Compile Data Set for Download or QSAR

Found 108 hits with Last Name = 'kakefuda' and Initial = 'a'   

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
Vasopressin V1a receptor (RAT)	BDBM50108501 (2-Methyl-furan-3-carboxylic acid (4-{5-[2-(4-dimet...) Show SMILES CN(C)C1CCN(CC1)C(=O)\C=C1/c2ccccc2N(CCC1(F)F)C(=O)c1ccc(NC(=O)c2ccoc2C)cc1 Show InChI InChI=1S/C32H34F2N4O4/c1-21-25(14-19-42-21)30(40)35-23-10-8-22(9-11-23)31(41)38-18-15-32(33,34)27(26-6-4-5-7-28(26)38)20-29(39)37-16-12-24(13-17-37)36(2)3/h4-11,14,19-20,24H,12-13,15-18H2,1-3H3,(H,35,40)/b27-20+	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.102	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Evaluated for the binding affinity towards vasopressin (V1A) receptor in rat liver membrane using [3H]AVP as radioligand				Bioorg Med Chem Lett 12: 229-32 (2001) BindingDB Entry DOI: 10.7270/Q2R78FQP
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (RAT)	BDBM50108498 (Biphenyl-2-carboxylic acid (4-{5-[2-(4-dimethylami...) Show SMILES CN(C)C1CCN(CC1)C(=O)\C=C1\c2ccccc2N(CCC1(F)F)C(=O)c1ccc(NC(=O)c2ccccc2-c2ccccc2)cc1 Show InChI InChI=1S/C39H38F2N4O3/c1-43(2)30-20-23-44(24-21-30)36(46)26-34-33-14-8-9-15-35(33)45(25-22-39(34,40)41)38(48)28-16-18-29(19-17-28)42-37(47)32-13-7-6-12-31(32)27-10-4-3-5-11-27/h3-19,26,30H,20-25H2,1-2H3,(H,42,47)/b34-26-	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.160	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at Vasopressin V1a receptor, performed using [3H]-AVP on rat liver				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (Homo sapiens (Human))	BDBM50114031 ((2S)-1-[(2R,3S)-5-chloro-3-(2-chlorophenyl)-1-(3,4...) Show SMILES COc1ccc(cc1OC)S(=O)(=O)N1[C@@H](C(=O)N2CCC[C@H]2C(N)=O)[C@](O)(c2cc(Cl)ccc12)c1ccccc1Cl |r| Show InChI InChI=1S/C28H27Cl2N3O7S/c1-39-23-12-10-17(15-24(23)40-2)41(37,38)33-21-11-9-16(29)14-19(21)28(36,18-6-3-4-7-20(18)30)25(33)27(35)32-13-5-8-22(32)26(31)34/h3-4,6-7,9-12,14-15,22,25,36H,5,8,13H2,1-2H3,(H2,31,34)/t22-,25-,28+/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents	PubMed	0.530	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at cloned human Vasopressin V1a receptor stably expressed in CHO cells, using [3H]-AVP as radioligand				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (Homo sapiens (Human))	BDBM50108498 (Biphenyl-2-carboxylic acid (4-{5-[2-(4-dimethylami...) Show SMILES CN(C)C1CCN(CC1)C(=O)\C=C1\c2ccccc2N(CCC1(F)F)C(=O)c1ccc(NC(=O)c2ccccc2-c2ccccc2)cc1 Show InChI InChI=1S/C39H38F2N4O3/c1-43(2)30-20-23-44(24-21-30)36(46)26-34-33-14-8-9-15-35(33)45(25-22-39(34,40)41)38(48)28-16-18-29(19-17-28)42-37(47)32-13-7-6-12-31(32)27-10-4-3-5-11-27/h3-19,26,30H,20-25H2,1-2H3,(H,42,47)/b34-26-	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.620	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at cloned human Vasopressin V1a receptor stably expressed in CHO cells, using [3H]-AVP as radioligand				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (RAT)	BDBM50108498 (Biphenyl-2-carboxylic acid (4-{5-[2-(4-dimethylami...) Show SMILES CN(C)C1CCN(CC1)C(=O)\C=C1\c2ccccc2N(CCC1(F)F)C(=O)c1ccc(NC(=O)c2ccccc2-c2ccccc2)cc1 Show InChI InChI=1S/C39H38F2N4O3/c1-43(2)30-20-23-44(24-21-30)36(46)26-34-33-14-8-9-15-35(33)45(25-22-39(34,40)41)38(48)28-16-18-29(19-17-28)42-37(47)32-13-7-6-12-31(32)27-10-4-3-5-11-27/h3-19,26,30H,20-25H2,1-2H3,(H,42,47)/b34-26-	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.620	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Evaluated for the binding affinity towards vasopressin (V1A) receptor in rat liver membrane using [3H]AVP as radioligand				Bioorg Med Chem Lett 12: 229-32 (2001) BindingDB Entry DOI: 10.7270/Q2R78FQP
					More data for this Ligand-Target Pair
Vasopressin V2 receptor (Rattus norvegicus (Rat))	BDBM50108498 (Biphenyl-2-carboxylic acid (4-{5-[2-(4-dimethylami...) Show SMILES CN(C)C1CCN(CC1)C(=O)\C=C1\c2ccccc2N(CCC1(F)F)C(=O)c1ccc(NC(=O)c2ccccc2-c2ccccc2)cc1 Show InChI InChI=1S/C39H38F2N4O3/c1-43(2)30-20-23-44(24-21-30)36(46)26-34-33-14-8-9-15-35(33)45(25-22-39(34,40)41)38(48)28-16-18-29(19-17-28)42-37(47)32-13-7-6-12-31(32)27-10-4-3-5-11-27/h3-19,26,30H,20-25H2,1-2H3,(H,42,47)/b34-26-	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.770	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at Vasopressin V2 receptor, performed using [3H]-AVP on rat kidney				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (Homo sapiens (Human))	BDBM50114033 (CHEMBL86667 | {4-[2-(3-Biphenyl-4-yl-5-methyl-[1,2...) Show SMILES Cc1nnc(-c2ccc(cc2)-c2ccccc2)n1-c1c(C)cccc1OCc1ccc(cc1)C(=O)N1CCC(CC1)N1CCCCC1 |(15.01,-.52,;13.48,-.29,;12.92,1.14,;11.39,1.05,;10.99,-.44,;9.57,-1,;9.33,-2.53,;7.9,-3.09,;6.69,-2.13,;6.92,-.61,;8.35,-.03,;5.26,-2.69,;4.05,-1.71,;2.62,-2.27,;2.38,-3.81,;3.58,-4.77,;5.02,-4.21,;12.29,-1.27,;12.45,-2.79,;11.2,-3.7,;9.8,-3.07,;11.36,-5.22,;12.77,-5.85,;14.02,-4.94,;13.86,-3.42,;15.1,-2.51,;16.53,-3.05,;16.79,-4.56,;18.23,-5.09,;18.49,-6.6,;17.32,-7.6,;15.87,-7.06,;15.59,-5.55,;17.57,-9.12,;19.02,-9.65,;16.39,-10.1,;17.53,-11.13,;17.18,-12.65,;15.71,-13.11,;14.59,-12.07,;14.92,-10.56,;15.48,-14.61,;16.67,-15.57,;16.44,-17.09,;15.01,-17.63,;13.82,-16.67,;14.05,-15.17,)| Show InChI InChI=1S/C40H43N5O2/c1-29-10-9-13-37(38(29)45-30(2)41-42-39(45)34-20-18-33(19-21-34)32-11-5-3-6-12-32)47-28-31-14-16-35(17-15-31)40(46)44-26-22-36(23-27-44)43-24-7-4-8-25-43/h3,5-6,9-21,36H,4,7-8,22-28H2,1-2H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.01	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at cloned human Vasopressin V1a receptor stably expressed in CHO