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TargetSialidase-2
LigandBDBM4994
Substrate/Competitorn/a
Meas. Tech.ChEMBL_679988 (CHEMBL1280936)
IC50>6000000±n/a nM
Citation Hata, KKoseki, KYamaguchi, KMoriya, SSuzuki, YYingsakmongkon, SHirai, GSodeoka, Mvon Itzstein, MMiyagi, T Limited inhibitory effects of oseltamivir and zanamivir on human sialidases. Antimicrob Agents Chemother52:3484-91 (2008) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Sialidase-2
Name:Sialidase-2
Synonyms:Cytosolic sialidase | N-acetyl-alpha-neuraminidase 2 | NEU2 | NEUR2_HUMAN | Sialidase 2 | Sialidase-2
Type:PROTEIN
Mol. Mass.:42256.20
Organism:Homo sapiens (Human)
Description:ChEMBL_960638
Residue:380
Sequence:
MASLPVLQKESVFQSGAHAYRIPALLYLPGQQSLLAFAEQRASKKDEHAELIVLRRGDYD
APTHQVQWQAQEVVAQARLDGHRSMNPCPLYDAQTGTLFLFFIAIPGQVTEQQQLQTRAN
VTRLCQVTSTDHGRTWSSPRDLTDAAIGPAYREWSTFAVGPGHCLQLHDRARSLVVPAYA
YRKLHPIQRPIPSAFCFLSHDHGRTWARGHFVAQDTLECQVAEVETGEQRVVTLNARSHL
RARVQAQSTNDGLDFQESQLVKKLVEPPPQGCQGSVISFPSPRSGPGSPAQWLLYTHPTH
SWQRADLGAYLNPRPPAPEAWSEPVLLAKGSCAYSDLQSMGTGPDGSPLFGCLYEANDYE
EIVFLMFTLKQAFPAEYLPQ
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM4994
n/a
NameBDBM4994
Synonyms:(3R,4R,5S)-5-amino-4-acetamido-3-(pentan-3-yloxy)cyclohex-1-ene-1-carboxylic acid | CHEMBL674 | GS4071 | Oseltamivir carboxylate
TypeSmall organic molecule
Emp. Form.C14H24N2O4
Mol. Mass.284.3514
SMILESCCC(CC)O[C@@H]1C=C(C[C@H](N)[C@H]1NC(C)=O)C(O)=O |r,c:7|
Structure
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