Compile Data Set for Download or QSAR

Found 420 hits with Last Name = 'bambal' and Initial = 'r'   

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
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176918 ((2S)-aminobutyryl-(2S)-indoline carboxylic acid pr...) Show SMILES CCCNC(=O)[C@@H]1Cc2ccccc2N1C(=O)[C@@H](N)CC |r| Show InChI InChI=1S/C16H23N3O2/c1-3-9-18-15(20)14-10-11-7-5-6-8-13(11)19(14)16(21)12(17)4-2/h5-8,12,14H,3-4,9-10,17H2,1-2H3,(H,18,20)/t12-,14-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50121282 ((S)-1-((S)-2-aminobutanoyl)-N-butylindoline-2-carb...) Show SMILES CCCCNC(=O)[C@@H]1Cc2ccccc2N1C(=O)[C@@H](N)CC Show InChI InChI=1S/C17H25N3O2/c1-3-5-10-19-16(21)15-11-12-8-6-7-9-14(12)20(15)17(22)13(18)4-2/h6-9,13,15H,3-5,10-11,18H2,1-2H3,(H,19,21)/t13-,15-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	7	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176940 ((2S)-aminobutyryl-(2S)-indoline carboxylic acid et...) Show SMILES CCNC(=O)[C@@H]1Cc2ccccc2N1C(=O)[C@@H](N)CC |r| Show InChI InChI=1S/C15H21N3O2/c1-3-11(16)15(20)18-12-8-6-5-7-10(12)9-13(18)14(19)17-4-2/h5-8,11,13H,3-4,9,16H2,1-2H3,(H,17,19)/t11-,13-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	12	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176934 ((2S)-aminobutyryl-L-proline n-butylamide | CHEMBL2...) Show SMILES CCCCNC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CC |r| Show InChI InChI=1S/C13H25N3O2/c1-3-5-8-15-12(17)11-7-6-9-16(11)13(18)10(14)4-2/h10-11H,3-9,14H2,1-2H3,(H,15,17)/t10-,11-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	80	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176913 ((2S)-aminobutyryl-L-proline n-propylamide | CHEMBL...) Show SMILES CCCNC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CC |r| Show InChI InChI=1S/C12H23N3O2/c1-3-7-14-11(16)10-6-5-8-15(10)12(17)9(13)4-2/h9-10H,3-8,13H2,1-2H3,(H,14,16)/t9-,10-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	80	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176939 ((2S)-1-((S)-2-aminobutanoyl)-4-benzyl-N-butylpyrro...) Show SMILES CCCCNC(=O)[C@@H]1CC(Cc2ccccc2)CN1C(=O)[C@@H](N)CC |r| Show InChI InChI=1S/C20H31N3O2/c1-3-5-11-22-19(24)18-13-16(12-15-9-7-6-8-10-15)14-23(18)20(25)17(21)4-2/h6-10,16-18H,3-5,11-14,21H2,1-2H3,(H,22,24)/t16?,17-,18-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	140	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176936 ((2S)-aminobutyryl-L-proline n-pentylamide | CHEMBL...) Show SMILES CCCCCNC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CC |r| Show InChI InChI=1S/C14H27N3O2/c1-3-5-6-9-16-13(18)12-8-7-10-17(12)14(19)11(15)4-2/h11-12H,3-10,15H2,1-2H3,(H,16,18)/t11-,12-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	270	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176927 ((2S)-aminobutyryl-L-proline 3-methylthiopropylamid...) Show SMILES CC[C@H](N)C(=O)N1CCC[C@H]1C(=O)NCCCSC |r| Show InChI InChI=1S/C13H25N3O2S/c1-3-10(14)13(18)16-8-4-6-11(16)12(17)15-7-5-9-19-2/h10-11H,3-9,14H2,1-2H3,(H,15,17)/t10-,11-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	