cells, using [3H]-AVP as radioligand				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (Homo sapiens (Human))	BDBM50114028 (1-{6-[2-(3-Biphenyl-4-yl-5-methyl-[1,2,4]triazol-4...) Show SMILES CN1CCN(CCCCCCOc2ccccc2-n2c(C)nnc2-c2ccc(cc2)-c2ccccc2)CC1 |(27.25,-2.68,;25.78,-2.25,;24.66,-3.31,;23.19,-2.88,;22.83,-1.38,;21.58,-2.29,;20.18,-1.64,;18.92,-2.53,;17.52,-1.89,;16.26,-2.77,;14.86,-2.13,;13.62,-3.02,;13.76,-4.55,;15.14,-5.18,;15.28,-6.72,;14.02,-7.59,;12.64,-6.96,;12.51,-5.42,;11.12,-4.78,;10.9,-3.25,;11.88,-2.08,;9.38,-2.99,;8.66,-4.36,;9.75,-5.46,;9.49,-6.98,;8.05,-7.52,;7.79,-9.03,;8.98,-10,;10.41,-9.48,;10.68,-7.96,;8.71,-11.52,;7.28,-12.06,;7,-13.57,;8.19,-14.56,;9.64,-14.02,;9.91,-12.51,;23.93,-.31,;25.4,-.75,)| Show InChI InChI=1S/C32H39N5O/c1-26-33-34-32(29-18-16-28(17-19-29)27-12-6-5-7-13-27)37(26)30-14-8-9-15-31(30)38-25-11-4-3-10-20-36-23-21-35(2)22-24-36/h5-9,12-19H,3-4,10-11,20-25H2,1-2H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.04	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at cloned human Vasopressin V1a receptor stably expressed in CHO cells, using [3H]-AVP as radioligand				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (Homo sapiens (Human))	BDBM50114034 (1'-{6-[2-(3-Biphenyl-4-yl-5-methyl-[1,2,4]triazol-...) Show SMILES Cc1nnc(-c2ccc(cc2)-c2ccccc2)n1-c1ccccc1OCCCCCCN1CCC(CC1)N1CCCCC1 |(6.93,-1.75,;5.55,-2.43,;4.25,-1.61,;3.06,-2.57,;3.62,-4.01,;2.78,-5.3,;1.24,-5.23,;.4,-6.52,;1.1,-7.87,;2.64,-7.96,;3.48,-6.68,;.26,-9.17,;.96,-10.54,;.12,-11.84,;-1.42,-11.74,;-2.11,-10.37,;-1.28,-9.08,;5.16,-3.93,;6.17,-5.07,;5.68,-6.54,;6.69,-7.68,;8.2,-7.38,;8.69,-5.91,;7.66,-4.77,;8.15,-3.3,;9.52,-2.62,;10.8,-3.48,;12.18,-2.78,;13.46,-3.65,;14.84,-2.95,;16.13,-3.81,;17.5,-3.13,;19.04,-3.27,;19.93,-2.04,;19.3,-.63,;17.76,-.47,;16.87,-1.73,;20.09,.67,;19.39,2.01,;20.21,3.3,;21.73,3.24,;22.45,1.91,;21.63,.61,)| Show InChI InChI=1S/C37H47N5O/c1-30-38-39-37(33-20-18-32(19-21-33)31-14-6-4-7-15-31)42(30)35-16-8-9-17-36(35)43-29-13-3-2-10-24-40-27-22-34(23-28-40)41-25-11-5-12-26-41/h4,6-9,14-21,34H,2-3,5,10-13,22-29H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.05	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at cloned human Vasopressin V1a receptor stably expressed in CHO cells, using [3H]-AVP as radioligand				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V2 receptor (Homo sapiens (Human))	BDBM50108498 (Biphenyl-2-carboxylic acid (4-{5-[2-(4-dimethylami...) Show SMILES CN(C)C1CCN(CC1)C(=O)\C=C1\c2ccccc2N(CCC1(F)F)C(=O)c1ccc(NC(=O)c2ccccc2-c2ccccc2)cc1 Show InChI InChI=1S/C39H38F2N4O3/c1-43(2)30-20-23-44(24-21-30)36(46)26-34-33-14-8-9-15-35(33)45(25-22-39(34,40)41)38(48)28-16-18-29(19-17-28)42-37(47)32-13-7-6-12-31(32)27-10-4-3-5-11-27/h3-19,26,30H,20-25H2,1-2H3,(H,42,47)/b34-26-	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.19	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at cloned human Vasopressin V2 receptor stably expressed in CHO cells, using [3H]-AVP as radioligand				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V2 receptor (Rattus norvegicus (Rat))	BDBM50108498 (Biphenyl-2-carboxylic acid (4-{5-[2-(4-dimethylami...) Show SMILES CN(C)C1CCN(CC1)C(=O)\C=C1\c2ccccc2N(CCC1(F)F)C(=O)c1ccc(NC(=O)c2ccccc2-c2ccccc2)cc1 Show InChI InChI=1S/C39H38F2N4O3/c1-43(2)30-20-23-44(24-21-30)36(46)26-34-33-14-8-9-15-35(33)45(25-22-39(34,40)41)38(48)28-16-18-29(19-17-28)42-37(47)32-13-7-6-12-31(32)27-10-4-3-5-11-27/h3-19,26,30H,20-25H2,1-2H3,(H,42,47)/b34-26-	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Evaluated for the binding affinity towards vasopressin (V2) receptor in rat kidney membrane using [3H]AVP as radioligand				Bioorg Med Chem Lett 12: 229-32 (2001) BindingDB Entry DOI: 10.7270/Q2R78FQP
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (RAT)	BDBM50114031 ((2S)-1-[(2R,3S)-5-chloro-3-(2-chlorophenyl)-1-(3,4...) Show SMILES COc1ccc(cc1OC)S(=O)(=O)N1[C@@H](C(=O)N2CCC[C@H]2C(N)=O)[C@](O)(c2cc(Cl)ccc12)c1ccccc1Cl |r| Show InChI InChI=1S/C28H27Cl2N3O7S/c1-39-23-12-10-17(15-24(23)40-2)41(37,38)33-21-11-9-16(29)14-19(21)28(36,18-6-3-4-7-20(18)30)25(33)27(35)32-13-5-8-22(32)26(31)34/h3-4,6-7,9-12,14-15,22,25,36H,5,8,13H2,1-2H3,(H2,31,34)/t22-,25-,28+/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents	PubMed	1.43	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at Vasopressin V1a receptor, performed using [3H]-AVP on rat liver				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (Homo sapiens (Human))	BDBM50114025 (4-{4-[2-(3-Biphenyl-4-yl-5-methyl-[1,2,4]triazol-4...) Show SMILES Cc1nnc(-c2ccc(cc2)-c2ccccc2)n1-c1ccccc1OCCCCC1CCNCC1 |(10.8,-.03,;9.42,-.73,;8.13,.11,;6.93,-.86,;7.49,-2.29,;6.65,-3.59,;5.11,-3.5,;4.27,-4.8,;4.97,-6.16,;6.51,-6.25,;7.35,-4.96,;4.13,-7.44,;4.83,-8.82,;3.99,-10.11,;2.45,-10.03,;1.76,-8.65,;2.59,-7.36,;9.02,-2.22,;10.03,-3.36,;9.54,-4.82,;10.56,-5.97,;12.07,-5.66,;12.55,-4.19,;11.54,-3.05,;12.01,-1.59,;13.38,-.92,;14.67,-1.76,;16.04,-1.08,;17.32,-1.93,;17.23,-3.46,;18.55,-4.27,;18.49,-5.81,;17.14,-6.53,;15.83,-5.73,;15.88,-4.2,)| Show InChI InChI=1S/C30H34N4O/c1-23-32-33-30(27-16-14-26(15-17-27)25-10-3-2-4-11-25)34(23)28-12-5-6-13-29(28)35-22-8-7-9-24-18-20-31-21-19-24/h2-6,10-17,24,31H,7-9,18-22H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	2.12	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at cloned human Vasopressin V1a receptor stably expressed in CHO cells, using [3H]-AVP as radioligand				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (RAT)	BDBM50108493 (2-Methyl-furan-3-carboxylic acid [4-({2-[4-([1,4']...) Show SMILES CN(C(=O)c1ccc(NC(=O)c2ccoc2C)cc1)c1ccc(C)cc1OCc1ccc(cc1)C(=O)N1CCC(CC1)N1CCCCC1 Show InChI InChI=1S/C39H44N4O5/c1-27-7-16-35(41(3)38(45)30-12-14-32(15-13-30)40-37(44)34-19-24-47-28(34)2)36(25-27)48-26-29-8-10-31(11-9-29)39(46)43-22-17-33(18-23-43)42-20-5-4-6-21-42/h7-16,19,24-25,33H,4-6,17-18,20-23,26H2,1-3H3,(H,40,44)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	2.90	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Evaluated for the binding affinity towards vasopressin (V1A) receptor in rat liver membrane using [3H]AVP as radioligand				Bioorg Med Chem Lett 12: 229-32 (2001) BindingDB Entry DOI: 10.7270/Q2R78FQP
