Reaction Details |
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Target | Carboxypeptidase B2 |
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Ligand | BDBM50226599 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_452077 (CHEMBL901238) |
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Ki | 250±n/a nM |
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Citation | Bunnage, ME; Blagg, J; Steele, J; Owen, DR; Allerton, C; McElroy, AB; Miller, D; Ringer, T; Butcher, K; Beaumont, K; Evans, K; Gray, AJ; Holland, SJ; Feeder, N; Moore, RS; Brown, DG Discovery of potent& selective inhibitors of activated thrombin-activatable fibrinolysis inhibitor for the treatment of thrombosis. J Med Chem50:6095-103 (2007) [PubMed] Article |
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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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BDBM50226599 |
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n/a |
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Name | BDBM50226599 |
Synonyms: | (S)-2-(2-aminoethylamino)-3-(1-ethyl-1H-imidazol-4-yl)propanoic acid | CHEMBL235277 |
Type | Small organic molecule |
Emp. Form. | C10H18N4O2 |
Mol. Mass. | 226.2755 |
SMILES | CCn1cnc(C[C@H](NCCN)C(O)=O)c1 |
Structure |
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