Reaction Details |
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Target | Alpha-galactosidase A |
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Ligand | BDBM50150470 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1558581 (CHEMBL3774070) |
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Ki | >2000000±n/a nM |
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Citation | Thonhofer, M; Weber, P; Santana, AG; Fischer, R; Pabst, BM; Paschke, E; Schalli, M; Stütz, AE; Tschernutter, M; Windischhofer, W; Withers, SG Synthesis of C-5a-chain extended derivatives of 4-epi-isofagomine: Powerfulß-galactosidase inhibitors and low concentration activators of GM1-gangliosidosis-related human lysosomalß-galactosidase. Bioorg Med Chem Lett26:1438-42 (2016) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Alpha-galactosidase A |
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Name: | Alpha-galactosidase A |
Synonyms: | AGAL_HUMAN | Alpha-D-galactosidase A | Alpha-D-galactoside galactohydrolase | Alpha-galactosidase A | Alpha-glucosidase A (α-Gal A) | GLA | INN=Agalsidase | Melibiase |
Type: | Protein |
Mol. Mass.: | 48760.21 |
Organism: | Homo sapiens (Human) |
Description: | n/a |
Residue: | 429 |
Sequence: | MQLRNPELHLGCALALRFLALVSWDIPGARALDNGLARTPTMGWLHWERFMCNLDCQEEP
DSCISEKLFMEMAELMVSEGWKDAGYEYLCIDDCWMAPQRDSEGRLQADPQRFPHGIRQL
ANYVHSKGLKLGIYADVGNKTCAGFPGSFGYYDIDAQTFADWGVDLLKFDGCYCDSLENL
ADGYKHMSLALNRTGRSIVYSCEWPLYMWPFQKPNYTEIRQYCNHWRNFADIDDSWKSIK
SILDWTSFNQERIVDVAGPGGWNDPDMLVIGNFGLSWNQQVTQMALWAIMAAPLFMSNDL
RHISPQAKALLQDKDVIAINQDPLGKQGYQLRQGDNFEVWERPLSGLAWAVAMINRQEIG
GPRSYTIAVASLGKGVACNPACFITQLLPVKRKLGFYEWTSRLRSHINPTGTVLLQLENT
MQMSLKDLL
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BDBM50150470 |
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n/a |
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Name | BDBM50150470 |
Synonyms: | CHEMBL3771185 |
Type | Small organic molecule |
Emp. Form. | C22H33N3O5S |
Mol. Mass. | 451.58 |
SMILES | CN(C)c1cccc2c(cccc12)S(=O)(=O)NCCCC[C@H]1NC[C@@H](O)[C@@H](O)[C@H]1CO |r| |
Structure |
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