Reaction Details |
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Target | Oligo-1,6-glucosidase IMA1 |
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Ligand | BDBM23406 |
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Substrate/Competitor | n/a |
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Meas. Tech. | α-Glucosidase Assay |
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pH | 6.8±n/a |
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IC50 | 3.825e+4± 1.2e+2 nM |
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Comments | extracted |
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Citation | Riaz, S; Khan, IU; Bajda, M; Ashraf, M; Qurat-Ul-Ain, null; Shaukat, A; Rehman, TU; Mutahir, S; Hussain, S; Mustafa, G; Yar, M Pyridine sulfonamide as a small key organic molecule for the potential treatment of type-II diabetes mellitus and Alzheimer's disease: In vitro studies against yeast a-glucosidase, acetylcholinesterase and butyrylcholinesterase. Bioorg Chem63:64-71 (2015) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Oligo-1,6-glucosidase IMA1 |
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Name: | Oligo-1,6-glucosidase IMA1 |
Synonyms: | α-glucosidase | Alpha-glucosidase | Alpha-glucosidase (α-glucosidase) | IMA1 | MALX3_YEAST | Oligo-1,6-glucosidase |
Type: | Protein |
Mol. Mass.: | 68577.59 |
Organism: | Saccharomyces cerevisiae S288c (Baker's yeast) |
Description: | n/a |
Residue: | 589 |
Sequence: | MTISSAHPETEPKWWKEATFYQIYPASFKDSNDDGWGDMKGIASKLEYIKELGADAIWIS
PFYDSPQDDMGYDIANYEKVWPTYGTNEDCFALIEKTHKLGMKFITDLVINHCSSEHEWF
KESRSSKTNPKRDWFFWRPPKGYDAEGKPIPPNNWKSYFGGSAWTFDEKTQEFYLRLFCS
TQPDLNWENEDCRKAIYESAVGYWLDHGVDGFRIDVGSLYSKVVGLPDAPVVDKNSTWQS
SDPYTLNGPRIHEFHQEMNQFIRNRVKDGREIMTVGEMQHASDETKRLYTSASRHELSEL
FNFSHTDVGTSPLFRYNLVPFELKDWKIALAELFRYINGTDCWSTIYLENHDQPRSITRF
GDDSPKNRVISGKLLSVLLSALTGTLYVYQGQELGQINFKNWPVEKYEDVEIRNNYNAIK
EEHGENSEEMKKFLEAIALISRDHARTPMQWSREEPNAGFSGPSAKPWFYLNDSFREGIN
VEDEIKDPNSVLNFWKEALKFRKAHKDITVYGYDFEFIDLDNKKLFSFTKKYNNKTLFAA
LNFSSDATDFKIPNDDSSFKLEFGNYPKKEVDASSRTLKPWEGRIYISE
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BDBM23406 |
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n/a |
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Name | BDBM23406 |
Synonyms: | (3R,4R,5S,6R)-5-{[(2R,3R,4R,5S,6R)-5-{[(2R,3R,4S,5S,6R)-3,4-dihydroxy-6-methyl-5-{[(1S,4R,5S,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)cyclohex-2-en-1-yl]amino}oxan-2-yl]oxy}-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6-(hydroxymethyl)oxane-2,3,4-triol | Acarbose | US11292789, Acarbose |
Type | Carbohydrate |
Emp. Form. | C25H43NO18 |
Mol. Mass. | 645.6048 |
SMILES | C[C@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@H](O[C@@H]3[C@@H](CO)OC(O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1N[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O |t:37| |
Structure |
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