Found 205 hits with Last Name = 'rosenblum' and Initial = 'js' 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 |
Dipeptidyl peptidase 4
(Homo sapiens (Human)) | BDBM50050513
((R)-1-((S)-2-amino-3-methylbutanoyl)pyrrolidin-2-y...)Show InChI InChI=1S/C9H19BN2O3/c1-6(2)8(11)9(13)12-5-3-4-7(12)10(14)15/h6-8,14-15H,3-5,11H2,1-2H3/t7-,8-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 0.100 | n/a | n/a | n/a | n/a | n/a | n/a |
Tufts University School of Medicine
Curated by ChEMBL
| Assay Description Inhibition of human DPP4 |
Bioorg Med Chem Lett 17: 507-10 (2007)
Article DOI: 10.1016/j.bmcl.2006.10.012 BindingDB Entry DOI: 10.7270/Q2T43SQH |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 4
(Homo sapiens (Human)) | BDBM50050517
(Boronic acid derivative | CHEMBL305170 | N-alkyl G...)Show InChI InChI=1S/C9H19BN2O3/c1-6(2)8(11)9(13)12-5-3-4-7(12)10(14)15/h6-8,14-15H,3-5,11H2,1-2H3/t7-,8+/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid PDB UniChem
Similars
| Article PubMed
| n/a | n/a | 0.300 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against human DPP4 using Gly-Pro-AMC in fluorometric assay |
Bioorg Med Chem Lett 15: 4239-42 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.075 BindingDB Entry DOI: 10.7270/Q2CJ8D2F |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 4
(Homo sapiens (Human)) | BDBM50171552
((S)-2-(S)-Amino-1-(2-boron-dihydroxide-pyrrolidine...)Show InChI InChI=1S/C9H19BN2O3/c1-6(2)8(11)9(13)12-5-3-4-7(12)10(14)15/h6-8,14-15H,3-5,11H2,1-2H3/t7-,8+/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 0.300 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences
Curated by ChEMBL
| Assay Description Inhibitory concentration against human dipeptidylpeptidase 4 |
Bioorg Med Chem Lett 15: 4256-60 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.076 BindingDB Entry DOI: 10.7270/Q2RR1XSW |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 2
(Homo sapiens (Human)) | BDBM50171546
((S)-2,4-Diamino-N-((R)-1-boron-dihydroxide-pentyl)...)Show InChI InChI=1S/C9H22BN3O3/c1-2-3-4-8(10(15)16)13-9(14)7(12)5-6-11/h7-8,15-16H,2-6,11-12H2,1H3,(H,13,14)/t7-,8+/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 0.480 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences
Curated by ChEMBL
| Assay Description Inhibitory concentration against human dipeptidylpeptidase 7 |
Bioorg Med Chem Lett 15: 4256-60 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.076 BindingDB Entry DOI: 10.7270/Q2RR1XSW |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 2
(Homo sapiens (Human)) | BDBM50196928
((R)-1-((S)-2,4-diaminobutanamido)pentylboronic aci...)Show InChI InChI=1S/C9H22BN3O3/c1-2-3-4-8(10(15)16)13-9(14)7(12)5-6-11/h7-8,15-16H,2-6,11-12H2,1H3,(H,13,14)/t7-,8-/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 0.480 | n/a | n/a | n/a | n/a | n/a | n/a |
Tufts University School of Medicine
Curated by ChEMBL
| Assay Description Inhibition of human DPP2 |
Bioorg Med Chem Lett 17: 507-10 (2007)
Article DOI: 10.1016/j.bmcl.2006.10.012 BindingDB Entry DOI: 10.7270/Q2T43SQH |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 2
(Homo sapiens (Human)) | BDBM50171555
((S)-2,4-Diamino-1-(2-boron-dihydroxide-pyrrolidin-...)Show InChI InChI=1S/C8H18BN3O3/c10-4-3-6(11)8(13)12-5-1-2-7(12)9(14)15/h6-7,14-15H,1-5,10-11H2/t6-,7+/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 0.720 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences
Curated by ChEMBL
| Assay Description Inhibitory concentration against human dipeptidylpeptidase 7 |
Bioorg Med Chem Lett 15: 4256-60 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.076 BindingDB Entry DOI: 10.7270/Q2RR1XSW |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 4
(Homo sapiens (Human)) | BDBM50171653
(CHEMBL196120 | N-alkyl Gly-boro-Pro derivative)Show InChI InChI=1S/C7H15BN2O3/c1-5(9)7(11)10-4-2-3-6(10)8(12)13/h5-6,12-13H,2-4,9H2,1H3/t5-,6+/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 0.800 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against human DPP4 using Gly-Pro-AMC in fluorometric assay |
