Reaction Details |
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Target | Sialidase |
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Ligand | BDBM50317435 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_631812 (CHEMBL1111005) |
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Ki | 1210±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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BDBM50317435 |
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n/a |
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Name | BDBM50317435 |
Synonyms: | CHEMBL1096406 | Erythribyssin O |
Type | Small organic molecule |
Emp. Form. | C21H18O5 |
Mol. Mass. | 350.3646 |
SMILES | [#6]\[#6](-[#6])=[#6]\[#6]-c1c(-[#8])ccc2c3-[#6]-[#8]-c4cc(-[#8])c(-[#6]=O)cc4-c3oc12 |
Structure |
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