Compile Data Set for Download or QSAR

Found 44 hits with Last Name = 'bonnier' and Initial = 'b'   

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
Sodium-dependent noradrenaline transporter (Homo sapiens (Human))	BDBM50180524 ((R)-2-(2-methoxyphenyl)-1-((S)-morpholin-2-yl)-1-p...) Show SMILES COc1ccccc1C[C@](O)([C@@H]1CNCCO1)c1ccccc1 Show InChI InChI=1S/C19H23NO3/c1-22-17-10-6-5-7-15(17)13-19(21,16-8-3-2-4-9-16)18-14-20-11-12-23-18/h2-10,18,20-21H,11-14H2,1H3/t18-,19+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	3.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Eli Lilly and Company Curated by ChEMBL					Assay Description Binding affinity to NET				Bioorg Med Chem Lett 16: 2022-5 (2006) Article DOI: 10.1016/j.bmcl.2005.12.061 BindingDB Entry DOI: 10.7270/Q21J9BJ5
					More data for this Ligand-Target Pair
Sodium-dependent noradrenaline transporter (Homo sapiens (Human))	BDBM50180521 ((R)-2-biphenyl-2-yl-1-(S)-morpholin-2-yl-1-phenyl-...) Show SMILES O[C@@](Cc1ccccc1-c1ccccc1)([C@@H]1CNCCO1)c1ccccc1 Show InChI InChI=1S/C24H25NO2/c26-24(21-12-5-2-6-13-21,23-18-25-15-16-27-23)17-20-11-7-8-14-22(20)19-9-3-1-4-10-19/h1-14,23,25-26H,15-18H2/t23-,24+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	3.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Eli Lilly and Company Curated by ChEMBL					Assay Description Binding affinity to NET				Bioorg Med Chem Lett 16: 2022-5 (2006) Article DOI: 10.1016/j.bmcl.2005.12.061 BindingDB Entry DOI: 10.7270/Q21J9BJ5
					More data for this Ligand-Target Pair
Sodium-dependent noradrenaline transporter (Homo sapiens (Human))	BDBM50180531 ((R)-2-(2-ethoxyphenyl)-1-((S)-morpholin-2-yl)-1-ph...) Show SMILES CCOc1ccccc1C[C@](O)([C@@H]1CNCCO1)c1ccccc1 Show InChI InChI=1S/C20H25NO3/c1-2-23-18-11-7-6-8-16(18)14-20(22,17-9-4-3-5-10-17)19-15-21-12-13-24-19/h3-11,19,21-22H,2,12-15H2,1H3/t19-,20+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	5.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Eli Lilly and Company Curated by ChEMBL					Assay Description Binding affinity to NET				Bioorg Med Chem Lett 16: 2022-5 (2006) Article DOI: 10.1016/j.bmcl.2005.12.061 BindingDB Entry DOI: 10.7270/Q21J9BJ5
					More data for this Ligand-Target Pair
Sodium-dependent noradrenaline transporter (Homo sapiens (Human))	BDBM50180526 ((R)-2-(2-isopropoxyphenyl)-1-((S)-morpholin-2-yl)-...) Show SMILES CC(C)Oc1ccccc1C[C@](O)([C@@H]1CNCCO1)c1ccccc1 Show InChI InChI=1S/C21H27NO3/c1-16(2)25-19-11-7-6-8-17(19)14-21(23,18-9-4-3-5-10-18)20-15-22-12-13-24-20/h3-11,16,20,22-23H,12-15H2,1-2H3/t20-,21+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	7.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Eli Lilly and Company Curated by ChEMBL					Assay Description Binding affinity to NET				Bioorg Med Chem Lett 16: 2022-5 (2006) Article DOI: 10.1016/j.bmcl.2005.12.061 BindingDB Entry DOI: 10.7270/Q21J9BJ5
					More data for this Ligand-Target Pair
Sodium-dependent noradrenaline transporter (Homo sapiens (Human))	BDBM50180526 ((R)-2-(2-isopropoxyphenyl)-1-((S)-morpholin-2-yl)-...) Show SMILES CC(C)Oc1ccccc1C[C@](O)([C@@H]1CNCCO1)c1ccccc1 Show InChI InChI=1S/C21H27NO3/c1-16(2)25-19-11-7-6-8-17(19)14-21(23,18-9-4-3-5-10-18)20-15-22-12-13-24-20/h3-11,16,20,22-23H,12-15H2,1-2H3/t20-,21+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	7.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Eli Lilly and Company Curated by ChEMBL					Assay Description Binding affinity to NET				Bioorg Med Chem Lett 16: 2022-5 (2006) Article DOI: 10.1016/j.bmcl.2005.12.061 BindingDB Entry DOI: 10.7270/Q21J9BJ5
					More data for this Ligand-Target Pair
Sodium-dependent noradrenaline transporter (Homo sapiens (Human))	BDBM50180523 ((R)-2-(2-bromophenyl)-1-((S)-morpholin-2-yl)-1-phe...) Show SMILES O[C@@](Cc1ccccc1Br)([C@@H]1CNCCO1)c1ccccc1 Show InChI InChI=1S/C18H20BrNO2/c19-16-9-5-4-6-14(16)12-18(21,15-7-2-1-3-8-15)17-13-20-10-11-22-17/h1-9,17,20-21H,10-13H2/t17-,18+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	11.9	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Eli Lilly and Company Curated by ChEMBL					Assay Description Binding affinity to NET				Bioorg Med Chem Lett 16: 2022-5 (2006) Article DOI: 10.1016/j.bmcl.2005.12.061 BindingDB Entry DOI: 10.7270/Q21J9BJ5