Bioorg Med Chem Lett 15: 4239-42 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.075 BindingDB Entry DOI: 10.7270/Q2CJ8D2F |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 2
(Homo sapiens (Human)) | BDBM50196929
((S)-2,4-diamino-1-((3aR,6aR)-hexahydrocyclopenta[b...)Show InChI InChI=1S/C11H21N3O/c12-6-4-9(13)11(15)14-7-5-8-2-1-3-10(8)14/h8-10H,1-7,12-13H2/t8-,9+,10-/m1/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 0.880 | n/a | n/a | n/a | n/a | n/a | n/a |
Tufts University School of Medicine
Curated by ChEMBL
| Assay Description Inhibition of human DPP2 |
Bioorg Med Chem Lett 17: 507-10 (2007)
Article DOI: 10.1016/j.bmcl.2006.10.012 BindingDB Entry DOI: 10.7270/Q2T43SQH |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 4
(Homo sapiens (Human)) | BDBM50171556
((R)-1-((S)-2-amino-3-methylbutanamido)ethylboronic...)Show InChI InChI=1S/C7H17BN2O3/c1-4(2)6(9)7(11)10-5(3)8(12)13/h4-6,12-13H,9H2,1-3H3,(H,10,11)/t5-,6-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
| Article PubMed
| n/a | n/a | 0.890 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences
Curated by ChEMBL
| Assay Description Inhibitory concentration against human dipeptidylpeptidase 4 |
Bioorg Med Chem Lett 15: 4256-60 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.076 BindingDB Entry DOI: 10.7270/Q2RR1XSW |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 2
(Homo sapiens (Human)) | BDBM50171648
(CHEMBL372180 | N-alkyl Gly-boro-Pro derivative)Show SMILES CCCCCC12CCC(CC1)(CC2)NCC(=O)N1CCC[C@H]1B(O)O Show InChI InChI=1S/C19H35BN2O3/c1-2-3-4-7-18-8-11-19(12-9-18,13-10-18)21-15-17(23)22-14-5-6-16(22)20(24)25/h16,21,24-25H,2-15H2,1H3/t16-,18?,19?/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against human DPP7 using Ala-Pro-AMC in fluorometric assay |
Bioorg Med Chem Lett 15: 4239-42 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.075 BindingDB Entry DOI: 10.7270/Q2CJ8D2F |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 2
(Homo sapiens (Human)) | BDBM50171649
(CHEMBL196933 | N-alkyl Gly-boro-Pro derivative)Show InChI InChI=1S/C13H25BN2O3/c17-13(16-9-5-8-12(16)14(18)19)10-15-11-6-3-1-2-4-7-11/h11-12,15,18-19H,1-10H2/t12-/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.80 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against human DPP7 using Ala-Pro-AMC in fluorometric assay |
Bioorg Med Chem Lett 15: 4239-42 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.075 BindingDB Entry DOI: 10.7270/Q2CJ8D2F |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 2
(Homo sapiens (Human)) | BDBM50171548
((S)-2-(S)-Amino-1-(2-boron-dihydroxide-pyrrolidin-...)Show InChI InChI=1S/C10H21BN2O3/c1-2-3-5-8(12)10(14)13-7-4-6-9(13)11(15)16/h8-9,15-16H,2-7,12H2,1H3/t8-,9+/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences
Curated by ChEMBL
| Assay Description Inhibitory concentration against human dipeptidylpeptidase 7 |
Bioorg Med Chem Lett 15: 4256-60 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.076 BindingDB Entry DOI: 10.7270/Q2RR1XSW |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 9
(Homo sapiens (Human)) | BDBM50050513
((R)-1-((S)-2-amino-3-methylbutanoyl)pyrrolidin-2-y...)Show InChI InChI=1S/C9H19BN2O3/c1-6(2)8(11)9(13)12-5-3-4-7(12)10(14)15/h6-8,14-15H,3-5,11H2,1-2H3/t7-,8-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 2 | n/a | n/a | n/a | n/a | n/a | n/a |
Tufts University School of Medicine
Curated by ChEMBL
| Assay Description Inhibition of human DPP9 |
Bioorg Med Chem Lett 17: 507-10 (2007)
Article DOI: 10.1016/j.bmcl.2006.10.012 BindingDB Entry DOI: 10.7270/Q2T43SQH |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 9
(Homo sapiens (Human)) | BDBM50171552
((S)-2-(S)-Amino-1-(2-boron-dihydroxide-pyrrolidine...)Show InChI InChI=1S/C9H19BN2O3/c1-6(2)8(11)9(13)12-5-3-4-7(12)10(14)15/h6-8,14-15H,3-5,11H2,1-2H3/t7-,8+/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences
