Compile Data Set for Download or QSAR

Found 17 hits with Last Name = 'harms' and Initial = 'h'   

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
Carboxypeptidase A1 (Homo sapiens (Human))	BDBM50478894 (Anabaenopeptin G) Show SMILES [H][C@]1(NC(=O)[C@H](CCc2ccc(O)cc2)N(C)C(=O)[C@H](CCc2ccc(O)cc2)NC(=O)[C@@]([H])(NC(=O)[C@@H](CCCCNC1=O)NC(=O)N[C@@H](Cc1ccc(O)cc1)C(O)=O)[C@@H](C)CC)[C@@H](C)CC |r| Show InChI InChI=1S/C49H67N7O11/c1-6-29(3)41-45(62)50-27-9-8-10-37(52-49(67)53-39(48(65)66)28-33-15-23-36(59)24-16-33)43(60)54-42(30(4)7-2)46(63)51-38(25-17-31-11-19-34(57)20-12-31)47(64)56(5)40(44(61)55-41)26-18-32-13-21-35(58)22-14-32/h11-16,19-24,29-30,37-42,57-59H,6-10,17-18,25-28H2,1-5H3,(H,50,62)(H,51,63)(H,54,60)(H,55,61)(H,65,66)(H2,52,53,67)/t29-,30-,37+,38-,39-,40-,41-,42-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of carboxypeptidase A (unknown origin) assessed as reduction in hydrolysis of hippuryl-L-phenylalanine using hippuryl-L-phenylalanine as s...				Citation and Details Article DOI: 10.1016/j.bmcl.2016.09.008 BindingDB Entry DOI: 10.7270/Q2XP78MX
					More data for this Ligand-Target Pair
Carboxypeptidase A1 (Bos taurus (bovine))	BDBM50478892 (Anabaenopeptin T) Show SMILES [H][C@]1(NC(=O)[C@H](CCc2ccc(O)cc2)N(C)C(=O)[C@H](CCc2ccc(O)cc2)NC(=O)[C@@H](NC(=O)[C@@H](CCCCNC1=O)NC(=O)N[C@@H]([C@@H](C)CC)C(O)=O)C(C)C)[C@@H](C)CC |r| Show InChI InChI=1S/C45H67N7O10/c1-8-27(5)37-41(57)46-25-11-10-12-33(48-45(62)51-38(44(60)61)28(6)9-2)39(55)49-36(26(3)4)42(58)47-34(23-17-29-13-19-31(53)20-14-29)43(59)52(7)35(40(56)50-37)24-18-30-15-21-32(54)22-16-30/h13-16,19-22,26-28,33-38,53-54H,8-12,17-18,23-25H2,1-7H3,(H,46,57)(H,47,58)(H,49,55)(H,50,56)(H,60,61)(H2,48,51,62)/t27-,28-,33+,34-,35-,36-,37-,38-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of carboxypeptidase A in bovine pancreas assessed as reduction in hydrolysis of hippuryl-L-phenylalanine using hippuryl-L-phenylalanine as...				Citation and Details Article DOI: 10.1016/j.bmcl.2016.09.008 BindingDB Entry DOI: 10.7270/Q2XP78MX
					More data for this Ligand-Target Pair
Carboxypeptidase A1 (Homo sapiens (Human))	BDBM50478893 (Anabaenopeptin H) Show SMILES [H][C@]1(NC(=O)[C@H](CCc2ccc(O)cc2)N(C)C(=O)[C@H](CCc2ccc(O)cc2)NC(=O)[C@@]([H])(NC(=O)[C@@H](CCCCNC1=O)NC(=O)N[C@@H](CCCNC(N)=N)C(O)=O)[C@@H](C)CC)[C@@H](C)CC |r| Show InChI InChI=1S/C46H70N10O10/c1-6-27(3)37-41(61)49-25-9-8-11-33(52-46(66)53-35(44(64)65)12-10-26-50-45(47)48)39(59)54-38(28(4)7-2)42(62)51-34(23-17-29-13-19-31(57)20-14-29)43(63)56(5)36(40(60)55-37)24-18-30-15-21-32(58)22-16-30/h13-16,19-22,27-28,33-38,57-58H,6-12,17-18,23-26H2,1-5H3,(H,49,61)(H,51,62)(H,54,59)(H,55,60)(H,64,65)(H4,47,48,50)(H2,52,53,66)/t27-,28-,33+,34-,35-,36-,37-,38-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of carboxypeptidase A (unknown origin) assessed as reduction in hydrolysis of hippuryl-L-phenylalanine using hippuryl-L-phenylalanine as s...				Citation and Details Article DOI: 10.1016/j.bmcl.2016.09.008 BindingDB Entry DOI: 10.7270/Q2XP78MX
