Reaction Details |
| Report a problem with these data |
Target | Carboxypeptidase B2 |
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Ligand | BDBM81905 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Inhibition Assay |
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Ki | 7.4e+3±n/a nM |
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Citation | Fernández, D; Avilés, FX; Vendrell, J Aromatic organic compounds as scaffolds for metallocarboxypeptidase inhibitor design. Chem Biol Drug Des73:75-82 (2009) [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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BDBM81905 |
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n/a |
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Name | BDBM81905 |
Synonyms: | 1-(3,4-dihydroisoquinolin-1(1H)-yl)-2-(5-(3,5-dimethylphenyl)-1,3,4-oxadiazol-2-ylthio)ethanone, 4 |
Type | Small organic molecule |
Emp. Form. | C21H21N3O2S |
Mol. Mass. | 379.475 |
SMILES | Cc1cc(C)cc(c1)-c1nnc(SCC(=O)N2CCCc3ccccc23)o1 |
Structure |
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