					More data for this Ligand-Target Pair
Sodium-dependent noradrenaline transporter (Homo sapiens (Human))	BDBM50180525 ((R)-2-(2-chlorophenyl)-1-((S)-morpholin-2-yl)-1-ph...) Show SMILES O[C@@](Cc1ccccc1Cl)([C@@H]1CNCCO1)c1ccccc1 Show InChI InChI=1S/C18H20ClNO2/c19-16-9-5-4-6-14(16)12-18(21,15-7-2-1-3-8-15)17-13-20-10-11-22-17/h1-9,17,20-21H,10-13H2/t17-,18+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	30	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Eli Lilly and Company Curated by ChEMBL					Assay Description Binding affinity to NET				Bioorg Med Chem Lett 16: 2022-5 (2006) Article DOI: 10.1016/j.bmcl.2005.12.061 BindingDB Entry DOI: 10.7270/Q21J9BJ5
					More data for this Ligand-Target Pair
Sodium-dependent noradrenaline transporter (Homo sapiens (Human))	BDBM50180522 ((R)-1-((S)-morpholin-2-yl)-1-phenyl-2-(2-(trifluor...) Show SMILES O[C@@](Cc1ccccc1SC(F)(F)F)([C@@H]1CNCCO1)c1ccccc1 Show InChI InChI=1S/C19H20F3NO2S/c20-19(21,22)26-16-9-5-4-6-14(16)12-18(24,15-7-2-1-3-8-15)17-13-23-10-11-25-17/h1-9,17,23-24H,10-13H2/t17-,18+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	54.4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Eli Lilly and Company Curated by ChEMBL					Assay Description Binding affinity to NET				Bioorg Med Chem Lett 16: 2022-5 (2006) Article DOI: 10.1016/j.bmcl.2005.12.061 BindingDB Entry DOI: 10.7270/Q21J9BJ5
					More data for this Ligand-Target Pair
Sodium-dependent noradrenaline transporter (Homo sapiens (Human))	BDBM50180524 ((R)-2-(2-methoxyphenyl)-1-((S)-morpholin-2-yl)-1-p...) Show SMILES COc1ccccc1C[C@](O)([C@@H]1CNCCO1)c1ccccc1 Show InChI InChI=1S/C19H23NO3/c1-22-17-10-6-5-7-15(17)13-19(21,16-8-3-2-4-9-16)18-14-20-11-12-23-18/h2-10,18,20-21H,11-14H2,1H3/t18-,19+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	56	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Eli Lilly and Company Curated by ChEMBL					Assay Description Binding affinity to NET				Bioorg Med Chem Lett 16: 2022-5 (2006) Article DOI: 10.1016/j.bmcl.2005.12.061 BindingDB Entry DOI: 10.7270/Q21J9BJ5
					More data for this Ligand-Target Pair
Sodium-dependent noradrenaline transporter (Homo sapiens (Human))	BDBM50180527 ((R)-1-((S)-morpholin-2-yl)-1,2-diphenylethanol | C...) Show SMILES O[C@@](Cc1ccccc1)([C@@H]1CNCCO1)c1ccccc1 Show InChI InChI=1S/C18H21NO2/c20-18(16-9-5-2-6-10-16,17-14-19-11-12-21-17)13-15-7-3-1-4-8-15/h1-10,17,19-20H,11-14H2/t17-,18+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	148	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Eli Lilly and Company Curated by ChEMBL					Assay Description Binding affinity to NET				Bioorg Med Chem Lett 16: 2022-5 (2006) Article DOI: 10.1016/j.bmcl.2005.12.061 BindingDB Entry DOI: 10.7270/Q21J9BJ5
					More data for this Ligand-Target Pair
Sodium-dependent noradrenaline transporter (Homo sapiens (Human))	BDBM50180524 ((R)-2-(2-methoxyphenyl)-1-((S)-morpholin-2-yl)-1-p...) Show SMILES COc1ccccc1C[C@](O)([C@@H]1CNCCO1)c1ccccc1 Show InChI InChI=1S/C19H23NO3/c1-22-17-10-6-5-7-15(17)13-19(21,16-8-3-2-4-9-16)18-14-20-11-12-23-18/h2-10,18,20-21H,11-14H2,1H3/t18-,19+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	156	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Eli Lilly and Company Curated by ChEMBL					Assay Description Binding affinity to NET				Bioorg Med Chem Lett 16: 2022-5 (2006) Article DOI: 10.1016/j.bmcl.2005.12.061 BindingDB Entry DOI: 10.7270/Q21J9BJ5
					More data for this Ligand-Target Pair
Sodium-dependent noradrenaline transporter (Homo sapiens (Human))	BDBM50180524 ((R)-2-(2-methoxyphenyl)-1-((S)-morpholin-2-yl)-1-p...) Show SMILES COc1ccccc1C[C@](O)([C@@H]1CNCCO1)c1ccccc1 Show InChI InChI=1S/C19H23NO3/c1-22-17-10-6-5-7-15(17)13-19(21,16-8-3-2-4-9-16)18-14-20-11-12-23-18/h2-10,18,20-21H,11-14H2,1H3/t18-,19+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	161	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Eli Lilly and Company Curated by ChEMBL					Assay Description Binding affinity to NET				Bioorg Med Chem Lett 16: 2022-5 (2006) Article DOI: 10.1016/j.bmcl.2005.12.061 BindingDB Entry DOI: 10.7270/Q21J9BJ5
