Compile Data Set for Download or QSAR

Found 810 hits with Last Name = 'huang' and Initial = 'k'   

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
Apelin receptor (Homo sapiens (Human))	BDBM50556826 (CHEMBL4745863) Show SMILES CCCCCCCCCCCCCCCC(=O)N[C@@H](CCC(=O)N[C@@H](CS)C(=O)N[C@@H](CCSC)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)N1CCC[C@H]1C(N)=O)C(O)=O |r| Show InChI	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	0.220	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Displacement of [Glp65, Nle75, Tyr77][125I]-apelin13 from human APJ receptor expressed in HEK293 cells incubated for 1 hr by gamma counting based rad...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01913 BindingDB Entry DOI: 10.7270/Q2BG2SNB
					More data for this Ligand-Target Pair
Apelin receptor (Homo sapiens (Human))	BDBM50556827 (CHEMBL4748838) Show SMILES CSCC[C@H](NC(=O)[C@H](CS)NC(=O)CC[C@H](NC(=O)CCOCCOCCOCCOCCOCCOCCN)C(O)=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)N1CCC[C@H]1C(N)=O |r| Show InChI	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	0.25	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Displacement of [Glp65, Nle75, Tyr77][125I]-apelin13 from human APJ receptor expressed in HEK293 cells incubated for 1 hr by gamma counting based rad...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01913 BindingDB Entry DOI: 10.7270/Q2BG2SNB
					More data for this Ligand-Target Pair
Apelin receptor (Homo sapiens (Human))	BDBM50556825 (CHEMBL4787784) Show SMILES CCCCCCCCCCCCCCCC(=O)N[C@@H](CCC(=O)NCCCC[C@H](N)C(=O)N[C@@H](CS)C(=O)N[C@@H](CCSC)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)N1CCC[C@H]1C(N)=O)C(O)=O |r| Show InChI	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	0.460	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Displacement of [Glp65, Nle75, Tyr77][125I]-apelin13 from human APJ receptor expressed in HEK293 cells incubated for 1 hr by gamma counting based rad...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01913 BindingDB Entry DOI: 10.7270/Q2BG2SNB
					More data for this Ligand-Target Pair
Apelin receptor (Homo sapiens (Human))	BDBM50556828 (CHEMBL4798771) Show SMILES CCCCCCCCCCCCCCCC(=O)N[C@@H](CCC(=O)NCCCC[C@H](NC(=O)CCC(=O)N[C@@H](CS)C(=O)N[C@@H](CCSC)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)N1CCC[C@H]1C(N)=O)C(=O)N[C@@H](CS)C(=O)N[C@@H](CCSC)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)N1CCC[C@H]1C(N)=O)C(O)=O |r| Show InChI	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	0.600	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Displacement of [Glp65, Nle75, Tyr77][125I]-apelin13 from human APJ receptor expressed in HEK293 cells incubated for 1 hr by gamma counting based rad...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01913 BindingDB Entry DOI: 10.7270/Q2BG2SNB
					More data for this Ligand-Target Pair
Sodium-dependent serotonin transporter (Homo sapiens (Human))	BDBM50297420 ((Z)-N-Methyl-2-(naphthalen-1-yloxy)-2-(thiophen-2-...) Show SMILES CNC[C@@H]1C[C@@]1(Oc1cccc2ccccc12)c1cccs1 |r| Show InChI InChI=1S/C19H19NOS/c1-20-13-15-12-19(15,18-10-5-11-22-18)21-17-9-4-7-14-6-2-3-8-16(14)17/h2-11,15,20H,12-13H2,1H3/t15-,19-/m0/s1	PDB KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.01	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Oregon State University Curated by ChEMBL					Assay Description Inhibition of [3H]serotonin reuptake at serotonin transporter				J Med Chem 52: 5872-9 (2009) Article DOI: 10.1021/jm900847b BindingDB Entry DOI: 10.7270/Q26Q1XBR
					More data for this Ligand-Target Pair
Sodium-dependent serotonin transporter (Homo sapiens (Human))	BDBM50297420 ((Z)-N-Methyl-2-(naphthalen-1-yloxy)-2-(thiophen-2-...) Show SMILES CNC[C@@H]1C[C@@]1(Oc1cccc2ccccc12)c1cccs1 |r| Show InChI InChI=1S/C19H19NOS/c1-20-13-15-12-19(15,18-10-5-11-22-18)21-17-9-4-7-14-6-2-3-8-16(14)17/h2-11,15,20H,12-13H2,1H3/t15-,19-/m0/s1	PDB KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Oregon State University Curated by ChEMBL					Assay Description Inhibition of [3H]serotonin reuptake at serotonin transporter				J Med Chem 52: 5872-9 (2009) Article DOI: 10.1021/jm900847b BindingDB Entry DOI: 10.7270/Q26Q1XBR