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (Homo sapiens (Human))	BDBM50114032 (CHEMBL86577 | {4-[2-(3-Biphenyl-4-yl-5-methyl-[1,2...) Show SMILES CN1CCN(CC1)C(=O)c1ccc(COc2ccccc2-n2c(C)nnc2-c2ccc(cc2)-c2ccccc2)cc1 |(15.94,-10.56,;16.17,-9.05,;17.64,-8.58,;17.99,-7.08,;16.85,-6.05,;15.38,-6.5,;15.04,-8,;18.02,-5.05,;19.47,-5.59,;17.76,-3.54,;16.31,-3,;16.06,-1.48,;17.25,-.5,;16.99,1.02,;15.54,1.54,;14.3,.65,;14.47,-.89,;13.23,-1.8,;11.82,-1.17,;11.66,.37,;12.9,1.26,;12.74,2.8,;13.93,3.78,;15.46,3.54,;13.37,5.2,;11.84,5.11,;11.45,3.61,;10.02,3.05,;8.81,4.02,;7.38,3.45,;7.16,1.93,;8.35,.97,;9.79,1.53,;5.71,1.37,;5.47,-.16,;4.04,-.71,;2.83,.25,;3.08,1.79,;4.52,2.34,;18.69,-1.04,;18.95,-2.55,)| Show InChI InChI=1S/C34H33N5O2/c1-25-35-36-33(29-18-16-28(17-19-29)27-8-4-3-5-9-27)39(25)31-10-6-7-11-32(31)41-24-26-12-14-30(15-13-26)34(40)38-22-20-37(2)21-23-38/h3-19H,20-24H2,1-2H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	3.03	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at cloned human Vasopressin V1a receptor stably expressed in CHO cells, using [3H]-AVP as radioligand				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (Homo sapiens (Human))	BDBM50114045 (1-{5-[2-(3-Biphenyl-4-yl-5-methyl-[1,2,4]triazol-4...) Show SMILES CN1CCN(CCCCCOc2ccccc2-n2c(C)nnc2-c2ccc(cc2)-c2ccccc2)CC1 |(24.7,-5.65,;23.67,-4.52,;22.16,-4.86,;21.11,-3.74,;21.58,-2.29,;20.18,-1.64,;18.92,-2.53,;17.52,-1.89,;16.26,-2.78,;14.86,-2.13,;13.62,-3.02,;13.76,-4.55,;15.14,-5.19,;15.28,-6.72,;14.02,-7.59,;12.64,-6.96,;12.51,-5.42,;11.12,-4.78,;10.9,-3.25,;11.88,-2.08,;9.38,-2.99,;8.66,-4.36,;9.75,-5.46,;9.49,-6.98,;8.05,-7.52,;7.79,-9.03,;8.98,-10,;10.41,-9.48,;10.68,-7.96,;8.71,-11.52,;9.91,-12.51,;9.64,-14.02,;8.19,-14.56,;7,-13.57,;7.28,-12.06,;23.07,-1.92,;24.12,-3.06,)| Show InChI InChI=1S/C31H37N5O/c1-25-32-33-31(28-17-15-27(16-18-28)26-11-5-3-6-12-26)36(25)29-13-7-8-14-30(29)37-24-10-4-9-19-35-22-20-34(2)21-23-35/h3,5-8,11-18H,4,9-10,19-24H2,1-2H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	4.09	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at cloned human Vasopressin V1a receptor stably expressed in CHO cells, using [3H]-AVP as radioligand				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (Homo sapiens (Human))	BDBM50114038 (1-{7-[2-(3-Biphenyl-4-yl-5-methyl-[1,2,4]triazol-4...) Show SMILES CN1CCN(CCCCCCCOc2ccccc2-n2c(C)nnc2-c2ccc(cc2)-c2ccccc2)CC1 |(27.36,-5.41,;26.31,-4.28,;24.82,-4.63,;23.77,-3.51,;24.24,-2.04,;22.84,-1.4,;21.58,-2.29,;20.18,-1.64,;18.92,-2.53,;17.52,-1.89,;16.26,-2.77,;14.86,-2.13,;13.62,-3.02,;13.76,-4.55,;15.14,-5.18,;15.28,-6.72,;14.02,-7.59,;12.64,-6.96,;12.51,-5.42,;11.12,-4.78,;10.9,-3.25,;11.88,-2.08,;9.38,-2.99,;8.66,-4.36,;9.75,-5.46,;9.49,-6.98,;8.05,-7.52,;7.79,-9.03,;8.98,-10,;10.41,-9.48,;10.68,-7.96,;8.71,-11.52,;9.91,-12.51,;9.64,-14.02,;8.19,-14.56,;7,-13.57,;7.28,-12.06,;25.73,-1.68,;26.78,-2.81,)| Show InChI InChI=1S/C33H41N5O/c1-27-34-35-33(30-19-17-29(18-20-30)28-13-7-6-8-14-28)38(27)31-15-9-10-16-32(31)39-26-12-5-3-4-11-21-37-24-22-36(2)23-25-37/h6-10,13-20H,3-5,11-12,21-26H2,1-2H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	4.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at cloned human Vasopressin V1a receptor stably expressed in CHO cells, using [3H]-AVP as radioligand				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (RAT)	BDBM50108494 (2-Methyl-furan-3-carboxylic acid (4-{[2-(6-[1,4']b...) Show SMILES CN(C(=O)c1ccc(NC(=O)c2ccoc2C)cc1)c1ccc(C)cc1OCCCCCC(=O)N1CCC(CC1)N1CCCCC1 Show InChI InChI=1S/C37H48N4O5/c1-27-11-16-33(39(3)37(44)29-12-14-30(15-13-29)38-36(43)32-19-25-45-28(32)2)34(26-27)46-24-9-4-6-10-35(42)41-22-17-31(18-23-41)40-20-7-5-8-21-40/h11-16,19,25-26,31H,4-10,17-18,20-24H2,1-3H3,(H,38,43)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Evaluated for the binding affinity towards vasopressin (V1A) receptor in rat liver membrane using [3H]AVP as radioligand				Bioorg Med Chem Lett 12: 229-32 (2001) BindingDB Entry DOI: 10.7270/Q2R78FQP
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (RAT)	BDBM50108495 (1N-methyl-1N-{4-methyl-2-[6-(4-methylhexahydro-1-p...) Show SMILES CCc1nccn1-c1ccccc1C(=O)Nc1ccc(cc1)C(=O)N(C)c1ccc(C)cc1OCCCCCC(=O)N1CCN(C)CC1 Show InChI InChI=1S/C38H46N6O4/c1-5-35-39-20-21-44(35)32-12-9-8-11-31(32)37(46)40-30-17-15-29(16-18-30)38(47)42(4)33-19-14-28(2)27-34(33)48-26-10-6-7-13-36(45)43-24-22-41(3)23-25-43/h8-9,11-12,14-21,27H,5-7,10,13,22-26H2,1-4H3,(H,40,46)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	5.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Evaluated for the binding affinity towards vasopressin (V1A) receptor in rat liver membrane using [3H]AVP as radioligand				Bioorg Med Chem Lett 12: 229-32 (2001) BindingDB Entry DOI: 10.7270/Q2R78FQP
