Reaction Details |
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Target | Neuraminidase |
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Ligand | BDBM50500018 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1541519 (CHEMBL3744082) |
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IC50 | 10600±n/a nM |
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Citation | Boechat, Fda C; Sacramento, CQ; Cunha, AC; Sagrillo, FS; Nogueira, CM; Fintelman-Rodrigues, N; Santos-Filho, O; Riscado, CS; Forezi, Lda S; Faro, LV; Brozeguini, L; Marques, IP; Ferreira, VF; Souza, TM; de Souza, MC 1,2,3-Triazolyl-4-oxoquinolines: A feasible beginning for promising chemical structures to inhibit oseltamivir-resistant influenza A and B viruses. Bioorg Med Chem23:7777-84 (2015) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Neuraminidase |
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Name: | Neuraminidase |
Synonyms: | NA | NRAM_I33A0 |
Type: | PROTEIN |
Mol. Mass.: | 49687.56 |
Organism: | Influenza A virus |
Description: | ChEMBL_1347422 |
Residue: | 453 |
Sequence: | MNPNQKIITIGSICMVVGIISLILQIGNIISIWISHSIQTGNQNHTGICNQGIITYNVVA
GQDSTSVILTGNSSLCPIRGWAIHSKDNGIRIGSKGDVFVIREPFISCSHLECRTFFLTQ
GALLNDKHSNGTVKDRSPYRALMSCPVGEAPSPYNSRFESVAWSASACHDGMGWLTIGIS
GPDNGAVAVLKYNGIITETIKSWRKKILRTQESECTCVNGSCFTIMTDGPSNGLASYKIF
KIEKGKVTKSIELNAPNSHYEECSCYPDTGKVMCVCRDNWHGSNRPWVSFDQNLDYQIGY
ICSGVFGDNPRPKDGPGSCGPVSADGANGVKGFSYRYGNGVWIGRTKSDSSRHGFEMIWD
PNGWTETDSRFSVRQDVVAMTDRSGYSGSFVQHPELTGLDCMRPCFWVELIRGRPEEETI
WTSGSIISFCGVNSDTVDWSWPDGAELPFTIDK
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BDBM50500018 |
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n/a |
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Name | BDBM50500018 |
Synonyms: | CHEMBL3740548 |
Type | Small organic molecule |
Emp. Form. | C22H24N4O3 |
Mol. Mass. | 392.451 |
SMILES | CCOC(=O)c1cn(CC)c2ccc(cc2c1=O)-n1cc(nn1)C1=CCCCC1 |t:26| |
Structure |
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