Curated by ChEMBL
| Assay Description Inhibitory concentration against human dipeptidylpeptidase 9 using FP-TAMRA incubated for 30 min |
Bioorg Med Chem Lett 15: 4256-60 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.076 BindingDB Entry DOI: 10.7270/Q2RR1XSW |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 2
(Homo sapiens (Human)) | BDBM50171645
(2-Cyclodecylamino-1-pyrrolidin-1-yl--2-borandihydr...)Show InChI InChI=1S/C16H31BN2O3/c20-16(19-12-8-11-15(19)17(21)22)13-18-14-9-6-4-2-1-3-5-7-10-14/h14-15,18,21-22H,1-13H2/t15-/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2.20 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against human DPP7 using Ala-Pro-AMC in fluorometric assay |
Bioorg Med Chem Lett 15: 4239-42 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.075 BindingDB Entry DOI: 10.7270/Q2CJ8D2F |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 2
(Homo sapiens (Human)) | BDBM50171558
(2,6-Diamino-hexanoic acid ((R)-1-boron-dihydroxide...)Show InChI InChI=1S/C11H26BN3O3/c1-2-3-7-10(12(17)18)15-11(16)9(14)6-4-5-8-13/h9-10,17-18H,2-8,13-14H2,1H3,(H,15,16)/t9-,10+/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 3.70 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences
Curated by ChEMBL
| Assay Description Inhibitory concentration against human dipeptidylpeptidase 7 |
Bioorg Med Chem Lett 15: 4256-60 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.076 BindingDB Entry DOI: 10.7270/Q2RR1XSW |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 2
(Homo sapiens (Human)) | BDBM50171650
(2-Cyclooctonylamino-1-pyrrolidin-1-yl--2-borandihy...)Show InChI InChI=1S/C14H27BN2O3/c18-14(17-10-6-9-13(17)15(19)20)11-16-12-7-4-2-1-3-5-8-12/h12-13,16,19-20H,1-11H2/t13-/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 4 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against human DPP7 using Ala-Pro-AMC in fluorometric assay |
Bioorg Med Chem Lett 15: 4239-42 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.075 BindingDB Entry DOI: 10.7270/Q2CJ8D2F |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 2
(Homo sapiens (Human)) | BDBM50171656
(2-Cyclohexylamino-1-pyrrolidin-1-yl--2-borandihydr...)Show InChI InChI=1S/C12H23BN2O3/c16-12(9-14-10-5-2-1-3-6-10)15-8-4-7-11(15)13(17)18/h10-11,14,17-18H,1-9H2/t11-/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 4.10 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against human DPP7 using Ala-Pro-AMC in fluorometric assay |
Bioorg Med Chem Lett 15: 4239-42 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.075 BindingDB Entry DOI: 10.7270/Q2CJ8D2F |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 4
(Homo sapiens (Human)) | BDBM50171548
((S)-2-(S)-Amino-1-(2-boron-dihydroxide-pyrrolidin-...)Show InChI InChI=1S/C10H21BN2O3/c1-2-3-5-8(12)10(14)13-7-4-6-9(13)11(15)16/h8-9,15-16H,2-7,12H2,1H3/t8-,9+/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 4.5 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences
Curated by ChEMBL
| Assay Description Inhibitory concentration against human dipeptidylpeptidase 4 |
Bioorg Med Chem Lett 15: 4256-60 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.076 BindingDB Entry DOI: 10.7270/Q2RR1XSW |
More data for this Ligand-Target Pair | |
Prolyl endopeptidase FAP
(Homo sapiens (Human)) | BDBM50171647
(CHEMBL373269 | N-alkyl Gly-boro-Pro derivative)Show SMILES OB(O)[C@H]1CCCN1C(=O)CNC12CC3CC(CC(C3)C1)C2 |TLB:15:16:20:14.13.19,THB:17:18:13:16.21.15,17:16:13:18.20.19,15:14:20:16.21.17| Show InChI InChI=1S/C16H27BN2O3/c20-15(19-3-1-2-14(19)17(21)22)10-18-16-7-11-4-12(8-16)6-13(5-11)9-16/h11-14,18,21-22H,1-10H2/t11?,12?,13?,14-,16?/m1/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 4.60 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against human FAP using Lys-Pro-AMC in fluorometric assay |