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (RAT)	BDBM50108499 (1N-methyl-1N-{4-methyl-2-[4-(4-methylhexahydro-1-p...) Show SMILES CCc1nccn1-c1ccccc1C(=O)Nc1ccc(cc1)C(=O)N(C)c1ccc(C)cc1OCc1ccc(cc1)C(=O)N1CCN(C)CC1 Show InChI InChI=1S/C40H42N6O4/c1-5-37-41-20-21-46(37)34-9-7-6-8-33(34)38(47)42-32-17-15-30(16-18-32)39(48)44(4)35-19-10-28(2)26-36(35)50-27-29-11-13-31(14-12-29)40(49)45-24-22-43(3)23-25-45/h6-21,26H,5,22-25,27H2,1-4H3,(H,42,47)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	7.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Evaluated for the binding affinity towards vasopressin (V1A) receptor in rat liver membrane using [3H]AVP as radioligand				Bioorg Med Chem Lett 12: 229-32 (2001) BindingDB Entry DOI: 10.7270/Q2R78FQP
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (Homo sapiens (Human))	BDBM50114037 (4-{3-[2-(3-Biphenyl-4-yl-5-methyl-[1,2,4]triazol-4...) Show SMILES Cc1nnc(-c2ccc(cc2)-c2ccccc2)n1-c1ccccc1OCCCC1CCNCC1 |(9.43,-1.75,;8.05,-2.43,;6.76,-1.61,;5.56,-2.57,;6.12,-4.01,;5.28,-5.3,;3.74,-5.22,;2.9,-6.51,;3.6,-7.87,;5.14,-7.96,;5.98,-6.68,;2.76,-9.17,;3.46,-10.54,;2.62,-11.83,;1.08,-11.74,;.38,-10.36,;1.22,-9.08,;7.65,-3.93,;8.66,-5.07,;8.17,-6.54,;9.2,-7.68,;10.71,-7.38,;11.18,-5.91,;10.17,-4.77,;10.64,-3.31,;12.02,-2.62,;13.3,-3.47,;14.68,-2.78,;15.96,-3.65,;17.31,-2.9,;18.63,-3.72,;18.57,-5.26,;17.22,-5.98,;15.91,-5.18,)| Show InChI InChI=1S/C29H32N4O/c1-22-31-32-29(26-15-13-25(14-16-26)24-9-3-2-4-10-24)33(22)27-11-5-6-12-28(27)34-21-7-8-23-17-19-30-20-18-23/h2-6,9-16,23,30H,7-8,17-21H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	7.84	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at cloned human Vasopressin V1a receptor stably expressed in CHO cells, using [3H]-AVP as radioligand				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (Homo sapiens (Human))	BDBM50114041 (CHEMBL316093 | {4-[2-(3-Biphenyl-4-yl-5-methyl-[1,...) Show SMILES CN1CCN(CC1)C(=O)c1ccc(COc2cccc(C)c2-n2c(C)nnc2-c2ccc(cc2)-c2ccccc2)cc1 |(15.47,-14.61,;15.71,-13.11,;14.58,-12.06,;14.91,-10.56,;16.38,-10.1,;17.53,-11.13,;17.18,-12.65,;17.57,-9.12,;19.02,-9.65,;17.31,-7.6,;18.49,-6.6,;18.23,-5.09,;16.78,-4.56,;16.52,-3.04,;15.09,-2.51,;13.85,-3.42,;14.02,-4.94,;12.76,-5.85,;11.36,-5.22,;11.2,-3.7,;9.8,-3.07,;12.45,-2.79,;12.29,-1.27,;13.48,-.29,;15.01,-.52,;12.92,1.14,;11.38,1.05,;10.99,-.44,;9.56,-1,;9.33,-2.53,;7.9,-3.09,;6.69,-2.13,;6.92,-.61,;8.35,-.03,;5.26,-2.69,;4.05,-1.71,;2.62,-2.27,;2.38,-3.81,;3.58,-4.77,;5.02,-4.21,;15.59,-5.54,;15.86,-7.06,)| Show InChI InChI=1S/C35H35N5O2/c1-25-8-7-11-32(42-24-27-12-14-31(15-13-27)35(41)39-22-20-38(3)21-23-39)33(25)40-26(2)36-37-34(40)30-18-16-29(17-19-30)28-9-5-4-6-10-28/h4-19H,20-24H2,1-3H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	8.09	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at cloned human Vasopressin V1a receptor stably expressed in CHO cells, using [3H]-AVP as radioligand				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (RAT)	BDBM50108500 (2-Methyl-furan-3-carboxylic acid [4-(methyl-{4-met...) Show SMILES CN(C(=O)c1ccc(NC(=O)c2ccoc2C)cc1)c1ccc(C)cc1OCCCCCC(=O)N1CCN(C)CC1 Show InChI InChI=1S/C32H40N4O5/c1-23-9-14-28(29(22-23)41-20-7-5-6-8-30(37)36-18-16-34(3)17-19-36)35(4)32(39)25-10-12-26(13-11-25)33-31(38)27-15-21-40-24(27)2/h9-15,21-22H,5-8,16-20H2,1-4H3,(H,33,38)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	8.80	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Evaluated for the binding affinity towards vasopressin (V1A) receptor in rat liver membrane using [3H]AVP as radioligand				Bioorg Med Chem Lett 12: 229-32 (2001) BindingDB Entry DOI: 10.7270/Q2R78FQP
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (Homo sapiens (Human))	BDBM50114043 (3-Biphenyl-4-yl-4-[2-(6-imidazol-1-yl-hexyloxy)-ph...) Show SMILES Cc1nnc(-c2ccc(cc2)-c2ccccc2)n1-c1ccccc1OCCCCCCn1ccnc1 |(8.16,-1.75,;6.79,-2.43,;5.49,-1.61,;4.3,-2.57,;4.86,-4.01,;4.02,-5.3,;2.47,-5.22,;1.64,-6.51,;2.34,-7.87,;3.86,-7.96,;4.71,-6.68,;1.5,-9.16,;2.2,-10.54,;1.35,-11.83,;-.19,-11.74,;-.88,-10.36,;-.04,-9.08,;6.39,-3.93,;7.4,-5.07,;6.91,-6.54,;7.93,-7.68,;9.43,-7.38,;9.92,-5.91,;8.89,-4.77,;9.38,-3.3,;10.75,-2.62,;12.03,-3.47,;13.41,-2.78,;14.69,-3.65,;16.08,-2.95,;17.36,-3.81,;18.73,-3.12,;18.98,-1.61,;20.51,-1.38,;21.18,-2.76,;20.09,-3.83,)| Show InChI InChI=1S/C30H31N5O/c1-24-32-33-30(27-17-15-26(16-18-27)25-11-5-4-6-12-25)35(24)28-13-7-8-14-29(28)36-22-10-3-2-9-20-34-21-19-31-23-34/h4-8,11-19,21,23H,2-3,9-10,20,22H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	9.06	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at cloned human Vasopressin V1a receptor stably expressed in CHO cells, using [3H]-AVP as radioligand				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (Homo sapiens (Human))	BDBM50114040 (6-[2-(3-Biphenyl-4-yl-5-methyl-[1,2,4]triazol-4-yl...) Show SMILES CN1CCN(CC1)C(=O)CCCCCOc1ccccc1-n1c(C)nnc1-c1ccc(cc1)-c1ccccc1 |(17.72,4.65,;16.39,3.89,;16.5,2.35,;15.21,1.49,;13.84,2.17,;13.74,3.71,;15.01,4.57,;12.56,1.32,;12.65,-.22,;11.17,2,;9.89,1.16,;8.51,1.84,;7.22,.98,;5.84,1.67,;4.56,.82,;4.07,-.64,;5.1,-1.78,;4.61,-3.26,;3.11,-3.56,;2.09,-2.41,;2.58,-.96,;1.55,.19,;1.96,1.68,;3.34,2.38,;.66,2.52,;-.53,1.56,;.03,.11,;-.81,-1.18,;-2.36,-1.11,;-3.19,-2.39,;-2.49,-3.76,;-.96,-3.84,;-.12,-2.56,;-3.33,-5.06,;-2.63,-6.43,;-3.48,-7.72,;-5.02,-7.64,;-5.72,-6.25,;-4.88,-4.96,)| Show InChI InChI=1S/C32H37N5O2/c1-25-33-34-32(28-18-16-27(17-19-28)26-11-5-3-6-12-26)37(25)29-13-8-9-14-30(29)39-24-10-4-7-15-31(38)36-22-20-35(2)21-23-36/h3,5-6,8-9,11-14,16-19H,4,7,10,15,20-24H2,1-2H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	9.16	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at cloned human Vasopressin V1a receptor stably expressed in CHO cells, using [3H]-AVP