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase FKBP4 (Homo sapiens (Human))	BDBM50022815 ((3S,6S,9S,12R,15S,18S,21S,24S,30S,33S)-30-ethyl-33...) Show SMILES CC[C@@H]1NC(=O)[C@H]([C@H](O)[C@H](C)C\C=C\C)N(C)C(=O)[C@H](C(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](NC(=O)[C@H](CC(C)C)N(C)C(=O)CN(C)C1=O)C(C)C |r| Show InChI InChI=1S/C62H111N11O12/c1-25-27-28-40(15)52(75)51-56(79)65-43(26-2)58(81)67(18)33-48(74)68(19)44(29-34(3)4)55(78)66-49(38(11)12)61(84)69(20)45(30-35(5)6)54(77)63-41(16)53(76)64-42(17)57(80)70(21)46(31-36(7)8)59(82)71(22)47(32-37(9)10)60(83)72(23)50(39(13)14)62(85)73(51)24/h25,27,34-47,49-52,75H,26,28-33H2,1-24H3,(H,63,77)(H,64,76)(H,65,79)(H,66,78)/b27-25+/t40-,41+,42-,43+,44+,45+,46+,47+,49+,50+,51+,52-/m1/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE KEGG MMDB PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	16	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against hCyp-18 PPIase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase A (Homo sapiens (Human))	BDBM50369811 (CHEMBL1790316) Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@H](C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)CC(C)C)C(=O)NCc1ccccc1 Show InChI InChI=1S/C34H50N8O6/c1-6-22(4)30(34(48)36-17-24-11-8-7-9-12-24)41-33(47)27-13-10-14-42(27)29(44)19-37-31(45)23(5)39-32(46)26(16-25-18-35-20-38-25)40-28(43)15-21(2)3/h7-9,11-12,18,20-23,26-27,30H,6,10,13-17,19H2,1-5H3,(H,35,38)(H,36,48)(H,37,45)(H,39,46)(H,40,43)(H,41,47)/t22-,23-,26-,27-,30-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	6.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against human Peptidyl-prolyl isomerase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase FKBP4 (Homo sapiens (Human))	BDBM50068939 ((E)-(9S,12S,13R,14S,17R,21S,23S,24R,25S,27S)-17-Et...) Show SMILES CC[C@@H]1\C=C(C)\C[C@H](C)C[C@H](OC)[C@H]2O[C@](O)([C@H](C)C[C@@H]2OC)C(=O)C(=O)N2CCCC[C@H]2C(=O)O[C@@H]([C@H](C)[C@@H](O)CC1=O)C(\C)=C\[C@@H]1CC[C@@H](O)[C@@H](C1)OC |c:3| Show InChI InChI=1S/C43H69NO12/c1-10-30-18-24(2)17-25(3)19-36(53-8)39-37(54-9)21-27(5)43(51,56-39)40(48)41(49)44-16-12-11-13-31(44)42(50)55-38(28(6)33(46)23-34(30)47)26(4)20-29-14-15-32(45)35(22-29)52-7/h18,20,25,27-33,35-39,45-46,51H,10-17,19,21-23H2,1-9H3/b24-18+,26-20+/t25-,27+,28+,29-,30+,31-,32+,33-,35+,36-,37-,38+,39+,43+/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid PDB UniChem Patents Similars	PubMed	n/a	n/a	8.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against hCyp-18 PPIase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase FKBP4 (Homo sapiens (Human))	BDBM50087860 (1-(2-{2-[3-(3H-Imidazol-4-yl)-2-(3-methyl-butyryla...) Show SMILES CCC(C)[C@H](NC(=O)[C@@H]1CCN(C1)C(=O)CNC(=O)[C@H](C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)CC(C)C)C(=O)NCc1ccccc1 Show InChI InChI=1S/C34H50N8O6/c1-6-22(4)30(34(48)36-16-24-10-8-7-9-11-24)41-32(46)25-12-13-42(19-25)29(44)18-37-31(45)23(5)39-33(47)27(15-26-17-35-20-38-26)40-28(43)14-21(2)3/h7-11,17,20-23,25,27,30H,6,12-16,18-19H2,1-5H3,(H,35,38)(H,36,48)(H,37,45)(H,39,47)(H,40,43)(H,41,46)/t22?,23-,25+,27-,30-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.80E+4	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against hCyp-18 PPIase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase A (Homo sapiens (Human))	BDBM50369808 (CHEMBL1793898) Show SMILES CC(C)CC(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](C)C(=O)NCC(=O)N1CCC[C@H]1C(=O)NC1(CCCC1)C(=O)NCc1ccccc1 Show InChI InChI=1S/C34H48N8O6/c1-22(2)16-28(43)40-26(17-25-19-35-21-38-25)31(46)39-23(3)30(45)36-20-29(44)42-15-9-12-27(42)32(47)41-34(13-7-8-14-34)33(48)37-18-24-10-5-4-6-11-24/h4-6,10-11,19,21-23,26-27H,7-9,12-18,20H2,1-3H3,(H,35,38)(H,36,45)(H,37,48)(H,39,46)(H,40,43)(H,41,47)/t23-,26-,27-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	9.