Reaction Details |
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Target | Sialidase-4 |
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Ligand | BDBM50343685 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_745979 (CHEMBL1775278) |
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IC50 | >1000000±n/a nM |
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Citation | Albohy, A; Mohan, S; Zheng, RB; Pinto, BM; Cairo, CW Inhibitor selectivity of a new class of oseltamivir analogs against viral neuraminidase over human neuraminidase enzymes. Bioorg Med Chem19:2817-22 (2011) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Sialidase-4 |
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Name: | Sialidase-4 |
Synonyms: | NEU4 | NEUR4_HUMAN | Sialidase 4 |
Type: | PROTEIN |
Mol. Mass.: | 51579.82 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_960637 |
Residue: | 484 |
Sequence: | MGVPRTPSRTVLFERERTGLTYRVPSLLPVPPGPTLLAFVEQRLSPDDSHAHRLVLRRGT
LAGGSVRWGALHVLGTAALAEHRSMNPCPVHDAGTGTVFLFFIAVLGHTPEAVQIATGRN
AARLCCVASRDAGLSWGSARDLTEEAIGGAVQDWATFAVGPGHGVQLPSGRLLVPAYTYR
VDRRECFGKICRTSPHSFAFYSDDHGRTWRCGGLVPNLRSGECQLAAVDGGQAGSFLYCN
ARSPLGSRVQALSTDEGTSFLPAERVASLPETAWGCQGSIVGFPAPAPNRPRDDSWSVGP
GSPLQPPLLGPGVHEPPEEAAVDPRGGQVPGGPFSRLQPRGDGPRQPGPRPGVSGDVGSW
TLALPMPFAAPPQSPTWLLYSHPVGRRARLHMGIRLSQSPLDPRSWTEPWVIYEGPSGYS
DLASIGPAPEGGLVFACLYESGARTSYDEISFCTFSLREVLENVPASPKPPNLGDKPRGC
CWPS
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BDBM50343685 |
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n/a |
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Name | BDBM50343685 |
Synonyms: | (3S,4R,5R)-4-Acetamido-5-(1-ethylpropoxy)-3-[4-(1-hydroxy-1-methylethyl)[1,2,3]triazol-1-yl]cyclohex-1-ene-1-carboxylic Acid | (3S,4R,5R)-4-acetamido-3-(4-(2-hydroxypropan-2-yl)-1H-1,2,3-triazol-1-yl)-5-(pentan-3-yloxy)cyclohex-1-enecarboxylic acid | CHEMBL1270232 |
Type | Small organic molecule |
Emp. Form. | C19H30N4O5 |
Mol. Mass. | 394.4653 |
SMILES | CCC(CC)O[C@@H]1CC(=C[C@@H]([C@H]1NC(C)=O)n1cc(nn1)C(C)(C)O)C(O)=O |r,c:8| |
Structure |
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