300	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176935 ((2S,4S)-1-((S)-2-aminobutanoyl)-N-butyl-4-fluoropy...) Show SMILES CCCCNC(=O)[C@@H]1C[C@H](F)CN1C(=O)[C@@H](N)CC |r| Show InChI InChI=1S/C13H24FN3O2/c1-3-5-6-16-12(18)11-7-9(14)8-17(11)13(19)10(15)4-2/h9-11H,3-8,15H2,1-2H3,(H,16,18)/t9-,10-,11-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	320	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176945 ((2S)-aminobutyryl-L-proline isobutylamide | CHEMBL...) Show SMILES CC[C@H](N)C(=O)N1CCC[C@H]1C(=O)NCC(C)C |r| Show InChI InChI=1S/C13H25N3O2/c1-4-10(14)13(18)16-7-5-6-11(16)12(17)15-8-9(2)3/h9-11H,4-8,14H2,1-3H3,(H,15,17)/t10-,11-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	320	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176922 ((2S)-aminobutyryl-(2S)-indoline carboxylic acid me...) Show SMILES CC[C@H](N)C(=O)N1[C@@H](Cc2ccccc12)C(=O)NC |r| Show InChI InChI=1S/C14H19N3O2/c1-3-10(15)14(19)17-11-7-5-4-6-9(11)8-12(17)13(18)16-2/h4-7,10,12H,3,8,15H2,1-2H3,(H,16,18)/t10-,12-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	340	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176914 ((2S)-aminobutyryl-L-proline-(2S)-methylbutylamide ...) Show SMILES CC[C@H](C)CNC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CC |r| Show InChI InChI=1S/C14H27N3O2/c1-4-10(3)9-16-13(18)12-7-6-8-17(12)14(19)11(15)5-2/h10-12H,4-9,15H2,1-3H3,(H,16,18)/t10-,11-,12-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	500	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176932 ((2S)-aminobutyryl-L-prolinamide | CHEMBL224063) Show SMILES CC[C@H](N)C(=O)N1CCC[C@H]1C(N)=O |r| Show InChI InChI=1S/C9H17N3O2/c1-2-6(10)9(14)12-5-3-4-7(12)8(11)13/h6-7H,2-5,10H2,1H3,(H2,11,13)/t6-,7-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	570	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176920 ((S)-1-((S)-2-amino-3-methylbutanoyl)-N-butylpyrrol...) Show SMILES CCCCNC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)C(C)C |r| Show InChI InChI=1S/C14H27N3O2/c1-4-5-8-16-13(18)11-7-6-9-17(11)14(19)12(15)10(2)3/h10-12H,4-9,15H2,1-3H3,(H,16,18)/t11-,12-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	570	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176928 (CHEMBL375490 | L-valyl-L-proline hexylamide) Show SMILES CCCCCCNC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)C(C)C |r| Show InChI InChI=1S/C16H31N3O2/c1-4-5-6-7-10-18-15(20)13-9-8-11-19(13)16(21)14(17)12(2)3/h12-14H,4-11,17H2,1-3H3,(H,18,20)/t13-,14-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	900	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50085083 (2-{[1-(2-Amino-3-methyl-pentanoyl)-pyrrolidine-2-c...) Show SMILES CCC(C)C(N)C(=O)N1CCCC1C(=O)NC(C(C)CC)C(O)=O Show InChI InChI=1S/C17H31N3O4/c1-5-10(3)13(18)16(22)20-9-7-8-12(20)15(21)19-14(17(23)24)11(4)6-2/h10-14H,5-9,18H2,1-4H3,(H,19,21)(H,23,24)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	PubMed	1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition potency against Cholecystokinin-8-Inactivating Peptidase (Serine Peptidase).				J Med Chem 43: 664-74 (2000) BindingDB Entry DOI: 10.7270/Q2RX9CTG