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against human Peptidyl-prolyl isomerase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase A (Homo sapiens (Human))	BDBM50369806 (CHEMBL1790326) Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@H](C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(C)=O)C(C)C)C(=O)NCc1ccccc1 Show InChI InChI=1S/C36H53N9O7/c1-7-22(4)31(35(51)38-17-25-12-9-8-10-13-25)44-34(50)28-14-11-15-45(28)29(47)19-39-32(48)23(5)41-33(49)27(16-26-18-37-20-40-26)43-36(52)30(21(2)3)42-24(6)46/h8-10,12-13,18,20-23,27-28,30-31H,7,11,14-17,19H2,1-6H3,(H,37,40)(H,38,51)(H,39,48)(H,41,49)(H,42,46)(H,43,52)(H,44,50)/t22-,23-,27-,28-,30-,31-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.15E+5	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against human Peptidyl-prolyl isomerase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase A (Homo sapiens (Human))	BDBM50369804 (CHEMBL1790324) Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@H](C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)CC(C)C)C(=O)N[C@H](C)C(N)=O Show InChI InChI=1S/C30H49N9O7/c1-7-17(4)25(30(46)35-18(5)26(31)42)38-29(45)22-9-8-10-39(22)24(41)14-33-27(43)19(6)36-28(44)21(12-20-13-32-15-34-20)37-23(40)11-16(2)3/h13,15-19,21-22,25H,7-12,14H2,1-6H3,(H2,31,42)(H,32,34)(H,33,43)(H,35,46)(H,36,44)(H,37,40)(H,38,45)/t17-,18+,19-,21-,22-,25-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.65E+5	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against human Peptidyl-prolyl isomerase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase A (Homo sapiens (Human))	BDBM50369803 (CHEMBL1790327) Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@H](C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](N)C(C)C)C(=O)NCc1ccccc1 Show InChI InChI=1S/C34H51N9O6/c1-6-21(4)29(34(49)37-16-23-11-8-7-9-12-23)42-32(47)26-13-10-14-43(26)27(44)18-38-30(45)22(5)40-31(46)25(15-24-17-36-19-39-24)41-33(48)28(35)20(2)3/h7-9,11-12,17,19-22,25-26,28-29H,6,10,13-16,18,35H2,1-5H3,(H,36,39)(H,37,49)(H,38,45)(H,40,46)(H,41,48)(H,42,47)/t21-,22-,25-,26-,28-,29-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.60E+5	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against human Peptidyl-prolyl isomerase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase A (Homo sapiens (Human))	BDBM50369816 (CHEMBL1790319) Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@H](C)NC(=O)[C@H](Cc1cnc[nH]1)NC(C)=O)C(=O)NCc1ccccc1 Show InChI InChI=1S/C31H44N8O6/c1-5-19(2)27(31(45)33-15-22-10-7-6-8-11-22)38-30(44)25-12-9-13-39(25)26(41)17-34-28(42)20(3)36-29(43)24(37-21(4)40)14-23-16-32-18-35-23/h6-8,10-11,16,18-20,24-25,27H,5,9,12-15,17H2,1-4H3,(H,32,35)(H,33,45)(H,34,42)(H,36,43)(H,37,40)(H,38,44)/t19-,20-,24-,25-,27-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.80E+5	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against human Peptidyl-prolyl isomerase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase FKBP4 (Homo sapiens (Human))	BDBM50369809 (CHEMBL1790321) Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@H](C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(C)=O)C(C)C)C(=O)NCCc1ccccc1 Show InChI InChI=1S/C37H55N9O7/c1-7-23(4)32(36(52)39-16-15-26-12-9-8-10-13-26)45-35(51)29-14-11-17-46(29)30(48)20-40-33(49)24(5)42-34(50)28(18-27-19-38-21-41-27)44-37(53)31(22(2)3)43-25(6)47/h8-10,12-13,19,21-24,28-29,31-32H,7,11,14-18,20H2,1-6H3,(H,38,41)(H,39,52)(H,40,49)(H,42,50)(H,43,47)(H,44,53)(H,45,51)/t23-,24-,28-,29-,31-,32-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.25E+5	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against hCyp-18 PPIase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase FKBP4 (Homo sapiens (Human))	BDBM50369810 (CHEMBL1790320) Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@H](C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(C)=O)C(C)C)C(=O)NCC(c1ccccc1)c1ccccc1 Show InChI