eRF3b/GSPT2
- [1]. Zhouravleva G, et al. Termination of translation in eukaryotes is governed by two interacting polypeptide chain release factors, eRF1 and eRF3. EMBO Journal. 1995;14(16):4065-4072. [Content Brief]
- [2]. Kisselev L, et al. Termination of translation: interplay of mRNA, rRNAs, and release factors. EMBO Journal. 2002;21(7):175-182.
- [3]. Chauvin C, et al. Involvement of human release factors eRF3a and eRF3b in translation termination and nonsense-mediated mRNA decay. Molecular and Cellular Biology. 2005;25(14):5801-5811. [Content Brief]
- [4]. Hoshino S, et al. The eukaryotic polypeptide chain release factor (eRF3/GSPT) carrying the translation termination signal promotes GTPase activity of eRF1. RNA. 1999;5(3):362-376. [Content Brief]
- [5]. Le Goff X, et al. Overexpression of human eRF3a and eRF3b proteins: differential effects on translation termination and nonsense-mediated mRNA decay. Molecular and Cellular Biology. 2002;22(16):6101-6110. [Content Brief]
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eRF3b/GSPT2 Related Products (5)
Related Products (5)
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SJ6986
0 ImagesSJ6986 is a potent, selective and orally active GSPT1/2 Molecular Glue degrader, with a DC50 of 2.1 nM (Dmax 99%) for GSPT1. -
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GT19630
0 ImagesGT19630 is an orally active c-Myc PROTAC targeted degrader based on the cereblon E3 ubiquitin ligase, with an IC50 of 1.5 nM against human c-Myc. GT19630 mediates the degradation of MYC, GSPT1, GSPT2, CK1 alpha, N-Myc, B7-H3 and XIAP, and disrupts the MYC-GSPT1 synergistic regulatory feedback loop. GT19630 inhibits cell proliferation, blocks S-phase progression of the cell cycle, promotes cell apoptosis, reduces cell migration capacity, induces integrated stress response, and blocks oxidative phosphorylation by inhibiting the TCA cycle. GT19630 can be used in the research of Myc-driven hematological cancers, small cell lung cancer, breast cancer, TP53-mutant cancers, and venetoclax-resistant cancers. -
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MDEG-541
0 ImagesCat. No.: HY-150259Purity: 98.68%MDEG-541 is a PROTAC degrader targeting MYC, GSPT1/2 and PLK1. MDEG-541 induces degradation via proteasome- and ubiquitin-dependent pathways. MDEG-541 exhibits anti-tumor activity in gastrointestinal cancer cells and patient-derived organoids. MDEG-541 can be used for the research of gastrointestinal cancer. -
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KMG-1068
0 ImagesKMG-1068 is a molecular glue degrader that induces proteasomal degradation of GSPT1 and GSPT2 with DC50 values of 126.7 nM and 42.2 nM, respectively. KMG-1068 binds to the C-terminal IMiD-binding site of CRBN, forms ternary complexes with GSPT1 and GSPT2, and mediates proteasomal degradation of target proteins via the CRL4 ubiquitination pathway. KMG-1068 is applicable to research related to acute myeloid leukemia. -
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GSPT2 degrader-1
0 ImagesCat. No.: HY-177744CAS No.: 3093413-09-0GSPT2 degrader-1 (compound 619) is a selective molecular glue GSPT2 degrader targeting GSPT2. GSPT2 degrader-1 contains Thalidomide (HY-14658) and the linker of MDEG-541 (HY-150259). GSPT2 degrader-1 induces the degradation, but not GSPT1 or myelocytomatosis oncogene (MYC). GSPT2 degrader-1 can be used for research of gastrointestinal cancer. -
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