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176926 (CHEMBL224628 | L-norvalyl-L-prolinamide) Show SMILES CCC[C@H](N)C(=O)N1CCC[C@H]1C(N)=O |r| Show InChI InChI=1S/C10H19N3O2/c1-2-4-7(11)10(15)13-6-3-5-8(13)9(12)14/h7-8H,2-6,11H2,1H3,(H2,12,14)/t7-,8-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176919 (CHEMBL388843 | L-norleucyl-L-prolinamide) Show SMILES CCCC[C@H](N)C(=O)N1CCC[C@H]1C(N)=O |r| Show InChI InChI=1S/C11H21N3O2/c1-2-3-5-8(12)11(16)14-7-4-6-9(14)10(13)15/h8-9H,2-7,12H2,1H3,(H2,13,15)/t8-,9-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176925 (CHEMBL224340 | L-leucyl-L-prolinamide) Show SMILES CC(C)C[C@H](N)C(=O)N1CCC[C@H]1C(N)=O |r| Show InChI InChI=1S/C11H21N3O2/c1-7(2)6-8(12)11(16)14-5-3-4-9(14)10(13)15/h7-9H,3-6,12H2,1-2H3,(H2,13,15)/t8-,9-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	2.10E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176943 ((S)-1-((S)-2-aminopropanoyl)pyrrolidine-2-carboxam...) Show SMILES C[C@H](N)C(=O)N1CCC[C@H]1C(N)=O |r| Show InChI InChI=1S/C8H15N3O2/c1-5(9)8(13)11-4-2-3-6(11)7(10)12/h5-6H,2-4,9H2,1H3,(H2,10,12)/t5-,6-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	2.10E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50085116 (2-(2-Amino-3-methyl-butyrylamino)-pentanoic acid b...) Show SMILES CCCCNC(=O)C(CCC)NC(=O)C(N)C(C)C Show InChI InChI=1S/C14H29N3O2/c1-5-7-9-16-13(18)11(8-6-2)17-14(19)12(15)10(3)4/h10-12H,5-9,15H2,1-4H3,(H,16,18)(H,17,19)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition potency against Cholecystokinin-8-Inactivating Peptidase (Serine Peptidase).				J Med Chem 43: 664-74 (2000) BindingDB Entry DOI: 10.7270/Q2RX9CTG
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50085127 (2-{[1-(2-Amino-propionyl)-pyrrolidine-2-carbonyl]-...) Show SMILES CC(N)C(=O)N1CCCC1C(=O)NC(C)C(O)=O Show InChI InChI=1S/C11H19N3O4/c1-6(12)10(16)14-5-3-4-8(14)9(15)13-7(2)11(17)18/h6-8H,3-5,12H2,1-2H3,(H,13,15)(H,17,18)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	3.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition potency against Cholecystokinin-8-Inactivating Peptidase (Serine Peptidase).				J Med Chem 43: 664-74 (2000) BindingDB Entry DOI: 10.7270/Q2RX9CTG
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176931 (CHEMBL376375 | L-valyl-L-proline benzylamide) Show SMILES CC(C)[C@H](N)C(=O)N1CCC[C@H]1C(=O)NCc1ccccc1 |r| Show InChI InChI=1S/C17H25N3O2/c1-12(2)15(18)17(22)20-10-6-9-14(20)16(21)19-11-13-7-4-3-5-8-13/h3-5,7-8,12,14-15H,6,9-11,18H2,1-2H3,(H,19,21)/t14-,15-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176924 (CHEMBL224341 | L-isoleucyl-L-prolinamide) Show SMILES CCC(C)[C@H](N)C(=O)N1CCC[C@H]1C(N)=O |r| Show InChI InChI=1S/C11H21N3O2/c1-3-7(2)9(12)11(16)14-6-4-5-8(14)10(13)15/h7-9H,3-6,12H2,1-2H3,(H2,13,15)/t7?,8-,9-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176930 ((2S)-aminobutyryl-L-proline (R)-sec-butylamide | C...) Show SMILES