Načítá se...
Bridged Analogues for p53-Dependent Cancer Therapy Obtained by S-Alkylation
A small library of anticancer, cell-permeating, stapled peptides based on potent dual-specific antagonist of p53–MDM2/MDMX interactions, PMI-N8A, was synthesized, characterized and screened for anticancer activity against human colorectal cancer cell line, HCT-116. Employed synthetic modifications i...
Uloženo v:
| Vydáno v: | Int J Pept Res Ther |
|---|---|
| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2015
|
| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4779441/ https://ncbi.nlm.nih.gov/pubmed/26957954 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10989-015-9487-3 |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|