(CN(C[C@@H]1CN1CCC(CC1)N(CC=C)C(=O)Cc1ccc(F)cc1)C(=O)C1CCCC1)c1ccccc1 |r| Show InChI InChI=1S/C33H42FN3O3/c1-2-18-37(31(38)21-25-12-14-29(34)15-13-25)30-16-19-35(20-17-30)22-28-23-36(32(39)26-8-6-7-9-26)24-33(28,40)27-10-4-3-5-11-27/h2-5,10-15,26,28,30,40H,1,6-9,16-24H2/t28-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	11	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50325320 (CHEMBL1222770 | N-allyl-N-(1-(((3S,4R)-1-(cyclopen...) Show SMILES CNS(=O)(=O)c1ccc(CC(=O)N(CC=C)C2CCN(C[C@H]3CN(C[C@]3(O)c3ccc(F)cc3)C(=O)C3CCCC3)CC2)cc1 |r| Show InChI InChI=1S/C34H45FN4O5S/c1-3-18-39(32(40)21-25-8-14-31(15-9-25)45(43,44)36-2)30-16-19-37(20-17-30)22-28-23-38(33(41)26-6-4-5-7-26)24-34(28,42)27-10-12-29(35)13-11-27/h3,8-15,26,28,30,36,42H,1,4-7,16-24H2,2H3/t28-,34-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	11.2	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibition of human CCR5 expressed in CHO cells assessed as inhibition of RANTES-stimulated [35S]GTPgammaS binding				Bioorg Med Chem Lett 20: 5334-6 (2010) Article DOI: 10.1016/j.bmcl.2010.05.046 BindingDB Entry DOI: 10.7270/Q2J67H49
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50325323 (4-((3-allyl-3-((1R,3S,5S)-8-(((3S,4R)-1-(cyclopent...) Show SMILES CN(C)S(=O)(=O)c1ccc(CNC(=O)N(CC=C)[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@H]2CN(C[C@]2(O)c2cccc(F)c2)C(=O)C2CCCC2)cc1 |r,THB:26:25:18.24.19:22.21| Show InChI InChI=1S/C37H50FN5O5S/c1-4-18-42(36(45)39-22-26-12-16-34(17-13-26)49(47,48)40(2)3)33-20-31-14-15-32(21-33)43(31)24-29-23-41(35(44)27-8-5-6-9-27)25-37(29,46)28-10-7-11-30(38)19-28/h4,7,10-13,16-17,19,27,29,31-33,46H,1,5-6,8-9,14-15,18,20-25H2,2-3H3,(H,39,45)/t29-,31-,32+,33+,37+/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	11.4	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibition of human CCR5 expressed in CHO cells assessed as inhibition of RANTES-stimulated [35S]GTPgammaS binding				Bioorg Med Chem Lett 20: 5334-6 (2010) Article DOI: 10.1016/j.bmcl.2010.05.046 BindingDB Entry DOI: 10.7270/Q2J67H49
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50325326 (1-allyl-1-((1R,3R,5S)-8-(((3S,4R)-1-(cyclopentanec...) Show SMILES O[C@@]1(CN(C[C@@H]1CN1[C@H]2CC[C@@H]1C[C@H](C2)N(CC=C)C(=O)NCc1ccc(cc1)C(F)(F)F)C(=O)C1CCCC1)c1cccc(F)c1 |r,THB:6:7:13.12.14:10.9| Show InChI InChI=1S/C36H44F4N4O3/c1-2-16-43(34(46)41-20-24-10-12-26(13-11-24)36(38,39)40)32-18-30-14-15-31(19-32)44(30)22-28-21-42(33(45)25-6-3-4-7-25)23-35(28,47)27-8-5-9-29(37)17-27/h2,5,8-13,17,25,28,30-32,47H,1,3-4,6-7,14-16,18-23H2,(H,41,46)/t28-,30-,31+,32-,35+/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	14.3	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibition of human CCR5 expressed in CHO cells assessed as inhibition of RANTES-stimulated [35S]GTPgammaS binding				Bioorg Med Chem Lett 20: 5334-6 (2010) Article DOI: 10.1016/j.bmcl.2010.05.046 BindingDB Entry DOI: 10.7270/Q2J67H49
