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TargetGlycogen synthase kinase-3 beta
LigandBDBM50166289
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1672653 (CHEMBL4022682)
IC50 200±n/a nM
Citation Wagman, ASBoyce, RSBrown, SPFang, EGoff, DJansen, JMLe, VPLevine, BHNg, SCNi, ZJNuss, JMPfister, KBRamurthy, SRenhowe, PARing, DBShu, WSubramanian, SZhou, XAShafer, CMHarrison, SDJohnson, KWBussiere, DE Synthesis, Binding Mode, and Antihyperglycemic Activity of Potent and Selective (5-Imidazol-2-yl-4-phenylpyrimidin-2-yl)[2-(2-pyridylamino)ethyl]amine Inhibitors of Glycogen Synthase Kinase 3. J Med Chem60:8482-8514 (2017) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Glycogen synthase kinase-3 beta
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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  Blast E-value cutoff:
BDBM50166289
n/a
NameBDBM50166289
Synonyms:CHEBI:43645 | CHEMBL216543
TypeSmall organic molecule
Emp. Form.C16H11N3O2
Mol. Mass.277.2774
SMILESO\N=C1\C(\Nc2ccccc\12)=C1\C(=O)Nc2ccccc12
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: