Reaction Details |
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Target | Cathepsin G |
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Ligand | BDBM50329819 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_464561 (CHEMBL933247) |
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IC50 | 2110±n/a nM |
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Citation | Dorsey, BD; Iqbal, M; Chatterjee, S; Menta, E; Bernardini, R; Bernareggi, A; Cassarà, PG; D'Arasmo, G; Ferretti, E; De Munari, S; Oliva, A; Pezzoni, G; Allievi, C; Strepponi, I; Ruggeri, B; Ator, MA; Williams, M; Mallamo, JP Discovery of a potent, selective, and orally active proteasome inhibitor for the treatment of cancer. J Med Chem51:1068-72 (2008) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Cathepsin G |
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Name: | Cathepsin G |
Synonyms: | CATG_HUMAN | CG | CTSG |
Type: | PROTEIN |
Mol. Mass.: | 28860.08 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_1469016 |
Residue: | 255 |
Sequence: | MQPLLLLLAFLLPTGAEAGEIIGGRESRPHSRPYMAYLQIQSPAGQSRCGGFLVREDFVL
TAAHCWGSNINVTLGAHNIQRRENTQQHITARRAIRHPQYNQRTIQNDIMLLQLSRRVRR
NRNVNPVALPRAQEGLRPGTLCTVAGWGRVSMRRGTDTLREVQLRVQRDRQCLRIFGSYD
PRRQICVGDRRERKAAFKGDSGGPLLCNNVAHGIVSYGKSSGVPPEVFTRVSSFLPWIRT
TMRSFKLLDQMETPL
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BDBM50329819 |
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n/a |
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Name | BDBM50329819 |
Synonyms: | (R)-1-((2S,3R)-3-hydroxy-2-(6-phenylpicolinamido)butanamido)-3-methylbutylboronic acid | CEP-18770 | CHEMBL270515 | [(1R)-1-[[(2S,3R)-3-hydroxy-2-[(6-phenylpyridine-2-carbonyl)amino]-1-oxobutyl]amino]-3-methylbutyl]boronic acid |
Type | Small organic molecule |
Emp. Form. | C21H28BN3O5 |
Mol. Mass. | 413.275 |
SMILES | CC(C)C[C@H](NC(=O)[C@@H](NC(=O)c1cccc(n1)-c1ccccc1)[C@@H](C)O)B(O)O |
Structure |
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