Reaction Details |
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Target | Beta-galactosidase |
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Ligand | BDBM50153478 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_305559 (CHEMBL828578) |
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IC50 | <1000000±n/a nM |
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Citation | Ogawa, S; Funayama, S; Okazaki, K; Ishizuka, F; Sakata, Y; Doi, F Synthesis of 5a-carba-hexopyranoses and hexopyranosylamines, as well as 5a,5a'-dicarbadisaccharides, from 3,8-dioxatricyclo[4.2.1.0(2,4)]nonan-9-ol: glycosidase inhibitory activity of N-substituted 5a-carba-beta-gluco- and beta-galactopyranosylamines, and derivatives thereof. Bioorg Med Chem Lett14:5183-8 (2004) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Beta-galactosidase |
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Name: | Beta-galactosidase |
Synonyms: | β-galactosidase | BGAL_BOVIN | Beta-galactosidase/Glucosylceramidase | GLB1 |
Type: | Protein |
Mol. Mass.: | 73420.88 |
Organism: | Bos taurus (Bovine) |
Description: | n/a |
Residue: | 653 |
Sequence: | MPGVVRLLALLLVPLLLGSARGLHNATQRTFQIDYRRNRFLKDGQPFRYISGSIHYFRVP
RFYWKDRLLKMKMAGLNAIQTYVAWNFHELQPGRYNFSGDHDVEHFIQLAHELGLLVILR
PGPYICAEWDMGGLPAWLLEKKSIVLRSSDPDYLAAVDKWLGVLLPKMRPLLYKNGGPII
TVQVENEYGSYLSCDYDYLRFLQKRFHDHLGEDVLLFTTDGVNERLLQCGALQGLYATVD
FSPGTNLTAAFMLQRKFEPTGPLVNSEFYTGWLDHWGQRHSTVSSKAVAFTLHDMLALGA
NVNMYMFIGGTNFAYWNGANIPYQPQPTSYDYDAPLSEAGDLTEKYFALRDIIQKFAKVP
EGPIPPSTPKFAYGKVALNKLKTVEDALNILCPSGPIKSVYPLTFIDVKQYFGFVLYRTM
LPEDCSDPTPLSSPLSGVHDRAYVSVNGVAQGILERESVITLNITGKAGATLDLLVENMG
RVNYGSSINDFKGLVSNLTLGSKILTNWEIFPLDMEDAVRSHLGTWGGRDRGYHNKARAH
SPPTYALPTFYVGNFTIPSGIADLPQDTFIQFPGWTKGQVWINGFNLGRYWPVRGPQMTL
FVPQHILVTSTPNTIVVLELEHAPCQDGGPELCTVEFVDKPVFRTVQTHRHAN
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BDBM50153478 |
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n/a |
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Name | BDBM50153478 |
Synonyms: | CHEMBL185536 | N-(2,3,4-Trihydroxy-5-hydroxymethyl-cyclohexyl)-acetamide |
Type | Small organic molecule |
Emp. Form. | C9H17NO5 |
Mol. Mass. | 219.235 |
SMILES | CC(=O)NC1CC(CO)C(O)C(O)C1O |
Structure |
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