CC[C@@H](C)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CC |r| Show InChI InChI=1S/C13H25N3O2/c1-4-9(3)15-12(17)11-7-6-8-16(11)13(18)10(14)5-2/h9-11H,4-8,14H2,1-3H3,(H,15,17)/t9-,10+,11+/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.50E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176938 (CHEMBL388062 | alpha-methylalanyl-L-proline butyla...) Show SMILES CCCCNC(=O)[C@@H]1CCCN1C(=O)C(C)(C)N |r| Show InChI InChI=1S/C13H25N3O2/c1-4-5-8-15-11(17)10-7-6-9-16(10)12(18)13(2,3)14/h10H,4-9,14H2,1-3H3,(H,15,17)/t10-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	5.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176944 (1-((S)-2-aminobutanoyl)-N-butylazepane-2-carboxami...) Show SMILES CCCCNC(=O)C1CCCCCN1C(=O)[C@@H](N)CC |r| Show InChI InChI=1S/C15H29N3O2/c1-3-5-10-17-14(19)13-9-7-6-8-11-18(13)15(20)12(16)4-2/h12-13H,3-11,16H2,1-2H3,(H,17,19)/t12-,13?/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	6.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176929 (CHEMBL375933 | L-valyl-L-prolinamide) Show SMILES CC(C)[C@H](N)C(=O)N1CCC[C@H]1C(N)=O |r| Show InChI InChI=1S/C10H19N3O2/c1-6(2)8(11)10(15)13-5-3-4-7(13)9(12)14/h6-8H,3-5,11H2,1-2H3,(H2,12,14)/t7-,8-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	6.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50085111 (2-Amino-hexanoic acid (1-methylcarbamoyl-pentyl)-a...) Show SMILES CCCCC(N)C(=O)NC(CCCC)C(=O)NC Show InChI InChI=1S/C13H27N3O2/c1-4-6-8-10(14)12(17)16-11(9-7-5-2)13(18)15-3/h10-11H,4-9,14H2,1-3H3,(H,15,18)(H,16,17)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	9.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition potency against Cholecystokinin-8-Inactivating Peptidase (Serine Peptidase).				J Med Chem 43: 664-74 (2000) BindingDB Entry DOI: 10.7270/Q2RX9CTG
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50085117 (2-Amino-N-[2-(4-hydroxy-phenyl)-1-methylcarbamoyl-...) Show SMILES CNC(=O)C(Cc1ccc(O)cc1)NC(=O)C(N)C(C)C Show InChI InChI=1S/C15H23N3O3/c1-9(2)13(16)15(21)18-12(14(20)17-3)8-10-4-6-11(19)7-5-10/h4-7,9,12-13,19H,8,16H2,1-3H3,(H,17,20)(H,18,21)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition potency against Cholecystokinin-8-Inactivating Peptidase (Serine Peptidase).				J Med Chem 43: 664-74 (2000) BindingDB Entry DOI: 10.7270/Q2RX9CTG
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176923 ((2S)-aminobutyryl-(R)-pipecolinic acid amide | CHE...) Show SMILES CC[C@H](N)C(=O)N1CCCC[C@@H]1C(N)=O |r| Show InChI InChI=1S/C10H19N3O2/c1-2-7(11)10(15)13-6-4-3-5-8(13)9(12)14/h7-8H,2-6,11H2,1H3,(H2,12,14)/t7-,8+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.20E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50085075 (2-[2-(2-Amino-propionylamino)-propionylamino]-prop...) Show SMILES CC(N)C(=O)NC(C)C(=O)NC(C)C(O)=O Show InChI InChI=1S/C9H17N3O4/c1-4(10)7(13)11-5(2)8(14)12-6(3)9(15)16/h4-6H,10H2,1-3H3,(H,11,13)(H,12,14)(H,15,16)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	1.40E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition potency against Cholecystokinin-8-Inactivating Peptidase (Serine Peptidase).				J Med Chem 43: 664-74 (2000) BindingDB Entry DOI: 10.7270/Q2RX9CTG
