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19 similar compounds to monomer 12165

Compile data set for download or QSAR
Wt: 331.3
BDBM12166
Wt: 347.8
BDBM12167
Wt: 381.3
BDBM12168
Wt: 327.4
BDBM12169
Wt: 382.2
BDBM12170
Wt: 301.3
BDBM12172
Wt: 331.3
BDBM12175
Wt: 331.3
BDBM12176
Wt: 338.4
BDBM12178
Wt: 366.4
BDBM12179
Wt: 352.4
BDBM50205213
Wt: 231.2
BDBM50243316
Wt: 321.4
BDBM50243317
Wt: 411.5
BDBM50243318
Wt: 321.4
BDBM50243242
Displayed 1 to 15 (of 19 total )  |  Next  |  Last  >>

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 57 hits for monomerid = 12166,12167,12168,12169,12170,12172,12175,12176,12178,12179,50205213,50243316,50243317,50243318,50243242   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Dipeptidyl peptidase 4


(Homo sapiens (Human))
BDBM12166
PNG
(5-fluoro-2-{[(3S,5S)-5-(pyrrolidin-1-ylcarbonyl)py...)
Show SMILES Fc1ccc2CN(Cc2c1)C(=O)[C@@H]1CN[C@@H](C1)C(=O)N1CCCC1
Show InChI InChI=1S/C18H22FN3O2/c19-15-4-3-12-10-22(11-14(12)7-15)17(23)13-8-16(20-9-13)18(24)21-5-1-2-6-21/h3-4,7,13,16,20H,1-2,5-6,8-11H2/t13-,16-/m0/s1
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n/an/a 73n/an/an/an/a8.037



National Health Research Institutes



Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase IX


(Homo sapiens (Human))
BDBM50243242
PNG
(((2S,4S)-4-(benzylamino)pyrrolidin-2-yl)(isoindoli...)
Show SMILES O=C([C@@H]1C[C@@H](CN1)NCc1ccccc1)N1Cc2ccccc2C1
Show InChI InChI=1S/C20H23N3O/c24-20(23-13-16-8-4-5-9-17(16)14-23)19-10-18(12-22-19)21-11-15-6-2-1-3-7-15/h1-9,18-19,21-22H,10-14H2/t18-,19-/m0/s1
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n/an/a 1.31E+4n/an/an/an/an/an/a



University of Antwerp

Curated by ChEMBL


Assay Description
Inhibition of DPP9 (unknown origin)


Bioorg Med Chem Lett 18: 4159-62 (2008)


Article DOI: 10.1016/j.bmcl.2008.05.079
BindingDB Entry DOI: 10.7270/Q2KS6RC4
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 4


(Homo sapiens (Human))
BDBM12168
PNG
(2-{[(3S,5S)-5-(pyrrolidin-1-ylcarbonyl)pyrrolidin-...)
Show SMILES FC(F)(F)c1ccc2CN(Cc2c1)C(=O)[C@@H]1CN[C@@H](C1)C(=O)N1CCCC1
Show InChI InChI=1S/C19H22F3N3O2/c20-19(21,22)15-4-3-12-10-25(11-14(12)7-15)17(26)13-8-16(23-9-13)18(27)24-5-1-2-6-24/h3-4,7,13,16,23H,1-2,5-6,8-11H2/t13-,16-/m0/s1
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n/an/a 73n/an/an/an/a8.037



National Health Research Institutes



Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 4


(Homo sapiens (Human))
BDBM12169
PNG
(5-methyl-2-{[(3S,5S)-5-(pyrrolidin-1-ylcarbonyl)py...)
Show SMILES Cc1ccc2CN(Cc2c1)C(=O)[C@@H]1CN[C@@H](C1)C(=O)N1CCCC1
Show InChI InChI=1S/C19H25N3O2/c1-13-4-5-14-11-22(12-16(14)8-13)18(23)15-9-17(20-10-15)19(24)21-6-2-3-7-21/h4-5,8,15,17,20H,2-3,6-7,9-12H2,1H3/t15-,17-/m0/s1
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n/an/a 72n/an/an/an/a8.037



National Health Research Institutes



Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 4


(Homo sapiens (Human))
BDBM12170
PNG
(5,6-dichloro-2-{[(3S,5S)-5-(pyrrolidin-1-ylcarbony...)
Show SMILES Clc1cc2CN(Cc2cc1Cl)C(=O)[C@@H]1CN[C@@H](C1)C(=O)N1CCCC1
Show InChI InChI=1S/C18H21Cl2N3O2/c19-14-5-12-9-23(10-13(12)6-15(14)20)17(24)11-7-16(21-8-11)18(25)22-3-1-2-4-22/h5-6,11,16,21H,1-4,7-10H2/t11-,16-/m0/s1
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n/an/a 144n/an/an/an/a8.037



