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Science 383 , eadi5798 (2024). Covalent and noncovalent inhibitors of BTK have revolutionized the treatment of these cancers. Covalent and noncovalent inhibitors of BTK have revolutionized the treatment of these cancers. Skye Montoya et al.
Options for cell-based proteindegrader assays Interest is growing in the use of targeted-proteindegradation to induce the breakdown of disease-causing proteins after treatment with small molecule drugs.
Sygnature Discovery identifies potent SHP2 degrader compounds using its proprietary targetedproteindegrader platform, CHARMED, in collaboration with Japanese specialty chemical company, UBE Corporation. UBE Corporation: www.ube.com
I studied Natural Sciences at the University of Cambridge, where I was exposed to a range of disciplines from chemistry to physiology, specialising in my last year in biochemistry. Pushing the boundaries of science always opens the door to new, impactful developments, although there are always challenges along the way.
NYSE: PFE) today announced a global collaboration to develop and commercialize ARV-471, an investigational oral PROTAC® (PROteolysis TArgeting Chimera) estrogen receptor proteindegrader. Despite advancements in oncology in recent years, considerable unmet need persists in the treatment of HR+ breast cancer.
a leading biotechnology company developing small molecule therapeutics based on its proprietary uSMITE platform of targetedproteindegradation technology, today announced that the company’s internal program to develop selective degraders that target key proteins within the TRK family has been published by the Journal of Medicinal Chemistry.
The companies will receive priority admission or renewal for one year of lab bench space with access to core facilities at the MBC BioLabs life sciences incubator, including access to Amgen ‘s scientific experts and business leaders to help advance their scientific programs.
Recent promising results from a Phase 2/3 trial support the use of a single oral dose of brain-penetrant acoziborole (SCYX-7158) for HAT treatment. The need to achieve CNS target coverage with a single dose makes the HAT field an excellent source of case studies for improving brain penetration, with three examples noted below.
These fields are moving at remarkable speed and have huge potential to transform treatments. Combining multiple strands of exciting science in a single location for unrestricted knowledge-sharing is what this is all about,” said Dr Thomas Lundbäck, Senior Director, Mechanistic and Structural Biology, Discovery Sciences, AstraZeneca.
Antibody-drug conjugates (ADCs) have been a groundbreaking approach to cancer treatment with their ability to deliver cytotoxic drugs directly to diseased cells while sparing healthy tissues. This targeted delivery allows enhanced therapeutic efficacy while reducing the harmful side effects commonly associated with traditional chemotherapy.
However, in recent years, huge leaps have been made in drug discovery ranging from novel technologies unearthing new techniques for small molecule development to new modalities like targetedproteindegradation that are beginning to open the door to a promising wave of transcription factor-directed therapeutic candidates.
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