Loading...
The affinity of RSK for cylitol analogues of SL0101 is critically dependent on the B-ring C-4′-hydroxy†
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 g...
Na minha lista:
| Udgivet i: | Chem Commun (Camb) |
|---|---|
| Main Authors: | , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2020
|
| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7285658/ https://ncbi.nlm.nih.gov/pubmed/32048692 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1039/d0cc00128g |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|