National Health Research Institutes



Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 4


(Homo sapiens (Human))
BDBM12172
PNG
((3S,5S)-N-benzyl-5-(pyrrolidin-1-ylcarbonyl)pyrrol...)
Show SMILES O=C(NCc1ccccc1)[C@@H]1CN[C@@H](C1)C(=O)N1CCCC1
Show InChI InChI=1S/C17H23N3O2/c21-16(19-11-13-6-2-1-3-7-13)14-10-15(18-12-14)17(22)20-8-4-5-9-20/h1-3,6-7,14-15,18H,4-5,8-12H2,(H,19,21)/t14-,15-/m0/s1
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n/an/a 1.96E+3n/an/an/an/a8.037



National Health Research Institutes



Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 4


(Homo sapiens (Human))
BDBM12175
PNG
(2-{[(3S,5S)-5-{[(3S)-3-fluoropyrrolidin-1-yl]carbo...)
Show SMILES F[C@H]1CCN(C1)C(=O)[C@@H]1C[C@@H](CN1)C(=O)N1Cc2ccccc2C1
Show InChI InChI=1S/C18H22FN3O2/c19-15-5-6-21(11-15)18(24)16-7-14(8-20-16)17(23)22-9-12-3-1-2-4-13(12)10-22/h1-4,14-16,20H,5-11H2/t14-,15-,16-/m0/s1
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n/an/a 245n/an/an/an/a8.037



National Health Research Institutes



Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 4


(Homo sapiens (Human))
BDBM12176
PNG
(2-{[(3S,5S)-5-{[(3R)-3-fluoropyrrolidin-1-yl]carbo...)
Show SMILES F[C@@H]1CCN(C1)C(=O)[C@@H]1C[C@@H](CN1)C(=O)N1Cc2ccccc2C1
Show InChI InChI=1S/C18H22FN3O2/c19-15-5-6-21(11-15)18(24)16-7-14(8-20-16)17(23)22-9-12-3-1-2-4-13(12)10-22/h1-4,14-16,20H,5-11H2/t14-,15+,16-/m0/s1
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n/an/a 228n/an/an/an/a8.037



National Health Research Institutes



Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 4


(Homo sapiens (Human))
BDBM12178
PNG
((2S)-1-{[(2S,4S)-4-(2,3-dihydro-1H-isoindol-2-ylca...)
Show SMILES O=C([C@@H]1CN[C@@H](C1)C(=O)N1CCC[C@H]1C#N)N1Cc2ccccc2C1
Show InChI InChI=1S/C19H22N4O2/c20-9-16-6-3-7-23(16)19(25)17-8-15(10-21-17)18(24)22-11-13-4-1-2-5-14(13)12-22/h1-2,4-5,15-17,21H,3,6-8,10-12H2/t15-,16-,17-/m0/s1
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n/an/a 1.70n/an/an/an/a8.037



National Health Research Institutes



Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 4


(Homo sapiens (Human))
BDBM12179
PNG
((2S)-1-{[(2S,4S)-4-(2,3-dihydro-1H-isoindol-2-ylca...)
Show SMILES CC1(C)N[C@@H](C[C@@H]1C(=O)N1Cc2ccccc2C1)C(=O)N1CCC[C@H]1C#N
Show InChI InChI=1S/C21H26N4O2/c1-21(2)17(19(26)24-12-14-6-3-4-7-15(14)13-24)10-18(23-21)20(27)25-9-5-8-16(25)11-22/h3-4,6-7,16-18,23H,5,8-10,12-13H2,1-2H3/t16-,17+,18-/m0/s1
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n/an/a 984n/an/an/an/a8.037



National Health Research Institutes



Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase VIII


(Homo sapiens (Human))
BDBM12166
PNG
(5-fluoro-2-{[(3S,5S)-5-(pyrrolidin-1-ylcarbonyl)py...)
Show SMILES Fc1ccc2CN(Cc2c1)C(=O)[C@@H]1CN[C@@H](C1)C(=O)N1CCCC1
Show InChI InChI=1S/C18H22FN3O2/c19-15-4-3-12-10-22(11-14(12)7-15)17(23)13-8-16(20-9-13)18(24)21-5-1-2-6-21/h3-4,7,13,16,20H,1-2,5-6,8-11H2/t13-,16-/m0/s1
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n/an/a>2.00E+4n/an/an/an/an/an/a



National Health Research Institutes



Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase VIII


(Homo sapiens (Human))
BDBM12167
PNG
(5-chloro-2-{[(3S,5S)-5-(pyrrolidin-1-ylcarbonyl)py...)
Show SMILES Clc1ccc2CN(Cc2c1)C(=O)[C@@H]1CN[C@@H](C1)C(=O)N1CCCC1
Show InChI InChI=1S/C18H22ClN3O2/c19-15-4-3-12-10-22(11-14(12)7-15)17(23)13-8-16(20-9-13)18(24)21-5-1-2-6-21/h3-4,7,13,16,20H,1-2,5-6,8-11H2/t13-,16-/m0/s1
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n/an/a>2.00E+4n/an/an/an/an/an/a