					More data for this Ligand-Target Pair
Carboxypeptidase A1 (Homo sapiens (Human))	BDBM50558425 (CHEMBL4746522) Show SMILES CC(C)[C@@H]1NC(=O)[C@@H](CCCCNC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](C)N(C)C(=O)[C@H](CCc2ccc(O)cc2)NC1=O)NC(N)=O |r| Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.74E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of carboxypeptidase A (unknown origin) assessed as reduction in degradation of N-(4-methoxyphenylazoformyl)-Phe-OH using N-(4-methoxypheny...				Citation and Details Article DOI: 10.1016/j.bmcl.2016.09.008 BindingDB Entry DOI: 10.7270/Q2XP78MX
					More data for this Ligand-Target Pair
N-arachidonyl glycine receptor (Homo sapiens (Human))	BDBM50448075 (CHEMBL1258979) Show SMILES CC(C)=C[C@H]1C[C@]2(C)[C@H](CC[C@@]3(C)[C@H]2CC[C@H]2Cc4c([nH]c5ccccc45)[C@]32C)O1 |r,wU:11.11,6.6,8.33,13.14,wD:16.17,27.32,4.3,(32.2,-12.88,;30.67,-12.87,;29.92,-11.54,;29.89,-14.18,;28.36,-14.17,;27.46,-12.9,;25.97,-13.36,;25.95,-11.85,;25.95,-14.93,;24.6,-15.69,;23.27,-14.91,;23.28,-13.37,;23.27,-11.84,;24.63,-12.61,;24.63,-11.06,;23.29,-10.28,;21.95,-11.05,;20.48,-10.57,;19.59,-11.84,;20.48,-13.08,;19.57,-14.32,;18.11,-13.84,;16.79,-14.61,;15.46,-13.84,;15.46,-12.31,;16.78,-11.54,;18.11,-12.3,;21.95,-12.6,;21.94,-14.13,;27.43,-15.42,)| Show InChI InChI=1S/C28H37NO/c1-17(2)14-19-16-26(3)23-11-10-18-15-21-20-8-6-7-9-22(20)29-25(21)28(18,5)27(23,4)13-12-24(26)30-19/h6-9,14,18-19,23-24,29H,10-13,15-16H2,1-5H3/t18-,19-,23-,24-,26-,27-,28+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.91E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inverse agonist activity at human GPR18 expressed in CHO cells assessed as inhibition of 7.5 uM THC-mediated beta-arrestin recruitment after 90 mins ...				J Nat Prod 77: 673-7 (2014) Article DOI: 10.1021/np400850g BindingDB Entry DOI: 10.7270/Q2154JJZ
					More data for this Ligand-Target Pair
G-protein coupled receptor 55 (Homo sapiens (Human))	BDBM50448073 (CHEMBL3120631) Show SMILES CC(C)=CCC[C@]1(C)[C@H](CC[C@@]2(C)[C@H]1CC[C@H]1Cc3c([nH]c4ccccc34)[C@]21C)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O |r,wU:30.34,39.45,37.42,32.37,13.14,11.11,6.6,8.33,wD:35.40,16.17,27.32,6.5,(20.66,-6.65,;19.17,-6.25,;18.78,-4.76,;18.09,-7.35,;16.6,-6.94,;15.51,-8.04,;14.03,-7.64,;14.78,-6.3,;14,-9.19,;12.65,-9.94,;11.33,-9.15,;11.35,-7.61,;11.35,-6.07,;12.7,-6.86,;12.71,-5.32,;11.38,-4.53,;10.05,-5.29,;8.59,-4.81,;7.68,-6.06,;8.57,-7.31,;7.68,-8.55,;6.21,-8.08,;4.87,-8.86,;3.54,-8.09,;3.54,-6.54,;4.87,-5.77,;6.21,-6.53,;10.04,-6.84,;10.02,-8.37,;15.33,-9.98,;15.37,-11.51,;14.06,-12.32,;14.1,-13.84,;12.79,-14.65,;11.44,-13.92,;15.45,-14.58,;15.48,-16.11,;16.75,-13.78,;18.1,-14.51,;16.71,-12.24,;18.02,-11.44,)| Show