Reaction Details |
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Target | Beta-galactosidase |
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Ligand | BDBM50403936 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_39390 (CHEMBL659248) |
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IC50 | 12000±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: | Acid beta-galactosidase | BGAL_HUMAN | ELNR1 | Elastin receptor 1 | GLB1 | Lactase |
Type: | PROTEIN |
Mol. Mass.: | 76074.43 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_215886 |
Residue: | 677 |
Sequence: | MPGFLVRILPLLLVLLLLGPTRGLRNATQRMFEIDYSRDSFLKDGQPFRYISGSIHYSRV
PRFYWKDRLLKMKMAGLNAIQTYVPWNFHEPWPGQYQFSEDHDVEYFLRLAHELGLLVIL
RPGPYICAEWEMGGLPAWLLEKESILLRSSDPDYLAAVDKWLGVLLPKMKPLLYQNGGPV
ITVQVENEYGSYFACDFDYLRFLQKRFRHHLGDDVVLFTTDGAHKTFLKCGALQGLYTTV
DFGTGSNITDAFLSQRKCEPKGPLINSEFYTGWLDHWGQPHSTIKTEAVASSLYDILARG
ASVNLYMFIGGTNFAYWNGANSPYAAQPTSYDYDAPLSEAGDLTEKYFALRNIIQKFEKV
PEGPIPPSTPKFAYGKVTLEKLKTVGAALDILCPSGPIKSLYPLTFIQVKQHYGFVLYRT
TLPQDCSNPAPLSSPLNGVHDRAYVAVDGIPQGVLERNNVITLNITGKAGATLDLLVENM
GRVNYGAYINDFKGLVSNLTLSSNILTDWTIFPLDTEDAVRSHLGGWGHRDSGHHDEAWA
HNSSNYTLPAFYMGNFSIPSGIPDLPQDTFIQFPGWTKGQVWINGFNLGRYWPARGPQLT
LFVPQHILMTSAPNTITVLELEWAPCSSDDPELCAVTFVDRPVIGSSVTYDHPSKPVEKR
LMPPPPQKNKDSWLDHV
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BDBM50403936 |
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n/a |
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Name | BDBM50403936 |
Synonyms: | CHEMBL2114148 |
Type | Small organic molecule |
Emp. Form. | C12H17NO5 |
Mol. Mass. | 255.2671 |
SMILES | CCOC(=O)c1cc(oc1C)[C@H]1NC[C@@H](O)[C@H]1O |r| |
Structure |
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