Reaction Details |
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Target | Pancreatic alpha-amylase |
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Ligand | BDBM50120842 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1516316 (CHEMBL3618756) |
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Ki | 15±n/a nM |
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Citation | Al-Asri, J; Fazekas, E; Lehoczki, G; Perdih, A; Görick, C; Melzig, MF; Gyémánt, G; Wolber, G; Mortier, J From carbohydrates to drug-like fragments: Rational development of novela-amylase inhibitors. Bioorg Med Chem23:6725-32 (2015) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Pancreatic alpha-amylase |
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Name: | Pancreatic alpha-amylase |
Synonyms: | 1,4-alpha-D-glucan glucanohydrolase | AMY2A | AMYP_HUMAN | PA | Pancreatic α-amylase (HPA) | Pancreatic alpha-amylase | Pancreatic alpha-amylase (HPA) |
Type: | Protein |
Mol. Mass.: | 57709.71 |
Organism: | Homo sapiens (Human) |
Description: | n/a |
Residue: | 511 |
Sequence: | MKFFLLLFTIGFCWAQYSPNTQQGRTSIVHLFEWRWVDIALECERYLAPKGFGGVQVSPP
NENVAIYNPFRPWWERYQPVSYKLCTRSGNEDEFRNMVTRCNNVGVRIYVDAVINHMCGN
AVSAGTSSTCGSYFNPGSRDFPAVPYSGWDFNDGKCKTGSGDIENYNDATQVRDCRLTGL
LDLALEKDYVRSKIAEYMNHLIDIGVAGFRLDASKHMWPGDIKAILDKLHNLNSNWFPAG
SKPFIYQEVIDLGGEPIKSSDYFGNGRVTEFKYGAKLGTVIRKWNGEKMSYLKNWGEGWG
FVPSDRALVFVDNHDNQRGHGAGGASILTFWDARLYKMAVGFMLAHPYGFTRVMSSYRWP
RQFQNGNDVNDWVGPPNNNGVIKEVTINPDTTCGNDWVCEHRWRQIRNMVIFRNVVDGQP
FTNWYDNGSNQVAFGRGNRGFIVFNNDDWSFSLTLQTGLPAGTYCDVISGDKINGNCTGI
KIYVSDDGKAHFSISNSAEDPFIAIHAESKL
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BDBM50120842 |
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n/a |
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Name | BDBM50120842 |
Synonyms: | CHEMBL3618489 |
Type | Small organic molecule |
Emp. Form. | C56H94N2O40 |
Mol. Mass. | 1435.335 |
SMILES | [H][C@]1(O[C@@H]2[C@@H](CO)O[C@H](O[C@]3([H])[C@@H](CO)O[C@H](O[C@]4([H])[C@@H](CO)O[C@H](O[C@]5([H])[C@@H](CO)O[C@H](O)[C@H](O)[C@H]5O)[C@H](O)[C@H]4O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)O[C@H](C)[C@@H](N[C@H]2C=C(CO)[C@@H](O[C@@]3([H])O[C@H](CO)[C@@H](O[C@@]4([H])O[C@H](C)[C@@H](N[C@H]5C=C(CO)[C@@H](O)[C@H](O)[C@H]5O)[C@H](O)[C@H]4O)[C@H](O)[C@H]3O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O |r,t:60,82| |
Structure |
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