Reaction Details |
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Target | Sialidase-3 |
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Ligand | BDBM50559928 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2070711 (CHEMBL4726245) |
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IC50 | >1000000±n/a nM |
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Citation | La Rocca, P; Rota, P; Piccoli, M; Cirillo, F; Ghiroldi, A; Franco, V; Allevi, P; Anastasia, 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 |
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More Info.: | Get all data from this article, Assay Method |
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Sialidase-3 |
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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
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BDBM50559928 |
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n/a |
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Name | BDBM50559928 |
Synonyms: | CHEMBL4764169 |
Type | Small organic molecule |
Emp. Form. | C15H24KNO8 |
Mol. Mass. | 385.4513 |
SMILES | [K;v0+].[H][C@]1([#8][C@@]([#8]-[#6]-[#6]-[#6]-[#6])([#6]=[#6]-[#6@H]1-[#7]-[#6](-[#6])=O)[#6](-[#8-])=O)[#6@H](-[#8])-[#6@H](-[#8])-[#6]-[#8] |r,c:9| |
Structure |
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