National Health Research Institutes



Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase VIII


(Homo sapiens (Human))
BDBM12168
PNG
(2-{[(3S,5S)-5-(pyrrolidin-1-ylcarbonyl)pyrrolidin-...)
Show SMILES FC(F)(F)c1ccc2CN(Cc2c1)C(=O)[C@@H]1CN[C@@H](C1)C(=O)N1CCCC1
Show InChI InChI=1S/C19H22F3N3O2/c20-19(21,22)15-4-3-12-10-25(11-14(12)7-15)17(26)13-8-16(23-9-13)18(27)24-5-1-2-6-24/h3-4,7,13,16,23H,1-2,5-6,8-11H2/t13-,16-/m0/s1
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n/an/a>2.00E+4n/an/an/an/an/an/a



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Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase VIII


(Homo sapiens (Human))
BDBM12169
PNG
(5-methyl-2-{[(3S,5S)-5-(pyrrolidin-1-ylcarbonyl)py...)
Show SMILES Cc1ccc2CN(Cc2c1)C(=O)[C@@H]1CN[C@@H](C1)C(=O)N1CCCC1
Show InChI InChI=1S/C19H25N3O2/c1-13-4-5-14-11-22(12-16(14)8-13)18(23)15-9-17(20-10-15)19(24)21-6-2-3-7-21/h4-5,8,15,17,20H,2-3,6-7,9-12H2,1H3/t15-,17-/m0/s1
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n/an/a>2.00E+4n/an/an/an/an/an/a



National Health Research Institutes



Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase VIII


(Homo sapiens (Human))
BDBM12170
PNG
(5,6-dichloro-2-{[(3S,5S)-5-(pyrrolidin-1-ylcarbony...)
Show SMILES Clc1cc2CN(Cc2cc1Cl)C(=O)[C@@H]1CN[C@@H](C1)C(=O)N1CCCC1
Show InChI InChI=1S/C18H21Cl2N3O2/c19-14-5-12-9-23(10-13(12)6-15(14)20)17(24)11-7-16(21-8-11)18(25)22-3-1-2-4-22/h5-6,11,16,21H,1-4,7-10H2/t11-,16-/m0/s1
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n/an/a 1.22E+4n/an/an/an/an/an/a



National Health Research Institutes



Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase VIII


(Homo sapiens (Human))
BDBM12172
PNG
((3S,5S)-N-benzyl-5-(pyrrolidin-1-ylcarbonyl)pyrrol...)
Show SMILES O=C(NCc1ccccc1)[C@@H]1CN[C@@H](C1)C(=O)N1CCCC1
Show InChI InChI=1S/C17H23N3O2/c21-16(19-11-13-6-2-1-3-7-13)14-10-15(18-12-14)17(22)20-8-4-5-9-20/h1-3,6-7,14-15,18H,4-5,8-12H2,(H,19,21)/t14-,15-/m0/s1
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n/an/a>2.00E+4n/an/an/an/an/an/a



National Health Research Institutes



Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase VIII


(Homo sapiens (Human))
BDBM12175
PNG
(2-{[(3S,5S)-5-{[(3S)-3-fluoropyrrolidin-1-yl]carbo...)
Show SMILES F[C@H]1CCN(C1)C(=O)[C@@H]1C[C@@H](CN1)C(=O)N1Cc2ccccc2C1
Show InChI InChI=1S/C18H22FN3O2/c19-15-5-6-21(11-15)18(24)16-7-14(8-20-16)17(23)22-9-12-3-1-2-4-13(12)10-22/h1-4,14-16,20H,5-11H2/t14-,15-,16-/m0/s1
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n/an/a>2.00E+4n/an/an/an/an/an/a



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Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase VIII


(Homo sapiens (Human))
BDBM12176
PNG
(2-{[(3S,5S)-5-{[(3R)-3-fluoropyrrolidin-1-yl]carbo...)
Show SMILES F[C@@H]1CCN(C1)C(=O)[C@@H]1C[C@@H](CN1)C(=O)N1Cc2ccccc2C1
Show InChI InChI=1S/C18H22FN3O2/c19-15-5-6-21(11-15)18(24)16-7-14(8-20-16)17(23)22-9-12-3-1-2-4-13(12)10-22/h1-4,14-16,20H,5-11H2/t14-,15+,16-/m0/s1
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n/an/a>2.00E+4n/an/an/an/an/an/a



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Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase VIII


(Homo sapiens (Human))
BDBM12178
PNG
((2S)-1-{[(2S,4S)-4-(2,3-dihydro-1H-isoindol-2-ylca...)
Show SMILES O=C([C@@H]1CN[C@@H](C1)C(=O)N1CCC[C@H]1C#N)N1Cc2ccccc2C1
Show InChI InChI=1S/C19H22N4O2/c20-9-16-6-3-7-23(16)19(25)17-8-15(10-21-17)18(24)22-11-13-4-1-2-5-14(13)12-22/h1-2,4-5,15-17,21H,3,6-8,10-12H2/t15-,16-,17-/m0/s1
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n/an/a 2.73E+3n/an/an/an/an/an/a



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Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase VIII