Bioorg Med Chem Lett 15: 4239-42 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.075 BindingDB Entry DOI: 10.7270/Q2CJ8D2F |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 9
(Homo sapiens (Human)) | BDBM50171548
((S)-2-(S)-Amino-1-(2-boron-dihydroxide-pyrrolidin-...)Show InChI InChI=1S/C10H21BN2O3/c1-2-3-5-8(12)10(14)13-7-4-6-9(13)11(15)16/h8-9,15-16H,2-7,12H2,1H3/t8-,9+/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 4.60 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences
Curated by ChEMBL
| Assay Description Inhibitory concentration against human dipeptidylpeptidase 9 using FP-TAMRA incubated for 30 min |
Bioorg Med Chem Lett 15: 4256-60 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.076 BindingDB Entry DOI: 10.7270/Q2RR1XSW |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 2
(Homo sapiens (Human)) | BDBM50171553
(2,5-Diamino-pentanoic acid ((R)-1-boron-dihydroxid...)Show InChI InChI=1S/C10H24BN3O3/c1-2-3-6-9(11(16)17)14-10(15)8(13)5-4-7-12/h8-9,16-17H,2-7,12-13H2,1H3,(H,14,15)/t8-,9+/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 4.70 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences
Curated by ChEMBL
| Assay Description Inhibitory concentration against human dipeptidylpeptidase 7 |
Bioorg Med Chem Lett 15: 4256-60 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.076 BindingDB Entry DOI: 10.7270/Q2RR1XSW |
More data for this Ligand-Target Pair | |
Serine/threonine-protein kinase PLK1
(Homo sapiens (Human)) | BDBM15234
((1R,3R,5S,9R,18S)-18-(methoxymethyl)-1,5-dimethyl-...)Show SMILES [H][C@@]12CCC(=O)[C@@]1(C)C[C@@H](OC(C)=O)C1=C2C(=O)c2occ3c2[C@]1(C)[C@@H](COC)OC3=O |r,c:15| Show InChI InChI=1S/C23H24O8/c1-10(24)30-13-7-22(2)12(5-6-14(22)25)16-18(13)23(3)15(9-28-4)31-21(27)11-8-29-20(17(11)23)19(16)26/h8,12-13,15H,5-7,9H2,1-4H3/t12-,13+,15+,22-,23-/m0/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL DrugBank MCE KEGG PC cid PC sid PDB UniChem
Patents
Similars
| DrugBank Article PubMed
| n/a | n/a | 5.80 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibition of AX7503 binding to recombinant Plk1 (unknown origin) by Western blot |
J Biol Chem 282: 2505-11 (2007)
Article DOI: 10.1074/jbc.M609603200 BindingDB Entry DOI: 10.7270/Q2QV3M8X |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 2
(Homo sapiens (Human)) | BDBM50171653
(CHEMBL196120 | N-alkyl Gly-boro-Pro derivative)Show InChI InChI=1S/C7H15BN2O3/c1-5(9)7(11)10-4-2-3-6(10)8(12)13/h5-6,12-13H,2-4,9H2,1H3/t5-,6+/m1/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 6.30 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against human DPP7 using Ala-Pro-AMC in fluorometric assay |
Bioorg Med Chem Lett 15: 4239-42 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.075 BindingDB Entry DOI: 10.7270/Q2CJ8D2F |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 9
(Homo sapiens (Human)) | BDBM50171555
((S)-2,4-Diamino-1-(2-boron-dihydroxide-pyrrolidin-...)Show InChI InChI=1S/C8H18BN3O3/c10-4-3-6(11)8(13)12-5-1-2-7(12)9(14)15/h6-7,14-15H,1-5,10-11H2/t6-,7+/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 6.70 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences
Curated by ChEMBL
| Assay Description Inhibitory concentration against human dipeptidylpeptidase 9 using FP-TAMRA incubated for 30 min |
Bioorg Med Chem Lett 15: 4256-60 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.076 BindingDB Entry DOI: 10.7270/Q2RR1XSW |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 4
(Homo sapiens (Human)) | BDBM50171649
(CHEMBL196933 | N-alkyl Gly-boro-Pro derivative)Show InChI InChI=1S/C13H25BN2O3/c17-13(16-9-5-8-12(16)14(18)19)10-15-11-6-3-1-2-4-7-11/h11-12,15,18-19H,1-10H2/t12-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 7.80 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against human DPP4 using Gly-Pro-AMC in fluorometric assay |
Bioorg Med Chem Lett 15: 4239-42 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.075 BindingDB Entry DOI: 10.7270/Q2CJ8D2F |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 2