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435111 (US10584120, Compound 45) Show SMILES O=C1NC(=O)N(C1c1ccc(cc1)-c1nnn(CC2CC2)n1)c1ccc2[nH]cnc2c1 Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435105 (US10584120, Compound 39) Show SMILES O=C1NC(=O)N(C1c1ccc(cc1)-c1cnc(s1)C1CC1)c1ccc2[nH]cnc2c1 Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435104 (US10584120, Compound 38) Show SMILES O=C1NC(=O)N(C1c1ccc(cc1)-c1csc(n1)C1CC1)c1ccc2[nH]cnc2c1 Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Sodium-dependent noradrenaline transporter (Homo sapiens (Human))	BDBM50297420 ((Z)-N-Methyl-2-(naphthalen-1-yloxy)-2-(thiophen-2-...) Show SMILES CNC[C@@H]1C[C@@]1(Oc1cccc2ccccc12)c1cccs1 |r| Show InChI InChI=1S/C19H19NOS/c1-20-13-15-12-19(15,18-10-5-11-22-18)21-17-9-4-7-14-6-2-3-8-16(14)17/h2-11,15,20H,12-13H2,1H3/t15-,19-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.16	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Oregon State University Curated by ChEMBL					Assay Description Inhibition of [3H]norepinephrine reuptake at norepinephrine transporter				J Med Chem 52: 5872-9 (2009) Article DOI: 10.1021/jm900847b BindingDB Entry DOI: 10.7270/Q26Q1XBR
					More data for this Ligand-Target Pair
Sodium-dependent noradrenaline transporter (Homo sapiens (Human))	BDBM50297420 ((Z)-N-Methyl-2-(naphthalen-1-yloxy)-2-(thiophen-2-...) Show SMILES CNC[C@@H]1C[C@@]1(Oc1cccc2ccccc12)c1cccs1 |r| Show InChI InChI=1S/C19H19NOS/c1-20-13-15-12-19(15,18-10-5-11-22-18)21-17-9-4-7-14-6-2-3-8-16(14)17/h2-11,15,20H,12-13H2,1H3/t15-,19-/m0/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.16	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Oregon State University Curated by ChEMBL					Assay Description Inhibition of [3H]norepinephrine reuptake at norepinephrine transporter				J Med Chem 52: 5872-9 (2009) Article DOI: 10.1021/jm900847b BindingDB Entry DOI: 10.7270/Q26Q1XBR
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435108 (US10584120, Compound 42) Show SMILES CCCn1nnc(n1)-c1ccc(cc1)C1N(C(=O)NC1=O)c1ccc2[nH]cnc2c1 Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Sodium-dependent dopamine transporter (Homo sapiens (Human))	BDBM22165 (1-{2-[bis(4-fluorophenyl)methoxy]ethyl}-4-(3-pheny...) Show SMILES Fc1ccc(cc1)C(OCCN1CCN(CCCc2ccccc2)CC1)c1ccc(F)cc1 Show InChI InChI=1S/C28H32F2N2O/c29-26-12-8-24(9-13-26)28(25-10-14-27(30)15-11-25)33-22-21-32-19-17-31(18-20-32)16-4-7-23-5-2-1-3-6-23/h1-3,5-6,8-15,28H,4,7,16-22H2	NCI pathway Reactome pathway KEGG UniProtKB/SwissProt DrugBank GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents Similars	Article PubMed	5.07	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Oregon State University Curated by ChEMBL					Assay Description Inhibition of [3H]dopamine reuptake at dopamine transporter				J Med Chem 52: 5872-9 (2009) Article DOI: 10.1021/jm900847b BindingDB Entry DOI: 10.7270/Q26Q1XBR
					More data for this Ligand-Target Pair
Apelin receptor (Homo sapiens (Human))	BDBM50556824 (CHEMBL4746142) Show SMILES CSCC[C@H](NC(=O)[C@@H](N)CS)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)N1CCC[C@H]1C(N)=O |r| Show InChI	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	5.10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Displacement of [Glp65, Nle75, Tyr77][125I]-apelin13 from human APJ receptor expressed in HEK293 cells incubated for 1 hr by gamma counting based rad...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01913 BindingDB Entry DOI: 10.7270/Q2BG2SNB
					More data for this Ligand-Target Pair