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50085085 (2-(2-Amino-3-methyl-butyrylamino)-hexanoic acid bu...) Show SMILES CCCCNC(=O)C(CCCC)NC(=O)C(N)C(C)C Show InChI InChI=1S/C15H31N3O2/c1-5-7-9-12(14(19)17-10-8-6-2)18-15(20)13(16)11(3)4/h11-13H,5-10,16H2,1-4H3,(H,17,19)(H,18,20)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	1.40E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition potency against Cholecystokinin-8-Inactivating Peptidase (Serine Peptidase).				J Med Chem 43: 664-74 (2000) BindingDB Entry DOI: 10.7270/Q2RX9CTG
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176915 ((2S)-aminobutyryl-L-proline (S)-sec-butylamide | C...) Show SMILES CC[C@H](C)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CC |r| Show InChI InChI=1S/C13H25N3O2/c1-4-9(3)15-12(17)11-7-6-8-16(11)13(18)10(14)5-2/h9-11H,4-8,14H2,1-3H3,(H,15,17)/t9-,10-,11-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176921 ((2S)-aminobutyryl-(2S)-azetidine carboxamide | CHE...) Show SMILES CC[C@H](N)C(=O)N1CC[C@H]1C(N)=O |r| Show InChI InChI=1S/C8H15N3O2/c1-2-5(9)8(13)11-4-3-6(11)7(10)12/h5-6H,2-4,9H2,1H3,(H2,10,12)/t5-,6-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50085074 (2-Amino-N-(1-butylcarbamoyl-2-phenyl-ethyl)-3-meth...) Show SMILES CCCCNC(=O)C(Cc1ccccc1)NC(=O)C(N)C(C)C Show InChI InChI=1S/C18H29N3O2/c1-4-5-11-20-17(22)15(12-14-9-7-6-8-10-14)21-18(23)16(19)13(2)3/h6-10,13,15-16H,4-5,11-12,19H2,1-3H3,(H,20,22)(H,21,23)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition potency against Cholecystokinin-8-Inactivating Peptidase (Serine Peptidase).				J Med Chem 43: 664-74 (2000) BindingDB Entry DOI: 10.7270/Q2RX9CTG
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50085106 (2-[2-(2-Amino-acetylamino)-3-(1H-indol-3-yl)-propi...) Show SMILES CSCCC(NC(=O)C(Cc1c[nH]c2ccccc12)NC(=O)CN)C(O)=O Show InChI InChI=1S/C18H24N4O4S/c1-27-7-6-14(18(25)26)22-17(24)15(21-16(23)9-19)8-11-10-20-13-5-3-2-4-12(11)13/h2-5,10,14-15,20H,6-9,19H2,1H3,(H,21,23)(H,22,24)(H,25,26)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition potency against Cholecystokinin-8-Inactivating Peptidase (Serine Peptidase).				J Med Chem 43: 664-74 (2000) BindingDB Entry DOI: 10.7270/Q2RX9CTG
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50085102 (2-Amino-3-methyl-N-(1-methylcarbamoyl-2-phenyl-eth...) Show SMILES CNC(=O)C(Cc1ccccc1)NC(=O)C(N)C(C)C Show InChI InChI=1S/C15H23N3O2/c1-10(2)13(16)15(20)18-12(14(19)17-3)9-11-7-5-4-6-8-11/h4-8,10,12-13H,9,16H2,1-3H3,(H,17,19)(H,18,20)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	2.20E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition potency against Cholecystokinin-8-Inactivating Peptidase (Serine Peptidase).				J Med Chem 43: 664-74 (2000) BindingDB Entry DOI: 10.7270/Q2RX9CTG