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321704 (CHEMBL1172438 | N-allyl-N-(1-(((3S,4R)-1-(cyclopen...) Show SMILES COc1ccc(CC(=O)N(CC=C)C2CCN(C[C@H]3CN(C[C@]3(O)c3ccccc3)C(=O)C3CCCC3)CC2)cc1 |r| Show InChI InChI=1S/C34H45N3O4/c1-3-19-37(32(38)22-26-13-15-31(41-2)16-14-26)30-17-20-35(21-18-30)23-29-24-36(33(39)27-9-7-8-10-27)25-34(29,40)28-11-5-4-6-12-28/h3-6,11-16,27,29-30,40H,1,7-10,17-25H2,2H3/t29-,34-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	15	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321708 (CHEMBL1169819 | N-allyl-2-(4-bromophenyl)-N-(1-(((...) Show SMILES O[C@@]1(CN(C[C@@H]1CN1CCC(CC1)N(CC=C)C(=O)Cc1ccc(Br)cc1)C(=O)C1CCCC1)c1ccccc1 |r| Show InChI InChI=1S/C33H42BrN3O3/c1-2-18-37(31(38)21-25-12-14-29(34)15-13-25)30-16-19-35(20-17-30)22-28-23-36(32(39)26-8-6-7-9-26)24-33(28,40)27-10-4-3-5-11-27/h2-5,10-15,26,28,30,40H,1,6-9,16-24H2/t28-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	18	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
Integrase (Human immunodeficiency virus 1)	BDBM50482807 (CHEMBL1222998) Show SMILES Oc1c(nc2ccc(cn2c1=O)N1CCOCC1)-c1ncc(Cc2ccc(F)cc2)s1 Show InChI InChI=1S/C22H19FN4O3S/c23-15-3-1-14(2-4-15)11-17-12-24-21(31-17)19-20(28)22(29)27-13-16(5-6-18(27)25-19)26-7-9-30-10-8-26/h1-6,12-13,28H,7-11H2	PDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	20	n/a	n/a	n/a	n/a	n/a	n/a
Avexa Ltd Curated by ChEMBL					Assay Description Inhibition of HIV-1 integrase-mediated 3'-processing and strand transfer activity				Bioorg Med Chem Lett 20: 5909-12 (2010) Article DOI: 10.1016/j.bmcl.2010.07.081 BindingDB Entry DOI: 10.7270/Q2XW4NNV
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321688 (4-bromobenzyl allyl(1-(((3S,4R)-1-(cyclopentanecar...) Show SMILES O[C@@]1(CN(C[C@@H]1CN1CCC(CC1)N(CC=C)C(=O)OCc1ccc(Br)cc1)C(=O)C1CCCC1)c1ccccc1 |r| Show InChI InChI=1S/C33H42BrN3O4/c1-2-18-37(32(39)41-23-25-12-14-29(34)15-13-25)30-16-19-35(20-17-30)21-28-22-36(31(38)26-8-6-7-9-26)24-33(28,40)27-10-4-3-5-11-27/h2-5,10-15,26,28,30,40H,1,6-9,16-24H2/t28-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	20	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
Integrase (Human immunodeficiency virus 1)	BDBM50479890 (CHEMBL522653) Show SMILES CCN(C(=O)C(=O)N1CCOCC1)c1cccn2c1nc(C(=O)NCc1ccc(F)cc1)c(O)c2=O Show InChI InChI=1S/C24H24FN5O6/c1-2-29(24(35)23(34)28-10-12-36-13-11-28)17-4-3-9-30-20(17)27-18(19(31)22(30)33)21(32)26-14-15-5-7-16(25)8-6-15/h3-9,31H,2,10-14H2,1H3,(H,26,32)	PDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	25	n/a	n/a	n/a	n/a	n/a	n/a
Avexa Ltd Curated by ChEMBL					Assay Description Inhibition of HIV1 integrase 3'-strand transfer				Bioorg Med Chem Lett 20: 5913-7 (2010) Article DOI: 10.1016/j.bmcl.2010.07.079 BindingDB Entry DOI: 10.7270/Q22N5533
