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TargetSialidase-3
LigandBDBM50559931
Substrate/Competitorn/a
Meas. Tech.ChEMBL_2070711 (CHEMBL4726245)
IC50 3900±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:
BDBM50559931
n/a
NameBDBM50559931
Synonyms:CHEMBL4745230
TypeSmall organic molecule
Emp. Form.C11H14F3NO8
Mol. Mass.345.226
SMILES[H][C@]1(OC(=C[C@H](O)[C@H]1NC(=O)C(F)(F)F)C(O)=O)[C@H](O)[C@H](O)CO |r,c:3|
Structure
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