Reaction Details |
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Target | Proteasome subunit beta type-7 |
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Ligand | BDBM50007206 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1338348 (CHEMBL3240084) |
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IC50 | 46±n/a nM |
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Citation | Kawamura, S; Unno, Y; Asai, A; Arisawa, M; Shuto, S Structurally novel highly potent proteasome inhibitors created by the structure-based hybridization of nonpeptidic belactosin derivatives and peptide boronates. J Med Chem57:2726-35 (2014) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Proteasome subunit beta type-7 |
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Name: | Proteasome subunit beta type-7 |
Synonyms: | Macropain chain Z | Multicatalytic endopeptidase complex chain Z | PSB7_HUMAN | PSMB7 | Proteasome subunit Z | Z |
Type: | PROTEIN |
Mol. Mass.: | 29968.13 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_106197 |
Residue: | 277 |
Sequence: | MAAVSVYAPPVGGFSFDNCRRNAVLEADFAKRGYKLPKVRKTGTTIAGVVYKDGIVLGAD
TRATEGMVVADKNCSKIHFISPNIYCCGAGTAADTDMTTQLISSNLELHSLSTGRLPRVV
TANRMLKQMLFRYQGYIGAALVLGGVDVTGPHLYSIYPHGSTDKLPYVTMGSGSLAAMAV
FEDKFRPDMEEEEAKNLVSEAIAAGIFNDLGSGSNIDLCVISKNKLDFLRPYTVPNKKGT
RLGRYRCEKGTTAVLTEKITPLEIEVLEETVQTMDTS
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BDBM50007206 |
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n/a |
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Name | BDBM50007206 |
Synonyms: | CHEMBL3237867 |
Type | Small organic molecule |
Emp. Form. | C42H62BN3O7 |
Mol. Mass. | 731.769 |
SMILES | [H][C@@]12C[C@@]([H])(C1(C)C)[C@]1(C)OB(O[C@]1([H])C2)[C@H](CC(C)C)NC(=O)[C@H](CCC(=O)NCCCC(COCc1ccccc1)COCc1ccccc1)NC(C)=O |r| |
Structure |
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