Reaction Details |
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Target | Aminopeptidase B |
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Ligand | BDBM50010212 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1344423 (CHEMBL3258373) |
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IC50 | >860000±n/a nM |
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Citation | Nishizawa, R; Saino, T; Takita, T; Suda, H; Aoyagi, T Synthesis and structure-activity relationships of bestatin analogues, inhibitors of aminopeptidase B. J Med Chem20:510-5 (1977) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Aminopeptidase B |
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Name: | Aminopeptidase B |
Synonyms: | AMPB_RAT | Ap-B | Arginine aminopeptidase | Arginyl aminopeptidase | Cytosol aminopeptidase IV | Rnpep |
Type: | PROTEIN |
Mol. Mass.: | 72609.93 |
Organism: | Rattus norvegicus |
Description: | ChEMBL_1344423 |
Residue: | 650 |
Sequence: | MESSGPSSCHSAARRPLHSAQAVDVASASSFRAFEILHLHLDLRAEFGPPGPGPGSRGLN
GKATLELRCLLPEGASELRLDSHSCLEVMAATLLRGQPGDQQQLTEPVPFHTQPFSHYGQ
ALCVVFPKPCCAAERFRLELTYRVGEGPGVCWLAPEQTAGKKKPFVYTQGQAVLNRAFFP
CFDTPAVKCTYSALVEVPDGFTAVMSASTWERRGPNKFFFQMSQPIPSYLIALAIGDLAS
AEVGPRSRVWAEPCLIEAAKEEYNGVIEEFLATGEKLFGPYVWGRYDLLFMPPSFPFGGM
ENPCLTFVTPCLLAGDRSLADVIIHEISHSWFGNLVTNANWGEFWLNEGFTMYAQRRIST
ILFGAAYTCLEAATGRALLRQHMDVSGEENPLNKLRVKIEPGVDPDDTYNETPYEKGYCF
VSYLAHLVGDQEQFDKFLKAYVDEFKFQSILAEDFLEFYLEYFPELKKKGVDSIPGFEFN
RWLNTPGWPPYLPDLSPGDSLMKPAEELAELWAASEPDMQAIEAVAISTWKTYQLVYFLD
KILQKSPLPPGNVKKLGETYPKISNAQNAELRLRWGQIILKNDHQEEFWKVKDFLQSQGK
QKYTLPLYHAMMGGSEMARTLAKETFSATASQLHSNVVNYVQQILAPKGS
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BDBM50010212 |
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n/a |
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Name | BDBM50010212 |
Synonyms: | CHEMBL3251680 |
Type | Small organic molecule |
Emp. Form. | C15H20N2O4 |
Mol. Mass. | 292.3303 |
SMILES | N[C@H](Cc1ccccc1)[C@H](O)C(=O)N1CCC[C@H]1C(O)=O |r| |
Structure |
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