(Homo sapiens (Human)) | BDBM50171657
(2-(Bicyclo[3.2.1]oct-6-ylamino)-1-((S)-2-dihydroxy...)Show SMILES OC(O)[C@@H]1CCCN1C(=O)CNC1CC2CC1CCC2 |TLB:11:12:15:17.18.19| Show InChI InChI=1S/C15H26N2O3/c18-14(17-6-2-5-13(17)15(19)20)9-16-12-8-10-3-1-4-11(12)7-10/h10-13,15-16,19-20H,1-9H2/t10?,11?,12?,13-/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 8 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against human DPP7 using Ala-Pro-AMC in fluorometric assay |
Bioorg Med Chem Lett 15: 4239-42 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.075 BindingDB Entry DOI: 10.7270/Q2CJ8D2F |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 4
(Homo sapiens (Human)) | BDBM50171647
(CHEMBL373269 | N-alkyl Gly-boro-Pro derivative)Show SMILES OB(O)[C@H]1CCCN1C(=O)CNC12CC3CC(CC(C3)C1)C2 |TLB:15:16:20:14.13.19,THB:17:18:13:16.21.15,17:16:13:18.20.19,15:14:20:16.21.17| Show InChI InChI=1S/C16H27BN2O3/c20-15(19-3-1-2-14(19)17(21)22)10-18-16-7-11-4-12(8-16)6-13(5-11)9-16/h11-14,18,21-22H,1-10H2/t11?,12?,13?,14-,16?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 8 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against human DPP4 using Gly-Pro-AMC in fluorometric assay |
Bioorg Med Chem Lett 15: 4239-42 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.075 BindingDB Entry DOI: 10.7270/Q2CJ8D2F |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 2
(Homo sapiens (Human)) | BDBM50171559
((S)-2,3-Diamino-N-((R)-1-boron-dihydroxide-pentyl)...)Show InChI InChI=1S/C8H20BN3O3/c1-2-3-4-7(9(14)15)12-8(13)6(11)5-10/h6-7,14-15H,2-5,10-11H2,1H3,(H,12,13)/t6-,7+/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 8.20 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences
Curated by ChEMBL
| Assay Description Inhibitory concentration against human dipeptidylpeptidase 7 |
Bioorg Med Chem Lett 15: 4256-60 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.076 BindingDB Entry DOI: 10.7270/Q2RR1XSW |
More data for this Ligand-Target Pair | |
Prolyl endopeptidase FAP
(Homo sapiens (Human)) | BDBM50171552
((S)-2-(S)-Amino-1-(2-boron-dihydroxide-pyrrolidine...)Show InChI InChI=1S/C9H19BN2O3/c1-6(2)8(11)9(13)12-5-3-4-7(12)10(14)15/h6-8,14-15H,3-5,11H2,1-2H3/t7-,8+/m1/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 11 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences
Curated by ChEMBL
| Assay Description Inhibitory concentration against human fibroblast activation protein alpha |
Bioorg Med Chem Lett 15: 4256-60 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.076 BindingDB Entry DOI: 10.7270/Q2RR1XSW |
More data for this Ligand-Target Pair | |
Prolyl endopeptidase FAP
(Homo sapiens (Human)) | BDBM50050517
(Boronic acid derivative | CHEMBL305170 | N-alkyl G...)Show InChI InChI=1S/C9H19BN2O3/c1-6(2)8(11)9(13)12-5-3-4-7(12)10(14)15/h6-8,14-15H,3-5,11H2,1-2H3/t7-,8+/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid PDB UniChem
Similars
| Article PubMed
| n/a | n/a | 11 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against human FAP using Lys-Pro-AMC in fluorometric assay |
Bioorg Med Chem Lett 15: 4239-42 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.075 BindingDB Entry DOI: 10.7270/Q2CJ8D2F |
More data for this Ligand-Target Pair | |
Glycogen synthase kinase-3 beta
(Homo sapiens (Human)) | BDBM50354779
(CHEMBL1834330)Show SMILES Nc1c(F)c(NCCNc2ccccn2)c2OCC3(CCCC3)n3cc(C(O)=O)c(=O)c1c23 Show InChI InChI=1S/C23H24FN5O4/c24-16-17(25)15-19-21(18(16)28-10-9-27-14-5-1-4-8-26-14)33-12-23(6-2-3-7-23)29(19)11-13(20(15)30)22(31)32/h1,4-5,8,11,28H,2-3,6-7,9-10,12,25H2,(H,26,27)(H,31,32) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 12 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibition of human recombinant full length GSK3beta after 1 hrs by luminescence assay |
Bioorg Med Chem Lett 21: 5948-51 (2011)
Article DOI: 10.1016/j.bmcl.2011.07.073 BindingDB Entry DOI: 10.7270/Q23T9HMH |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 4
