Reaction Details |
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Target | Carboxypeptidase B2 |
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Ligand | BDBM173928 |
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Substrate/Competitor | n/a |
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Meas. Tech. | TAFI Activity Assay |
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pH | 7.4±n/a |
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Temperature | 298.15±n/a K |
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IC50 | 40±n/a nM |
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Comments | extracted |
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Citation | Kallus, C; Broenstrup, M; Evers, A; Globisch, A; Schreuder, H; Wagner, M Macrocyclic urea and sulfamide derivatives as inhibitors of TAFIa US Patent US9688645 Publication Date 6/27/2017 |
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More Info.: | Get all data from this article, Assay Method |
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Carboxypeptidase B2 |
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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: | MKLCSLAVLVPIVLFCEQHVFAFQSGQVLAALPRTSRQVQVLQNLTTTYEIVLWQPVTAD
LIVKKKQVHFFVNASDVDNVKAHLNVSGIPCSVLLADVEDLIQQQISNDTVSPRASASYY
EQYHSLNEIYSWIEFITERHPDMLTKIHIGSSFEKYPLYVLKVSGKEQAAKNAIWIDCGI
HAREWISPAFCLWFIGHITQFYGIIGQYTNLLRLVDFYVMPVVNVDGYDYSWKKNRMWRK
NRSFYANNHCIGTDLNRNFASKHWCEEGASSSSCSETYCGLYPESEPEVKAVASFLRRNI
NQIKAYISMHSYSQHIVFPYSYTRSKSKDHEELSLVASEAVRAIEKISKNTRYTHGHGSE
TLYLAPGGGDDWIYDLGIKYSFTIELRDTGTYGFLLPERYIKPTCREAFAAVSKIAWHVI
RNV
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BDBM173928 |
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n/a |
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Name | BDBM173928 |
Synonyms: | US9688645, 7-4 |
Type | Small organic molecule |
Emp. Form. | C26H34N6O6 |
Mol. Mass. | 526.5848 |
SMILES | CC(C)[C@H]1COCCNC(=O)c2ccc(C[C@@H](NC(=O)N[C@@H](Cc3ccc(N)nc3)C(O)=O)C(=O)N1)cc2 |r| |
Structure |
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