| Literature DB >> 32048692 |
Yu Li1, Pedro Seber2, Eric B Wright3, Sharia Yasmin4, Deborah A Lannigan5, George A O'Doherty1.
Abstract
Five cyclitol analogues of SL0101 with variable substitution at the C-4' position (i.e., OH, Cl, F, H, OMe) were synthesized. The series of analogues were evaluated for their ability to inhibit p90 ribosomal S6 kinase (RSK) activity. The study demonstrated the importance of the B-ring C-4' hydroxy group for RSK1/2 inhibition.Entities:
Year: 2020 PMID: 32048692 PMCID: PMC7285658 DOI: 10.1039/d0cc00128g
Source DB: PubMed Journal: Chem Commun (Camb) ISSN: 1359-7345 Impact factor: 6.222