Reaction Details |
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Target | Genome polyprotein |
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Ligand | BDBM22851 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_160894 |
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IC50 | 8200±n/a nM |
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Citation | Singh, SB; Graham, PL; Reamer, RA; Cordingley, MG Discovery, total synthesis, HRV 3C-protease inhibitory activity, and structure-activity relationships of 2-methoxystypandrone and its analogues. Bioorg Med Chem Lett11:3143-6 (2001) [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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BDBM22851 |
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n/a |
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Name | BDBM22851 |
Synonyms: | 1,2-Dione-Based Compound, 8 | 1,2-dihydronaphthalene-1,2-dione | 1,2-naphthoquinone | CHEMBL52347 | cid_10667 |
Type | Small organic molecule |
Emp. Form. | C10H6O2 |
Mol. Mass. | 158.1534 |
SMILES | O=C1C=Cc2ccccc2C1=O |c:2| |
Structure |
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