(Homo sapiens (Human)) | BDBM50171644
(CHEMBL427012 | N-alkyl Gly-boro-Pro derivative)Show SMILES OB(O)[C@H]1CCCN1C(=O)CNC1C2CC3CC(C2)CC1C3 |wU:3.2,TLB:11:12:19:15.21.16,14:15:19:13.12.18,THB:16:17:12:15.14.21,16:15:12:17.19.18,14:13:19:15.21.16,(14.33,-8.43,;13.44,-7.16,;14.08,-5.74,;11.88,-7.31,;11.1,-8.65,;9.61,-8.32,;9.44,-6.8,;10.85,-6.16,;11.13,-4.63,;12.58,-4.12,;9.96,-3.64,;8.51,-4.15,;7.17,-4.92,;7.17,-6.47,;6.14,-7.73,;4.74,-7.17,;3.24,-7.59,;4.43,-6.32,;5.77,-6.81,;4.43,-4.83,;5.77,-4.35,;4.74,-5.58,)| Show InChI InChI=1S/C16H27BN2O3/c20-15(19-3-1-2-14(19)17(21)22)9-18-16-12-5-10-4-11(7-12)8-13(16)6-10/h10-14,16,18,21-22H,1-9H2/t10?,11?,12?,13?,14-,16?/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 12 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against human DPP4 using Gly-Pro-AMC in fluorometric assay |
Bioorg Med Chem Lett 15: 4239-42 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.075 BindingDB Entry DOI: 10.7270/Q2CJ8D2F |
More data for this Ligand-Target Pair | |
Glycogen synthase kinase-3 beta
(Homo sapiens (Human)) | BDBM50354765
(CHEMBL1834315)Show SMILES Nc1c(F)c(NCCNc2ccccn2)cc2n(cc(C(O)=O)c(=O)c12)C1CC1 Show InChI InChI=1S/C20H20FN5O3/c21-17-13(23-7-8-25-15-3-1-2-6-24-15)9-14-16(18(17)22)19(27)12(20(28)29)10-26(14)11-4-5-11/h1-3,6,9-11,23H,4-5,7-8,22H2,(H,24,25)(H,28,29) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 13 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibition of human recombinant full length GSK3beta after 1 hrs by luminescence assay |
Bioorg Med Chem Lett 21: 5948-51 (2011)
Article DOI: 10.1016/j.bmcl.2011.07.073 BindingDB Entry DOI: 10.7270/Q23T9HMH |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 8
(Homo sapiens (Human)) | BDBM50171552
((S)-2-(S)-Amino-1-(2-boron-dihydroxide-pyrrolidine...)Show InChI InChI=1S/C9H19BN2O3/c1-6(2)8(11)9(13)12-5-3-4-7(12)10(14)15/h6-8,14-15H,3-5,11H2,1-2H3/t7-,8+/m1/s1 | PDB
KEGG
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 15 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences
Curated by ChEMBL
| Assay Description Inhibitory concentration against human dipeptidylpeptidase 8 using FP-TAMRA incubated for 30 min |
Bioorg Med Chem Lett 15: 4256-60 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.076 BindingDB Entry DOI: 10.7270/Q2RR1XSW |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 2
(Homo sapiens (Human)) | BDBM50171651
(2-Cyclopentylamino-1-pyrrolidin-1-yl--2-borandihyd...)Show InChI InChI=1S/C11H21BN2O3/c15-11(8-13-9-4-1-2-5-9)14-7-3-6-10(14)12(16)17/h9-10,13,16-17H,1-8H2/t10-/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 15 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against human DPP7 using Ala-Pro-AMC in fluorometric assay |
Bioorg Med Chem Lett 15: 4239-42 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.075 BindingDB Entry DOI: 10.7270/Q2CJ8D2F |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 4
(Homo sapiens (Human)) | BDBM50171555
((S)-2,4-Diamino-1-(2-boron-dihydroxide-pyrrolidin-...)Show InChI InChI=1S/C8H18BN3O3/c10-4-3-6(11)8(13)12-5-1-2-7(12)9(14)15/h6-7,14-15H,1-5,10-11H2/t6-,7+/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 15 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences
Curated by ChEMBL
| Assay Description Inhibitory concentration against human dipeptidylpeptidase 4 |
Bioorg Med Chem Lett 15: 4256-60 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.076 BindingDB Entry DOI: 10.7270/Q2RR1XSW |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 8
(Homo sapiens (Human)) | BDBM50050513
((R)-1-((S)-2-amino-3-methylbutanoyl)pyrrolidin-2-y...)Show InChI InChI=1S/C9H19BN2O3/c1-6(2)8(11)9(13)12-5-3-4-7(12)10(14)15/h6-8,14-15H,3-5,11H2,1-2H3/t7-,8-/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 17 | n/a | n/a | n/a | n/a | n/a | n/a |
Tufts University School of Medicine
Curated by ChEMBL
| Assay Description Inhibition of human DPP8 |
