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TargetSialidase
LigandBDBM26655
Substrate/Competitorn/a
Meas. Tech.ChEMBL_606760 (CHEMBL1065350)
IC50 800±n/a nM
Citation Jeong, HJRyu, YBPark, SJKim, JHKwon, HJKim, JHPark, KHRho, MCLee, WS Neuraminidase inhibitory activities of flavonols isolated from Rhodiola rosea roots and their in vitro anti-influenza viral activities. Bioorg Med Chem17:6816-23 (2009) [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:
BDBM26655
n/a
NameBDBM26655
Synonyms:2-(3,4-dihydroxyphenyl)-3,5,7,8-tetrahydroxy-4H-chromen-4-one | CHEMBL253570 | Gossypetin (23) | gossypetin
TypeFlavonoid
Emp. Form.C15H10O8
Mol. Mass.318.2351
SMILESOc1ccc(cc1O)-c1oc2c(O)c(O)cc(O)c2c(=O)c1O
Structure
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