(Homo sapiens (Human))
BDBM12179
PNG
((2S)-1-{[(2S,4S)-4-(2,3-dihydro-1H-isoindol-2-ylca...)
Show SMILES CC1(C)N[C@@H](C[C@@H]1C(=O)N1Cc2ccccc2C1)C(=O)N1CCC[C@H]1C#N
Show InChI InChI=1S/C21H26N4O2/c1-21(2)17(19(26)24-12-14-6-3-4-7-15(14)13-24)10-18(23-21)20(27)25-9-5-8-16(25)11-22/h3-4,6-7,16-18,23H,5,8-10,12-13H2,1-2H3/t16-,17+,18-/m0/s1
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n/an/a>2.00E+4n/an/an/an/an/an/a



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Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 2 (DPP II)


(Homo sapiens (Human))
BDBM12166
PNG
(5-fluoro-2-{[(3S,5S)-5-(pyrrolidin-1-ylcarbonyl)py...)
Show SMILES Fc1ccc2CN(Cc2c1)C(=O)[C@@H]1CN[C@@H](C1)C(=O)N1CCCC1
Show InChI InChI=1S/C18H22FN3O2/c19-15-4-3-12-10-22(11-14(12)7-15)17(23)13-8-16(20-9-13)18(24)21-5-1-2-6-21/h3-4,7,13,16,20H,1-2,5-6,8-11H2/t13-,16-/m0/s1
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Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 2 (DPP II)


(Homo sapiens (Human))
BDBM12167
PNG
(5-chloro-2-{[(3S,5S)-5-(pyrrolidin-1-ylcarbonyl)py...)
Show SMILES Clc1ccc2CN(Cc2c1)C(=O)[C@@H]1CN[C@@H](C1)C(=O)N1CCCC1
Show InChI InChI=1S/C18H22ClN3O2/c19-15-4-3-12-10-22(11-14(12)7-15)17(23)13-8-16(20-9-13)18(24)21-5-1-2-6-21/h3-4,7,13,16,20H,1-2,5-6,8-11H2/t13-,16-/m0/s1
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Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 2 (DPP II)


(Homo sapiens (Human))
BDBM12168
PNG
(2-{[(3S,5S)-5-(pyrrolidin-1-ylcarbonyl)pyrrolidin-...)
Show SMILES FC(F)(F)c1ccc2CN(Cc2c1)C(=O)[C@@H]1CN[C@@H](C1)C(=O)N1CCCC1
Show InChI InChI=1S/C19H22F3N3O2/c20-19(21,22)15-4-3-12-10-25(11-14(12)7-15)17(26)13-8-16(23-9-13)18(27)24-5-1-2-6-24/h3-4,7,13,16,23H,1-2,5-6,8-11H2/t13-,16-/m0/s1
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Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 2 (DPP II)


(Homo sapiens (Human))
BDBM12169
PNG
(5-methyl-2-{[(3S,5S)-5-(pyrrolidin-1-ylcarbonyl)py...)
Show SMILES Cc1ccc2CN(Cc2c1)C(=O)[C@@H]1CN[C@@H](C1)C(=O)N1CCCC1
Show InChI InChI=1S/C19H25N3O2/c1-13-4-5-14-11-22(12-16(14)8-13)18(23)15-9-17(20-10-15)19(24)21-6-2-3-7-21/h4-5,8,15,17,20H,2-3,6-7,9-12H2,1H3/t15-,17-/m0/s1
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Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 2 (DPP II)


(Homo sapiens (Human))
BDBM12170
PNG
(5,6-dichloro-2-{[(3S,5S)-5-(pyrrolidin-1-ylcarbony...)
Show SMILES Clc1cc2CN(Cc2cc1Cl)C(=O)[C@@H]1CN[C@@H](C1)C(=O)N1CCCC1
Show InChI InChI=1S/C18H21Cl2N3O2/c19-14-5-12-9-23(10-13(12)6-15(14)20)17(24)11-7-16(21-8-11)18(25)22-3-1-2-4-22/h5-6,11,16,21H,1-4,7-10H2/t11-,16-/m0/s1
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Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 2 (DPP II)


(Homo sapiens (Human))
BDBM12172
PNG
((3S,5S)-N-benzyl-5-(pyrrolidin-1-ylcarbonyl)pyrrol...)
Show SMILES O=C(NCc1ccccc1)[C@@H]1CN[C@@H](C1)C(=O)N1CCCC1
Show InChI InChI=1S/C17H23N3O2/c21-16(19-11-13-6-2-1-3-7-13)14-10-15(18-12-14)17(22)20-8-4-5-9-20/h1-3,6-7,14-15,18H,4-5,8-12H2,(H,19,21)/t14-,15-/m0/s1
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Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 2 (DPP II)


(Homo sapiens (Human))
BDBM12175
PNG
(2-{[(3S,5S)-5-{[(3S)-3-fluoropyrrolidin-1-yl]carbo...)
Show SMILES F[C@H]1CCN(C1)C(=O)[C@@H]1C[C@@H](CN1)C(=O)N1Cc2ccccc2C1
Show InChI InChI=1S/C18H22FN3O2/c19-15-5-6-21(11-15)18(24)16-7-14(8-20-16)17(23)22-9-12-3-1-2-4-13(12)10-22/h1-4,14-16,20H,5-11H2/t14-,15-,16-/m0/s1
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Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 2 (DPP II)


