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BioWorld - Monday, June 15, 2026
Home » Topics » Drugs » Degradation inducer

Degradation inducer
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Cancer

Daiichi Sankyo patents SF-1 degradation inducers

March 23, 2026
Daiichi Sankyo Co. Ltd. has disclosed new proteolysis targeting chimera (PROTAC) compounds comprising an E3 ubiquitin ligase-binding moiety covalently linked to a steroidogenic factor 1 (SF-1)-targeting moiety. They are reported to be potentially useful for the treatment of primary aldosteronism, Cushing syndrome and cancer.
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3D structure model of α-synuclein
Neurology/psychiatric

New Danish research program targets α-synuclein in Parkinson’s

March 23, 2026
No Comments
A new Danish research project focused on Parkinson’s disease has received funding from Innovation Fund Denmark. The DESYNA (Degradation of Extracellular α-SYNuclein Aggregates) project aims to develop a new therapy targeting α-synuclein, the accumulation of which is a key driver of Parkinson’s disease.
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Cancer

Treeline Biosciences reports TEAD degraders

March 20, 2026
Treeline Biosciences Inc. has synthesized new proteolysis targeting chimera (PROTAC) compounds comprising an E3 ubiquitin ligase-binding moiety covalently linked to transcriptional enhancer factor TEF (TEAD)-targeting moiety potentially useful for the treatment of cancer.
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Immune

Innocare presents new VAV1 degradation inducers

March 19, 2026
Beijing Innocare Pharma Tech Co. Ltd. and Innocare Pharma Inc. have patented molecular glue degraders acting as VAV1 degradation inducers. They are reported to be useful for the treatment of autoimmune disease and inflammatory disorders.
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Cancer

University of Texas patents new YAP1 PROTACs

March 17, 2026
A University of Texas System patent describes new YAP1 degradation inducing proteolysis targeting chimeras (PROTACs) designed for use in the treatment of cancer.
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Immune

VAV1 degradation inducers reported in new Humanwell Healthcare patents

March 11, 2026
Humanwell Healthcare (Group) Co. Ltd. has divulged molecular glue degraders comprising cereblon (CRBN)-binding agents acting as proto-oncogene Vav (VAV1) degradation inducers. They are reported to be useful for the treatment of autoimmune disease, cancer, inflammatory bowel disease, multiple sclerosis, myasthenia gravis, periodontitis, psoriasis, rheumatoid arthritis and type I diabetes, among others.
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Cancer

Gilead Sciences discovers KRAS G12D mutant inhibitors

March 6, 2026
A patent from Gilead Sciences Inc. has divulged GTPase KRAS (G12D mutant) inhibitors and proteolysis targeting chimeras (PROTACS) comprising an E3 ubiquitin ligase-binding moiety covalently linked to a GTPase KRAS (G12D mutant)-targeting moiety through linker.
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Cancer

Risen Pharma synthesizes PROTAC KRAS degraders

March 5, 2026
A Risen (Shanghai) Pharma Eng Co. Ltd. and Risen (Suzhou) Pharma Tech Co. Ltd. patent describes the discovery of new proteolysis targeting chimera (PROTAC) compounds comprising a E3 ubiquitin ligase-binding moiety covalently linked to a GTPase KRAS-targeting moiety. They are reported to be useful for the treatment of cancer.
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Microscopic image of acute myeloid leukemia (AML) cells.
Cancer

Dual degrader shows activity in acute myeloid leukemia models

March 4, 2026
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Researchers in China reported the discovery and preclinical characterization of ZX-079, a novel BRD4/CBP PROTAC degrader.
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Leukemia illustration
Cancer

Newly described selective CDK6 degrader exhibits potential in leukemia models

March 3, 2026
No Comments
Researchers from Specally (Wuhan) Life Technology Co. Ltd. have disclosed the discovery and preclinical profile of WWZ-11-098, a non-palbociclib-based, selective cyclin-dependent kinase 6 (CDK6) degrader in models of leukemia.
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