InChI=1S/C43H59N9O7/c1-7-27(4)38(42(58)45-23-33(30-15-10-8-11-16-30)31-17-12-9-13-18-31)51-41(57)35-19-14-20-52(35)36(54)24-46-39(55)28(5)48-40(56)34(21-32-22-44-25-47-32)50-43(59)37(26(2)3)49-29(6)53/h8-13,15-18,22,25-28,33-35,37-38H,7,14,19-21,23-24H2,1-6H3,(H,44,47)(H,45,58)(H,46,55)(H,48,56)(H,49,53)(H,50,59)(H,51,57)/t27-,28-,34-,35-,37-,38-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.65E+5	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against hCyp-18 PPIase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase A (Homo sapiens (Human))	BDBM50369805 (CHEMBL1793899) Show SMILES CC(C)CC(=O)N[C@@H](Cc1cnc[nH]1)C(=O)NC(C)(C)C(=O)NCC(=O)N1CCC[C@H]1C(=O)NC1(CCCC1)C(=O)NCc1ccccc1 Show InChI InChI=1S/C35H50N8O6/c1-23(2)17-28(44)40-26(18-25-20-36-22-39-25)30(46)41-34(3,4)32(48)38-21-29(45)43-16-10-13-27(43)31(47)42-35(14-8-9-15-35)33(49)37-19-24-11-6-5-7-12-24/h5-7,11-12,20,22-23,26-27H,8-10,13-19,21H2,1-4H3,(H,36,39)(H,37,49)(H,38,48)(H,40,44)(H,41,46)(H,42,47)/t26-,27-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	5.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against human Peptidyl-prolyl isomerase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase A (Homo sapiens (Human))	BDBM50369817 (CHEMBL1793897) Show SMILES CC(C)[C@H](NC(C)=O)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](C)C(=O)NCC(=O)N1CCC[C@H]1C(=O)NC1(CCCC1)C(=O)N[C@@H](C)C(N)=O Show InChI InChI=1S/C32H50N10O8/c1-17(2)25(39-20(5)43)30(49)40-22(13-21-14-34-16-36-21)28(47)37-19(4)27(46)35-15-24(44)42-12-8-9-23(42)29(48)41-32(10-6-7-11-32)31(50)38-18(3)26(33)45/h14,16-19,22-23,25H,6-13,15H2,1-5H3,(H2,33,45)(H,34,36)(H,35,46)(H,37,47)(H,38,50)(H,39,43)(H,40,49)(H,41,48)/t18-,19-,22-,23-,25-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	6.80E+5	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against human Peptidyl-prolyl isomerase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase A (Homo sapiens (Human))	BDBM50087868 (1-(2-{2-[2-(2-Acetylamino-3-methyl-butyrylamino)-3...) Show SMILES CC[C@@H](C)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)CNC(=O)C(C)(C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(C)=O)C(C)C)C(=O)N[C@H](C)C(N)=O Show InChI InChI=1S/C33H54N10O8/c1-9-18(4)26(31(50)38-19(5)27(34)46)41-29(48)23-11-10-12-43(23)24(45)15-36-32(51)33(7,8)42-28(47)22(13-21-14-35-16-37-21)40-30(49)25(17(2)3)39-20(6)44/h14,16-19,22-23,25-26H,9-13,15H2,1-8H3,(H2,34,46)(H,35,37)(H,36,51)(H,38,50)(H,39,44)(H,40,49)(H,41,48)(H,42,47)/t18-,19-,22+,23+,25+,26-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	7.60E+5	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against human Peptidyl-prolyl isomerase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase A (Homo sapiens (Human))	BDBM50087875 (1-(2-{2-[2-(2-Acetylamino-3-methyl-butyrylamino)-3...) Show SMILES CC(C)[C@H](NC(C)=O)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](C)C(=O)NCC(=O)N1CCC[C@H]1C(=O)N[C@H](C(=O)N[C@H](C)C(N)=O)c1ccccc1 Show InChI InChI=1S/C34H48N10O8/c1-18(2)27(41-21(5)45)33(51)42-24(14-23-15-36-17-38-23)31(49)40-20(4)30(48)37-16-26(46)44-13-9-12-25(44)32(50)43-28(22-10-7-6-8-11-22)34(52)39-19(3)29(35)47/h6-8,10-11,15,17-20,24-25,27-28H,9,12-14,16H2,1-5H3,(H2,35,47)(H,36,38)(H,37,48)(H,39,52)(H,40,49)(H,41,45)(H,42,51)(H,43,50)/t19-,20+,24+,25+,27+,28+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	8.20E+5	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against human Peptidyl-prolyl isomerase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase FKBP4 (Homo sapiens (Human))	BDBM50087877 (CHEMBL298712 | N-[1-(1-Methyl-2-{2-[1-(4-nitro-phe...) Show SMILES C[C@H](NC(=O)CCC(O)=O)C(=O)N[C@@H](C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)Nc1ccc(cc1)[N+]([O-])=O Show InChI InChI=1S/C30H36N6O9/c1-18(31-25(37)14-15-26(38)39)27(40)32-19(2)30(43)35-16-6-9-24(35)29(42)34-23(17-20-7-4-3-5-8-20)28(41)33-21-10-12-22(13-11-21)36(44)45/h3-5,7-8,10-13,18-19,23-24H,6,9,14-17H2,1-2H3,(H,31,37)(H,32,40)(H,33,41)(H,34,42)(H,38,39)/t18-,19-,23-,24-/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG MMDB PC cid PC sid UniChem Similars	PubMed	n/a	n/a	8.