(Homo sapiens (Human))
BDBM12176
PNG
(2-{[(3S,5S)-5-{[(3R)-3-fluoropyrrolidin-1-yl]carbo...)
Show SMILES F[C@@H]1CCN(C1)C(=O)[C@@H]1C[C@@H](CN1)C(=O)N1Cc2ccccc2C1
Show InChI InChI=1S/C18H22FN3O2/c19-15-5-6-21(11-15)18(24)16-7-14(8-20-16)17(23)22-9-12-3-1-2-4-13(12)10-22/h1-4,14-16,20H,5-11H2/t14-,15+,16-/m0/s1
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n/an/a>2.00E+4n/an/an/an/an/an/a



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Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 2 (DPP II)


(Homo sapiens (Human))
BDBM12178
PNG
((2S)-1-{[(2S,4S)-4-(2,3-dihydro-1H-isoindol-2-ylca...)
Show SMILES O=C([C@@H]1CN[C@@H](C1)C(=O)N1CCC[C@H]1C#N)N1Cc2ccccc2C1
Show InChI InChI=1S/C19H22N4O2/c20-9-16-6-3-7-23(16)19(25)17-8-15(10-21-17)18(24)22-11-13-4-1-2-5-14(13)12-22/h1-2,4-5,15-17,21H,3,6-8,10-12H2/t15-,16-,17-/m0/s1
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n/an/a>2.00E+4n/an/an/an/an/an/a



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Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 2 (DPP II)


(Homo sapiens (Human))
BDBM12179
PNG
((2S)-1-{[(2S,4S)-4-(2,3-dihydro-1H-isoindol-2-ylca...)
Show SMILES CC1(C)N[C@@H](C[C@@H]1C(=O)N1Cc2ccccc2C1)C(=O)N1CCC[C@H]1C#N
Show InChI InChI=1S/C21H26N4O2/c1-21(2)17(19(26)24-12-14-6-3-4-7-15(14)13-24)10-18(23-21)20(27)25-9-5-8-16(25)11-22/h3-4,6-7,16-18,23H,5,8-10,12-13H2,1-2H3/t16-,17+,18-/m0/s1
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Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Fibroblast Activation Protein (FAP)


(Homo sapiens (Human))
BDBM12166
PNG
(5-fluoro-2-{[(3S,5S)-5-(pyrrolidin-1-ylcarbonyl)py...)
Show SMILES Fc1ccc2CN(Cc2c1)C(=O)[C@@H]1CN[C@@H](C1)C(=O)N1CCCC1
Show InChI InChI=1S/C18H22FN3O2/c19-15-4-3-12-10-22(11-14(12)7-15)17(23)13-8-16(20-9-13)18(24)21-5-1-2-6-21/h3-4,7,13,16,20H,1-2,5-6,8-11H2/t13-,16-/m0/s1
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n/an/a 1.36E+4n/an/an/an/an/an/a



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Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Fibroblast Activation Protein (FAP)


(Homo sapiens (Human))
BDBM12167
PNG
(5-chloro-2-{[(3S,5S)-5-(pyrrolidin-1-ylcarbonyl)py...)
Show SMILES Clc1ccc2CN(Cc2c1)C(=O)[C@@H]1CN[C@@H](C1)C(=O)N1CCCC1
Show InChI InChI=1S/C18H22ClN3O2/c19-15-4-3-12-10-22(11-14(12)7-15)17(23)13-8-16(20-9-13)18(24)21-5-1-2-6-21/h3-4,7,13,16,20H,1-2,5-6,8-11H2/t13-,16-/m0/s1
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n/an/a 7.95E+3n/an/an/an/an/an/a



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Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Fibroblast Activation Protein (FAP)


(Homo sapiens (Human))
BDBM12168
PNG
(2-{[(3S,5S)-5-(pyrrolidin-1-ylcarbonyl)pyrrolidin-...)
Show SMILES FC(F)(F)c1ccc2CN(Cc2c1)C(=O)[C@@H]1CN[C@@H](C1)C(=O)N1CCCC1
Show InChI InChI=1S/C19H22F3N3O2/c20-19(21,22)15-4-3-12-10-25(11-14(12)7-15)17(26)13-8-16(23-9-13)18(27)24-5-1-2-6-24/h3-4,7,13,16,23H,1-2,5-6,8-11H2/t13-,16-/m0/s1
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n/an/a>2.00E+4n/an/an/an/an/an/a



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Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Fibroblast Activation Protein (FAP)


(Homo sapiens (Human))
BDBM12169
PNG
(5-methyl-2-{[(3S,5S)-5-(pyrrolidin-1-ylcarbonyl)py...)
Show SMILES Cc1ccc2CN(Cc2c1)C(=O)[C@@H]1CN[C@@H](C1)C(=O)N1CCCC1
Show InChI InChI=1S/C19H25N3O2/c1-13-4-5-14-11-22(12-16(14)8-13)18(23)15-9-17(20-10-15)19(24)21-6-2-3-7-21/h4-5,8,15,17,20H,2-3,6-7,9-12H2,1H3/t15-,17-/m0/s1
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n/an/a 8.80E+3n/an/an/an/an/an/a



