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TargetSialidase
LigandBDBM5225
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1751542 (CHEMBL4186302)
IC50 65±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:
BDBM5225
n/a
NameBDBM5225
Synonyms:(3R,4R,5S)-5-amino-4-acetamido-3-[methyl(propyl)amino]cyclohex-1-ene-1-carboxylic acid | C3-Aza Carbocyclic Analogue 3a
TypeSmall organic molecule
Emp. Form.C13H23N3O3
Mol. Mass.269.34
SMILESCCCN(C)[C@@H]1C=C(C[C@H](N)[C@H]1NC(C)=O)C(O)=O |r,c:6|
Structure
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