Bioorg Med Chem Lett 17: 507-10 (2007)
Article DOI: 10.1016/j.bmcl.2006.10.012 BindingDB Entry DOI: 10.7270/Q2T43SQH |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 2
(Homo sapiens (Human)) | BDBM50171551
((S)-2-Amino-hexanoic acid ((R)-1-boron-dihydroxide...)Show InChI InChI=1S/C11H25BN2O3/c1-3-5-7-9(13)11(15)14-10(12(16)17)8-6-4-2/h9-10,16-17H,3-8,13H2,1-2H3,(H,14,15)/t9-,10+/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 18 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences
Curated by ChEMBL
| Assay Description Inhibitory concentration against human dipeptidylpeptidase 7 |
Bioorg Med Chem Lett 15: 4256-60 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.076 BindingDB Entry DOI: 10.7270/Q2RR1XSW |
More data for this Ligand-Target Pair | |
Glycogen synthase kinase-3 beta
(Homo sapiens (Human)) | BDBM50354767
(CHEMBL1834318)Show SMILES Nc1c(F)c(NCCNc2ccccn2)c(F)c2n(cc(C(O)=O)c(=O)c12)C1CCCC1 Show InChI InChI=1S/C22H23F2N5O3/c23-16-18(25)15-20(17(24)19(16)28-10-9-27-14-7-3-4-8-26-14)29(12-5-1-2-6-12)11-13(21(15)30)22(31)32/h3-4,7-8,11-12,28H,1-2,5-6,9-10,25H2,(H,26,27)(H,31,32) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 22 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibition of human recombinant full length GSK3beta after 1 hrs by luminescence assay |
Bioorg Med Chem Lett 21: 5948-51 (2011)
Article DOI: 10.1016/j.bmcl.2011.07.073 BindingDB Entry DOI: 10.7270/Q23T9HMH |
More data for this Ligand-Target Pair | |
Prolyl endopeptidase FAP
(Homo sapiens (Human)) | BDBM50050513
((R)-1-((S)-2-amino-3-methylbutanoyl)pyrrolidin-2-y...)Show InChI InChI=1S/C9H19BN2O3/c1-6(2)8(11)9(13)12-5-3-4-7(12)10(14)15/h6-8,14-15H,3-5,11H2,1-2H3/t7-,8-/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 24 | n/a | n/a | n/a | n/a | n/a | n/a |
Tufts University School of Medicine
Curated by ChEMBL
| Assay Description Inhibition of human FAP |
Bioorg Med Chem Lett 17: 507-10 (2007)
Article DOI: 10.1016/j.bmcl.2006.10.012 BindingDB Entry DOI: 10.7270/Q2T43SQH |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 4
(Homo sapiens (Human)) | BDBM50171657
(2-(Bicyclo[3.2.1]oct-6-ylamino)-1-((S)-2-dihydroxy...)Show SMILES OC(O)[C@@H]1CCCN1C(=O)CNC1CC2CC1CCC2 |TLB:11:12:15:17.18.19| Show InChI InChI=1S/C15H26N2O3/c18-14(17-6-2-5-13(17)15(19)20)9-16-12-8-10-3-1-4-11(12)7-10/h10-13,15-16,19-20H,1-9H2/t10?,11?,12?,13-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 25 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against human DPP4 using Gly-Pro-AMC in fluorometric assay |
Bioorg Med Chem Lett 15: 4239-42 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.075 BindingDB Entry DOI: 10.7270/Q2CJ8D2F |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 4
(Homo sapiens (Human)) | BDBM50171651
(2-Cyclopentylamino-1-pyrrolidin-1-yl--2-borandihyd...)Show InChI InChI=1S/C11H21BN2O3/c15-11(8-13-9-4-1-2-5-9)14-7-3-6-10(14)12(16)17/h9-10,13,16-17H,1-8H2/t10-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 25 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against human DPP4 using Gly-Pro-AMC in fluorometric assay |
Bioorg Med Chem Lett 15: 4239-42 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.075 BindingDB Entry DOI: 10.7270/Q2CJ8D2F |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 4
(Homo sapiens (Human)) | BDBM50171650
(2-Cyclooctonylamino-1-pyrrolidin-1-yl--2-borandihy...)Show InChI InChI=1S/C14H27BN2O3/c18-14(17-10-6-9-13(17)15(19)20)11-16-12-7-4-2-1-3-5-8-12/h12-13,16,19-20H,1-11H2/t13-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 27 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against human DPP4 using Gly-Pro-AMC in fluorometric assay |
Bioorg Med Chem Lett 15: 4239-42 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.075 BindingDB Entry DOI: 10.7270/Q2CJ8D2F |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 4
(Homo sapiens (Human)) | BDBM50171656
