Reaction Details |
| Report a problem with these data |
Target | Carboxypeptidase B2 |
---|
Ligand | BDBM50144337 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEBML_206146 |
---|
IC50 | 2±n/a nM |
---|
Citation | Nantermet, PG; Barrow, JC; Lindsley, SR; Young, M; Mao, SS; Carroll, S; Bailey, C; Bosserman, M; Colussi, D; McMasters, DR; Vacca, JP; Selnick, HG Imidazole acetic acid TAFIa inhibitors: SAR studies centered around the basic P(1)(') group. Bioorg Med Chem Lett14:2141-5 (2004) [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: | MKLCSLAVLVPIVLFCEQHVFAFQSGQVLAALPRTSRQVQVLQNLTTTYEIVLWQPVTAD
LIVKKKQVHFFVNASDVDNVKAHLNVSGIPCSVLLADVEDLIQQQISNDTVSPRASASYY
EQYHSLNEIYSWIEFITERHPDMLTKIHIGSSFEKYPLYVLKVSGKEQAAKNAIWIDCGI
HAREWISPAFCLWFIGHITQFYGIIGQYTNLLRLVDFYVMPVVNVDGYDYSWKKNRMWRK
NRSFYANNHCIGTDLNRNFASKHWCEEGASSSSCSETYCGLYPESEPEVKAVASFLRRNI
NQIKAYISMHSYSQHIVFPYSYTRSKSKDHEELSLVASEAVRAIEKISKNTRYTHGHGSE
TLYLAPGGGDDWIYDLGIKYSFTIELRDTGTYGFLLPERYIKPTCREAFAAVSKIAWHVI
RNV
|
|
|
BDBM50144337 |
---|
n/a |
---|
Name | BDBM50144337 |
Synonyms: | 3-(6-Amino-pyridin-3-yl)-2-[1-(4-methyl-pentyl)-1H-imidazol-4-yl]-propionic acid | CHEMBL70177 |
Type | Small organic molecule |
Emp. Form. | C17H24N4O2 |
Mol. Mass. | 316.3981 |
SMILES | CC(C)CCCn1cnc(c1)C(Cc1ccc(N)nc1)C(O)=O |
Structure |
|