Reaction Details |
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Target | Cytosol aminopeptidase |
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Ligand | BDBM23971 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_872713 (CHEMBL2185126) |
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Ki | 500±n/a nM |
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Citation | Albrecht, S; Salomon, E; Defoin, A; Tarnus, C Rapid and efficient synthesis of a novel series of substituted aminobenzosuberone derivatives as potent, selective, non-peptidic neutral aminopeptidase inhibitors. Bioorg Med Chem20:4942-53 (2012) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Cytosol aminopeptidase |
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Name: | Cytosol aminopeptidase |
Synonyms: | AMPL_BOVIN | LAP | LAP3 | LAPc | Leucine Aminopeptidase | Leucyl aminopeptidase |
Type: | Homohexamer |
Mol. Mass.: | 56288.28 |
Organism: | Bos taurus (bovine) |
Description: | Bovine kidney LAPc was purchased from Sigma Chemical Co. |
Residue: | 519 |
Sequence: | MFLLPLPAAARVAVRHLSVKRLWAPGPAAADMTKGLVLGIYSKEKEEDEPQFTSAGENFN
KLVSGKLREILNISGPPLKAGKTRTFYGLHEDFPSVVVVGLGKKTAGIDEQENWHEGKEN
IRAAVAAGCRQIQDLEIPSVEVDPCGDAQAAAEGAVLGLYEYDDLKQKRKVVVSAKLHGS
EDQEAWQRGVLFASGQNLARRLMETPANEMTPTKFAEIVEENLKSASIKTDVFIRPKSWI
EEQEMGSFLSVAKGSEEPPVFLEIHYKGSPNASEPPLVFVGKGITFDSGGISIKAAANMD
LMRADMGGAATICSAIVSAAKLDLPINIVGLAPLCENMPSGKANKPGDVVRARNGKTIQV
DNTDAEGRLILADALCYAHTFNPKVIINAATLTGAMDIALGSGATGVFTNSSWLWNKLFE
ASIETGDRVWRMPLFEHYTRQVIDCQLADVNNIGKYRSAGACTAAAFLKEFVTHPKWAHL
DIAGVMTNKDEVPYLRKGMAGRPTRTLIEFLFRFSQDSA
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BDBM23971 |
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n/a |
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Name | BDBM23971 |
Synonyms: | (2S)-2-[(2S,3R)-3-amino-2-hydroxy-4-phenylbutanamido]-4-methylpentanoic acid | Bestatin | CHEMBL29292 | Ubenimex |
Type | Small organic molecule |
Emp. Form. | C16H24N2O4 |
Mol. Mass. | 308.3728 |
SMILES | CC(C)C[C@H](NC(=O)[C@@H](O)[C@H](N)Cc1ccccc1)C(O)=O |
Structure |
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