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TargetMAP kinase-interacting serine/threonine-protein kinase 2
LigandBDBM50562613
Substrate/Competitorn/a
Meas. Tech.ChEMBL_2079583 (CHEMBL4735374)
IC50 8.0±n/a nM
Citation Dreas, AKucwaj-Brysz, KPyziak, KKulesza, UWincza, EFabritius, CHMichalik, KGabor-Worwa, EGo?as, AMilik, MMasiejczyk, MMajewska, EPy?niak, KWójcik-Trechci?ska, USandowska-Markiewicz, ZBrzózka, KOstrowski, JRzymski, TMikula, M Discovery of indazole-pyridinone derivatives as a novel class of potent and selective MNK1/2 kinase inhibitors that protecting against endotoxin-induced septic shock. Eur J Med Chem213:0 (2021) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
MAP kinase-interacting serine/threonine-protein kinase 2
Name:MAP kinase-interacting serine/threonine-protein kinase 2
Synonyms:GPRK7 | MAP kinase signal-integrating kinase 2 | MAP kinase-interacting serine/threonine-protein kinase 2 (MKNK2) | MAP kinase-interacting serine/threonine-protein kinase 2 (MnK2) | MAP-kinase interacting kinase 2 (MNK2) | MKNK2 | MKNK2_HUMAN | MNK2
Type:Protein
Mol. Mass.:51870.79
Organism:Homo sapiens (Human)
Description:Q9HBH9
Residue:465
Sequence:
MVQKKPAELQGFHRSFKGQNPFELAFSLDQPDHGDSDFGLQCSARPDMPASQPIDIPDAK
KRGKKKKRGRATDSFSGRFEDVYQLQEDVLGEGAHARVQTCINLITSQEYAVKIIEKQPG
HIRSRVFREVEMLYQCQGHRNVLELIEFFEEEDRFYLVFEKMRGGSILSHIHKRRHFNEL
EASVVVQDVASALDFLHNKGIAHRDLKPENILCEHPNQVSPVKICDFDLGSGIKLNGDCS
PISTPELLTPCGSAEYMAPEVVEAFSEEASIYDKRCDLWSLGVILYILLSGYPPFVGRCG
SDCGWDRGEACPACQNMLFESIQEGKYEFPDKDWAHISCAAKDLISKLLVRDAKQRLSAA
QVLQHPWVQGCAPENTLPTPMVLQRNSCAKDLTSFAAEAIAMNRQLAQHDEDLAEEEAAG
QGQPVLVRATSRCLQLSPPSQSKLAQRRQRASLSSAPVVLVGDHA
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  Blast E-value cutoff:
BDBM50562613
n/a
NameBDBM50562613
Synonyms:CHEMBL4785028
TypeSmall organic molecule
Emp. Form.C21H19N5O2
Mol. Mass.373.4079
SMILESCC(=O)Nc1cccc(Cn2cc(ccc2=O)-c2ccc3c(N)n[nH]c3c2)c1
Structure
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