Reaction Details |
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Target | Polymerase acidic protein |
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Ligand | BDBM50125822 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_823246 (CHEMBL2040664) |
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IC50 | 5100±n/a nM |
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Citation | Singh, SB; Tomassini, JE Synthesis of natural flutimide and analogous fully substituted pyrazine-2,6-diones, endonuclease inhibitors of influenza virus. J Org Chem66:5504-16 (2001) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Polymerase acidic protein |
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Name: | Polymerase acidic protein |
Synonyms: | Hepatitis C virus polyprotein | PA | PA/PB1 | PA_I34A1 | Polymerase acidic protein | RNA-directed RNA polymerase subunit P2 |
Type: | PROTEIN |
Mol. Mass.: | 82573.84 |
Organism: | Hepatitis C virus |
Description: | ChEMBL_64976 |
Residue: | 716 |
Sequence: | MEDFVRQCFNPMIVELAEKTMKEYGEDLKIETNKFAAICTHLEVCFMYSDFHFINEQGES
IIVELGDPNALLKHRFEIIEGRDRTMAWTVVNSICNTTGAEKPKFLPDLYDYKENRFIEI
GVTRREVHIYYLEKANKIKSEKTHIHIFSFTGEEMATKADYTLDEESRARIKTRLFTIRQ
EMASRGLWDSFRQSERGEETIEERFEITGTMRKLADQSLPPNFSSLENFRAYVDGFEPNG
YIEGKLSQMSKEVNARIEPFLKTTPRPLRLPNGPPCSQRSKFLLMDALKLSIEDPSHEGE
GIPLYDAIKCMRTFFGWKEPNVVKPHEKGINPNYLLSWKQVLAELQDIENEEKIPKTKNM
KKTSQLKWALGENMAPEKVDFDDCKDVGDLKQYDSDEPELRSLASWIQNEFNKACELTDS
SWIELDEIGEDVAPIEHIASMRRNYFTSEVSHCRATEYIMKGVYINTALLNASCAAMDDF
QLIPMISKCRTKEGRRKTNLYGFIIKGRSHLRNDTDVVNFVSMEFSLTDPRLEPHKWEKY
CVLEIGDMLIRSAIGQVSRPMFLYVRTNGTSKIKMKWGMEMRRCLLQSLQQIESMIEAES
SVKEKDMTKEFFENKSETWPIGESPKGVEESSIGKVCRTLLAKSVFNSLYASPQLEGFSA
ESRKLLLIVQALRDNLEPGTFDLGGLYEAIEECLINDPWVLLNASWFNSFLTHALS
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BDBM50125822 |
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n/a |
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Name | BDBM50125822 |
Synonyms: | 1-Hydroxy-5-isobutyl-3-isobutylidene-3H-pyrazine-2,6-dione | 1-hydroxy-5-isobutyl-3-(2-methylpropylidene)pyrazine-2,6(1H,3H)-dione | CHEMBL16320 |
Type | Small organic molecule |
Emp. Form. | C12H18N2O3 |
Mol. Mass. | 238.2829 |
SMILES | CC(C)C=c1[nH]c(=CC(C)C)c(=O)n(O)c1=O |w:3.2,7.7| |
Structure |
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