WebIC50: N/A Cycloheximide is an inhibitor of protein biosynthesis in eukaryotic organisms widely used in biomedical research to inhibit protein synthesis in eukaryotic cells studied in vitro. WebOct 1, 2024 · Paclitaxel, a new anti-tubulin drug, has been proved to be effective against breast carcinoma, head and neck carcinomas, ovarian carcinoma, and nonsmall-cell lung tumors [50]. It has been observed that paraptosis occurrs in human lung adenocarcinoma cells, such as ASTC-a-1 and the non-small cell lung cancer cell line, A549 [51].
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WebIC₅₀ & Target IC50: 532.5 nM (protein synthesis), 2.88 μM (RNA synthesis)[1] Cycloheximide (CHX) is the most common laboratory reagent used to inhibit protein synthesis. Cycloheximide has been shown to block the elongation phase of eukaryotic translation. Cycloheximide binds the ribosome and inhibits eEF2-In Vitro Product Data … WebCycloheximide是一种蛋白生物合成 (protein synthesis) 的抑制剂, IC50值为532.5 nM。. Cycloheximide (Naramycin A) 也是一种抗真菌 (antifungal) 素,Cycloheximide 还可抑制铁死亡 (ferroptosis) 并抑制自噬 (autophagy)。. 021-50967598 2118621495 [email protected]. high time grammar
APExBIO - Cycloheximide Antibiotic,inhibiter of protein …
WebCycloheximide is supplied as a crystalline solid. A stock solution may be made by dissolving the cycloheximide in the solvent of choice, which should be purged with an inert gas. Cycloheximide is soluble in organic solvents such as ethanol and DMSO. It is also soluble in water. WebMay 7, 2015 · A series of spirooxindole tetrahydrofuran derivatives 3 were obtained in moderate to good yields via oxindole derivatives 1 and β-arylacrylonitrile derivatives 2via base-mediated cascade [3 + 2] double Michael reactions under mild conditions and the application of this method in the synthesis of bio … WebCycloheximide is rapidly inactivated by direct light (especially ultra violet light) – never expose cycloheximide solutions, mixtures or plates to direct sun light – short exposure … high time grateful dead chords