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50325327 (4-((3-allyl-3-((1R,3R,5S)-8-(((3S,4R)-1-(cyclopent...) Show SMILES CNS(=O)(=O)c1ccc(CNC(=O)N(CC=C)[C@H]2C[C@@H]3CC[C@H](C2)N3C[C@H]2CN(C[C@]2(O)c2cccc(F)c2)C(=O)C2CCCC2)cc1 |r,THB:25:24:17.23.18:21.20| Show InChI InChI=1S/C36H48FN5O5S/c1-3-17-41(35(44)39-21-25-11-15-33(16-12-25)48(46,47)38-2)32-19-30-13-14-31(20-32)42(30)23-28-22-40(34(43)26-7-4-5-8-26)24-36(28,45)27-9-6-10-29(37)18-27/h3,6,9-12,15-16,18,26,28,30-32,38,45H,1,4-5,7-8,13-14,17,19-24H2,2H3,(H,39,44)/t28-,30-,31+,32-,36+/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	27.1	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibition of human CCR5 expressed in CHO cells assessed as inhibition of RANTES-stimulated [35S]GTPgammaS binding				Bioorg Med Chem Lett 20: 5334-6 (2010) Article DOI: 10.1016/j.bmcl.2010.05.046 BindingDB Entry DOI: 10.7270/Q2J67H49
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50325324 (1-allyl-1-((1R,3S,5S)-8-(((3S,4R)-1-(cyclopentanec...) Show SMILES O[C@@]1(CN(C[C@@H]1CN1[C@H]2CC[C@@H]1C[C@@H](C2)N(CC=C)C(=O)NCc1ccc(F)cc1)C(=O)C1CCCC1)c1cccc(F)c1 |r,THB:6:7:13.12.14:10.9| Show InChI InChI=1S/C35H44F2N4O3/c1-2-16-40(34(43)38-20-24-10-12-28(36)13-11-24)32-18-30-14-15-31(19-32)41(30)22-27-21-39(33(42)25-6-3-4-7-25)23-35(27,44)26-8-5-9-29(37)17-26/h2,5,8-13,17,25,27,30-32,44H,1,3-4,6-7,14-16,18-23H2,(H,38,43)/t27-,30-,31+,32+,35+/m1/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	30	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibition of human CCR5 expressed in CHO cells assessed as inhibition of RANTES-stimulated [35S]GTPgammaS binding				Bioorg Med Chem Lett 20: 5334-6 (2010) Article DOI: 10.1016/j.bmcl.2010.05.046 BindingDB Entry DOI: 10.7270/Q2J67H49
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321689 (4-(trifluoromethyl)benzyl allyl(1-(((3S,4R)-1-(cyc...) Show SMILES O[C@@]1(CN(C[C@@H]1CN1CCC(CC1)N(CC=C)C(=O)OCc1ccc(cc1)C(F)(F)F)C(=O)C1CCCC1)c1ccccc1 |r| Show InChI InChI=1S/C34H42F3N3O4/c1-2-18-40(32(42)44-23-25-12-14-28(15-13-25)34(35,36)37)30-16-19-38(20-17-30)21-29-22-39(31(41)26-8-6-7-9-26)24-33(29,43)27-10-4-3-5-11-27/h2-5,10-15,26,29-30,43H,1,6-9,16-24H2/t29-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>30	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50325316 (4-nitrobenzyl allyl(1-(((3S,4R)-1-(cyclopentanecar...) Show SMILES O[C@@]1(CN(C[C@@H]1CN1CCC(CC1)N(CC=C)C(=O)OCc1ccc(cc1)[N+]([O-])=O)C(=O)C1CCCC1)c1ccc(F)cc1 |r| Show InChI InChI=1S/C33H41FN4O6/c1-2-17-37(32(40)44-22-24-7-13-30(14-8-24)38(42)43)29-15-18-35(19-16-29)20-27-21-36(31(39)25-5-3-4-6-25)23-33(27,41)26-9-11-28(34)12-10-26/h2,7-14,25,27,29,41H,1,3-6,15-23H2/t27-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	30	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibition of human CCR5 expressed in CHO cells assessed as inhibition of RANTES-stimulated [35S]GTPgammaS binding				Bioorg Med Chem Lett 20: 5334-6 (2010) Article DOI: 10.1016/j.bmcl.2010.05.046 BindingDB Entry DOI: 10.7270/Q2J67H49
					More data for this Ligand-Target Pair
Integrase (Human immunodeficiency virus 1)	BDBM50482815 (CHEMBL1258726) Show SMILES Oc1c(nc2c(cc(cn2c1=O)N1CCOCC1)N1CCOC1=O)-c1ncc(Cc2ccc(F)cc2)[nH]1 Show InChI InChI=1S/C25H23FN6O5/c26-16-3-1-15(2-4-16)11-17-13-27-22(28-17)20-21(33)24(34)32-14-18(30-5-8-36-9-6-30)12-19(23(32)29-20)31-7-10-37-25(31)35/h1-4,12-14,33H,5-11H2,(H,27,28)	PDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	35	n/a	n/a	n/a	n/a	n/a	n/a