InChI InChI=1S/C34H49NO6/c1-19(2)9-8-15-32(3)25-13-12-20-17-22-21-10-6-7-11-23(21)35-30(22)34(20,5)33(25,4)16-14-26(32)41-31-29(39)28(38)27(37)24(18-36)40-31/h6-7,9-11,20,24-29,31,35-39H,8,12-18H2,1-5H3/t20-,24+,25-,26-,27+,28-,29-,31-,32-,33-,34+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Antagonist activity at human GPR55 expressed in CHO cells assessed as inhibition of LPI-mediated beta-arrestin recruitment after 90 mins by beta-gala...				J Nat Prod 77: 673-7 (2014) Article DOI: 10.1021/np400850g BindingDB Entry DOI: 10.7270/Q2154JJZ
					More data for this Ligand-Target Pair
G-protein coupled receptor 55 (Homo sapiens (Human))	BDBM50448076 (CHEMBL3120632) Show SMILES COC(C)(C)\C=C\C[C@]1(C)[C@@H](O)CC[C@@]2(C)[C@H]1CC[C@H]1Cc3c([nH]c4ccccc34)[C@]21C |r| Show InChI InChI=1S/C29H41NO2/c1-26(2,32-6)15-9-16-27(3)23-13-12-19-18-21-20-10-7-8-11-22(20)30-25(21)29(19,5)28(23,4)17-14-24(27)31/h7-11,15,19,23-24,30-31H,12-14,16-18H2,1-6H3/b15-9+/t19-,23-,24-,27-,28-,29+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Antagonist activity at human GPR55 expressed in CHO cells assessed as inhibition of LPI-mediated beta-arrestin recruitment after 90 mins by beta-gala...				J Nat Prod 77: 673-7 (2014) Article DOI: 10.1021/np400850g BindingDB Entry DOI: 10.7270/Q2154JJZ
					More data for this Ligand-Target Pair
G-protein coupled receptor 55 (Homo sapiens (Human))	BDBM50448075 (CHEMBL1258979) Show SMILES CC(C)=C[C@H]1C[C@]2(C)[C@H](CC[C@@]3(C)[C@H]2CC[C@H]2Cc4c([nH]c5ccccc45)[C@]32C)O1 |r,wU:11.11,6.6,8.33,13.14,wD:16.17,27.32,4.3,(32.2,-12.88,;30.67,-12.87,;29.92,-11.54,;29.89,-14.18,;28.36,-14.17,;27.46,-12.9,;25.97,-13.36,;25.95,-11.85,;25.95,-14.93,;24.6,-15.69,;23.27,-14.91,;23.28,-13.37,;23.27,-11.84,;24.63,-12.61,;24.63,-11.06,;23.29,-10.28,;21.95,-11.05,;20.48,-10.57,;19.59,-11.84,;20.48,-13.08,;19.57,-14.32,;18.11,-13.84,;16.79,-14.61,;15.46,-13.84,;15.46,-12.31,;16.78,-11.54,;18.11,-12.3,;21.95,-12.6,;21.94,-14.13,;27.43,-15.42,)| Show InChI InChI=1S/C28H37NO/c1-17(2)14-19-16-26(3)23-11-10-18-15-21-20-8-6-7-9-22(20)29-25(21)28(18,5)27(23,4)13-12-24(26)30-19/h6-9,14,18-19,23-24,29H,10-13,15-16H2,1-5H3/t18-,19-,23-,24-,26-,27-,28+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Antagonist activity at human GPR55 expressed in CHO cells assessed as inhibition of LPI-mediated beta-arrestin recruitment after 90 mins by beta-gala...				J Nat Prod 77: 673-7 (2014) Article DOI: 10.1021/np400850g BindingDB Entry DOI: 10.7270/Q2154JJZ
					More data for this Ligand-Target Pair
