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Cat. No. Product Name Information
PC-26557

PF-07293623

eIF4E inhibitor

PF-07293623 is a first-in-class, specific eukaryotic initiation factor 4E (eIF4E) cap-binding domain inhibitor, inhibits protein synthesis and disrupts eIF4E binding to the m7G cap.
PC-25745

EJC-i

EJC inhibitor, eIF4A3 inhibitor

EJC-i (eIF4A3 inhibitor 18, Exon Junction Complex inhibitor) is a selective ATP-competitive eIF4A3 ATPase inhibitor with IC50 of 0.97 uM and SPR KD of 0.2 uM, has excellent selectivity over other helicases, inhibits de novo Exon Junction Complex (EJC) assembly.
PC-24998

IBX-200

ISR modulator, GCN2 inhibitor

IBX-200 is a selective integrated stress response (ISR) modulator targeting stress sensor kinase GCN2, selectively eliminates ISR-high cells across diverse stressors.
PC-24689

1Ai-3638

eIF1A inhibitor

1Ai-3638 is a small molecule binder of eIF1A, blocks RPS10-eIF1A interaction and inhibits eIF1A association with the 48S in vitro and in cells.
PC-23755

Girolline

eIF5A modulator

Girolline (Girodazole) is a sequence-selective modulator of translation factor eIF5A, interferes with ribosome-eIF5A interaction and induces ribosome stalling, an anti-tumor agent as well as having activity against malaria.
PC-22966

eEF2K Degrader 36

eEF2K degrader

eEF2K Degrader 36 is a potent eEF2K degrader with binding KD of 330 nM, DC50 of 319 nM in MDA-MB-231 cells.
PC-22415

CR-1-31-B

eIF4A inhibitor

CR-1-31-B (CR-31) is a potent and specific eIF4A RNA helicase inhibitor, blocks translation of the MUC1-C oncoprotein.
PC-22002

DNL343

eIF2B activator

Evetifator (DNL343) is a potent, selective, and brain-penetrant eIF2B activator with IC50 of 3.2 nM in cellular ATF4 nano-Luciferase (nLuc) reporter assays.
PC-22001

ABBV-CLS-7262

eIF2B activator

ABBV-CLS-7262 (Fosigotifator) is a potent, selective eIF2B activator undergoing clinical development for ALS and vanishing white matter disease.
PC-21794

eEF2K degrader C1

eEF2K inhibitor

eEF2K degrader C1 is a small-molecule degrader of eEF2K, acts a molecular glue to enhance the interaction of eEF2K with the ubiquitin E3 ligase βTRCP, thereby promoting the proteasomal degradation of eEF2K.
PC-21728

Plitidepsin

eEF1A inhibitor

Plitidepsin (Aplidine, PM90001) is a potent anti-cancer agent by targeting eEF1A2 with KD value of 80 nM, shows antiviral activity against SARS-CoV-2 with IC90 of 0.88 nM.
PC-21688

MG-002

eIF4A inhibitor

MG-002 is a potent, second-generation, orally bioavailable eIF4A RNA helicase inhibitor, potently inhibits cap-dependent mRNA translation with IC50 of 43 nM.

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