Reaction Details |
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Target | Cathepsin B |
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Ligand | BDBM50286434 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_47409 |
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IC50 | 25000±n/a nM |
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Citation | Graybill, TL; Dolle, RE; Osifo, IK; Schmidt, SJ; Gregory, JS; Harris, AL; Miller, MS Inhibition of human erythrocyte calpain I by novel quinolinecarboxamides Bioorg Med Chem Lett5:387-392 (1995) 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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BDBM50286434 |
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n/a |
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Name | BDBM50286434 |
Synonyms: | 1-(2-Chloro-4-hydroxy-phenyl)-4-oxo-7-pyridin-4-yl-1,4-dihydro-quinoline-3-carboxylic acid amide | CHEMBL340384 |
Type | Small organic molecule |
Emp. Form. | C21H14ClN3O3 |
Mol. Mass. | 391.807 |
SMILES | NC(=O)c1cn(-c2ccc(O)cc2Cl)c2cc(ccc2c1=O)-c1ccncc1 |
Structure |
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