Reaction Details | |||
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Target | Carboxypeptidase B2 | ||
Ligand | BDBM50197529 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | ChEBML_1619507 | ||
IC50 | >30000±n/a nM | ||
Citation | Halland, N; Czech, J; Czechtizky, W; Evers, A; Follmann, M; Kohlmann, M; Schreuder, HA; Kallus, C Sulfamide as Zinc Binding Motif in Small Molecule Inhibitors of Activated Thrombin Activatable Fibrinolysis Inhibitor (TAFIa). J Med Chem59:9567-9573 (2016) [PubMed] Article | ||
More Info.: | Get all data from this article, Assay Method | ||
Carboxypeptidase B2 | |||
Name: | Carboxypeptidase B2 | ||
Synonyms: | CBPB2_HUMAN | CPB2 | CPU | Carboxypeptidase B2 | Carboxypeptidase B2 isoform A | Carboxypeptidase U | Plasma carboxypeptidase B | TAFI | Thrombin-activable fibrinolysis inhibitor | pCPB | ||
Type: | Enzyme | ||
Mol. Mass.: | 48432.74 | ||
Organism: | Homo sapiens (Human) | ||
Description: | Q96IY4 | ||
Residue: | 423 | ||
Sequence: |
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BDBM50197529 | |||
n/a | |||
Name | BDBM50197529 | ||
Synonyms: | CHEMBL3944308 | ||
Type | Small organic molecule | ||
Emp. Form. | C28H50N4O5S | ||
Mol. Mass. | 554.785 | ||
SMILES | CC1(C)[C@@H]2CC[C@@]1(C)[C@H](C2)NC(=O)[C@H](CC1CCCCC1)NS(=O)(=O)N[C@@H](CC1CCC(N)CC1)C(O)=O |r,wU:13.15,3.2,6.7,wD:26.29,8.11,THB:10:8:5.4:1,(19.19,-13.84,;19.2,-15.38,;17.7,-15.78,;20.04,-16.52,;19.39,-17.68,;19.32,-18.96,;20.22,-17.79,;20.62,-19.27,;21.62,-17.83,;21.61,-16.65,;22.96,-18.59,;24.29,-17.83,;24.29,-16.28,;25.63,-18.59,;25.63,-20.14,;24.29,-20.91,;22.96,-20.1,;21.62,-20.87,;21.6,-22.41,;22.93,-23.2,;24.29,-22.44,;26.98,-17.82,;28.33,-18.6,;27.22,-19.69,;29.41,-19.69,;29.68,-17.83,;31.03,-18.6,;31.03,-20.15,;32.36,-20.92,;32.35,-22.46,;33.68,-23.23,;35.01,-22.46,;36.34,-23.24,;35.02,-20.92,;33.68,-20.14,;32.36,-17.84,;33.69,-18.6,;32.36,-16.29,)| | ||
Structure |