Reaction Details | |||
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Target | Dipeptidyl peptidase 2 | ||
Ligand | BDBM50338440 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | ChEMBL_728290 (CHEMBL1687447) | ||
IC50 | 690±n/a nM | ||
Citation | Chen, P; Caldwell, CG; Ashton, W; Wu, JK; He, H; Lyons, KA; Thornberry, NA; Weber, AE Synthesis and evaluation of [(1R)-1-amino-2-(2,5-difluorophenyl)ethyl]cyclohexanes and 4-[(1R)-1-amino-2-(2,5-difluorophenyl)ethyl]piperidines as DPP-4 inhibitors. Bioorg Med Chem Lett21:1880-6 (2011) [PubMed] Article | ||
More Info.: | Get all data from this article, Assay Method | ||
Dipeptidyl peptidase 2 | |||
Name: | Dipeptidyl peptidase 2 | ||
Synonyms: | DAP II | DPP2 | DPP2_HUMAN | DPP7 | Dipeptidyl aminopeptidase II | Dipeptidyl peptidase 2 (DPP II) | Dipeptidyl peptidase 2 (DPP2) | Dipeptidyl peptidase II (DDP-II) | Dipeptidyl peptidase II (DPP II) | Dipeptidyl peptidase II (DPP2) | Dipeptidyl peptidase II and dipeptidyl peptidase IV (DPP2 and DPP4) | QPP | carboxytripeptidase | dipeptidyl arylamidase II | dipeptidyl(amino)peptidase II | dipeptidylarylamidase | ||
Type: | Protein | ||
Mol. Mass.: | 54339.29 | ||
Organism: | Homo sapiens (Human) | ||
Description: | Q9UHL4 | ||
Residue: | 492 | ||
Sequence: |
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BDBM50338440 | |||
n/a | |||
Name | BDBM50338440 | ||
Synonyms: | CHEMBL1682974 | trans-N-(4-((S)-1-amino-2-oxo-2-(thiazolidin-3-yl)ethyl)cyclohexyl)-4-(trifluoromethoxy)benzamide | ||
Type | Small organic molecule | ||
Emp. Form. | C19H24F3N3O3S | ||
Mol. Mass. | 431.472 | ||
SMILES | N[C@@H]([C@H]1CC[C@@H](CC1)NC(=O)c1ccc(OC(F)(F)F)cc1)C(=O)N1CCSC1 |r,wU:1.0,5.8,wD:2.1,(35.26,-24.16,;35.27,-25.7,;36.6,-26.47,;36.6,-28.01,;37.93,-28.77,;39.26,-28.01,;39.26,-26.47,;37.93,-25.69,;40.59,-28.78,;41.93,-28.01,;41.93,-26.47,;43.26,-28.78,;43.25,-30.32,;44.58,-31.09,;45.92,-30.32,;47.25,-31.09,;47.25,-32.63,;48.59,-33.4,;45.92,-33.4,;47.24,-34.17,;45.92,-28.78,;44.59,-28.01,;33.93,-26.48,;33.94,-28.02,;32.6,-25.71,;31.19,-26.33,;30.16,-25.19,;30.92,-23.86,;32.43,-24.17,)| | ||
Structure |