Sodium-dependent noradrenaline transporter (Homo sapiens (Human))	BDBM35229 (3-(10,11-dihydro-5H-dibenzo[b,f]azepin-5-yl)-N-met...) Show SMILES CNCCCN1c2ccccc2CCc2ccccc12 Show InChI InChI=1S/C18H22N2/c1-19-13-6-14-20-17-9-4-2-7-15(17)11-12-16-8-3-5-10-18(16)20/h2-5,7-10,19H,6,11-14H2,1H3	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	DrugBank Article PubMed	5.11	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Oregon State University Curated by ChEMBL					Assay Description Inhibition of [3H]norepinephrine reuptake at norepinephrine transporter				J Med Chem 52: 5872-9 (2009) Article DOI: 10.1021/jm900847b BindingDB Entry DOI: 10.7270/Q26Q1XBR
					More data for this Ligand-Target Pair
Apelin receptor (Homo sapiens (Human))	BDBM50556829 (CHEMBL4743589) Show SMILES CSCC[C@H](NC(=O)[C@H](CS)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H]1CCC(=O)N1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@H]1C(=O)N[C@@H](Cc1ccccc1)C(=O)N1CCC[C@H]1C(N)=O |r| Show InChI	PDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem	Article PubMed	5.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Displacement of [Glp65, Nle75, Tyr77][125I]-apelin13 from human APJ receptor expressed in HEK293 cells incubated for 1 hr by gamma counting based rad...				Citation and Details Article DOI: 10.1021/acs.jmedchem.0c01913 BindingDB Entry DOI: 10.7270/Q2BG2SNB
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435128 (US10584120, Compound 62) Show SMILES COCc1cc(cs1)-c1ccc(C2CNC(=O)N2c2ccc3[nH]cnc3c2)c(F)c1F Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435114 (US10584120, Compound 47) Show SMILES O=C1NC(=O)N(C1c1ccc(cc1)-c1nnn(CC#C)n1)c1ccc2[nH]cnc2c1 Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435123 (US10584120, Compound 56) Show SMILES Fc1c(F)c(ccc1[C@H]1CNC(=O)N1c1ccc2[nH]cnc2c1)-c1csc(c1)C(F)(F)F |r| Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	7	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435126 (US10584120, Compound 60) Show SMILES Cc1cc(cs1)-c1ccc(C2CNC(=O)N2c2ccc3[nH]cnc3c2)c(F)c1F Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	7	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Sodium-dependent serotonin transporter (Homo sapiens (Human))	BDBM50297418 ((E)-N-Methyl-2-(naphthalen-1-yloxy)-2-(thiophen-2-...) Show SMILES CNC[C@H]1C[C@@]1(Oc1cccc2ccccc12)c1cccs1 |r| Show InChI InChI=1S/C19H19NOS/c1-20-13-15-12-19(15,18-10-5-11-22-18)21-17-9-4-7-14-6-2-3-8-16(14)17/h2-11,15,20H,12-13H2,1H3/t15-,19+/m1/s1	PDB KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	7.47	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Oregon State University Curated by ChEMBL					Assay Description Inhibition of [3H]serotonin reuptake at serotonin transporter				J Med Chem 52: 5872-9 (2009) Article DOI: 10.1021/jm900847b BindingDB Entry DOI: 10.7270/Q26Q1XBR
					More data for this Ligand-Target Pair
Sodium-dependent serotonin transporter (Homo sapiens (Human))	BDBM50297418 ((E)-N-Methyl-2-(naphthalen-1-yloxy)-2-(thiophen-2-...) Show SMILES CNC[C@H]1C[C@@]1(Oc1cccc2ccccc12)c1cccs1 |r| Show InChI InChI=1S/C19H19NOS/c1-20-13-15-12-19(15,18-10-5-11-22-18)21-17-9-4-7-14-6-2-3-8-16(14)17/h2-11,15,20H,12-13H2,1H3/t15-,19+/m1/s1	PDB KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	7.47	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Oregon State University Curated by ChEMBL					Assay Description Inhibition of [3H]serotonin reuptake at serotonin transporter				J Med Chem 52: 5872-9 (2009) Article DOI: 10.1021/jm900847b BindingDB Entry DOI: 10.7270/Q26Q1XBR
					More data for this Ligand-Target Pair
Sodium-dependent serotonin transporter (Homo sapiens (Human))	BDBM50010859 (CHEMBL11 | IMIPRAMINE HYDROCHLORIDE | IMIPRAMINE P...) Show SMILES CN(C)CCCN1c2ccccc2CCc2ccccc12 Show InChI InChI=1S/C19H24N2/c1-20(2)14-7-15-21-18-10-5-3-8-16(18)12-13-17-9-4-6-11-19(17)21/h3-6,8-11H,7,12-15H2,1-2H3	PDB KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid PDB UniChem Patents Similars	DrugBank PDB Article PubMed	7.57	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Oregon State University Curated by ChEMBL					Assay Description Inhibition of [3H]serotonin reuptake at serotonin transporter				J Med Chem 52: 5872-9 (2009) Article DOI: 10.1021/jm900847b BindingDB Entry DOI: 10.7270/Q26Q1XBR