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against hCyp-18 PPIase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase A (Homo sapiens (Human))	BDBM50087882 (1-(2-{2-[2-(2-Acetylamino-3-methyl-butyrylamino)-3...) Show SMILES CC[C@@H](C)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@H](C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(C)=O)C(C)C)C(=O)N[C@H](C)C(N)=O Show InChI InChI=1S/C32H52N10O8/c1-8-17(4)26(32(50)37-18(5)27(33)45)41-30(48)23-10-9-11-42(23)24(44)14-35-28(46)19(6)38-29(47)22(12-21-13-34-15-36-21)40-31(49)25(16(2)3)39-20(7)43/h13,15-19,22-23,25-26H,8-12,14H2,1-7H3,(H2,33,45)(H,34,36)(H,35,46)(H,37,50)(H,38,47)(H,39,43)(H,40,49)(H,41,48)/t17-,18-,19+,22+,23+,25+,26-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	8.50E+5	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against human Peptidyl-prolyl isomerase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase A (Homo sapiens (Human))	BDBM50087855 (1-(2-{2-[2-(2-Acetylamino-3-methyl-butyrylamino)-3...) Show SMILES CC(C)[C@H](NC(C)=O)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](C)C(=O)NCC(=O)N1CCC[C@H]1C(=O)N[C@@H](C(=O)N[C@H](C)C(N)=O)c1ccccc1 Show InChI InChI=1S/C34H48N10O8/c1-18(2)27(41-21(5)45)33(51)42-24(14-23-15-36-17-38-23)31(49)40-20(4)30(48)37-16-26(46)44-13-9-12-25(44)32(50)43-28(22-10-7-6-8-11-22)34(52)39-19(3)29(35)47/h6-8,10-11,15,17-20,24-25,27-28H,9,12-14,16H2,1-5H3,(H2,35,47)(H,36,38)(H,37,48)(H,39,52)(H,40,49)(H,41,45)(H,42,51)(H,43,50)/t19-,20+,24+,25+,27+,28-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	9.70E+5	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against human Peptidyl-prolyl isomerase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase A (Homo sapiens (Human))	BDBM50369812 (CHEMBL1790308) Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@H](C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(=O)CCC(O)=O)C(C)C)C(=O)N[C@H](C)C(N)=O Show InChI InChI=1S/C34H54N10O10/c1-7-18(4)28(34(54)39-19(5)29(35)49)43-32(52)23-9-8-12-44(23)25(46)15-37-30(50)20(6)40-31(51)22(13-21-14-36-16-38-21)41-33(53)27(17(2)3)42-24(45)10-11-26(47)48/h14,16-20,22-23,27-28H,7-13,15H2,1-6H3,(H2,35,49)(H,36,38)(H,37,50)(H,39,54)(H,40,51)(H,41,53)(H,42,45)(H,43,52)(H,47,48)/t18-,19+,20-,22-,23-,27-,28-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against human Peptidyl-prolyl isomerase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase A (Homo sapiens (Human))	BDBM50087854 (2-{[1-(2-{2-[2-(2-Acetylamino-3-methyl-butyrylamin...) Show SMILES CC(C)[C@H](NC(C)=O)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](C)C(=O)NCC(=O)N1CCC[C@H]1C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H](C)C(N)=O Show InChI InChI=1S/C31H49N11O9/c1-15(2)25(39-18(5)43)31(51)41-21(11-19-12-34-14-36-19)29(49)38-17(4)27(47)35-13-24(45)42-10-6-7-22(42)30(50)40-20(8-9-23(32)44)28(48)37-16(3)26(33)46/h12,14-17,20-22,25H,6-11,13H2,1-5H3,(H2,32,44)(H2,33,46)(H,34,36)(H,35,47)(H,37,48)(H,38,49)(H,39,43)(H,40,50)(H,41,51)/t16-,17+,20+,21+,22+,25+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.30E+6	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against human Peptidyl-prolyl isomerase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase A (Homo sapiens (Human))	BDBM50369807 (CHEMBL1790325) Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@H](C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](NC(C)=O)C(C)C)C(=O)NC(c1ccccc1)c1ccccc1 Show InChI InChI=1S/C42H57N9O7/c1-7-26(4)36(42(58)50-37(29-15-10-8-11-16-29)30-17-12-9-13-18-30)49-40(56)33-19-14-20-51(33)34(53)23-44-38(54)27(5)46-39(55)32(21-31-22-43-24-45-31)48-41(57)35(25(2)3)47-28(6)52/h8-13,15-18,22,24-27,32-33,35-37H,7,14,19-21,23H2,1-6H3,(H,43,45)(H,44,54)(H,46,55)(H,47,52)(H,48,57)(H,49,56)(H,50,58)/t26-,27-,32-,33-,35-,36-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.50E+6	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against human Peptidyl-prolyl