Výzva V souladu s tím porcelán rocaglamide a Panoráma odpuštěno Tichomořské ostrovy
The traditional Chinese medical compound Rocaglamide protects nonmalignant primary cells from DNA damage-induced toxicity by inhibition of p53 expression | Cell Death & Disease
Rocaglamide (NSC 326408, Roc-A, Rocaglamide A, CAS Number: 84573-16-0) | Cayman Chemical
Reanalysis of ribosome profiling datasets reveals a function of rocaglamide A in perturbing the dynamics of translation elongation via eIF4A | Nature Communications
Molecular mechanisms and anti‐cancer aspects of the medicinal phytochemicals rocaglamides (=flavaglines) - Li‐Weber - 2015 - International Journal of Cancer - Wiley Online Library
Evidence for a Functionally Relevant Rocaglamide Binding Site on the eIF4A–RNA Complex | ACS Chemical Biology
Total Synthesis of (±)-Rocaglamide via Oxidation-Initiated Nazarov Cyclization | The Journal of Organic Chemistry
Rocaglamide, silvestrol and structurally related bioactive compounds from Aglaia species - Natural Product Reports (RSC Publishing)
Rocaglamide A - List of Frontiers' open access articles
Rocaglamide, inhibitor of NF-kappaB activation (CAS 84573-16-0) (ab142130)
ROCAGLAMIDE | 84573-16-0
Cancers | Free Full-Text | Identification of Cardiac Glycosides as Novel Inhibitors of eIF4A1-Mediated Translation in Triple-Negative Breast Cancer Cells
A double on the Rocs with a twist: Rocaglamide A targets multiple DEAD-box helicases to inhibit translation initiation - ScienceDirect
Rocaglamide | CAS# 84573-16-0 | 1863 | BioVision, Inc.
Structures of the natural rocaglates silvestrol and rocaglamide A... | Download Scientific Diagram
Rocaglamide A - List of Frontiers' open access articles
Rocaglamide overcomes tumor necrosis factor‑related apoptosis‑inducing ligand resistance in hepatocellular carcinoma cells by attenuating the inhibition of caspase‑8 through cellular FLICE‑like‑inhibitory protein downregulation
Rocaglamide | C29H31NO7 | CID 331783 - PubChem
Rocaglamide | NF-κB | HSP | PERK | TargetMol
Rocaglamide Derivatives Are Potent Inhibitors of NF-κB Activation in T-cells - ScienceDirect