as radioligand				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (RAT)	BDBM50114034 (1'-{6-[2-(3-Biphenyl-4-yl-5-methyl-[1,2,4]triazol-...) Show SMILES Cc1nnc(-c2ccc(cc2)-c2ccccc2)n1-c1ccccc1OCCCCCCN1CCC(CC1)N1CCCCC1 |(6.93,-1.75,;5.55,-2.43,;4.25,-1.61,;3.06,-2.57,;3.62,-4.01,;2.78,-5.3,;1.24,-5.23,;.4,-6.52,;1.1,-7.87,;2.64,-7.96,;3.48,-6.68,;.26,-9.17,;.96,-10.54,;.12,-11.84,;-1.42,-11.74,;-2.11,-10.37,;-1.28,-9.08,;5.16,-3.93,;6.17,-5.07,;5.68,-6.54,;6.69,-7.68,;8.2,-7.38,;8.69,-5.91,;7.66,-4.77,;8.15,-3.3,;9.52,-2.62,;10.8,-3.48,;12.18,-2.78,;13.46,-3.65,;14.84,-2.95,;16.13,-3.81,;17.5,-3.13,;19.04,-3.27,;19.93,-2.04,;19.3,-.63,;17.76,-.47,;16.87,-1.73,;20.09,.67,;19.39,2.01,;20.21,3.3,;21.73,3.24,;22.45,1.91,;21.63,.61,)| Show InChI InChI=1S/C37H47N5O/c1-30-38-39-37(33-20-18-32(19-21-33)31-14-6-4-7-15-31)42(30)35-16-8-9-17-36(35)43-29-13-3-2-10-24-40-27-22-34(23-28-40)41-25-11-5-12-26-41/h4,6-9,14-21,34H,2-3,5,10-13,22-29H2,1H3	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	9.69	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at Vasopressin V1a receptor, performed using [3H]-AVP on rat liver				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (Homo sapiens (Human))	BDBM50114029 (1-{8-[2-(3-Biphenyl-4-yl-5-methyl-[1,2,4]triazol-4...) Show SMILES CN1CCN(CCCCCCCCOc2ccccc2-n2c(C)nnc2-c2ccc(cc2)-c2ccccc2)CC1 |(24.67,-8.17,;24.58,-6.63,;23.19,-5.95,;23.09,-4.42,;24.38,-3.58,;24.24,-2.04,;22.84,-1.4,;21.58,-2.29,;20.18,-1.64,;18.92,-2.53,;17.52,-1.89,;16.26,-2.77,;14.86,-2.13,;13.62,-3.02,;13.76,-4.55,;15.14,-5.18,;15.28,-6.72,;14.02,-7.59,;12.64,-6.96,;12.51,-5.42,;11.12,-4.78,;10.9,-3.25,;11.88,-2.08,;9.38,-2.99,;8.66,-4.36,;9.75,-5.46,;9.49,-6.98,;8.05,-7.52,;7.79,-9.03,;8.98,-10,;10.41,-9.48,;10.68,-7.96,;8.71,-11.52,;9.91,-12.51,;9.64,-14.02,;8.19,-14.56,;7,-13.57,;7.28,-12.06,;25.75,-4.24,;25.85,-5.78,)| Show InChI InChI=1S/C34H43N5O/c1-28-35-36-34(31-20-18-30(19-21-31)29-14-8-7-9-15-29)39(28)32-16-10-11-17-33(32)40-27-13-6-4-3-5-12-22-38-25-23-37(2)24-26-38/h7-11,14-21H,3-6,12-13,22-27H2,1-2H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	13.2	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at cloned human Vasopressin V1a receptor stably expressed in CHO cells, using [3H]-AVP as radioligand				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (Homo sapiens (Human))	BDBM50114039 (1-{6-[2-(3-Biphenyl-4-yl-5-methyl-[1,2,4]triazol-4...) Show SMILES Cc1nnc(-c2ccc(cc2)-c2ccccc2)n1-c1ccccc1OCCCCCCN1CCCCC1 |(9.29,-1.39,;7.83,-1.97,;6.55,-1.15,;5.37,-2.08,;5.92,-3.51,;5.02,-4.76,;5.68,-6.17,;4.76,-7.42,;3.23,-7.27,;2.58,-5.86,;3.49,-4.61,;2.33,-8.52,;2.97,-9.93,;2.07,-11.18,;.52,-11.06,;-.12,-9.64,;.78,-8.39,;7.45,-3.44,;8.55,-4.53,;8.14,-5.99,;9.24,-7.08,;10.72,-6.68,;11.12,-5.22,;10.03,-4.13,;10.44,-2.63,;11.94,-2.23,;12.33,-.75,;13.82,-.36,;14.22,1.13,;15.68,1.53,;16.09,3.01,;17.57,3.39,;18.67,2.32,;20.12,2.71,;20.53,4.19,;19.44,5.28,;17.96,4.88,)| Show InChI InChI=1S/C32H38N4O/c1-26-33-34-32(29-20-18-28(19-21-29)27-14-6-4-7-15-27)36(26)30-16-8-9-17-31(30)37-25-13-3-2-10-22-35-23-11-5-12-24-35/h4,6-9,14-21H,2-3,5,10-13,22-25H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	13.9	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at cloned human Vasopressin V1a receptor stably expressed in CHO cells, using [3H]-AVP as radioligand				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (RAT)	BDBM50114028 (1-{6-[2-(3-Biphenyl-4-yl-5-methyl-[1,2,4]triazol-4...) Show SMILES CN1CCN(CCCCCCOc2ccccc2-n2c(C)nnc2-c2ccc(cc2)-c2ccccc2)CC1 |(27.25,-2.68,;25.78,-2.25,;24.66,-3.31,;23.19,-2.88,;22.83,-1.38,;21.58,-2.29,;20.18,-1.64,;18.92,-2.53,;17.52,-1.89,;16.26,-2.77,;14.86,-2.13,;13.62,-3.02,;13.76,-4.55,;15.14,-5.18,;15.28,-6.72,;14.02,-7.59,;12.64,-6.96,;12.51,-5.42,;11.12,-4.78,;10.9,-3.25,;11.88,-2.08,;9.38,-2.99,;8.66,-4.36,;9.75,-5.46,;9.49,-6.98,;8.05,-7.52,;7.79,-9.03,;8.98,-10,;10.41,-9.48,;10.68,-7.96,;8.71,-11.52,;7.28,-12.06,;7,-13.57,;8.19,-14.56,;9.64,-14.02,;9.91,-12.51,;23.93,-.31,;25.4,-.75,)| Show InChI InChI=1S/C32H39N5O/c1-26-33-34-32(29-18-16-28(17-19-29)27-12-6-5-7-13-27)37(26)30-14-8-9-15-31(30)38-25-11-4-3-10-20-36-23-21-35(2)22-24-36/h5-9,12-19H,3-4,10-11,20-25H2,1-2H3	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	17.3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at Vasopressin V1a receptor, performed using [3H]-AVP on rat liver				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (RAT)	BDBM50029644 (CHEMBL296908 | N-(3-(4-(4-(2-oxo-3,4-dihydroquinol...) Show SMILES CC(=O)NCCCOc1ccc(cc1)C(=O)N1CCC(CC1)N1C(=O)CCc2ccccc12 Show InChI InChI=1S/C26H31N3O4/c1-19(30)27-15-4-18-33-23-10-7-21(8-11-23)26(32)28-16-13-22(14-17-28)29-24-6-3-2-5-20(24)9-12-25(29)31/h2-3,5-8,10-11,22H,4,9,12-18H2,1H3,(H,27,30)	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	PubMed	23.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at Vasopressin V1a receptor, performed using [3H]-AVP on rat liver				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (RAT)	BDBM50029644 (CHEMBL296908 | N-(3-(4-(4-(2-oxo-3,4-dihydroquinol...) Show SMILES CC(=O)NCCCOc1ccc(cc1)C(=O)N1CCC(CC1)N1C(=O)CCc2ccccc12 Show InChI InChI=1S/C26H31N3O4/c1-19(30)27-15-4-18-33-23-10-7-21(8-11-23)26(32)28-16-13-22(14-17-28)29-24-6-3-2-5-20(24)9-12-25(29)31/h2-3,5-8,10-11,22H,4,9,12-18H2,1H3,(H,27,30)	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	PubMed	24	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Evaluated for the binding affinity towards Vasopressin V1a receptor in rat liver membrane using [3H]AVP as radioligand				Bioorg Med Chem Lett 12: 229-32 (2001) BindingDB Entry DOI: 10.7270/Q2R78FQP