G-protein coupled receptor 55 (Homo sapiens (Human))	BDBM50448074 (Emindole Sb) Show SMILES CC(C)=CCC[C@]1(C)[C@@H](O)CC[C@@]2(C)[C@H]1CC[C@H]1Cc3c([nH]c4ccccc34)[C@]21C |r,wU:12.12,6.6,8.8,14.15,wD:17.18,28.33,6.5,(7.26,-25.92,;7.27,-24.39,;8.61,-23.64,;5.95,-23.62,;5.97,-22.09,;4.62,-21.3,;3.28,-22.08,;3.27,-20.55,;3.27,-23.63,;4.61,-24.41,;1.92,-24.4,;.59,-23.61,;.6,-22.07,;.59,-20.54,;1.94,-21.31,;1.95,-19.76,;.6,-18.98,;-.73,-19.75,;-2.2,-19.27,;-3.1,-20.54,;-2.21,-21.78,;-3.12,-23.02,;-4.58,-22.54,;-5.91,-23.31,;-7.23,-22.54,;-7.23,-21.01,;-5.91,-20.24,;-4.58,-21,;-.73,-21.3,;-.75,-22.83,)| Show InChI InChI=1S/C28H39NO/c1-18(2)9-8-15-26(3)23-13-12-19-17-21-20-10-6-7-11-22(20)29-25(21)28(19,5)27(23,4)16-14-24(26)30/h6-7,9-11,19,23-24,29-30H,8,12-17H2,1-5H3/t19-,23-,24-,26-,27-,28+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Antagonist activity at human GPR55 expressed in CHO cells assessed as inhibition of LPI-mediated beta-arrestin recruitment after 90 mins by beta-gala...				J Nat Prod 77: 673-7 (2014) Article DOI: 10.1021/np400850g BindingDB Entry DOI: 10.7270/Q2154JJZ
					More data for this Ligand-Target Pair
N-arachidonyl glycine receptor (Homo sapiens (Human))	BDBM50448073 (CHEMBL3120631) Show SMILES CC(C)=CCC[C@]1(C)[C@H](CC[C@@]2(C)[C@H]1CC[C@H]1Cc3c([nH]c4ccccc34)[C@]21C)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]1O |r,wU:30.34,39.45,37.42,32.37,13.14,11.11,6.6,8.33,wD:35.40,16.17,27.32,6.5,(20.66,-6.65,;19.17,-6.25,;18.78,-4.76,;18.09,-7.35,;16.6,-6.94,;15.51,-8.04,;14.03,-7.64,;14.78,-6.3,;14,-9.19,;12.65,-9.94,;11.33,-9.15,;11.35,-7.61,;11.35,-6.07,;12.7,-6.86,;12.71,-5.32,;11.38,-4.53,;10.05,-5.29,;8.59,-4.81,;7.68,-6.06,;8.57,-7.31,;7.68,-8.55,;6.21,-8.08,;4.87,-8.86,;3.54,-8.09,;3.54,-6.54,;4.87,-5.77,;6.21,-6.53,;10.04,-6.84,;10.02,-8.37,;15.33,-9.98,;15.37,-11.51,;14.06,-12.32,;14.1,-13.84,;12.79,-14.65,;11.44,-13.92,;15.45,-14.58,;15.48,-16.11,;16.75,-13.78,;18.1,-14.51,;16.71,-12.24,;18.02,-11.44,)| Show InChI InChI=1S/C34H49NO6/c1-19(2)9-8-15-32(3)25-13-12-20-17-22-21-10-6-7-11-23(21)35-30(22)34(20,5)33(25,4)16-14-26(32)41-31-29(39)28(38)27(37)24(18-36)40-31/h6-7,9-11,20,24-29,31,35-39H,8,12-18H2,1-5H3/t20-,24+,25-,26-,27+,28-,29-,31-,32-,33-,34+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Antagonist activity at human GPR18 expressed in CHO cells assessed as inhibition of 10 uM THC-mediated beta-arrestin recruitment after 90 mins by bet...				J Nat Prod 77: 673-7 (2014) Article DOI: 10.1021/np400850g BindingDB Entry DOI: 10.7270/Q2154JJZ
					More data for this Ligand-Target Pair
N-arachidonyl glycine receptor (Homo sapiens (Human))	BDBM50448074 (Emindole Sb) Show SMILES CC(C)=CCC[C@]1(C)[C@@H](O)CC[C@@]2(C)[C@H]1CC[C@H]1Cc3c([nH]c4ccccc34)[C@]21C |r,wU:12.12,6.6,8.8,14.15,wD:17.18,28.33,6.5,(7.26,-25.92,;7.27,-24.39,;8.61,-23.64,;5.95,-23.62,;5.97,-22.09,;4.62,-21.3,;3.28,-22.08,;3.27,-20.55,;3.27,-23.63,;4.61,-24.41,;1.92,-24.4,;.59,-23.61,;.6,-22.07,;.59,-20.54,;1.94,-21.31,;1.95,-19.76,;.6,-18.98,;-.73,-19.75,;-2.2,-19.27,;-3.1,-20.54,;-2.21,-21.78,;-3.12,-23.02,;-4.58,-22.54,;-5.91,-23.31,;-7.23,-22.54,;-7.23,-21.01,;-5.91,-20.24,;-4.58,-21,;-.73,-21.3,;-.75,-22.83,)| Show