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BioWorld - Monday, May 4, 2026
Home » Topics » Drugs » Degradation inducer

Degradation inducer
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Cancer

Gluetacs Therapeutics divulges new protein degradation inducers

Nov. 27, 2025
Gluetacs Therapeutics (Shanghai) Co. Ltd. has synthesized molecular glue degraders comprising cereblon (CRBN) binding agents and protein degradation moieties reported to be useful for the treatment of cancer, infections, autoimmune diseases, anemia, transplant rejection, diabetes, cardiovascular disorders and inflammatory disorders, among others.
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Cancer

Blueprint Medicines patents new CDK4 degradation inducers

Nov. 27, 2025
Blueprint Medicines Corp. has disclosed PROTAC compounds comprising an E3 ubiquitin ligase binding moiety covalently linked to a cyclin-dependent kinase 4 (CDK4)-targeting moiety potentially useful for the treatment of cancer.
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Breast cancer cell
Cancer

Novel PROTAC based on GDC-0810 against ER-positive breast cancer

Nov. 27, 2025
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In an effort to develop more effective estrogen receptor α (ERα) inhibitors, researchers at Nanjing University of Chinese Medicine and collaborators aimed to develop a proteolysis targeting chimera (PROTAC) against the receptor.
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Cancer

Nikang Therapeutics patents new CDK2 and CDK4 degradation inducers

Nov. 26, 2025
Nikang Therapeutics Inc. has disclosed proteolysis targeting chimera (PROTAC) compounds comprising an E3 ubiquitin ligase-binding moiety coupled to a cyclin-dependent kinase 2 (CDK2)- and/or CDK4-targeting moiety through a linker reported to be useful for the treatment of cancer.
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Neurology/psychiatric

Captor Therapeutics patents new Nek7 degradation inducers

Nov. 25, 2025
Captor Therapeutics Inc. has disclosed molecular glue degraders comprising a cereblon (CRBN) binding moiety acting as serine/threonine-protein kinase Nek7 degradation inducers reported to be useful for the treatment of amyotrophic lateral sclerosis, Still’s disease, Behçet’s disease, familial Mediterranean fever, Alzheimer’s disease, pulmonary arterial hypertension and more.
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Art concept for molecular glue degradation
Cancer

Vaxcellbio advances research in MYO1D-targeted degradation

Nov. 25, 2025
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Vaxcellbio Co. Ltd. has signed a research agreement with the Korea Drug Development Fund (KDDF) to pursue the discovery of next-generation targeted anticancer lead compounds based on degradation of the molecular motor protein MYO1D (myosin 1D).
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Cancer

New PLK1 degradation inducers disclosed in Crossfire Oncology patent

Nov. 21, 2025
Crossfire Oncology BV has divulged proteolysis targeting chimera (PROTAC) compounds comprising an E3 ubiquitin ligase binding moiety covalently linked to a serine/threonine-protein kinase PLK1 (STPK13) targeting moiety through a linker reported to be useful for the treatment of cancer, autoimmune diseases, transplant rejection, neurological disorders and inflammatory disorders.
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Cancer

New GSPT1/CSNK1A1 degradation inducers disclosed in Mindrank patent

Nov. 19, 2025
Mindrank Therapeutics (Suzhou) New Drug Research & Development Co. Ltd. has divulged molecular glue degraders comprising cereblon (CRBN) ligands acting as dual eukaryotic peptide chain release factor GTP-binding subunit ERF3A (GSPT1) and casein kinase 1 isoform α (CSNK1A1) degradation inducers. They are reported to be potentially useful for the treatment of cancer, Alzheimer’s disease, inflammatory disorders, autoimmune diseases and metabolic diseases.
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Breast cancer illustration
Cancer

CDK2 degraders show activity in HR+/HER2- and CCNE1-amplified breast tumors

Nov. 14, 2025
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During the AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics, scientists from Plexium Inc. presented the identification of a new class of potent, selective, cereblon (CRBN)-based molecular glue degraders of CDK2 using its proprietary monovalent degrader platform.
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Cancer

Shanghai Leadingtac Pharmaceutical divulges new KRAS G12D degradation inducers

Nov. 12, 2025
Shanghai Leadingtac Pharmaceutical Co. Ltd. has synthesized proteolysis targeting chimera (PROTAC) compounds comprising an E3 ubiquitin ligase-binding moiety covalently linked to a GTPase KRAS (G12D mutant)-targeting moiety via a linker reported to be useful for the treatment of cancer.
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