Avexa Ltd Curated by ChEMBL					Assay Description Inhibition of HIV-1 integrase-mediated 3'-processing and strand transfer activity				Bioorg Med Chem Lett 20: 5909-12 (2010) Article DOI: 10.1016/j.bmcl.2010.07.081 BindingDB Entry DOI: 10.7270/Q2XW4NNV
					More data for this Ligand-Target Pair
Integrase (Human immunodeficiency virus 1)	BDBM50482808 (CHEMBL1222997) Show SMILES Oc1c(nc2c(cc(cn2c1=O)N1CCOCC1)N1CCCS1(=O)=O)-c1ncc(Cc2ccc(F)cc2)s1 Show InChI InChI=1S/C25H24FN5O5S2/c26-17-4-2-16(3-5-17)12-19-14-27-24(37-19)21-22(32)25(33)30-15-18(29-7-9-36-10-8-29)13-20(23(30)28-21)31-6-1-11-38(31,34)35/h2-5,13-15,32H,1,6-12H2	PDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	36	n/a	n/a	n/a	n/a	n/a	n/a
Avexa Ltd Curated by ChEMBL					Assay Description Inhibition of HIV-1 integrase-mediated 3'-processing and strand transfer activity				Bioorg Med Chem Lett 20: 5909-12 (2010) Article DOI: 10.1016/j.bmcl.2010.07.081 BindingDB Entry DOI: 10.7270/Q2XW4NNV
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321686 (4-(methylsulfonyl)benzyl allyl(1-(((3S,4R)-1-(cycl...) Show SMILES CS(=O)(=O)c1ccc(COC(=O)N(CC=C)C2CCN(C[C@H]3CN(C[C@]3(O)c3ccccc3)C(=O)C3CCCC3)CC2)cc1 |r| Show InChI InChI=1S/C34H45N3O6S/c1-3-19-37(33(39)43-24-26-13-15-31(16-14-26)44(2,41)42)30-17-20-35(21-18-30)22-29-23-36(32(38)27-9-7-8-10-27)25-34(29,40)28-11-5-4-6-12-28/h3-6,11-16,27,29-30,40H,1,7-10,17-25H2,2H3/t29-,34-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	37	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50321693 (1-allyl-3-benzyl-1-(1-(((3S,4R)-1-(cyclopentanecar...) Show SMILES O[C@@]1(CN(C[C@@H]1CN1CCC(CC1)N(CC=C)C(=O)NCc1ccccc1)C(=O)C1CCCC1)c1ccccc1 |r| Show InChI InChI=1S/C33H44N4O3/c1-2-19-37(32(39)34-22-26-11-5-3-6-12-26)30-17-20-35(21-18-30)23-29-24-36(31(38)27-13-9-10-14-27)25-33(29,40)28-15-7-4-8-16-28/h2-8,11-12,15-16,27,29-30,40H,1,9-10,13-14,17-25H2,(H,34,39)/t29-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	38	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Antagonist activity at CCR5 expressed in CHO cells assessed as inhibition of RANTES-induced [35S]GTPgamma binding by scintillation proximity assay				Bioorg Med Chem Lett 20: 4012-4 (2010) Article DOI: 10.1016/j.bmcl.2010.05.102 BindingDB Entry DOI: 10.7270/Q2H132Z4
					More data for this Ligand-Target Pair
C-C chemokine receptor type 5 (Homo sapiens (Human))	BDBM50325318 (1-allyl-1-(1-(((3S,4R)-1-(cyclopentanecarbonyl)-4-...) Show SMILES O[C@@]1(CN(C[C@@H]1CN1CCC(CC1)N(CC=C)C(=O)NCc1ccc(cc1)C(F)(F)F)C(=O)C1CCCC1)c1ccc(F)cc1 |r| Show InChI InChI=1S/C34H42F4N4O3/c1-2-17-42(32(44)39-20-24-7-9-27(10-8-24)34(36,37)38)30-15-18-40(19-16-30)21-28-22-41(31(43)25-5-3-4-6-25)23-33(28,45)26-11-13-29(35)14-12-26/h2,7-14,25,28,30,45H,1,3-6,15-23H2,(H,39,44)/t28-,33-/m0/s1	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	38.3	n/a	n/a	n/a	n/a	n/a	n/a
