Reaction Details |
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Target | Neuraminidase |
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Ligand | BDBM5014 |
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Substrate/Competitor | BDBM4702 |
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Meas. Tech. | Neuraminidase Inhibition Assay |
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IC50 | 2300±n/a nM |
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Citation | Lew, W; Wu, H; Mendel, DB; Escarpe, PA; Chen, X; Laver, WG; Graves, BJ; Kim, CU A new series of C3-aza carbocyclic influenza neuraminidase inhibitors: synthesis and inhibitory activity. Bioorg Med Chem Lett8:3321-4 (1998) [PubMed] Article |
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More Info.: | Get all data from this article, Solution Info, Assay Method |
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Neuraminidase |
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Name: | Neuraminidase |
Synonyms: | Influenza A Virus Neuraminidase | NA | NRAM_I34A1 | Neuraminidase | Neuraminidase A |
Type: | Enzyme |
Mol. Mass.: | 50124.14 |
Organism: | Influenza A virus (A/Puerto Rico/8/34/Mount Sinai(H1N1)) |
Description: | P03468 |
Residue: | 454 |
Sequence: | MNPNQKIITIGSICLVVGLISLILQIGNIISIWISHSIQTGSQNHTGICNQNIITYKNST
WVKDTTSVILTGNSSLCPIRGWAIYSKDNSIRIGSKGDVFVIREPFISCSHLECRTFFLT
QGALLNDKHSNGTVKDRSPYRALMSCPVGEAPSPYNSRFESVAWSASACHDGMGWLTIGI
SGPDNGAVAVLKYNGIITETIKSWRKKILRTQESECACVNGSCFTIMTDGPSDGLASYKI
FKIEKGKVTKSIELNAPNSHYEECSCYPDTGKVMCVCRDNWHGSNRPWVSFDQNLDYQIG
YICSGVFGDNPRPEDGTGSCGPVYVDGANGVKGFSYRYGNGVWIGRTKSHSSRHGFEMIW
DPNGWTETDSKFSVRQDVVAMTDWSGYSGSFVQHPELTGLDCMRPCFWVELIRGRPKEKT
IWTSASSISFCGVNSDTVDWSWPDGAELPFSIDK
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BDBM5014 |
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BDBM4702 |
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Name | BDBM5014 |
Synonyms: | (3R,4R,5S)-5-amino-4-acetamido-2-methyl-3-(pentan-3-yloxy)cyclohex-1-ene-1-carboxylic acid | C2-Substituted Carbocyclic Analogue 4 | Carbocyclic Analogue 64 |
Type | Small organic molecule |
Emp. Form. | C15H26N2O4 |
Mol. Mass. | 298.3779 |
SMILES | CCC(CC)O[C@H]1[C@H](NC(C)=O)[C@@H](N)CC(C(O)=O)=C1C |r,c:18| |
Structure |
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