Reaction Details |
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Target | Cathepsin B |
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Ligand | BDBM110194 |
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Substrate/Competitor | n/a |
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Meas. Tech. | Cathepsin B Inhibition Assay |
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pH | 5.5±n/a |
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Temperature | 310.15±n/a K |
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IC50 | 8.459e+4± 375 nM |
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Comments | extracted |
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Citation | Baek, KH; Karki, R; Lee, ES; Na, Y; Kwon, Y Synthesis and investigation of dihydroxychalcones as calpain and cathepsin inhibitors. Bioorg Chem51:24-30 (2013) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Cathepsin B |
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Name: | Cathepsin B |
Synonyms: | APP secretase | APPS | CATB_HUMAN | CPSB | CTSB | Cathepsin B heavy chain | Cathepsin B light chain | Cathepsin B1 |
Type: | Enzyme |
Mol. Mass.: | 37819.69 |
Organism: | Homo sapiens (Human) |
Description: | gi_63102437 |
Residue: | 339 |
Sequence: | MWQLWASLCCLLVLANARSRPSFHPLSDELVNYVNKRNTTWQAGHNFYNVDMSYLKRLCG
TFLGGPKPPQRVMFTEDLKLPASFDAREQWPQCPTIKEIRDQGSCGSCWAFGAVEAISDR
ICIHTNAHVSVEVSAEDLLTCCGSMCGDGCNGGYPAEAWNFWTRKGLVSGGLYESHVGCR
PYSIPPCEHHVNGSRPPCTGEGDTPKCSKICEPGYSPTYKQDKHYGYNSYSVSNSEKDIM
AEIYKNGPVEGAFSVYSDFLLYKSGVYQHVTGEMMGGHAIRILGWGVENGTPYWLVANSW
NTDWGDNGFFKILRGQDHCGIESEVVAGIPRTDQYWEKI
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BDBM110194 |
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n/a |
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Name | BDBM110194 |
Synonyms: | 1-(3,5-Dihydroxyphenyl)-3-(furan-2-yl)propenone (21) |
Type | Small organic molecule |
Emp. Form. | C13H10O4 |
Mol. Mass. | 230.2161 |
SMILES | Oc1cc(O)cc(c1)C(=O)\C=C\c1ccco1 |
Structure |
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