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BioWorld - Saturday, June 13, 2026
Home » GSPT1 degradation inducers

Articles Tagged with ''GSPT1 degradation inducers''

Cancer

Sichuan Kelun-Biotech prepares GSPT1-degrading PROTACs

June 3, 2026
Sichuan Kelun-Biotech Biopharmaceutical Co. Ltd. has reported new proteolysis targeting chimera (PROTACs) compounds comprising a cereblon E3 ubiquitin ligase-binding moiety covalently linked to a eukaryotic peptide chain release factor GTP-binding subunit ERF3A (GSPT1)-targeting moiety potentially useful for the treatment of cancer.
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Cancer

Beijing Innocare Pharma Tech discloses new GSPT1 degradation inducers

April 30, 2026
Beijing Innocare Pharma Tech Co. Ltd. has synthesized new antibody-drug conjugates comprising antibody or antigen-binding fragment covalently linked to eukaryotic peptide chain release factor GTP-binding subunit ERF3A (GSPT1) degradation inducer potentially useful for the treatment of cancer.
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Cancer

Ruijin Hospital and Shanghai Jiao Tong University discover GSPT1 degradation inducers

April 22, 2026
Researchers from Ruijin Hospital and Shanghai Jiao Tong University have patented molecular glue degraders, specifically eukaryotic peptide chain release factor GTP-binding subunit ERF3A (GSPT1) degradation inducers that are potentially useful for the treatment of cancer, autoimmune disease and inflammatory disorders.
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Cancer

Shanghai Haiyan and Yangtze River Pharmaceutical discover GSPT1 -degrading PROTACs

Jan. 29, 2026
Shanghai Haiyan Pharmaceutical Technology Co. Ltd. and Yangtze River Pharmaceutical Group have divulged new isoindoline proteolysis targeting chimeric (PROTAC) compounds comprising cereblon (CRBN) ligands covalently linked to a eukaryotic peptide chain release factor GTP-binding subunit ERF3A (GSPT1)-targeting moiety. They are reported to be useful for the treatment of cancer.
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AI generated, 3D rendering of protein degradation
Cancer

Oral GSPT1 degraders show potent antitumor activity

Dec. 2, 2025
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G1 to S phase transition 1 (GSPT1) is a protein involved in cell cycle progression, translation termination, and protein homeostasis, and its overexpression has been implicated in various cancers. Although GSPT1 is considered a promising therapeutic target, the lack of conventional ligand-binding pockets has historically rendered it undruggable.
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Cancer

Chia Tai Tianqing Pharmaceutical divulges new GSPT1 degradation inducers

Aug. 27, 2025
Chia Tai Tianqing Pharmaceutical Group Co. Ltd. has synthesized proteolysis targeting chimera (PROTAC) compounds comprising an E3 ubiquitin ligase binding moiety covalently linked to a eukaryotic peptide chain release factor GTP-binding subunit ERF3A (GSPT1) targeting moiety via a linker reported to be useful for the treatment of cancer.
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Cancer

Primelink Biotherapeutics presents new GSPT1 degradation inducers

July 31, 2025
Primelink Biotherapeutics (Shenzhen) Co. Ltd. has discovered molecular glue degraders acting as eukaryotic peptide chain release factor GTP-binding subunit ERF3A (GSPT1) degradation inducers reported to be useful for the treatment of cancer.
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Cancer

Beijing Innocare Pharma Tech discloses new molecular glue degraders

July 25, 2025
Beijing Innocare Pharma Tech Co. Ltd. has patented molecular glue degrader compounds acting as eukaryotic peptide chain release factor GTP-binding subunit ERF3A (GSPT1) degradation inducers reported to be useful for the treatment of cancer, autoimmune diseases, inflammation, neurodegenerative and dermatological disorders.
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Cancer

Protier Biotech develops new GSPT1 degradation inducers

June 11, 2025
Protier Biotech Inc. has patented protein/nucleic acid degraders comprising cereblon (CRBN)-binding agents covalently bound to a eukaryotic peptide chain release factor GTP-binding subunit ERF3A (GSPT1)-targeting moiety via linker.
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Cancer

Chinese researchers divulge new GSPT1 degradation inducers

May 22, 2025
Scientists at Ascentage Pharma (Suzhou) Co. Ltd. and China Pharmaceutical University have synthesized molecular glue degrader compounds acting as eukaryotic peptide chain release factor GTP-binding subunit ERF3A (GSPT1)/CRBN interaction inducers for GSPT1 degradation reported to be useful for the treatment of cancer, viral infections, aging, immunological disorders and neurological disorders.
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