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TargetSialidase-3
LigandBDBM50559925
Substrate/Competitorn/a
Meas. Tech.ChEMBL_2070711 (CHEMBL4726245)
IC50>1000000±n/a nM
Citation La Rocca, PRota, PPiccoli, MCirillo, FGhiroldi, AFranco, VAllevi, PAnastasia, L 2?-3,4-Unsaturated sialic acid derivatives: Synthesis optimization, and biological evaluation as Newcastle disease virus hemagglutinin-neuraminidase inhibitors. Bioorg Med Chem28:0 (2020) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Sialidase-3
Name:Sialidase-3
Synonyms:NEU3 | NEUR3_HUMAN | Sialidase 3 | Sialidase-3
Type:PROTEIN
Mol. Mass.:48257.99
Organism:Homo sapiens (Human)
Description:ChEMBL_461856
Residue:428
Sequence:
MEEVTTCSFNSPLFRQEDDRGITYRIPALLYIPPTHTFLAFAEKRSTRRDEDALHLVLRR
GLRIGQLVQWGPLKPLMEATLPGHRTMNPCPVWEQKSGCVFLFFICVRGHVTERQQIVSG
RNAARLCFIYSQDAGCSWSEVRDLTEEVIGSELKHWATFAVGPGHGIQLQSGRLVIPAYT
YYIPSWFFCFQLPCKTRPHSLMIYSDDLGVTWHHGRLIRPMVTVECEVAEVTGRAGHPVL
YCSARTPNRCRAEALSTDHGEGFQRLALSRQLCEPPHGCQGSVVSFRPLEIPHRCQDSSS
KDAPTIQQSSPGSSLRLEEEAGTPSESWLLYSHPTSRKQRVDLGIYLNQTPLEAACWSRP
WILHCGPCGYSDLAALEEEGLFGCLFECGTKQECEQIAFRLFTHREILSHLQGDCTSPGR
NPSQFKSN
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50559925
n/a
NameBDBM50559925
Synonyms:CHEMBL4779317
TypeSmall organic molecule
Emp. Form.C13H20KNO8
Mol. Mass.357.3981
SMILES[K;v0+].[H][C@]1([#8][C@@]([#8]-[#6]-[#6])([#6]=[#6]-[#6@H]1-[#7]-[#6](-[#6])=O)[#6](-[#8-])=O)[#6@H](-[#8])-[#6@H](-[#8])-[#6]-[#8] |r,c:7|
Structure
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