Reaction Details |
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Target | Mannosyl-oligosaccharide glucosidase |
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Ligand | BDBM193876 |
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Substrate/Competitor | n/a |
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Meas. Tech. | α-Glucosidase inhibition assay |
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pH | 6.8±n/a |
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IC50 | 1.5824e+5± 3.41e+3 nM |
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Comments | extracted |
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Citation | Özil, M; Emirik, M; Etlik, SY; Ülker, S; Kahveci, B A simple and efficient synthesis of novel inhibitors of alpha-glucosidase based on benzimidazole skeleton and molecular docking studies. Bioorg Chem68:226-35 (2016) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Mannosyl-oligosaccharide glucosidase |
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Name: | Mannosyl-oligosaccharide glucosidase |
Synonyms: | CWH41 | CWH41_YEAST | GLS1 | alpha-Glucosidase (α-glucosidase) |
Type: | Protein |
Mol. Mass.: | 96475.51 |
Organism: | Saccharomyces cerevisiae (Yeast) |
Description: | n/a |
Residue: | 833 |
Sequence: | MLISKSKMFKTFWILTSIVLLASATVDISKLQEFEEYQKFTNESLLWAPYRSNCYFGMRP
RYVHESPLIMGIMWFNSLSQDGLHSLRHFATPQDKLQKYGWEVYDPRIGGKEVFIDEKNN
LNLTVYFVKSKNGENWSVRVQGEPLDPKRPSTASVVLYFSQNGGEIDGKSSLAMIGHDGP
NDMKFFGYSKELGEYHLTVKDNFGHYFKNPEYETMEVAPGSDCSKTSHLSLQIPDKEVWK
ARDVFQSLVSDSIRDILEKEETKQRPADLIPSVLTIRNLYNFNPGNFHYIQKTFDLTKKD
GFQFDITYNKLGTTQSISTREQVTELITWSLNEINARFDKQFSFGEGPDSIESVEVKRRF
ALETLSNLLGGIGYFYGNQLIDRETEFDESQFTEIKLLNAKEEGPFELFTSVPSRGFFPR
GFYWDEGFHLLQIMEYDFDLAFEILASWFEMIEDDSGWIAREIILGNEARSKVPQEFQVQ
NPNIANPPTLLLAFSEMLSRAIENIGDFNSDSYHQVMFNSRTAKFMTNNLEANPGLLTEY
AKKIYPKLLKHYNWFRKSQTGLIDEYEEILEDEGIWDKIHKNEVYRWVGRTFTHCLPSGM
DDYPRAQPPDVAELNVDALAWVGVMTRSMKQIAHVLKLTQDEQRYAQIEQEVVENLDLLH
WSENDNCYCDISIDPEDDEIREFVCHEGYVSVLPFALKLIPKNSPKLEKVVALMSDPEKI
FSDYGLLSLSRQDDYFGKDENYWRGPIWMNINYLCLDAMRYYYPEVILDVAGEASNAKKL
YQSLKINLSNNIYKVWEEQGYCYENYSPIDGHGTGAEHFTGWTALVVNILGRF
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BDBM193876 |
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n/a |
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Name | BDBM193876 |
Synonyms: | 5-{[2-(2,4-Dichlorobenzyl)-1H-benzimidazol-1-yl]methyl}-N-phenyl-1,3,4-thiadiazol-2-amine (8a) |
Type | Small organic molecule |
Emp. Form. | C23H17Cl2N5S |
Mol. Mass. | 466.386 |
SMILES | Clc1ccc(Cc2nc3ccccc3n2Cc2nnc(Nc3ccccc3)s2)c(Cl)c1 |
Structure |
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