Reaction Details |
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Target | Glycogen synthase kinase-3 beta |
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Ligand | BDBM50382601 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_816539 (CHEMBL2025119) |
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IC50 | 1800±n/a nM |
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Citation | Palomo, V; Perez, DI; Perez, C; Morales-Garcia, JA; Soteras, I; Alonso-Gil, S; Encinas, A; Castro, A; Campillo, NE; Perez-Castillo, A; Gil, C; Martinez, A 5-imino-1,2,4-thiadiazoles: first small molecules as substrate competitive inhibitors of glycogen synthase kinase 3. J Med Chem55:1645-61 (2012) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Glycogen synthase kinase-3 beta |
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Name: | Glycogen synthase kinase-3 beta |
Synonyms: | GSK-3 beta | GSK-3, beta | GSK3B | GSK3B_HUMAN | Glycogen synthase kinase 3 beta (GSK3B) | Glycogen synthase kinase 3-beta (GSK3B) | Glycogen synthase kinase-3 beta (GSK-3B) | Glycogen synthase kinase-3 beta (GSK3 Beta) | Glycogen synthase kinase-3 beta (GSK3B) | Glycogen synthase kinase-3B (GSK-3B) | Glycogen synthase kinase-3beta (GSK3B) | Serine/threonine-protein kinase GSK3B |
Type: | Enzyme |
Mol. Mass.: | 46756.38 |
Organism: | Homo sapiens (Human) |
Description: | P49841 |
Residue: | 420 |
Sequence: | MSGRPRTTSFAESCKPVQQPSAFGSMKVSRDKDGSKVTTVVATPGQGPDRPQEVSYTDTK
VIGNGSFGVVYQAKLCDSGELVAIKKVLQDKRFKNRELQIMRKLDHCNIVRLRYFFYSSG
EKKDEVYLNLVLDYVPETVYRVARHYSRAKQTLPVIYVKLYMYQLFRSLAYIHSFGICHR
DIKPQNLLLDPDTAVLKLCDFGSAKQLVRGEPNVSYICSRYYRAPELIFGATDYTSSIDV
WSAGCVLAELLLGQPIFPGDSGVDQLVEIIKVLGTPTREQIREMNPNYTEFKFPQIKAHP
WTKVFRPRTPPEAIALCSRLLEYTPTARLTPLEACAHSFFDELRDPNVKLPNGRDTPALF
NFTTQELSSNPPLATILIPPHARIQAAASTPTNATAASDANTGDRGQTNNAASASASNST
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BDBM50382601 |
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n/a |
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Name | BDBM50382601 |
Synonyms: | CHEMBL2022422 | CHEMBL2024360 |
Type | Small organic molecule |
Emp. Form. | C18H17N3O2S |
Mol. Mass. | 339.411 |
SMILES | CCOC(=O)C\N=c1/nc(-c2ccccc2)n(s1)-c1ccccc1 |
Structure |
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