(2-Cyclohexylamino-1-pyrrolidin-1-yl--2-borandihydr...)Show InChI InChI=1S/C12H23BN2O3/c16-12(9-14-10-5-2-1-3-6-10)15-8-4-7-11(15)13(17)18/h10-11,14,17-18H,1-9H2/t11-/m0/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 27 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against human DPP4 using Gly-Pro-AMC in fluorometric assay |
Bioorg Med Chem Lett 15: 4239-42 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.075 BindingDB Entry DOI: 10.7270/Q2CJ8D2F |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 8
(Homo sapiens (Human)) | BDBM50171548
((S)-2-(S)-Amino-1-(2-boron-dihydroxide-pyrrolidin-...)Show InChI InChI=1S/C10H21BN2O3/c1-2-3-5-8(12)10(14)13-7-4-6-9(13)11(15)16/h8-9,15-16H,2-7,12H2,1H3/t8-,9+/m0/s1 | PDB
KEGG
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 30 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences
Curated by ChEMBL
| Assay Description Inhibitory concentration against human dipeptidylpeptidase 8 using FP-TAMRA incubated for 30 min |
Bioorg Med Chem Lett 15: 4256-60 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.076 BindingDB Entry DOI: 10.7270/Q2RR1XSW |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 2
(Homo sapiens (Human)) | BDBM50050513
((R)-1-((S)-2-amino-3-methylbutanoyl)pyrrolidin-2-y...)Show InChI InChI=1S/C9H19BN2O3/c1-6(2)8(11)9(13)12-5-3-4-7(12)10(14)15/h6-8,14-15H,3-5,11H2,1-2H3/t7-,8-/m0/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 30 | n/a | n/a | n/a | n/a | n/a | n/a |
Tufts University School of Medicine
Curated by ChEMBL
| Assay Description Inhibition of human DPP2 |
Bioorg Med Chem Lett 17: 507-10 (2007)
Article DOI: 10.1016/j.bmcl.2006.10.012 BindingDB Entry DOI: 10.7270/Q2T43SQH |
More data for this Ligand-Target Pair | |
Glycogen synthase kinase-3 beta
(Homo sapiens (Human)) | BDBM50354773
(CHEMBL1834324)Show SMILES CC(C)[C@@H]1COc2c(NCCNc3ccccn3)c(F)c(N)c3c2n1cc(C(O)=O)c3=O |r| Show InChI InChI=1S/C22H24FN5O4/c1-11(2)13-10-32-21-18(27-8-7-26-14-5-3-4-6-25-14)16(23)17(24)15-19(21)28(13)9-12(20(15)29)22(30)31/h3-6,9,11,13,27H,7-8,10,24H2,1-2H3,(H,25,26)(H,30,31)/t13-/m0/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 31 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibition of human recombinant full length GSK3beta after 1 hrs by luminescence assay |
Bioorg Med Chem Lett 21: 5948-51 (2011)
Article DOI: 10.1016/j.bmcl.2011.07.073 BindingDB Entry DOI: 10.7270/Q23T9HMH |
More data for this Ligand-Target Pair | |
Glycogen synthase kinase-3 beta
(Homo sapiens (Human)) | BDBM50354764
(CHEMBL1834125)Show SMILES COc1c(NCCNc2cccc3ccccc23)c(F)c(N)c2c1n(cc(C(O)=O)c2=O)C1CC1 Show InChI InChI=1S/C26H25FN4O4/c1-35-25-22(30-12-11-29-18-8-4-6-14-5-2-3-7-16(14)18)20(27)21(28)19-23(25)31(15-9-10-15)13-17(24(19)32)26(33)34/h2-8,13,15,29-30H,9-12,28H2,1H3,(H,33,34) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 31 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibition of human recombinant full length GSK3beta after 1 hrs by luminescence assay |
Bioorg Med Chem Lett 21: 5948-51 (2011)
Article DOI: 10.1016/j.bmcl.2011.07.073 BindingDB Entry DOI: 10.7270/Q23T9HMH |
More data for this Ligand-Target Pair | |
Dipeptidyl peptidase 2
(Homo sapiens (Human)) | BDBM50171652
(CHEMBL381444 | N-alkyl Gly-boro-Pro derivative)Show SMILES CC12CC3(C)CC(C)(C1)CC(C2)(C3)NCC(=O)N1CCC[C@@H]1B(O)O |TLB:0:1:9:3.12.5,4:3:9:1.11.8,4:3:11:6.9.8,5:3:11:6.9.8,THB:2:1:9:3.12.5,2:3:9:1.11.8,5:6:11:3.12.2| Show InChI InChI=1S/C19H33BN2O3/c1-16-8-17(2)10-18(3,9-16)13-19(11-16,12-17)21-7-15(23)22-6-4-5-14(22)20(24)25/h14,21,24-25H,4-13H2,1-3H3/t14-,16?,17?,18?,19?/m1/s1 | PDB MMDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 35 | n/a | n/a | n/a | n/a | n/a | n/a |
ActivX Biosciences, Inc.
Curated by ChEMBL
| Assay Description Inhibitory activity against human DPP7 using Ala-Pro-AMC in fluorometric assay |
Bioorg Med Chem Lett 15: 4239-42 (2005)
Article DOI: 10.1016/j.bmcl.2005.06.075 BindingDB Entry DOI: 10.7270/Q2CJ8D2F |
More data for this Ligand-Target Pair | |