Abstract:
:The synthesis of new meridianin derivatives substituted at the C-5 position of the 2-aminopyrimidine ring by various aryl groups and substituted or not by a methyl group on the indole nitrogen is described. These compounds were tested for their kinase inhibitory potencies toward five kinases (CDK5/p25, CK1delta/epsilon, GSK-3alpha/beta, Dyrk1A and Erk2) as well as their in vitro antiproliferative activities toward a human fibroblast primary culture and two human solid cancer cell lines (MCF-7 and PA 1).
journal_name
Bioorg Med Chemjournal_title
Bioorganic & medicinal chemistryauthors
Akue-Gedu R,Debiton E,Ferandin Y,Meijer L,Prudhomme M,Anizon F,Moreau Pdoi
10.1016/j.bmc.2009.05.017subject
Has Abstractpub_date
2009-07-01 00:00:00pages
4420-4issue
13eissn
0968-0896issn
1464-3391pii
S0968-0896(09)00460-Xjournal_volume
17pub_type
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