					More data for this Ligand-Target Pair				3D Structure (crystal)
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435112 (US10584120, Compound 46) Show SMILES FC(F)(F)Cn1nnc(n1)-c1ccc(cc1)C1N(C(=O)NC1=O)c1ccc2[nH]cnc2c1 Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	8	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435109 (US10584120, Compound 43) Show SMILES CC(C)n1nnc(n1)-c1ccc(cc1)C1N(C(=O)NC1=O)c1ccc2[nH]cnc2c1 Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	8	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435106 (US10584120, Compound 40) Show SMILES FC(F)(F)c1ncc(s1)-c1ccc(cc1)C1N(C(=O)NC1=O)c1ccc2[nH]cnc2c1 Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	9	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435116 (US10584120, Compound 49) Show SMILES CCC#CCn1nnc(n1)-c1ccc(cc1)C1N(C(=O)NC1=O)c1ccc2[nH]cnc2c1 Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435115 (US10584120, Compound 48) Show SMILES CC#CCn1nnc(n1)-c1ccc(cc1)C1N(C(=O)NC1=O)c1ccc2[nH]cnc2c1 Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435110 (US10584120, Compound 44) Show SMILES CC(C)Cn1nnc(n1)-c1ccc(cc1)C1N(C(=O)NC1=O)c1ccc2[nH]cnc2c1 Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435129 (US10584120, Compound 63) Show SMILES CCOCc1cc(cs1)-c1ccc(C2CNC(=O)N2c2ccc3[nH]cnc3c2)c(F)c1F Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	11	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435107 (US10584120, Compound 41) Show SMILES Cn1nnc(n1)-c1ccc(cc1)C1N(C(=O)NC1=O)c1ccc2[nH]cnc2c1 Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	12	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435130 (US10584120, Compound 64) Show SMILES COC(=O)c1cc(cs1)-c1ccc(C2CNC(=O)N2c2ccc3[nH]cnc3c2)c(F)c1F Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	13	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435117 (US10584120, Compound 50) Show SMILES Clc1ccc(Cn2nnc(n2)-c2ccc(cc2)C2N(C(=O)NC2=O)c2ccc3[nH]cnc3c2)cc1 Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	13	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435078 (US10584120, Compound 9) Show SMILES FC(F)(F)c1ncc(s1)-c1ccc(cc1)[C@H]1CNC(=O)N1c1ccc2[nH]cnc2c1 |r| Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	16	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435127 (US10584120, Compound 61) Show SMILES CCc1cc(cs1)-c1ccc(C2CNC(=O)N2c2ccc3[nH]cnc3c2)c(F)c1F Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	16	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435103 (US10584120, Compound 37) Show SMILES FC(F)(F)c1csc(n1)-c1ccc(cc1)C1N(C(=O)NC1=O)c1ccc2[nH]cnc2c1 Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	18	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435125 (US10584120, Compound 59) Show SMILES Fc1c(F)c(ccc1C1CNC(=O)N1c1ccc2[nH]cnc2c1)-c1csc(Cl)c1 Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	19	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435131 (US10584120, Compound 65) Show SMILES Fc1c(F)c(ccc1C1CNC(=O)N1c1ccc2[nH]cnc2c1)-c1ccsc1 Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435075 (US10584120, Compound 7) Show SMILES O=C1NCC(N1c1ccc2[nH]cnc2c1)c1ccc(cc1)-c1cnc(s1)C1CC1 Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	21	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435121 (US10584120, Compound 54) Show SMILES Fc1cc(ccc1-c1csc(c1)C(F)(F)F)[C@H]1CNC(=O)N1c1ccc2[nH]cnc2c1 |r| Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	23	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435118 (US10584120, Compound 51) Show SMILES COc1ccc(Cn2nnc(n2)-c2ccc(cc2)C2N(C(=O)NC2=O)c2ccc3[nH]cnc3c2)cc1 Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	24	