Chinese Academy of Sciences Curated by ChEMBL					Assay Description Inhibition of human CCR5 expressed in CHO cells assessed as inhibition of RANTES-stimulated [35S]GTPgammaS binding				Bioorg Med Chem Lett 20: 5334-6 (2010) Article DOI: 10.1016/j.bmcl.2010.05.046 BindingDB Entry DOI: 10.7270/Q2J67H49
					More data for this Ligand-Target Pair
Integrase (Human immunodeficiency virus 1)	BDBM50482809 (CHEMBL1222999) Show SMILES Oc1c(nc2c(Br)cc(cn2c1=O)N1CCOCC1)-c1ncc(Cc2ccc(F)cc2)s1 Show InChI InChI=1S/C22H18BrFN4O3S/c23-17-10-15(27-5-7-31-8-6-27)12-28-20(17)26-18(19(29)22(28)30)21-25-11-16(32-21)9-13-1-3-14(24)4-2-13/h1-4,10-12,29H,5-9H2	PDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	42	n/a	n/a	n/a	n/a	n/a	n/a
Avexa Ltd Curated by ChEMBL					Assay Description Inhibition of HIV-1 integrase-mediated 3'-processing and strand transfer activity				Bioorg Med Chem Lett 20: 5909-12 (2010) Article DOI: 10.1016/j.bmcl.2010.07.081 BindingDB Entry DOI: 10.7270/Q2XW4NNV
					More data for this Ligand-Target Pair
Integrase (Human immunodeficiency virus 1)	BDBM50482814 (CHEMBL1258050) Show SMILES Oc1c(nc2ccc(cn2c1=O)N1CCOCC1)-c1ncc(Cc2ccc(F)cc2)[nH]1 Show InChI InChI=1S/C22H20FN5O3/c23-15-3-1-14(2-4-15)11-16-12-24-21(25-16)19-20(29)22(30)28-13-17(5-6-18(28)26-19)27-7-9-31-10-8-27/h1-6,12-13,29H,7-11H2,(H,24,25)	PDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	45	n/a	n/a	n/a	n/a	n/a	n/a
Avexa Ltd Curated by ChEMBL					Assay Description Inhibition of HIV-1 integrase-mediated 3'-processing and strand transfer activity				Bioorg Med Chem Lett 20: 5909-12 (2010) Article DOI: 10.1016/j.bmcl.2010.07.081 BindingDB Entry DOI: 10.7270/Q2XW4NNV
					More data for this Ligand-Target Pair
Integrase (Human immunodeficiency virus 1)	BDBM50482816 (CHEMBL1258727) Show SMILES Oc1c(nc2c(cc(cn2c1=O)N1CCOCC1)N1CCCC1=O)-c1ncc(Cc2ccc(F)cc2)[nH]1 Show InChI InChI=1S/C26H25FN6O4/c27-17-5-3-16(4-6-17)12-18-14-28-24(29-18)22-23(35)26(36)33-15-19(31-8-10-37-11-9-31)13-20(25(33)30-22)32-7-1-2-21(32)34/h3-6,13-15,35H,1-2,7-12H2,(H,28,29)	PDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	47	n/a	n/a	n/a	n/a	n/a	n/a
Avexa Ltd Curated by ChEMBL					Assay Description Inhibition of HIV-1 integrase-mediated 3'-processing and strand transfer activity				Bioorg Med Chem Lett 20: 5909-12 (2010) Article DOI: 10.1016/j.bmcl.2010.07.081 BindingDB Entry DOI: 10.7270/Q2XW4NNV
					More data for this Ligand-Target Pair
Integrase (Human immunodeficiency virus 1)	BDBM50482810 (CHEMBL1258049) Show SMILES Oc1c(nc2ccc(cn2c1=O)N1CCOCC1)-c1ncc(Cc2ccc(F)cc2)o1 Show InChI InChI=1S/C22H19FN4O4/c23-15-3-1-14(2-4-15)11-17-12-24-21(31-17)19-20(28)22(29)27-13-16(5-6-18(27)25-19)26-7-9-30-10-8-26/h1-6,12-13,28H,7-11H2	PDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	59	n/a	n/a	n/a	n/a	n/a	n/a
Avexa Ltd Curated by ChEMBL					Assay Description Inhibition of HIV-1 integrase-mediated 3'-processing and strand transfer activity				Bioorg Med Chem Lett 20: 5909-12 (2010) Article DOI: 10.1016/j.bmcl.2010.07.081 BindingDB Entry DOI: 10.7270/Q2XW4NNV
					More data for this Ligand-Target Pair

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