| Reaction Details |
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 | Report a problem with these data |
| Target | Genome polyprotein |
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| Ligand | BDBM50075613 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_161099 (CHEMBL771560) |
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| EC50 | 600±n/a nM |
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| Citation |  Dragovich, PS; Prins, TJ; Zhou, R; Webber, SE; Marakovits, JT; Fuhrman, SA; Patick, AK; Matthews, DA; Lee, CA; Ford, CE; Burke, BJ; Rejto, PA; Hendrickson, TF; Tuntland, T; Brown, EL; Meador, JW; Ferre, RA; Harr, JE; Kosa, MB; Worland, ST Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitors. 4. Incorporation of P1 lactam moieties as L-glutamine replacements. J Med Chem42:1213-24 (1999) [PubMed] Article |
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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 |
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| Synonyms: | Human rhinovirus A protease | Human rhinovirus B 3A protease |
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| Type: | PROTEIN |
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| Mol. Mass.: | 44361.04 |
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| Organism: | Human rhinovirus B |
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| Description: | ChEMBL_158953 |
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| Residue: | 401 |
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| Sequence: | AFRPCNVNTKIGNAKCCPFVCGKAVTFKDRSTCSTYNLSSSLHHILEEDKRRRQVVDVMS
AIFQGPISLDAPPPPAIADLLQSVRTPRVIKYCQIIMGHPAECQVERDLNIANSIIAIIA
NIISIAGIIFVIYKLFCSLQGPYSGEPKPKTKVPERRVVAQGPEEEFGRSILKNNTCVIT
TGNGKFTGLGIHDRILIIPTHADPGREVQVNGVHTKVLDSYDLYNRDGVKLEITVIQLDR
NEKFRDIRKYIPETEDDYPECNLALSANQDEPTIIKVGDVVSYGNILLSGNQTARMLKYN
YPTKSGYCGGVLYKIGQILGIHVGGNGRDGFSAMLLRSYFTGQIKVNKHATECGLPDIQT
IHTPSKTKLQPSVFYDVFPGSKEPAVLTDNDPRLEVNFKEA
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| BDBM50075613 |
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| n/a |
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| Name | BDBM50075613 |
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| Synonyms: | (E)-(R)-4-[(S)-2-((S)-2-Benzyloxycarbonylamino-4-methyl-pentanoylamino)-3-phenyl-propionylamino]-5-(2-oxo-imidazolidin-1-yl)-pent-2-enoic acid ethyl ester | CHEMBL20239 |
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| Type | Small organic molecule |
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| Emp. Form. | C33H43N5O7 |
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| Mol. Mass. | 621.7238 |
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| SMILES | CCOC(=O)\C=C\[C@H](CN1CCNC1=O)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(C)C)NC(=O)OCc1ccccc1 |
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| Structure | 
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