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Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Fibroblast Activation Protein (FAP)


(Homo sapiens (Human))
BDBM12170
PNG
(5,6-dichloro-2-{[(3S,5S)-5-(pyrrolidin-1-ylcarbony...)
Show SMILES Clc1cc2CN(Cc2cc1Cl)C(=O)[C@@H]1CN[C@@H](C1)C(=O)N1CCCC1
Show InChI InChI=1S/C18H21Cl2N3O2/c19-14-5-12-9-23(10-13(12)6-15(14)20)17(24)11-7-16(21-8-11)18(25)22-3-1-2-4-22/h5-6,11,16,21H,1-4,7-10H2/t11-,16-/m0/s1
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n/an/a 5.13E+3n/an/an/an/an/an/a



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Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Fibroblast Activation Protein (FAP)


(Homo sapiens (Human))
BDBM12172
PNG
((3S,5S)-N-benzyl-5-(pyrrolidin-1-ylcarbonyl)pyrrol...)
Show SMILES O=C(NCc1ccccc1)[C@@H]1CN[C@@H](C1)C(=O)N1CCCC1
Show InChI InChI=1S/C17H23N3O2/c21-16(19-11-13-6-2-1-3-7-13)14-10-15(18-12-14)17(22)20-8-4-5-9-20/h1-3,6-7,14-15,18H,4-5,8-12H2,(H,19,21)/t14-,15-/m0/s1
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Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Fibroblast Activation Protein (FAP)


(Homo sapiens (Human))
BDBM12175
PNG
(2-{[(3S,5S)-5-{[(3S)-3-fluoropyrrolidin-1-yl]carbo...)
Show SMILES F[C@H]1CCN(C1)C(=O)[C@@H]1C[C@@H](CN1)C(=O)N1Cc2ccccc2C1
Show InChI InChI=1S/C18H22FN3O2/c19-15-5-6-21(11-15)18(24)16-7-14(8-20-16)17(23)22-9-12-3-1-2-4-13(12)10-22/h1-4,14-16,20H,5-11H2/t14-,15-,16-/m0/s1
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Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Fibroblast Activation Protein (FAP)


(Homo sapiens (Human))
BDBM12176
PNG
(2-{[(3S,5S)-5-{[(3R)-3-fluoropyrrolidin-1-yl]carbo...)
Show SMILES F[C@@H]1CCN(C1)C(=O)[C@@H]1C[C@@H](CN1)C(=O)N1Cc2ccccc2C1
Show InChI InChI=1S/C18H22FN3O2/c19-15-5-6-21(11-15)18(24)16-7-14(8-20-16)17(23)22-9-12-3-1-2-4-13(12)10-22/h1-4,14-16,20H,5-11H2/t14-,15+,16-/m0/s1
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n/an/a>2.00E+4n/an/an/an/an/an/a



National Health Research Institutes



Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Fibroblast Activation Protein (FAP)


(Homo sapiens (Human))
BDBM12178
PNG
((2S)-1-{[(2S,4S)-4-(2,3-dihydro-1H-isoindol-2-ylca...)
Show SMILES O=C([C@@H]1CN[C@@H](C1)C(=O)N1CCC[C@H]1C#N)N1Cc2ccccc2C1
Show InChI InChI=1S/C19H22N4O2/c20-9-16-6-3-7-23(16)19(25)17-8-15(10-21-17)18(24)22-11-13-4-1-2-5-14(13)12-22/h1-2,4-5,15-17,21H,3,6-8,10-12H2/t15-,16-,17-/m0/s1
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n/an/a 175n/an/an/an/an/an/a



National Health Research Institutes



Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Fibroblast Activation Protein (FAP)


(Homo sapiens (Human))
BDBM12179
PNG
((2S)-1-{[(2S,4S)-4-(2,3-dihydro-1H-isoindol-2-ylca...)
Show SMILES CC1(C)N[C@@H](C[C@@H]1C(=O)N1Cc2ccccc2C1)C(=O)N1CCC[C@H]1C#N
Show InChI InChI=1S/C21H26N4O2/c1-21(2)17(19(26)24-12-14-6-3-4-7-15(14)13-24)10-18(23-21)20(27)25-9-5-8-16(25)11-22/h3-4,6-7,16-18,23H,5,8-10,12-13H2,1-2H3/t16-,17+,18-/m0/s1
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n/an/a>2.00E+4n/an/an/an/an/an/a



National Health Research Institutes



Assay Description
The enzyme activity resulted in the liberation of free pNA at 405 nm. Reaction progress was monitored using a Molecular Devices SpectraMax Plus micro...