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (Homo sapiens (Human))	BDBM50114026 (1-{4-[2-(3-Biphenyl-4-yl-5-methyl-[1,2,4]triazol-4...) Show SMILES CN1CCN(CCCCOc2ccccc2-n2c(C)nnc2-c2ccc(cc2)-c2ccccc2)CC1 |(24.65,-.56,;23.17,-.92,;22.72,-2.39,;21.23,-2.76,;20.18,-1.64,;18.92,-2.53,;17.52,-1.89,;16.26,-2.78,;14.86,-2.13,;13.62,-3.02,;13.76,-4.55,;15.14,-5.19,;15.28,-6.72,;14.02,-7.59,;12.64,-6.96,;12.51,-5.42,;11.12,-4.78,;10.9,-3.25,;11.88,-2.08,;9.38,-2.99,;8.66,-4.36,;9.75,-5.46,;9.49,-6.98,;8.05,-7.52,;7.79,-9.03,;8.98,-10.01,;10.41,-9.48,;10.68,-7.96,;8.71,-11.52,;9.91,-12.51,;9.64,-14.02,;8.19,-14.56,;7,-13.57,;7.28,-12.06,;20.6,-.16,;22.09,.2,)| Show InChI InChI=1S/C30H35N5O/c1-24-31-32-30(27-16-14-26(15-17-27)25-10-4-3-5-11-25)35(24)28-12-6-7-13-29(28)36-23-9-8-18-34-21-19-33(2)20-22-34/h3-7,10-17H,8-9,18-23H2,1-2H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	29.1	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at cloned human Vasopressin V1a receptor stably expressed in CHO cells, using [3H]-AVP as radioligand				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (RAT)	BDBM50114033 (CHEMBL86667 | {4-[2-(3-Biphenyl-4-yl-5-methyl-[1,2...) Show SMILES Cc1nnc(-c2ccc(cc2)-c2ccccc2)n1-c1c(C)cccc1OCc1ccc(cc1)C(=O)N1CCC(CC1)N1CCCCC1 |(15.01,-.52,;13.48,-.29,;12.92,1.14,;11.39,1.05,;10.99,-.44,;9.57,-1,;9.33,-2.53,;7.9,-3.09,;6.69,-2.13,;6.92,-.61,;8.35,-.03,;5.26,-2.69,;4.05,-1.71,;2.62,-2.27,;2.38,-3.81,;3.58,-4.77,;5.02,-4.21,;12.29,-1.27,;12.45,-2.79,;11.2,-3.7,;9.8,-3.07,;11.36,-5.22,;12.77,-5.85,;14.02,-4.94,;13.86,-3.42,;15.1,-2.51,;16.53,-3.05,;16.79,-4.56,;18.23,-5.09,;18.49,-6.6,;17.32,-7.6,;15.87,-7.06,;15.59,-5.55,;17.57,-9.12,;19.02,-9.65,;16.39,-10.1,;17.53,-11.13,;17.18,-12.65,;15.71,-13.11,;14.59,-12.07,;14.92,-10.56,;15.48,-14.61,;16.67,-15.57,;16.44,-17.09,;15.01,-17.63,;13.82,-16.67,;14.05,-15.17,)| Show InChI InChI=1S/C40H43N5O2/c1-29-10-9-13-37(38(29)45-30(2)41-42-39(45)34-20-18-33(19-21-34)32-11-5-3-6-12-32)47-28-31-14-16-35(17-15-31)40(46)44-26-22-36(23-27-44)43-24-7-4-8-25-43/h3,5-6,9-21,36H,4,7-8,22-28H2,1-2H3	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	32.4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at Vasopressin V1a receptor, performed using [3H]-AVP on rat liver				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V2 receptor (Rattus norvegicus (Rat))	BDBM50108501 (2-Methyl-furan-3-carboxylic acid (4-{5-[2-(4-dimet...) Show SMILES CN(C)C1CCN(CC1)C(=O)\C=C1/c2ccccc2N(CCC1(F)F)C(=O)c1ccc(NC(=O)c2ccoc2C)cc1 Show InChI InChI=1S/C32H34F2N4O4/c1-21-25(14-19-42-21)30(40)35-23-10-8-22(9-11-23)31(41)38-18-15-32(33,34)27(26-6-4-5-7-28(26)38)20-29(39)37-16-12-24(13-17-37)36(2)3/h4-11,14,19-20,24H,12-13,15-18H2,1-3H3,(H,35,40)/b27-20+	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	34	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Evaluated for the binding affinity towards vasopressin (V2) receptor in rat kidney membrane using [3H]AVP as radioligand				Bioorg Med Chem Lett 12: 229-32 (2001) BindingDB Entry DOI: 10.7270/Q2R78FQP
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (Homo sapiens (Human))	BDBM50114042 (1-{3-[2-(3-Biphenyl-4-yl-5-methyl-[1,2,4]triazol-4...) Show SMILES CN1CCN(CCCOc2ccccc2-n2c(C)nnc2-c2ccc(cc2)-c2ccccc2)CC1 |(23.09,-4.46,;21.7,-3.81,;20.44,-4.7,;19.04,-4.06,;18.92,-2.53,;17.52,-1.89,;16.26,-2.77,;14.86,-2.13,;13.62,-3.02,;13.76,-4.55,;15.14,-5.18,;15.28,-6.72,;14.02,-7.59,;12.64,-6.96,;12.51,-5.42,;11.12,-4.78,;10.9,-3.25,;11.88,-2.08,;9.38,-2.99,;8.66,-4.36,;9.75,-5.46,;9.49,-6.98,;8.05,-7.52,;7.79,-9.03,;8.98,-10,;10.41,-9.48,;10.68,-7.96,;8.71,-11.52,;9.91,-12.51,;9.64,-14.02,;8.19,-14.56,;7,-13.57,;7.28,-12.06,;20.17,-1.63,;21.57,-2.29,)| Show InChI InChI=1S/C29H33N5O/c1-23-30-31-29(26-15-13-25(14-16-26)24-9-4-3-5-10-24)34(23)27-11-6-7-12-28(27)35-22-8-17-33-20-18-32(2)19-21-33/h3-7,9-16H,8,17-22H2,1-2H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	38.3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at cloned human Vasopressin V1a receptor stably expressed in CHO cells, using [3H]-AVP as radioligand				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (Homo sapiens (Human))	BDBM50114036 (1-{10-[2-(3-Biphenyl-4-yl-5-methyl-[1,2,4]triazol-...) Show SMILES CN1CCN(CCCCCCCCCCOc2ccccc2-n2c(C)nnc2-c2ccc(cc2)-c2ccccc2)CC1 |(27.33,-7.91,;27.23,-6.4,;25.85,-5.7,;25.76,-4.18,;27.03,-3.32,;26.89,-1.8,;25.49,-1.15,;24.24,-2.04,;22.84,-1.4,;21.58,-2.29,;20.18,-1.64,;18.92,-2.53,;17.52,-1.89,;16.26,-2.78,;14.86,-2.13,;13.62,-3.02,;13.76,-4.55,;15.14,-5.19,;15.28,-6.72,;14.02,-7.59,;12.64,-6.96,;12.51,-5.42,;11.12,-4.78,;10.9,-3.25,;11.88,-2.08,;9.38,-2.99,;8.66,-4.36,;9.75,-5.46,;9.49,-6.98,;8.05,-7.52,;7.79,-9.03,;8.98,-10.01,;10.41,-9.48,;10.68,-7.96,;8.71,-11.52,;9.91,-12.51,;9.64,-14.02,;8.19,-14.56,;7,-13.57,;7.28,-12.06,;28.41,-4,;28.51,-5.54,)| Show InChI InChI=1S/C36H47N5O/c1-30-37-38-36(33-22-20-32(21-23-33)31-16-10-9-11-17-31)41(30)34-18-12-13-19-35(34)42-29-15-8-6-4-3-5-7-14-24-40-27-25-39(2)26-28-40/h9-13,16-23H,3-8,14-15,24-29H2,1-2H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	39.4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at cloned human Vasopressin V1a receptor stably expressed in CHO cells, using [3H]-AVP as radioligand				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V2 receptor (Rattus norvegicus (Rat))	BDBM50108493 (2-Methyl-furan-3-carboxylic acid [4-({2-[4-([1,4']...) Show SMILES CN(C(=O)c1ccc(NC(=O)c2ccoc2C)cc1)c1ccc(C)cc1OCc1ccc(cc1)C(=O)N1CCC(CC1)N1CCCCC1 Show InChI InChI=1S/C39H44N4O5/c1-27-7-16-35(41(3)38(45)30-12-14-32(15-13-30)40-37(44)34-19-24-47-28(34)2)36(25-27)48-26-29-8-10-31(11-9-29)39(46)43-22-17-33(18-23-43)42-20-5-4-6-21-42/h7-16,19,24-25,33H,4-6,17-18,20-23,26H2,1-3H3,(H,40,44)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	42	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Evaluated for the binding affinity towards vasopressin (V2) receptor in rat kidney membrane using [3H]AVP as radioligand				Bioorg Med Chem Lett 12: 229-32 (2001) BindingDB Entry DOI: 10.7270/Q2R78FQP