InChI InChI=1S/C28H39NO/c1-18(2)9-8-15-26(3)23-13-12-19-17-21-20-10-6-7-11-22(20)29-25(21)28(19,5)27(23,4)16-14-24(26)30/h6-7,9-11,19,23-24,29-30H,8,12-17H2,1-5H3/t19-,23-,24-,26-,27-,28+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Antagonist activity at human GPR18 expressed in CHO cells assessed as inhibition of 10 uM THC-mediated beta-arrestin recruitment after 90 mins by bet...				J Nat Prod 77: 673-7 (2014) Article DOI: 10.1021/np400850g BindingDB Entry DOI: 10.7270/Q2154JJZ
					More data for this Ligand-Target Pair
Carboxypeptidase A1 (Homo sapiens (Human))	BDBM50478893 (Anabaenopeptin H) Show SMILES [H][C@]1(NC(=O)[C@H](CCc2ccc(O)cc2)N(C)C(=O)[C@H](CCc2ccc(O)cc2)NC(=O)[C@@]([H])(NC(=O)[C@@H](CCCCNC1=O)NC(=O)N[C@@H](CCCNC(N)=N)C(O)=O)[C@@H](C)CC)[C@@H](C)CC |r| Show InChI InChI=1S/C46H70N10O10/c1-6-27(3)37-41(61)49-25-9-8-11-33(52-46(66)53-35(44(64)65)12-10-26-50-45(47)48)39(59)54-38(28(4)7-2)42(62)51-34(23-17-29-13-19-31(57)20-14-29)43(63)56(5)36(40(60)55-37)24-18-30-15-21-32(58)22-16-30/h13-16,19-22,27-28,33-38,57-58H,6-12,17-18,23-26H2,1-5H3,(H,49,61)(H,51,62)(H,54,59)(H,55,60)(H,64,65)(H4,47,48,50)(H2,52,53,66)/t27-,28-,33+,34-,35-,36-,37-,38-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.02E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of carboxypeptidase A (unknown origin) assessed as reduction in degradation of N-(4-methoxyphenylazoformyl)-Phe-OH using N-(4-methoxypheny...				Citation and Details Article DOI: 10.1016/j.bmcl.2016.09.008 BindingDB Entry DOI: 10.7270/Q2XP78MX
					More data for this Ligand-Target Pair
Carboxypeptidase A1 (Homo sapiens (Human))	BDBM50558424 (Anabaenopeptin 908) Show SMILES [H][C@]1(NC(=O)[C@H](CCc2ccc(O)cc2)N(C)C(=O)[C@H](CCc2ccc(O)cc2)NC(=O)[C@@H](NC(=O)[C@@H](CCCCNC1=O)NC(=O)N[C@@H](CCCNC(N)=N)C(O)=O)C(C)C)[C@@H](C)CC |r| Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of carboxypeptidase A (unknown origin) assessed as reduction in degradation of N-(4-methoxyphenylazoformyl)-Phe-OH using N-(4-methoxypheny...				Citation and Details Article DOI: 10.1016/j.bmcl.2016.09.008 BindingDB Entry DOI: 10.7270/Q2XP78MX
					More data for this Ligand-Target Pair
N-arachidonyl glycine receptor (Homo sapiens (Human))	BDBM50448076 (CHEMBL3120632) Show SMILES COC(C)(C)\C=C\C[C@]1(C)[C@@H](O)CC[C@@]2(C)[C@H]1CC[C@H]1Cc3c([nH]c4ccccc34)[C@]21C |r| Show InChI InChI=1S/C29H41NO2/c1-26(2,32-6)15-9-16-27(3)23-13-12-19-18-21-20-10-7-8-11-22(20)30-25(21)29(19,5)28(23,4)17-14-24(27)31/h7-11,15,19,23-24,30-31H,12-14,16-18H2,1-6H3/b15-9+/t19-,23-,24-,27-,28-,29+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.34E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Bonn Curated by ChEMBL					Assay Description Inverse agonist activity at human GPR18 expressed in CHO cells assessed as inhibition of 7.5 uM THC-mediated beta-arrestin recruitment after 90 mins ...				J Nat Prod 77: 673-7 (2014) Article DOI: 10.1021/np400850g BindingDB Entry DOI: 10.7270/Q2154JJZ