Bioorg Med Chem Lett 16: 3268-72 (2006)


Article DOI: 10.1016/j.bmcl.2006.03.037
BindingDB Entry DOI: 10.7270/Q22805V8
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 4


(Homo sapiens (Human))
BDBM50205213
PNG
(2S)-1-{[(2S,4S,5S)-4-(1,3-dihydro-2H-isoindol-2-yl...)
Show SMILES C[C@@H]1N[C@@H](C[C@@H]1C(=O)N1Cc2ccccc2C1)C(=O)N1CCC[C@H]1C#N
Show InChI InChI=1S/C20H24N4O2/c1-13-17(19(25)23-11-14-5-2-3-6-15(14)12-23)9-18(22-13)20(26)24-8-4-7-16(24)10-21/h2-3,5-6,13,16-18,22H,4,7-9,11-12H2,1H3/t13-,16-,17-,18-/m0/s1
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n/an/a 5.60n/an/an/an/an/an/a



Minase Research Institute

Curated by ChEMBL


Assay Description
Inhibition of human DPP4


Bioorg Med Chem 15: 2631-50 (2007)


Article DOI: 10.1016/j.bmc.2007.01.041
BindingDB Entry DOI: 10.7270/Q2CV4HDR
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 2 (DPP II)


(Homo sapiens (Human))
BDBM50243318
PNG
(((2S,4R)-4-(dibenzylamino)pyrrolidin-2-yl)(isoindo...)
Show SMILES O=C([C@@H]1C[C@H](CN1)N(Cc1ccccc1)Cc1ccccc1)N1Cc2ccccc2C1
Show InChI InChI=1S/C27H29N3O/c31-27(30-19-23-13-7-8-14-24(23)20-30)26-15-25(16-28-26)29(17-21-9-3-1-4-10-21)18-22-11-5-2-6-12-22/h1-14,25-26,28H,15-20H2/t25-,26+/m1/s1
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n/an/a 4.50E+3n/an/an/an/an/an/a



University of Antwerp

Curated by ChEMBL


Assay Description
Inhibition of DPP2 (unknown origin)


Bioorg Med Chem Lett 18: 4159-62 (2008)


Article DOI: 10.1016/j.bmcl.2008.05.079
BindingDB Entry DOI: 10.7270/Q2KS6RC4
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 2 (DPP II)


(Homo sapiens (Human))
BDBM50243317
PNG
(((2S,4R)-4-(benzylamino)pyrrolidin-2-yl)(isoindoli...)
Show SMILES O=C([C@@H]1C[C@H](CN1)NCc1ccccc1)N1Cc2ccccc2C1
Show InChI InChI=1S/C20H23N3O/c24-20(23-13-16-8-4-5-9-17(16)14-23)19-10-18(12-22-19)21-11-15-6-2-1-3-7-15/h1-9,18-19,21-22H,10-14H2/t18-,19+/m1/s1
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n/an/a 3.50E+3n/an/an/an/an/an/a



University of Antwerp

Curated by ChEMBL


Assay Description
Inhibition of DPP2 (unknown origin)


Bioorg Med Chem Lett 18: 4159-62 (2008)


Article DOI: 10.1016/j.bmcl.2008.05.079
BindingDB Entry DOI: 10.7270/Q2KS6RC4
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 2 (DPP II)


(Homo sapiens (Human))
BDBM50243316
PNG
(((2S,4R)-4-aminopyrrolidin-2-yl)(isoindolin-2-yl)m...)
Show SMILES N[C@H]1CN[C@@H](C1)C(=O)N1Cc2ccccc2C1
Show InChI InChI=1S/C13H17N3O/c14-11-5-12(15-6-11)13(17)16-7-9-3-1-2-4-10(9)8-16/h1-4,11-12,15H,5-8,14H2/t11-,12+/m1/s1
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n/an/a 4.10E+4n/an/an/an/an/an/a



University of Antwerp

Curated by ChEMBL


Assay Description
Inhibition of DPP2 (unknown origin)


Bioorg Med Chem Lett 18: 4159-62 (2008)


Article DOI: 10.1016/j.bmcl.2008.05.079
BindingDB Entry DOI: 10.7270/Q2KS6RC4
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 2 (DPP II)


(Homo sapiens (Human))
BDBM50243242
PNG
(((2S,4S)-4-(benzylamino)pyrrolidin-2-yl)(isoindoli...)
Show SMILES O=C([C@@H]1C[C@@H](CN1)NCc1ccccc1)N1Cc2ccccc2C1
Show InChI InChI=1S/C20H23N3O/c24-20(23-13-16-8-4-5-9-17(16)14-23)19-10-18(12-22-19)21-11-15-6-2-1-3-7-15/h1-9,18-19,21-22H,10-14H2/t18-,19-/m0/s1
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n/an/a 3.40E+3n/an/an/an/an/an/a



University of Antwerp

Curated by ChEMBL


Assay Description
Inhibition of DPP2 (unknown origin)


Bioorg Med Chem Lett 18: 4159-62 (2008)


Article DOI: 10.1016/j.bmcl.2008.05.079
BindingDB Entry DOI: 10.7270/Q2KS6RC4
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 4