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (Homo sapiens (Human))	BDBM50114044 (4-{2-[2-(3-Biphenyl-4-yl-5-methyl-[1,2,4]triazol-4...) Show SMILES Cc1nnc(-c2ccc(cc2)-c2ccccc2)n1-c1ccccc1OCCC1CCNCC1 |(12.17,-.12,;10.79,-.82,;9.49,.02,;8.3,-.94,;8.86,-2.39,;8.02,-3.68,;6.47,-3.61,;5.64,-4.89,;6.34,-6.26,;7.87,-6.34,;8.71,-5.05,;5.5,-7.55,;6.2,-8.93,;5.35,-10.22,;3.81,-10.14,;3.11,-8.75,;3.96,-7.46,;10.4,-2.31,;11.41,-3.46,;10.92,-4.91,;11.94,-6.06,;13.44,-5.75,;13.93,-4.28,;12.9,-3.14,;13.39,-1.68,;14.76,-1,;16.05,-1.85,;15.96,-3.4,;14.56,-4.07,;14.47,-5.61,;15.75,-6.46,;17.13,-5.78,;17.24,-4.24,)| Show InChI InChI=1S/C28H30N4O/c1-21-30-31-28(25-13-11-24(12-14-25)23-7-3-2-4-8-23)32(21)26-9-5-6-10-27(26)33-20-17-22-15-18-29-19-16-22/h2-14,22,29H,15-20H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	55.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at cloned human Vasopressin V1a receptor stably expressed in CHO cells, using [3H]-AVP as radioligand				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (RAT)	BDBM50114032 (CHEMBL86577 | {4-[2-(3-Biphenyl-4-yl-5-methyl-[1,2...) Show SMILES CN1CCN(CC1)C(=O)c1ccc(COc2ccccc2-n2c(C)nnc2-c2ccc(cc2)-c2ccccc2)cc1 |(15.94,-10.56,;16.17,-9.05,;17.64,-8.58,;17.99,-7.08,;16.85,-6.05,;15.38,-6.5,;15.04,-8,;18.02,-5.05,;19.47,-5.59,;17.76,-3.54,;16.31,-3,;16.06,-1.48,;17.25,-.5,;16.99,1.02,;15.54,1.54,;14.3,.65,;14.47,-.89,;13.23,-1.8,;11.82,-1.17,;11.66,.37,;12.9,1.26,;12.74,2.8,;13.93,3.78,;15.46,3.54,;13.37,5.2,;11.84,5.11,;11.45,3.61,;10.02,3.05,;8.81,4.02,;7.38,3.45,;7.16,1.93,;8.35,.97,;9.79,1.53,;5.71,1.37,;5.47,-.16,;4.04,-.71,;2.83,.25,;3.08,1.79,;4.52,2.34,;18.69,-1.04,;18.95,-2.55,)| Show InChI InChI=1S/C34H33N5O2/c1-25-35-36-33(29-18-16-28(17-19-29)27-8-4-3-5-9-27)39(25)31-10-6-7-11-32(31)41-24-26-12-14-30(15-13-26)34(40)38-22-20-37(2)21-23-38/h3-19H,20-24H2,1-2H3	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	62.7	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at Vasopressin V1a receptor, performed using [3H]-AVP on rat liver				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V2 receptor (Rattus norvegicus (Rat))	BDBM50108500 (2-Methyl-furan-3-carboxylic acid [4-(methyl-{4-met...) Show SMILES CN(C(=O)c1ccc(NC(=O)c2ccoc2C)cc1)c1ccc(C)cc1OCCCCCC(=O)N1CCN(C)CC1 Show InChI InChI=1S/C32H40N4O5/c1-23-9-14-28(29(22-23)41-20-7-5-6-8-30(37)36-18-16-34(3)17-19-36)35(4)32(39)25-10-12-26(13-11-25)33-31(38)27-15-21-40-24(27)2/h9-15,21-22H,5-8,16-20H2,1-4H3,(H,33,38)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	73	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Evaluated for the binding affinity towards vasopressin (V2) receptor in rat kidney membrane using [3H]AVP as radioligand				Bioorg Med Chem Lett 12: 229-32 (2001) BindingDB Entry DOI: 10.7270/Q2R78FQP
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (RAT)	BDBM50366798 (CHEMBL1794053) Show SMILES Nc1nc(cs1)-c1ccc2NC(=O)C(=Cc3cc(Br)c(O)c(Br)c3)c2c1 Show InChI InChI=1S/C18H11Br2N3O2S/c19-12-4-8(5-13(20)16(12)24)3-11-10-6-9(15-7-26-18(21)23-15)1-2-14(10)22-17(11)25/h1-7,24H,(H2,21,23)(H,22,25)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	79	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Evaluated for the binding affinity towards vasopressin (V1A) receptor in rat liver membrane using [3H]AVP as radioligand				Bioorg Med Chem Lett 12: 229-32 (2001) BindingDB Entry DOI: 10.7270/Q2R78FQP
					More data for this Ligand-Target Pair
Vasopressin V2 receptor (Rattus norvegicus (Rat))	BDBM50108494 (2-Methyl-furan-3-carboxylic acid (4-{[2-(6-[1,4']b...) Show SMILES CN(C(=O)c1ccc(NC(=O)c2ccoc2C)cc1)c1ccc(C)cc1OCCCCCC(=O)N1CCC(CC1)N1CCCCC1 Show InChI InChI=1S/C37H48N4O5/c1-27-11-16-33(39(3)37(44)29-12-14-30(15-13-29)38-36(43)32-19-25-45-28(32)2)34(26-27)46-24-9-4-6-10-35(42)41-22-17-31(18-23-41)40-20-7-5-8-21-40/h11-16,19,25-26,31H,4-10,17-18,20-24H2,1-3H3,(H,38,43)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	95	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Evaluated for the binding affinity towards vasopressin (V2) receptor in rat kidney membrane using [3H]AVP as radioligand				Bioorg Med Chem Lett 12: 229-32 (2001) BindingDB Entry DOI: 10.7270/Q2R78FQP
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (Homo sapiens (Human))	BDBM50114035 (3-Biphenyl-4-yl-4-(2-methoxy-phenyl)-5-methyl-4H-[...) Show SMILES COc1ccccc1-n1c(C)nnc1-c1ccc(cc1)-c1ccccc1 |(18.22,-5.11,;16.73,-4.71,;15.64,-5.81,;16.04,-7.28,;14.95,-8.38,;13.47,-7.98,;13.07,-6.5,;14.17,-5.41,;13.77,-3.93,;14.8,-2.77,;16.34,-2.77,;14.01,-1.43,;12.51,-1.76,;12.35,-3.3,;11.02,-4.08,;9.68,-3.32,;8.36,-4.1,;8.37,-5.63,;9.7,-6.41,;11.04,-5.63,;7.04,-6.41,;7.04,-7.96,;5.69,-8.73,;4.36,-7.96,;4.36,-6.41,;5.69,-5.64,)| Show InChI InChI=1S/C22H19N3O/c1-16-23-24-22(25(16)20-10-6-7-11-21(20)26-2)19-14-12-18(13-15-19)17-8-4-3-5-9-17/h3-15H,1-2H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	120	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at cloned human Vasopressin V1a receptor stably expressed in CHO cells, using [3H]-AVP as radioligand				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V2 receptor (Rattus norvegicus (Rat))	BDBM50366798 (CHEMBL1794053) Show SMILES Nc1nc(cs1)-c1ccc2NC(=O)C(=Cc3cc(Br)c(O)c(Br)c3)c2c1 Show InChI InChI=1S/C18H11Br2N3O2S/c19-12-4-8(5-13(20)16(12)24)3-11-10-6-9(15-7-26-18(21)23-15)1-2-14(10)22-17(11)25/h1-7,24H,(H2,21,23)(H,22,25)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	168	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Evaluated for the binding affinity towards vasopressin (V2) receptor in rat kidney membrane using [3H]AVP as radioligand				Bioorg Med Chem Lett 12: 229-32 (2001) BindingDB Entry DOI: 10.7270/Q2R78FQP
