20 articles for thisTarget

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The following articles (labelled with PubMed ID or TBD) are for your review

PMID	Data	Article Title	Organization
25730262	195	10-iodo-11H-indolo[3,2-c]quinoline-6-carboxylic acids are selective inhibitors of DYRK1A.	Technische Universit£T Braunschweig
24798019	30	Acridone alkaloids from Glycosmis chlorosperma as DYRK1A inhibitors.	Institut De Chimie Des Substances Naturelles
24973661	10	9- and 11-substituted 4-azapaullones are potent and selective inhibitors of African trypanosoma.	Technische Universit£T Braunschweig
23454515	66	Chemical synthesis and biological validation of immobilized protein kinase inhibitory Leucettines.	Universit£
23642479	277	Small-molecule pyrimidine inhibitors of the cdc2-like (Clk) and dual specificity tyrosine phosphorylation-regulated (Dyrk) kinases: development of chemical probe ML315.	University of Kansas Specialized Chemistry Center
22982525	32	Synthesis and biological evaluation of selective and potent cyclin-dependent kinase inhibitors.	TBA
22998443	69	Selectivity, cocrystal structures, and neuroprotective properties of leucettines, a family of protein kinase inhibitors derived from the marine sponge alkaloid leucettamine B.	Cnrs
22809559	31	Synthesis and biological evaluation of analogs of the marine alkaloids granulatimide and isogranulatimide.	Universit£
22352892	42	Synthesis, biological evaluation, and molecular modeling of natural and unnatural flavonoidal alkaloids, inhibitors of kinases.	Institut De Chimie Des Substances Naturelles (Icsn)
18077363	314	A systematic interaction map of validated kinase inhibitors with Ser/Thr kinases.	University of Oxford
21615147	230	Leucettines, a class of potent inhibitors of cdc2-like kinases and dual specificity, tyrosine phosphorylation regulated kinases derived from the marine sponge leucettamine B: modulation of alternative pre-RNA splicing.	Universite£? De Rennes 1
30967303	3	Kinase inhibitions in pyrido[4,3-h] and [3,4-g]quinazolines: Synthesis, SAR and molecular modeling studies.	Universit£
30199702	24	A ?-glucuronidase-responsive albumin-binding prodrug for potential selective kinase inhibitor-based cancer chemotherapy.	Universit£
29778892	48	Structure-based design of novel quinoxaline-2-carboxylic acids and analogues as Pim-1 inhibitors.	University of Tours
29853332	50	Benzofuro[3,2-d]pyrimidines inspired from cercosporamide CaPkc1 inhibitor: Synthesis and evaluation of fluconazole susceptibility restoration.	Universit£
27721154	660	Exploration of the imidazo[1,2-b]pyridazine scaffold as a protein kinase inhibitor.	University of Paris
28487075	36	N-(1H-Pyrazol-3-yl)quinazolin-4-amines as a novel class of casein kinase 1?/? inhibitors: Synthesis, biological evaluation and molecular modeling studies.	Rajiv Gandhi Proudyogiki Vishwavidyalaya