Date published: 2025-11-7

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TCEAL5 Inhibitors

TCEAL5 Inhibitors primarily target different aspects of the transcription process and RNA processing, which could influence the function of TCEAL5. α-Amanitin and DRB directly target RNA polymerase II, crucial for transcription elongation, which might impact TCEAL5-related processes. Triptolide and Flavopiridol Hydrochloride disrupt the transcription elongation process by targeting the XPB subunit of TFIIH and CDK9, respectively. Actinomycin D interferes with RNA synthesis by binding to DNA, which could indirectly affect transcriptional processes involving TCEAL5. I-BET151 and JQ1 are known for their role in inhibiting BET bromodomain proteins, thereby impacting transcription regulation at the chromatin level.

Pladienolide B and KPT 330 affect RNA processing and nuclear export, respectively, both of which are crucial post-transcriptional regulation processes that could intersect with TCEAL5's function. Rocaglamide and Cordycepin target translation and RNA polyadenylation, further influencing gene expression regulation. Lastly, Burixafor's role as a CXCR4 antagonist suggests an impact on cell signaling pathways, which could have downstream effects on transcription regulation relevant to TCEAL5. These chemicals provide avenues to explore the transcriptional and post-transcriptional regulation that may be related to TCEAL5's function.

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