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Sodium-dependent noradrenaline transporter (Homo sapiens (Human))	BDBM50297421 (CHEMBL558525 | N-methyl-1-((1R,2R)-2-(naphthalen-1...) Show SMILES CNC[C@H]1C[C@]1(Oc1cccc2ccccc12)c1cccs1 |r| Show InChI InChI=1S/C19H19NOS/c1-20-13-15-12-19(15,18-10-5-11-22-18)21-17-9-4-7-14-6-2-3-8-16(14)17/h2-11,15,20H,12-13H2,1H3/t15-,19-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	27.8	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Oregon State University Curated by ChEMBL					Assay Description Inhibition of [3H]norepinephrine reuptake at norepinephrine transporter				J Med Chem 52: 5872-9 (2009) Article DOI: 10.1021/jm900847b BindingDB Entry DOI: 10.7270/Q26Q1XBR
					More data for this Ligand-Target Pair
Sodium-dependent serotonin transporter (Homo sapiens (Human))	BDBM50297421 (CHEMBL558525 | N-methyl-1-((1R,2R)-2-(naphthalen-1...) Show SMILES CNC[C@H]1C[C@]1(Oc1cccc2ccccc12)c1cccs1 |r| Show InChI InChI=1S/C19H19NOS/c1-20-13-15-12-19(15,18-10-5-11-22-18)21-17-9-4-7-14-6-2-3-8-16(14)17/h2-11,15,20H,12-13H2,1H3/t15-,19-/m1/s1	PDB KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	30.4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Oregon State University Curated by ChEMBL					Assay Description Inhibition of [3H]serotonin reuptake at serotonin transporter				J Med Chem 52: 5872-9 (2009) Article DOI: 10.1021/jm900847b BindingDB Entry DOI: 10.7270/Q26Q1XBR
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435102 (US10584120, Compound 36) Show SMILES FC(F)(F)c1cc(cs1)-c1ccc(cc1)[C@H]1CNC(=O)N1c1ccc2[nH]cnc2c1 |r| Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	32	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Sodium-dependent serotonin transporter (Homo sapiens (Human))	BDBM50297419 (CHEMBL558065 | N-methyl-1-((1S,2R)-2-(naphthalen-1...) Show SMILES CNC[C@@H]1C[C@]1(Oc1cccc2ccccc12)c1cccs1 |r| Show InChI InChI=1S/C19H19NOS/c1-20-13-15-12-19(15,18-10-5-11-22-18)21-17-9-4-7-14-6-2-3-8-16(14)17/h2-11,15,20H,12-13H2,1H3/t15-,19+/m0/s1	PDB KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	33.2	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Oregon State University Curated by ChEMBL					Assay Description Inhibition of [3H]serotonin reuptake at serotonin transporter				J Med Chem 52: 5872-9 (2009) Article DOI: 10.1021/jm900847b BindingDB Entry DOI: 10.7270/Q26Q1XBR
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435090 (US10584120, Compound 21) Show SMILES CC(C)n1nnc(n1)-c1ccc(cc1)C1CNC(=O)N1c1ccc2[nH]cnc2c1 Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	36	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435097 (US10584120, Compound 28) Show SMILES Fc1c(F)c(ccc1C1CNC(=O)N1c1ccc2[nH]cnc2c1)-c1csc(c1)C(F)(F)F Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	39	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435076 (US10584120, Compound 8) Show SMILES FC(F)(F)c1ncc(s1)-c1ccc(cc1)C1CNC(=O)N1c1ccc2[nH]cnc2c1 Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	49	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435072 (US10584120, Compound 1) Show SMILES O=C1NCC(N1c1ccc2[nH]cnc2c1)c1ccc(cc1)-c1nccs1 Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	53	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair
Glutaminyl-peptide cyclotransferase (Homo sapiens (Human))	BDBM435089 (US10584120, Compound 20) Show SMILES CCCn1nnc(n1)-c1ccc(cc1)C1CNC(=O)N1c1ccc2[nH]cnc2c1 Show InChI	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	US Patent	57	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Health Research Institutes; Academia Sinica US Patent					Assay Description An inhibition activity assay of QC inhibitors was conducted. See Huang et al., J. Biol. Chem. 2011, 286, 12439-12449. A reaction mixture containing 3...				US Patent US10584120 (2020) BindingDB Entry DOI: 10.7270/Q2ZK5K20
					More data for this Ligand-Target Pair

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