| Reaction Details |
|---|
 | Report a problem with these data |
| Target | Neuraminidase |
|---|
| Ligand | BDBM50526898 |
|---|
| Substrate/Competitor | n/a |
|---|
| Meas. Tech. | ChEMBL_1901692 (CHEMBL4403914) |
|---|
| IC50 | 440±n/a nM |
|---|
| Citation |  Ju, H; Xiu, S; Ding, X; Shang, M; Jia, R; Huang, B; Zhan, P; Liu, X Discovery of novel 1,2,3-triazole oseltamivir derivatives as potent influenza neuraminidase inhibitors targeting the 430-cavity. Eur J Med Chem187:0 (2020) [PubMed] Article |
|---|
| More Info.: | Get all data from this article, Assay Method |
|---|
| |
| Neuraminidase |
|---|
| 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
|
|
|
|---|
| BDBM50526898 |
|---|
| n/a |
|---|
| Name | BDBM50526898 |
|---|
| Synonyms: | CHEMBL4532651 |
|---|
| Type | Small organic molecule |
|---|
| Emp. Form. | C27H40N8O7 |
|---|
| Mol. Mass. | 588.6559 |
|---|
| SMILES | CCC(CC)O[C@@H]1C=C(C[C@H](N)[C@H]1NC(C)=O)C(=O)NCc1cn(nn1)[C@H]1C[C@@H](O[C@@H]1CO)n1cc(C)c(=O)[nH]c1=O |r,c:7| |
|---|
| Structure | 
|
|---|
Search and Browse