					More data for this Ligand-Target Pair
Carboxypeptidase A1 (Homo sapiens (Human))	BDBM50558424 (Anabaenopeptin 908) Show SMILES [H][C@]1(NC(=O)[C@H](CCc2ccc(O)cc2)N(C)C(=O)[C@H](CCc2ccc(O)cc2)NC(=O)[C@@H](NC(=O)[C@@H](CCCCNC1=O)NC(=O)N[C@@H](CCCNC(N)=N)C(O)=O)C(C)C)[C@@H](C)CC |r| Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	n/a	n/a	>2.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of carboxypeptidase A (unknown origin)				Citation and Details Article DOI: 10.1016/j.bmcl.2016.09.008 BindingDB Entry DOI: 10.7270/Q2XP78MX
					More data for this Ligand-Target Pair
Carboxypeptidase A1 (Homo sapiens (Human))	BDBM50089688 (ANABAENOPEPTIN B) Show SMILES CC(C)[C@@H]1NC(=O)[C@@H](CCCCNC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](C)N(C)C(=O)[C@H](CCc2ccc(O)cc2)NC1=O)NC(=O)N[C@@H](CCCNC(N)=N)C(O)=O |r| Show InChI InChI=1S/C41H60N10O9/c1-24(2)33-37(56)46-30(20-17-26-15-18-28(52)19-16-26)38(57)51(4)25(3)34(53)47-32(23-27-11-6-5-7-12-27)35(54)44-21-9-8-13-29(36(55)50-33)48-41(60)49-31(39(58)59)14-10-22-45-40(42)43/h5-7,11-12,15-16,18-19,24-25,29-33,52H,8-10,13-14,17,20-23H2,1-4H3,(H,44,54)(H,46,56)(H,47,53)(H,50,55)(H,58,59)(H4,42,43,45)(H2,48,49,60)/t25-,29+,30-,31-,32-,33-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of carboxypeptidase A (unknown origin) assessed as reduction in degradation of N-(4-methoxyphenylazoformyl)-Phe-OH using N-(4-methoxypheny...				Citation and Details Article DOI: 10.1016/j.bmcl.2016.09.008 BindingDB Entry DOI: 10.7270/Q2XP78MX
					More data for this Ligand-Target Pair
Carboxypeptidase A1 (Homo sapiens (Human))	BDBM50089687 (Anabaenopeptin F) Show SMILES [H][C@]1(NC(=O)[C@@H](CCCCNC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](C)N(C)C(=O)[C@H](CCc2ccc(O)cc2)NC1=O)NC(=O)N[C@@H](CCCNC(N)=N)C(O)=O)[C@@H](C)CC |r| Show InChI InChI=1S/C42H62N10O9/c1-5-25(2)34-38(57)47-31(21-18-27-16-19-29(53)20-17-27)39(58)52(4)26(3)35(54)48-33(24-28-12-7-6-8-13-28)36(55)45-22-10-9-14-30(37(56)51-34)49-42(61)50-32(40(59)60)15-11-23-46-41(43)44/h6-8,12-13,16-17,19-20,25-26,30-34,53H,5,9-11,14-15,18,21-24H2,1-4H3,(H,45,55)(H,47,57)(H,48,54)(H,51,56)(H,59,60)(H4,43,44,46)(H2,49,50,61)/t25-,26-,30+,31-,32-,33-,34-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of carboxypeptidase A (unknown origin) assessed as reduction in degradation of N-(4-methoxyphenylazoformyl)-Phe-OH using N-(4-methoxypheny...				Citation and Details Article DOI: 10.1016/j.bmcl.2016.09.008 BindingDB Entry DOI: 10.7270/Q2XP78MX
					More data for this Ligand-Target Pair