isomerase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase A (Homo sapiens (Human))	BDBM50087874 (1-(2-{2-[2-(2-Acetylamino-3-methyl-butyrylamino)-3...) Show SMILES CC(C)[C@H](NC(C)=O)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](C)C(=O)NCC(=O)N1CCC[C@H]1C(=O)N[C@@H](C(C)C)C(=O)N[C@H](C)C(N)=O Show InChI InChI=1S/C31H50N10O8/c1-15(2)24(38-19(7)42)31(49)39-21(11-20-12-33-14-35-20)28(46)37-18(6)27(45)34-13-23(43)41-10-8-9-22(41)29(47)40-25(16(3)4)30(48)36-17(5)26(32)44/h12,14-18,21-22,24-25H,8-11,13H2,1-7H3,(H2,32,44)(H,33,35)(H,34,45)(H,36,48)(H,37,46)(H,38,42)(H,39,49)(H,40,47)/t17-,18+,21+,22+,24+,25+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.50E+6	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against human Peptidyl-prolyl isomerase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase A (Homo sapiens (Human))	BDBM50369814 (CHEMBL1790322) Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@H](C)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@H](C)C(O)=O Show InChI InChI=1S/C25H40N8O7/c1-5-13(2)20(24(38)31-15(4)25(39)40)32-23(37)18-7-6-8-33(18)19(34)11-28-21(35)14(3)30-22(36)17(26)9-16-10-27-12-29-16/h10,12-15,17-18,20H,5-9,11,26H2,1-4H3,(H,27,29)(H,28,35)(H,30,36)(H,31,38)(H,32,37)(H,39,40)/t13-,14-,15+,17-,18-,20-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against human Peptidyl-prolyl isomerase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase A (Homo sapiens (Human))	BDBM50369813 (CHEMBL1790309) Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@H](C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](N)C(C)C)C(=O)N[C@H](C)C(N)=O Show InChI InChI=1S/C30H50N10O7/c1-7-16(4)24(30(47)36-17(5)25(32)42)39-28(45)21-9-8-10-40(21)22(41)13-34-26(43)18(6)37-27(44)20(11-19-12-33-14-35-19)38-29(46)23(31)15(2)3/h12,14-18,20-21,23-24H,7-11,13,31H2,1-6H3,(H2,32,42)(H,33,35)(H,34,43)(H,36,47)(H,37,44)(H,38,46)(H,39,45)/t16-,17+,18-,20-,21-,23-,24-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.10E+6	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against human Peptidyl-prolyl isomerase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase A (Homo sapiens (Human))	BDBM50087872 (2-(2-Acetylamino-3-methyl-butyrylamino)-pentanedio...) Show SMILES CC[C@@H](C)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(C)=O)C(C)C)C(=O)N[C@H](C)C(N)=O Show InChI InChI=1S/C31H53N9O9/c1-8-16(4)25(31(49)35-17(5)26(33)44)39-29(47)21-10-9-13-40(21)23(43)14-34-27(45)18(6)36-28(46)20(11-12-22(32)42)38-30(48)24(15(2)3)37-19(7)41/h15-18,20-21,24-25H,8-14H2,1-7H3,(H2,32,42)(H2,33,44)(H,34,45)(H,35,49)(H,36,46)(H,37,41)(H,38,48)(H,39,47)/t16-,17-,18+,20+,21+,24+,25-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.50E+6	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against human Peptidyl-prolyl isomerase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase A (Homo sapiens (Human))	BDBM50369815 (CHEMBL1790323) Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@H](C)NC(=O)CCc1cnc[nH]1)C(=O)N[C@H](C)C(N)=O Show InChI InChI=1S/C25H40N8O6/c1-5-14(2)21(25(39)31-15(3)22(26)36)32-24(38)18-7-6-10-33(18)20(35)12-28-23(37)16(4)30-19(34)9-8-17-11-27-13-29-17/h11,13-16,18,21H,5-10,12H2,1-4H3,(H2,26,36)(H,27,29)(H,28,37)(H,30,34)(H,31,39)(H,32,38)/t14-,15+,16-,18-,21-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.60E+6	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against human Peptidyl-prolyl isomerase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase A (Homo sapiens (Human))	BDBM50087866 (1-(2-{2-[2-(2-Acetylamino-3-methyl-butyrylamino)-3...) Show SMILES CC(C)[C@H](NC(C)=O)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](C)C(=O)NCC(=O)N1CCC[C@H]1C(=O)NCC(=O)N[C@H](C)C(N)=O Show InChI InChI=1S/C28H44N10O8/c1-14(2)23(36-17(5)39)28(46)37-19(9-18-10-30-13-33-18)26(44)35-16(4)25(43)32-12-22(41)38-8-6-7-20(38)27(45)31-11-21(40)34-15(3)24(29)42/h10,13-16,19-20,23H,6-9,11-12H2,1-5H3,(H2,29,42)(H,30,33)(H,31,45)(H,32,43)(H,34,40)(H,35,44)(H,36,39)(H,37,46)/t15-,16+,19+,20+,23+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.80E+6	