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50085093 (2-(2-Amino-3-methyl-butyrylamino)-pentanoic acid m...) Show SMILES CCCC(NC(=O)C(N)C(C)C)C(=O)NC Show InChI InChI=1S/C11H23N3O2/c1-5-6-8(10(15)13-4)14-11(16)9(12)7(2)3/h7-9H,5-6,12H2,1-4H3,(H,13,15)(H,14,16)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	2.80E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition potency against Cholecystokinin-8-Inactivating Peptidase (Serine Peptidase).				J Med Chem 43: 664-74 (2000) BindingDB Entry DOI: 10.7270/Q2RX9CTG
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50085101 (2-Amino-3-methyl-N-(methylcarbamoyl-phenyl-methyl)...) Show SMILES CNC(=O)C(NC(=O)C(N)C(C)C)c1ccccc1 Show InChI InChI=1S/C14H21N3O2/c1-9(2)11(15)13(18)17-12(14(19)16-3)10-7-5-4-6-8-10/h4-9,11-12H,15H2,1-3H3,(H,16,19)(H,17,18)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	2.90E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition potency against Cholecystokinin-8-Inactivating Peptidase (Serine Peptidase).				J Med Chem 43: 664-74 (2000) BindingDB Entry DOI: 10.7270/Q2RX9CTG
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50085078 (2-(2-Amino-3-methyl-butyrylamino)-hexanoic acid (3...) Show SMILES CCCCC(NC(=O)C(N)C(C)C)C(=O)NCCCc1ccccc1 Show InChI InChI=1S/C20H33N3O2/c1-4-5-13-17(23-20(25)18(21)15(2)3)19(24)22-14-9-12-16-10-7-6-8-11-16/h6-8,10-11,15,17-18H,4-5,9,12-14,21H2,1-3H3,(H,22,24)(H,23,25)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	2.90E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition potency against Cholecystokinin-8-Inactivating Peptidase (Serine Peptidase).				J Med Chem 43: 664-74 (2000) BindingDB Entry DOI: 10.7270/Q2RX9CTG
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50085129 (2-[2-(2-Amino-acetylamino)-3-methyl-butyrylamino]-...) Show SMILES CC(C)C(NC(=O)CN)C(=O)NC(Cc1ccccc1)C(O)=O Show InChI InChI=1S/C16H23N3O4/c1-10(2)14(19-13(20)9-17)15(21)18-12(16(22)23)8-11-6-4-3-5-7-11/h3-7,10,12,14H,8-9,17H2,1-2H3,(H,18,21)(H,19,20)(H,22,23)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	2.90E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition potency against Cholecystokinin-8-Inactivating Peptidase (Serine Peptidase).				J Med Chem 43: 664-74 (2000) BindingDB Entry DOI: 10.7270/Q2RX9CTG
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50085128 (2-Amino-3-methyl-N-(4-phenyl-butyl)-butyramide | C...) Show SMILES CC(C)[C@H](N)C(=O)NCCCCc1ccccc1 Show InChI InChI=1S/C15H24N2O/c1-12(2)14(16)15(18)17-11-7-6-10-13-8-4-3-5-9-13/h3-5,8-9,12,14H,6-7,10-11,16H2,1-2H3,(H,17,18)/t14-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	3.30E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition potency against Cholecystokinin-8-Inactivating Peptidase (Serine Peptidase).				J Med Chem 43: 664-74 (2000) BindingDB Entry DOI: 10.7270/Q2RX9CTG
