Reaction Details |
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Target | Chymotrypsin-like protease CTRL-1 |
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Ligand | BDBM50031440 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_49606 |
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IC50 | 6±n/a nM |
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Citation | Iqbal, M; Chatterjee, S; Kauer, JC; Mallamo, JP; Messina, PA; Reiboldt, A; Siman, R Potent α-ketocarbonyl and boronic ester derived inhibitors of proteasome Bioorg Med Chem Lett6:287-290 (1996) Article |
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More Info.: | Get all data from this article, Assay Method |
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Chymotrypsin-like protease CTRL-1 |
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Name: | Chymotrypsin-like protease CTRL-1 |
Synonyms: | CTRL | CTRL1 | CTRL_HUMAN |
Type: | PROTEIN |
Mol. Mass.: | 28008.18 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_49606 |
Residue: | 264 |
Sequence: | MLLLSLTLSLVLLGSSWGCGIPAIKPALSFSQRIVNGENAVLGSWPWQVSLQDSSGFHFC
GGSLISQSWVVTAAHCNVSPGRHFVVLGEYDRSSNAEPLQVLSVSRAITHPSWNSTTMNN
DVTLLKLASPAQYTTRISPVCLASSNEALTEGLTCVTTGWGRLSGVGNVTPAHLQQVALP
LVTVNQCRQYWGSSITDSMICAGGAGASSCQGDSGGPLVCQKGNTWVLIGIVSWGTKNCN
VRAPAVYTRVSKFSTWINQVIAYN
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BDBM50031440 |
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n/a |
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Name | BDBM50031440 |
Synonyms: | 1N-[4-amino(nitroimino)methylamino-1-(1-formyl-3-methylbutylcarbamoyl)butyl]-10-cyano-2-cyclopentyldecanamide | Alpha-ketocarbonyl derivative | CHEMBL74336 |
Type | Small organic molecule |
Emp. Form. | C28H49N7O5 |
Mol. Mass. | 563.7326 |
SMILES | CC(C)CC(NC(=O)C(CCCN=C(N)N[N+]([O-])=O)NC(=O)C(CCCCCCCCC#N)C1CCCC1)C=O |w:12.11| |
Structure |
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