Reaction Details |
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Target | Chymotrypsinogen B |
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Ligand | BDBM50055218 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_362488 (CHEMBL866986) |
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IC50 | 34000±n/a nM |
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Citation | Zhou, L; Liu, Y; Zhang, W; Wei, P; Huang, C; Pei, J; Yuan, Y; Lai, L Isatin compounds as noncovalent SARS coronavirus 3C-like protease inhibitors. J Med Chem49:3440-3 (2006) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Chymotrypsinogen B |
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Name: | Chymotrypsinogen B |
Synonyms: | A0A2R8YG87_HUMAN | Beta-chymotrypsin | CTRB1 | Chymotrypsin B chain A | Chymotrypsin B chain B | Chymotrypsin B chain C | Chymotrypsinogen B |
Type: | PROTEIN |
Mol. Mass.: | 27871.19 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_216634 |
Residue: | 263 |
Sequence: | MAFLWLLSCWALLGTTFGCGVPAIHPVLSGLSRIVNGEDAVPGSWPWQVSLQDKTGFHFC
GGSLISEDWVVTAAHCGVRTSDVVVAGEFDQGSDEENIQVLKIAKVFKNPKFSILTVNND
ITLLKLATPARFSQTVSAVCLPSADDDFPAGTLCATTGWGKTKYNANKTPDKLQQAALPL
LSNAECKKSWGRRITDVMICAGASGVSSCMGDSGGPLVCQKDGAWTLVGIVSWGSDTCST
SSPGVYARVTKLIPWVQKILAAN
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BDBM50055218 |
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n/a |
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Name | BDBM50055218 |
Synonyms: | 1-(2-naphthlmethyl) isatin-5-carboxamide | 1-Naphthalen-2-ylmethyl-2,3-dioxo-2,3-dihydro-1H-indole-5-carboxylic acid amide | CHEMBL358279 | acs.jmedchem.1c00409_ST.74 | med.21724, Compound 108 |
Type | Small organic molecule |
Emp. Form. | C20H14N2O3 |
Mol. Mass. | 330.3368 |
SMILES | NC(=O)c1ccc2N(Cc3ccc4ccccc4c3)C(=O)C(=O)c2c1 |
Structure |
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