(Homo sapiens (Human))
BDBM50243318
PNG
(((2S,4R)-4-(dibenzylamino)pyrrolidin-2-yl)(isoindo...)
Show SMILES O=C([C@@H]1C[C@H](CN1)N(Cc1ccccc1)Cc1ccccc1)N1Cc2ccccc2C1
Show InChI InChI=1S/C27H29N3O/c31-27(30-19-23-13-7-8-14-24(23)20-30)26-15-25(16-28-26)29(17-21-9-3-1-4-10-21)18-22-11-5-2-6-12-22/h1-14,25-26,28H,15-20H2/t25-,26+/m1/s1
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n/an/a>5.00E+5n/an/an/an/an/an/a



University of Antwerp

Curated by ChEMBL


Assay Description
Inhibition of DPP4 (unknown origin)


Bioorg Med Chem Lett 18: 4159-62 (2008)


Article DOI: 10.1016/j.bmcl.2008.05.079
BindingDB Entry DOI: 10.7270/Q2KS6RC4
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 4


(Homo sapiens (Human))
BDBM50243317
PNG
(((2S,4R)-4-(benzylamino)pyrrolidin-2-yl)(isoindoli...)
Show SMILES O=C([C@@H]1C[C@H](CN1)NCc1ccccc1)N1Cc2ccccc2C1
Show InChI InChI=1S/C20H23N3O/c24-20(23-13-16-8-4-5-9-17(16)14-23)19-10-18(12-22-19)21-11-15-6-2-1-3-7-15/h1-9,18-19,21-22H,10-14H2/t18-,19+/m1/s1
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n/an/a>1.00E+6n/an/an/an/an/an/a



University of Antwerp

Curated by ChEMBL


Assay Description
Inhibition of DPP4 (unknown origin)


Bioorg Med Chem Lett 18: 4159-62 (2008)


Article DOI: 10.1016/j.bmcl.2008.05.079
BindingDB Entry DOI: 10.7270/Q2KS6RC4
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 4


(Homo sapiens (Human))
BDBM50243316
PNG
(((2S,4R)-4-aminopyrrolidin-2-yl)(isoindolin-2-yl)m...)
Show SMILES N[C@H]1CN[C@@H](C1)C(=O)N1Cc2ccccc2C1
Show InChI InChI=1S/C13H17N3O/c14-11-5-12(15-6-11)13(17)16-7-9-3-1-2-4-10(9)8-16/h1-4,11-12,15H,5-8,14H2/t11-,12+/m1/s1
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n/an/a>5.00E+5n/an/an/an/an/an/a



University of Antwerp

Curated by ChEMBL


Assay Description
Inhibition of DPP4 (unknown origin)


Bioorg Med Chem Lett 18: 4159-62 (2008)


Article DOI: 10.1016/j.bmcl.2008.05.079
BindingDB Entry DOI: 10.7270/Q2KS6RC4
More data for this
Ligand-Target Pair
Dipeptidyl peptidase 4


(Homo sapiens (Human))
BDBM50243242
PNG
(((2S,4S)-4-(benzylamino)pyrrolidin-2-yl)(isoindoli...)
Show SMILES O=C([C@@H]1C[C@@H](CN1)NCc1ccccc1)N1Cc2ccccc2C1
Show InChI InChI=1S/C20H23N3O/c24-20(23-13-16-8-4-5-9-17(16)14-23)19-10-18(12-22-19)21-11-15-6-2-1-3-7-15/h1-9,18-19,21-22H,10-14H2/t18-,19-/m0/s1
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n/an/a>2.50E+5n/an/an/an/an/an/a



University of Antwerp

Curated by ChEMBL


Assay Description
Inhibition of DPP4 (unknown origin)


Bioorg Med Chem Lett 18: 4159-62 (2008)


Article DOI: 10.1016/j.bmcl.2008.05.079
BindingDB Entry DOI: 10.7270/Q2KS6RC4
More data for this
Ligand-Target Pair
Dipeptidyl peptidase VIII


(Homo sapiens (Human))
BDBM50243318
PNG
(((2S,4R)-4-(dibenzylamino)pyrrolidin-2-yl)(isoindo...)
Show SMILES O=C([C@@H]1C[C@H](CN1)N(Cc1ccccc1)Cc1ccccc1)N1Cc2ccccc2C1
Show InChI InChI=1S/C27H29N3O/c31-27(30-19-23-13-7-8-14-24(23)20-30)26-15-25(16-28-26)29(17-21-9-3-1-4-10-21)18-22-11-5-2-6-12-22/h1-14,25-26,28H,15-20H2/t25-,26+/m1/s1
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n/an/a 1.30E+4n/an/an/an/an/an/a



University of Antwerp

Curated by ChEMBL


Assay Description
Inhibition of DPP8 (unknown origin)


Bioorg Med Chem Lett 18: 4159-62 (2008)


Article DOI: 10.1016/j.bmcl.2008.05.079
BindingDB Entry DOI: 10.7270/Q2KS6RC4
More data for this
Ligand-Target Pair
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