Yüklüyor......

4,4′-unsymmetrically substituted 3,3′-biphenyl alpha helical proteomimetics as potential coactivator binding inhibitors

A series of unsymmetrically substituted biphenyl compounds was designed as alpha helical proteomimetics with the aim of inhibiting the binding of coactivator proteins to the nuclear hormone receptor coactivator binding domain. These compounds were synthesized in good overall yields in seven steps st...

Ful tanımlama

Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Bioorg Med Chem
Asıl Yazarlar: Weiser, Patrick T., Chang, Ching-Yi, McDonnell, Donald P., Hanson, Robert N.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2013
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4243926/
https://ncbi.nlm.nih.gov/pubmed/24360824
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bmc.2013.10.051
Etiketler: Etiketle
Etiket eklenmemiş, İlk siz ekleyin!