Reaction Details |
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Target | Sialidase |
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Ligand | BDBM4993 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1751542 (CHEMBL4186302) |
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IC50 | 10.0±n/a nM |
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Citation | Wang, Z; Cheng, LP; Zhang, XH; Pang, W; Li, L; Zhao, JL Design, synthesis and biological evaluation of novel oseltamivir derivatives as potent neuraminidase inhibitors. Bioorg Med Chem Lett27:5429-5435 (2017) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Sialidase |
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Name: | Sialidase |
Synonyms: | NANH_CLOPF | nanH |
Type: | PROTEIN |
Mol. Mass.: | 42808.79 |
Organism: | Clostridium perfringens |
Description: | ChEMBL_991336 |
Residue: | 382 |
Sequence: | MCNKNNTFEKNLDISHKPEPLILFNKDNNIWNSKYFRIPNIQLLNDGTILTFSDIRYNGP
DDHAYIDIASARSTDFGKTWSYNIAMKNNRIDSTYSRVMDSTTVITNTGRIILIAGSWNT
NGNWAMTTSTRRSDWSVQMIYSDDNGLTWSNKIDLTKDSSKVKNQPSNTIGWLGGVGSGI
VMDDGTIVMPAQISLRENNENNYYSLIIYSKDNGETWTMGNKVPNSNTSENMVIELDGAL
IMSTRYDYSGYRAAYISHDLGTTWEIYEPLNGKILTGKGSGCQGSFIKATTSNGHRIGLI
SAPKNTKGEYIRDNIAVYMIDFDDLSKGVQEICIPYPEDGNKLGGGYSCLSFKNNHLGIV
YEANGNIEYQDLTPYYSLINKQ
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BDBM4993 |
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n/a |
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Name | BDBM4993 |
Synonyms: | (3R,4R,5S)-5-amino-3-[(2S)-butan-2-yloxy]-4-acetamidocyclohex-1-ene-1-carboxylic acid | Carbocyclic Analogue 44 |
Type | Small organic molecule |
Emp. Form. | C13H22N2O4 |
Mol. Mass. | 270.3248 |
SMILES | CC[C@H](C)O[C@@H]1C=C(C[C@H](N)[C@H]1NC(C)=O)C(O)=O |r,c:6| |
Structure |
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