Reaction Details |
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Target | Sialidase |
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Ligand | BDBM50317428 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_631808 (CHEMBL1108201) |
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IC50 | 77100±n/a nM |
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Citation | Nguyen, PH; Nguyen, TN; Kang, KW; Ndinteh, DT; Mbafor, JT; Kim, YR; Oh, WK Prenylated pterocarpans as bacterial neuraminidase inhibitors. Bioorg Med Chem18:3335-44 (2010) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Sialidase |
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Name: | Sialidase |
Synonyms: | NANH_CLOPF | nanH |
Type: | PROTEIN |
Mol. Mass.: | 42808.79 |
Organism: | Clostridium perfringens |
Description: | ChEMBL_991336 |
Residue: | 382 |
Sequence: | MCNKNNTFEKNLDISHKPEPLILFNKDNNIWNSKYFRIPNIQLLNDGTILTFSDIRYNGP
DDHAYIDIASARSTDFGKTWSYNIAMKNNRIDSTYSRVMDSTTVITNTGRIILIAGSWNT
NGNWAMTTSTRRSDWSVQMIYSDDNGLTWSNKIDLTKDSSKVKNQPSNTIGWLGGVGSGI
VMDDGTIVMPAQISLRENNENNYYSLIIYSKDNGETWTMGNKVPNSNTSENMVIELDGAL
IMSTRYDYSGYRAAYISHDLGTTWEIYEPLNGKILTGKGSGCQGSFIKATTSNGHRIGLI
SAPKNTKGEYIRDNIAVYMIDFDDLSKGVQEICIPYPEDGNKLGGGYSCLSFKNNHLGIV
YEANGNIEYQDLTPYYSLINKQ
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BDBM50317428 |
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n/a |
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Name | BDBM50317428 |
Synonyms: | CHEMBL1099089 | Erythribyssin D |
Type | Small organic molecule |
Emp. Form. | C20H20O5 |
Mol. Mass. | 340.3698 |
SMILES | CC1(C)Oc2ccc3[C@@H]4COc5cc(O)ccc5[C@@H]4Oc3c2CC1O |r| |
Structure |
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