Reaction Details |
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Target | Sialidase |
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Ligand | BDBM50311585 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_772884 (CHEMBL1838287) |
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IC50 | 3350±n/a nM |
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Citation | Woo, HS; Kim, DW; Curtis-Long, MJ; Lee, BW; Lee, JH; Kim, JY; Kang, JE; Park, KH Potent inhibition of bacterial neuraminidase activity by pterocarpans isolated from the roots of Lespedeza bicolor. Bioorg Med Chem Lett21:6100-3 (2011) [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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BDBM50311585 |
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n/a |
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Name | BDBM50311585 |
Synonyms: | CHEMBL455372 | Erythrabyssin II | erybraedin C |
Type | Small organic molecule |
Emp. Form. | C25H28O4 |
Mol. Mass. | 392.4874 |
SMILES | [#6]\[#6](-[#6])=[#6]\[#6]-c1cc2-[#6@@H]-3-[#8]-c4c(ccc(-[#8])c4-[#6]\[#6]=[#6](\[#6])-[#6])-[#6@@H]-3-[#6]-[#8]-c2cc1-[#8] |r| |
Structure |
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