Ki Summary BindingDB logo
myBDB logout
Reaction Details
Report a problem with these data
TargetSialidase
LigandBDBM4993
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1751542 (CHEMBL4186302)
IC50 10.0±n/a nM
Citation Wang, ZCheng, LPZhang, XHPang, WLi, LZhao, JL Design, synthesis and biological evaluation of novel oseltamivir derivatives as potent neuraminidase inhibitors. Bioorg Med Chem Lett27:5429-5435 (2017) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Sialidase
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
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM4993
n/a
NameBDBM4993
Synonyms:(3R,4R,5S)-5-amino-3-[(2S)-butan-2-yloxy]-4-acetamidocyclohex-1-ene-1-carboxylic acid | Carbocyclic Analogue 44
TypeSmall organic molecule
Emp. Form.C13H22N2O4
Mol. Mass.270.3248
SMILESCC[C@H](C)O[C@@H]1C=C(C[C@H](N)[C@H]1NC(C)=O)C(O)=O |r,c:6|
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: