Reaction Details |
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Target | Genome polyprotein |
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Ligand | BDBM50084671 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_161095 (CHEMBL771556) |
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EC50 | 5±n/a nM |
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Citation | Leung, D; Abbenante, G; Fairlie, DP Protease inhibitors: current status and future prospects. J Med Chem43:305-41 (2000) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Genome polyprotein |
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Name: | Genome polyprotein |
Synonyms: | Human rhinovirus A protease | Human rhinovirus B 3A protease |
Type: | PROTEIN |
Mol. Mass.: | 44361.04 |
Organism: | Human rhinovirus B |
Description: | ChEMBL_158953 |
Residue: | 401 |
Sequence: | AFRPCNVNTKIGNAKCCPFVCGKAVTFKDRSTCSTYNLSSSLHHILEEDKRRRQVVDVMS
AIFQGPISLDAPPPPAIADLLQSVRTPRVIKYCQIIMGHPAECQVERDLNIANSIIAIIA
NIISIAGIIFVIYKLFCSLQGPYSGEPKPKTKVPERRVVAQGPEEEFGRSILKNNTCVIT
TGNGKFTGLGIHDRILIIPTHADPGREVQVNGVHTKVLDSYDLYNRDGVKLEITVIQLDR
NEKFRDIRKYIPETEDDYPECNLALSANQDEPTIIKVGDVVSYGNILLSGNQTARMLKYN
YPTKSGYCGGVLYKIGQILGIHVGGNGRDGFSAMLLRSYFTGQIKVNKHATECGLPDIQT
IHTPSKTKLQPSVFYDVFPGSKEPAVLTDNDPRLEVNFKEA
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BDBM50084671 |
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n/a |
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Name | BDBM50084671 |
Synonyms: | 4-{2-(4-Fluoro-benzyl)-7-methyl-5-[(5-methyl-isoxazole-3-carbonyl)-amino]-4-oxo-octanoylamino}-5-(2-oxo-pyrrolidin-3-yl)-pent-2-enoic acid ethyl ester(AG7088) | CHEMBL327058 |
Type | Small organic molecule |
Emp. Form. | C32H41FN4O7 |
Mol. Mass. | 612.6889 |
SMILES | CCOC(=O)\C=C\[C@H](C[C@@H]1CCNC1=O)NC(=O)[C@@H](CC(=O)[C@H](CC(C)C)NC(=O)c1cc(C)on1)Cc1ccc(F)cc1 |
Structure |
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