Reaction Details |
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Target | Alpha-glucosidase MAL12 |
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Ligand | BDBM181060 |
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Substrate/Competitor | n/a |
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Meas. Tech. | In vitro Assay of alpha-Glucosidasee Inhibitory Activity |
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pH | 6.8±n/a |
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IC50 | 2.522e+4± 3.2e+2 nM |
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Comments | extracted |
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Citation | Wang, G; He, D; Li, X; Li, J; Peng, Z Design, synthesis and biological evaluation of novel coumarin thiazole derivatives as a-glucosidase inhibitors. Bioorg Chem65:167-74 (2016) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Alpha-glucosidase MAL12 |
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Name: | Alpha-glucosidase MAL12 |
Synonyms: | α-Glucosidase | MAL12 | MAL12_YEAST | MAL1S | Maltase | alpha-Glucosidase (α-Glucosidase) |
Type: | Protein |
Mol. Mass.: | 68084.32 |
Organism: | Saccharomyces cerevisiae |
Description: | P53341 |
Residue: | 584 |
Sequence: | MTISDHPETEPKWWKEATIYQIYPASFKDSNNDGWGDLKGITSKLQYIKDLGVDAIWVCP
FYDSPQQDMGYDISNYEKVWPTYGTNEDCFELIDKTHKLGMKFITDLVINHCSTEHEWFK
ESRSSKTNPKRDWFFWRPPKGYDAEGKPIPPNNWKSFFGGSAWTFDETTNEFYLRLFASR
QVDLNWENEDCRRAIFESAVGFWLDHGVDGFRIDTAGLYSKRPGLPDSPIFDKTSKLQHP
NWGSHNGPRIHEYHQELHRFMKNRVKDGREIMTVGEVAHGSDNALYTSAARYEVSEVFSF
THVEVGTSPFFRYNIVPFTLKQWKEAIASNFLFINGTDSWATTYIENHDQARSITRFADD
SPKYRKISGKLLTLLECSLTGTLYVYQGQEIGQINFKEWPIEKYEDVDVKNNYEIIKKSF
GKNSKEMKDFFKGIALLSRDHSRTPMPWTKDKPNAGFTGPDVKPWFLLNESFEQGINVEQ
ESRDDDSVLNFWKRALQARKKYKELMIYGYDFQFIDLDSDQIFSFTKEYEDKTLFAALNF
SGEEIEFSLPREGASLSFILGNYDDTDVSSRVLKPWEGRIYLVK
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BDBM181060 |
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n/a |
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Name | BDBM181060 |
Synonyms: | (E)-N'-(4-Hydroxybenzylidene)-4-(2-oxo-2H-chromen-3-yl)thiazole-2-carbohydrazide (7c) |
Type | Small organic molecule |
Emp. Form. | C20H13N3O4S |
Mol. Mass. | 391.4 |
SMILES | Oc1ccc(\C=N\NC(=O)c2nc(cs2)-c2cc3ccccc3oc2=O)cc1 |
Structure |
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