Reaction Details |
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Target | Beta-galactosidase |
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Ligand | BDBM50220500 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_37281 (CHEMBL656030) |
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IC50 | 1000000±n/a nM |
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Citation | Moreno-Vargas, AJ; Demange, R; Fuentes, J; Robina, I; Vogel, P Synthesis of [(2S,3S,4R)-3,4-dihydroxypyrrolidin-2-yl]-5-methylfuran-4-carboxylic acid derivatives: new leads as selective beta-galactosidase inhibitors. Bioorg Med Chem Lett12:2335-9 (2002) [PubMed] |
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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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BDBM50220500 |
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n/a |
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Name | BDBM50220500 |
Synonyms: | CHEMBL3350286 |
Type | Small organic molecule |
Emp. Form. | C13H20N2O4 |
Mol. Mass. | 268.3089 |
SMILES | CC(C)NC(=O)c1cc(oc1C)[C@H]1NC[C@@H](O)[C@H]1O |r| |
Structure |
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