					More data for this Ligand-Target Pair
Vasopressin V2 receptor (Homo sapiens (Human))	BDBM50114031 ((2S)-1-[(2R,3S)-5-chloro-3-(2-chlorophenyl)-1-(3,4...) Show SMILES COc1ccc(cc1OC)S(=O)(=O)N1[C@@H](C(=O)N2CCC[C@H]2C(N)=O)[C@](O)(c2cc(Cl)ccc12)c1ccccc1Cl |r| Show InChI InChI=1S/C28H27Cl2N3O7S/c1-39-23-12-10-17(15-24(23)40-2)41(37,38)33-21-11-9-16(29)14-19(21)28(36,18-6-3-4-7-20(18)30)25(33)27(35)32-13-5-8-22(32)26(31)34/h3-4,6-7,9-12,14-15,22,25,36H,5,8,13H2,1-2H3,(H2,31,34)/t22-,25-,28+/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents	PubMed	178	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at cloned human Vasopressin V2 receptor stably expressed in CHO cells, using [3H]-AVP as radioligand				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (Homo sapiens (Human))	BDBM50114046 (1-{6-[3-(3-Biphenyl-4-yl-5-methyl-[1,2,4]triazol-4...) Show SMILES CN1CCN(CCCCCCOc2cccc(c2)-n2c(C)nnc2-c2ccc(cc2)-c2ccccc2)CC1 Show InChI InChI=1S/C32H39N5O/c1-26-33-34-32(29-17-15-28(16-18-29)27-11-6-5-7-12-27)37(26)30-13-10-14-31(25-30)38-24-9-4-3-8-19-36-22-20-35(2)21-23-36/h5-7,10-18,25H,3-4,8-9,19-24H2,1-2H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	214	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at cloned human Vasopressin V1a receptor stably expressed in CHO cells, using [3H]-AVP as radioligand				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V2 receptor (Rattus norvegicus (Rat))	BDBM50114031 ((2S)-1-[(2R,3S)-5-chloro-3-(2-chlorophenyl)-1-(3,4...) Show SMILES COc1ccc(cc1OC)S(=O)(=O)N1[C@@H](C(=O)N2CCC[C@H]2C(N)=O)[C@](O)(c2cc(Cl)ccc12)c1ccccc1Cl |r| Show InChI InChI=1S/C28H27Cl2N3O7S/c1-39-23-12-10-17(15-24(23)40-2)41(37,38)33-21-11-9-16(29)14-19(21)28(36,18-6-3-4-7-20(18)30)25(33)27(35)32-13-5-8-22(32)26(31)34/h3-4,6-7,9-12,14-15,22,25,36H,5,8,13H2,1-2H3,(H2,31,34)/t22-,25-,28+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents	PubMed	285	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at Vasopressin V2 receptor, performed using [3H]-AVP on rat kidney				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V1a receptor (RAT)	BDBM50108497 (2-Methyl-furan-3-carboxylic acid (4-{[4'-([1,4']bi...) Show SMILES CN(C(=O)c1ccc(NC(=O)c2ccoc2C)cc1)c1ccccc1-c1ccc(cc1)C(=O)N1CCC(CC1)N1CCCCC1 Show InChI InChI=1S/C37H40N4O4/c1-26-32(20-25-45-26)35(42)38-30-16-14-28(15-17-30)36(43)39(2)34-9-5-4-8-33(34)27-10-12-29(13-11-27)37(44)41-23-18-31(19-24-41)40-21-6-3-7-22-40/h4-5,8-17,20,25,31H,3,6-7,18-19,21-24H2,1-2H3,(H,38,42)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	335	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Evaluated for the binding affinity towards vasopressin (V1A) receptor in rat liver membrane using [3H]AVP as radioligand				Bioorg Med Chem Lett 12: 229-32 (2001) BindingDB Entry DOI: 10.7270/Q2R78FQP
					More data for this Ligand-Target Pair
Vasopressin V2 receptor (Rattus norvegicus (Rat))	BDBM50114032 (CHEMBL86577 | {4-[2-(3-Biphenyl-4-yl-5-methyl-[1,2...) Show SMILES CN1CCN(CC1)C(=O)c1ccc(COc2ccccc2-n2c(C)nnc2-c2ccc(cc2)-c2ccccc2)cc1 |(15.94,-10.56,;16.17,-9.05,;17.64,-8.58,;17.99,-7.08,;16.85,-6.05,;15.38,-6.5,;15.04,-8,;18.02,-5.05,;19.47,-5.59,;17.76,-3.54,;16.31,-3,;16.06,-1.48,;17.25,-.5,;16.99,1.02,;15.54,1.54,;14.3,.65,;14.47,-.89,;13.23,-1.8,;11.82,-1.17,;11.66,.37,;12.9,1.26,;12.74,2.8,;13.93,3.78,;15.46,3.54,;13.37,5.2,;11.84,5.11,;11.45,3.61,;10.02,3.05,;8.81,4.02,;7.38,3.45,;7.16,1.93,;8.35,.97,;9.79,1.53,;5.71,1.37,;5.47,-.16,;4.04,-.71,;2.83,.25,;3.08,1.79,;4.52,2.34,;18.69,-1.04,;18.95,-2.55,)| Show InChI InChI=1S/C34H33N5O2/c1-25-35-36-33(29-18-16-28(17-19-29)27-8-4-3-5-9-27)39(25)31-10-6-7-11-32(31)41-24-26-12-14-30(15-13-26)34(40)38-22-20-37(2)21-23-38/h3-19H,20-24H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	364	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Binding affinity at Vasopressin V2 receptor, performed using [3H]-AVP on rat kidney				J Med Chem 45: 2589-98 (2002) BindingDB Entry DOI: 10.7270/Q2NC60H9
					More data for this Ligand-Target Pair
Vasopressin V2 receptor (Rattus norvegicus (Rat))	BDBM50108499 (1N-methyl-1N-{4-methyl-2-[4-(4-methylhexahydro-1-p...) Show SMILES CCc1nccn1-c1ccccc1C(=O)Nc1ccc(cc1)C(=O)N(C)c1ccc(C)cc1OCc1ccc(cc1)C(=O)N1CCN(C)CC1 Show InChI InChI=1S/C40H42N6O4/c1-5-37-41-20-21-46(37)34-9-7-6-8-33(34)38(47)42-32-17-15-30(16-18-32)39(48)44(4)35-19-10-28(2)26-36(35)50-27-29-11-13-31(14-12-29)40(49)45-24-22-43(3)23-25-45/h6-21,26H,5,22-25,27H2,1-4H3,(H,42,47)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	445	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Yamanouchi Pharmaceutical Co. Ltd. Curated by ChEMBL					Assay Description Evaluated for the binding affinity towards vasopressin (V2) receptor in rat kidney membrane using [3H]AVP as radioligand				Bioorg Med Chem Lett 12: 229-32 (2001) BindingDB Entry DOI: 10.7270/Q2R78FQP
					More data for this Ligand-Target Pair

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