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176912 (CHEMBL225596 | L-valyl-L-proline cyclohexylmethyla...) Show SMILES CC(C)[C@H](N)C(=O)N1CCC[C@H]1C(=O)N(C)C1CCCCC1 |r| Show InChI InChI=1S/C17H31N3O2/c1-12(2)15(18)17(22)20-11-7-10-14(20)16(21)19(3)13-8-5-4-6-9-13/h12-15H,4-11,18H2,1-3H3/t14-,15-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.40E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176911 ((2S)-aminobutyryl-L-pipecolinic acid n-butylamide ...) Show SMILES CCCCNC(=O)[C@@H]1CCCCN1C(=O)[C@@H](N)CC |r| Show InChI InChI=1S/C14H27N3O2/c1-3-5-9-16-13(18)12-8-6-7-10-17(12)14(19)11(15)4-2/h11-12H,3-10,15H2,1-2H3,(H,16,18)/t11-,12-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.50E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176942 ((2S)-aminobutyryl-4-thia-L-prolinamide | CHEMBL375...) Show SMILES CC[C@H](N)C(=O)N1CSC[C@@H]1C(N)=O |r| Show InChI InChI=1S/C8H15N3O2S/c1-2-5(9)8(13)11-4-14-3-6(11)7(10)12/h5-6H,2-4,9H2,1H3,(H2,10,12)/t5-,6+/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50176916 ((2S)-aminobutyryl-(S)-nipecotamide | CHEMBL223665) Show SMILES CC[C@H](N)C(=O)N1CCC[C@@H](C1)C(N)=O |r| Show InChI InChI=1S/C10H19N3O2/c1-2-8(11)10(15)13-5-3-4-7(6-13)9(12)14/h7-8H,2-6,11H2,1H3,(H2,12,14)/t7-,8-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	4.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition of TPPII in rat cererbral membrane				J Med Chem 48: 7333-42 (2005) Article DOI: 10.1021/jm0500830 BindingDB Entry DOI: 10.7270/Q2KK9CMS
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50085099 (2-Amino-3-methyl-N-(2-methyl-1-methylcarbamoyl-pro...) Show SMILES CNC(=O)C(NC(=O)C(N)C(C)C)C(C)C Show InChI InChI=1S/C11H23N3O2/c1-6(2)8(12)10(15)14-9(7(3)4)11(16)13-5/h6-9H,12H2,1-5H3,(H,13,16)(H,14,15)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	4.60E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition potency against Cholecystokinin-8-Inactivating Peptidase (Serine Peptidase).				J Med Chem 43: 664-74 (2000) BindingDB Entry DOI: 10.7270/Q2RX9CTG
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50085073 (3-Amino-N-[1-(1-carboxy-3-methylsulfanyl-propylcar...) Show SMILES CSCCC(NC(=O)C(Cc1ccc(O)cc1)NC(=O)C(N)CC(O)=O)C(O)=O Show InChI InChI=1S/C18H25N3O7S/c1-29-7-6-13(18(27)28)20-17(26)14(8-10-2-4-11(22)5-3-10)21-16(25)12(19)9-15(23)24/h2-5,12-14,22H,6-9,19H2,1H3,(H,20,26)(H,21,25)(H,23,24)(H,27,28)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Similars	PubMed	5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition potency against Cholecystokinin-8-Inactivating Peptidase (Serine Peptidase).				J Med Chem 43: 664-74 (2000) BindingDB Entry DOI: 10.7270/Q2RX9CTG
					More data for this Ligand-Target Pair
Tripeptidyl-peptidase 2 (Rattus norvegicus)	BDBM50085082 (2-Amino-N-(1-butylcarbamoyl-2-cyclohexyl-ethyl)-3-...) Show SMILES CCCCNC(=O)C(CC1CCCCC1)NC(=O)C(N)C(C)C Show InChI InChI=1S/C18H35N3O2/c1-4-5-11-20-17(22)15(12-14-9-7-6-8-10-14)21-18(23)16(19)13(2)3/h13-16H,4-12,19H2,1-3H3,(H,20,22)(H,21,23)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	5.70E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University College London Curated by ChEMBL					Assay Description Inhibition potency against Cholecystokinin-8-Inactivating Peptidase (Serine Peptidase).				J Med Chem 43: 664-74 (2000) BindingDB Entry DOI: 10.7270/Q2RX9CTG
					More data for this Ligand-Target Pair

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