Reaction Details |
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Target | Proteasome subunit beta type-5 |
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Ligand | BDBM50199450 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_413589 (CHEMBL853870) |
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IC50 | >10000±n/a nM |
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Citation | Adsule, S; Barve, V; Chen, D; Ahmed, F; Dou, QP; Padhye, S; Sarkar, FH Novel Schiff base copper complexes of quinoline-2 carboxaldehyde as proteasome inhibitors in human prostate cancer cells. J Med Chem49:7242-6 (2006) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Proteasome subunit beta type-5 |
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Name: | Proteasome subunit beta type-5 |
Synonyms: | 20S proteasome chymotrypsin-like | 26S proteosome | LMPX | MB1 | PSB5_HUMAN | PSMB5 | Proteasome Macropain subunit MB1 | Proteasome subunit beta type-1/beta type-5 | X |
Type: | Protein |
Mol. Mass.: | 28480.96 |
Organism: | Homo sapiens (Human) |
Description: | n/a |
Residue: | 263 |
Sequence: | MALASVLERPLPVNQRGFFGLGGRADLLDLGPGSLSDGLSLAAPGWGVPEEPGIEMLHGT
TTLAFKFRHGVIVAADSRATAGAYIASQTVKKVIEINPYLLGTMAGGAADCSFWERLLAR
QCRIYELRNKERISVAAASKLLANMVYQYKGMGLSMGTMICGWDKRGPGLYYVDSEGNRI
SGATFSVGSGSVYAYGVMDRGYSYDLEVEQAYDLARRAIYQATYRDAYSGGAVNLYHVRE
DGWIRVSSDNVADLHEKYSGSTP
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BDBM50199450 |
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n/a |
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Name | BDBM50199450 |
Synonyms: | 1-(quinolin-2-ylmethylene)thiosemicarbazide | 2-(quinolin-2-ylmethylene)hydrazinecarbothioamide | CHEMBL215065 |
Type | Small organic molecule |
Emp. Form. | C11H10N4S |
Mol. Mass. | 230.289 |
SMILES | NC(=S)NN=Cc1ccc2ccccc2n1 |w:5.5| |
Structure |
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