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against human Peptidyl-prolyl isomerase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase A (Homo sapiens (Human))	BDBM50369818 (CHEMBL1790318) Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@H](C)NC(=O)CCc1cnc[nH]1)C(=O)NCc1ccccc1 Show InChI InChI=1S/C29H41N7O5/c1-4-19(2)26(29(41)31-15-21-9-6-5-7-10-21)35-28(40)23-11-8-14-36(23)25(38)17-32-27(39)20(3)34-24(37)13-12-22-16-30-18-33-22/h5-7,9-10,16,18-20,23,26H,4,8,11-15,17H2,1-3H3,(H,30,33)(H,31,41)(H,32,39)(H,34,37)(H,35,40)/t19-,20-,23-,26-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+7	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against human Peptidyl-prolyl isomerase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase A (Homo sapiens (Human))	BDBM50087873 (1-(2-{2-[2-(2-Acetylamino-3-methyl-butyrylamino)-3...) Show SMILES CC(C)[C@H](NC(C)=O)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](C)C(=O)NCC(=O)N1CCC[C@H]1C(=O)NC(C)(C)C(=O)N[C@H](C)C(N)=O Show InChI InChI=1S/C30H48N10O8/c1-15(2)23(37-18(5)41)28(47)38-20(11-19-12-32-14-34-19)26(45)35-17(4)25(44)33-13-22(42)40-10-8-9-21(40)27(46)39-30(6,7)29(48)36-16(3)24(31)43/h12,14-17,20-21,23H,8-11,13H2,1-7H3,(H2,31,43)(H,32,34)(H,33,44)(H,35,45)(H,36,48)(H,37,41)(H,38,47)(H,39,46)/t16-,17+,20+,21+,23+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+7	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against human Peptidyl-prolyl isomerase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase FKBP4 (Homo sapiens (Human))	BDBM50087861 (1-(2-{2-[2-(2-Acetylamino-3-methyl-butyrylamino)-5...) Show SMILES CC[C@@H](C)[C@@H](NC(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@H](C)NC(=O)[C@H](CCCN)NC(=O)[C@@H](NC(C)=O)C(C)C)C(=O)N[C@H](C)C(N)=O Show InChI InChI=1S/C31H55N9O8/c1-8-17(4)25(31(48)35-18(5)26(33)43)39-29(46)22-12-10-14-40(22)23(42)15-34-27(44)19(6)36-28(45)21(11-9-13-32)38-30(47)24(16(2)3)37-20(7)41/h16-19,21-22,24-25H,8-15,32H2,1-7H3,(H2,33,43)(H,34,44)(H,35,48)(H,36,45)(H,37,41)(H,38,47)(H,39,46)/t17-,18-,19+,21+,22+,24+,25-/m1/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+7	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against hCyp-18 PPIase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase A (Homo sapiens (Human))	BDBM50087857 (1-(2-{2-[3-(3H-Imidazol-4-yl)-2-(3-methyl-butyryla...) Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)CNC(=O)C(C)(C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)CC(C)C)C(=O)NCc1ccccc1 Show InChI InChI=1S/C35H52N8O6/c1-7-23(4)30(33(48)37-18-24-12-9-8-10-13-24)41-32(47)27-14-11-15-43(27)29(45)20-38-34(49)35(5,6)42-31(46)26(17-25-19-36-21-39-25)40-28(44)16-22(2)3/h8-10,12-13,19,21-23,26-27,30H,7,11,14-18,20H2,1-6H3,(H,36,39)(H,37,48)(H,38,49)(H,40,44)(H,41,47)(H,42,46)/t23-,26-,27-,30-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+7	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against human Peptidyl-prolyl isomerase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair
Peptidyl-prolyl cis-trans isomerase A (Homo sapiens (Human))	BDBM50087870 (4-{[1-(2-{2-[2-(2-Acetylamino-3-methyl-butyrylamin...) Show SMILES CC(C)[C@H](NC(C)=O)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](C)C(=O)NCC(=O)N1CCC[C@H]1C(=O)NC1(CCNCC1)C(=O)N[C@H](C)C(N)=O Show InChI InChI=1S/C32H51N11O8/c1-17(2)25(40-20(5)44)30(50)41-22(13-21-14-35-16-37-21)28(48)38-19(4)27(47)36-15-24(45)43-12-6-7-23(43)29(49)42-32(8-10-34-11-9-32)31(51)39-18(3)26(33)46/h14,16-19,22-23,25,34H,6-13,15H2,1-5H3,(H2,33,46)(H,35,37)(H,36,47)(H,38,48)(H,39,51)(H,40,44)(H,41,50)(H,42,49)/t18-,19+,22+,23+,25+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+7	n/a	n/a	n/a	n/a	n/a	n/a
D�partement D'Ing�nierie et D'Etudes des Prot�ines Curated by ChEMBL					Assay Description 50% inhibitory concentration of competitive binding against human Peptidyl-prolyl isomerase activity using uncoupled assay				J Med Chem 43: 1770-9 (2000) BindingDB Entry DOI: 10.7270/Q2SQ9135
					More data for this Ligand-Target Pair