Reaction Details |
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Target | Granzyme B |
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Ligand | BDBM50374384 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_469245 (CHEMBL948945) |
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Ki | 7±n/a nM |
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Citation | Maryanoff, BE; Costanzo, MJ Inhibitors of proteases and amide hydrolases that employ an alpha-ketoheterocycle as a key enabling functionality. Bioorg Med Chem16:1562-95 (2008) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Granzyme B |
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Name: | Granzyme B |
Synonyms: | CGL1 | CSPB | CTLA1 | GRAB_HUMAN | GRB | GZMB |
Type: | PROTEIN |
Mol. Mass.: | 27735.56 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_469245 |
Residue: | 247 |
Sequence: | MQPILLLLAFLLLPRADAGEIIGGHEAKPHSRPYMAYLMIWDQKSLKRCGGFLIRDDFVL
TAAHCWGSSINVTLGAHNIKEQEPTQQFIPVKRPIPHPAYNPKNFSNDIMLLQLERKAKR
TRAVQPLRLPSNKAQVKPGQTCSVAGWGQTAPLGKHSHTLQEVKMTVQEDRKCESDLRHY
YDSTIELCVGDPEIKKTSFKGDSGGPLVCNKVAQGIVSYGRNNGMPPRACTKVSSFVHWI
KKTMKRY
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BDBM50374384 |
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n/a |
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Name | BDBM50374384 |
Synonyms: | CHEMBL255387 |
Type | Small organic molecule |
Emp. Form. | C33H36N6O8 |
Mol. Mass. | 644.6743 |
SMILES | CC[C@H](C)[C@H](NC(C)=O)C(=O)N[C@H]1CCc2cccc3C[C@H](N(c23)C1=O)C(=O)N[C@@H](CC(O)=O)C(=O)c1nnc(o1)-c1ccccc1 |
Structure |
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