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TargetSialidase
LigandBDBM50442400
Substrate/Competitorn/a
Meas. Tech.ChEMBL_991336 (CHEMBL2443545)
IC50 300±n/a nM
Citation Wang, YCurtis-Long, MJYuk, HJKim, DWTan, XFPark, KH Bacterial neuraminidase inhibitory effects of prenylated isoflavones from roots of Flemingia philippinensis. Bioorg Med Chem21:6398-404 (2013) [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:
BDBM50442400
n/a
NameBDBM50442400
Synonyms:AURICULASIN
TypeSmall organic molecule
Emp. Form.C25H24O6
Mol. Mass.420.4545
SMILES[#6]\[#6](-[#6])=[#6]\[#6]-c1c2-[#8]C([#6])([#6])[#6]=[#6]-c2c(-[#8])c2c1occ(-c1ccc(-[#8])c(-[#8])c1)c2=O |c:11|
Structure
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