A team of chemists at the University of Cambridge has developed a powerful new method for adding single carbon atoms to ...

Atoms are the fundamental building blocks of everything around us, but their size is almost beyond comprehension. This ...

GSK said it is ending the development program for the small-molecule drug Belrestotug. The British pharmaceutical giant said Tuesday that the decision is based on a new interim analyses from phase ...

Vital Transformation’s research found that aggregate small molecule investments by companies valued at less than $2 billion dropped by 68% since the Inflation Reduction Act was introduced.

Now, researchers at the University of Gothenburg have discovered a small molecule that restores function in a defective mitochondrial enzyme, offering a new therapeutic avenue for diseases caused by ...

The Icahn School of Medicine at Mount Sinai launched the AI Small Molecule Drug Discovery Center which was created to integrate AI with traditional drug discovery methods to identify and design ...

Takeda has returned to BridGene Biosciences for another small-molecule collaboration—this time focused on immunology as well as neurology. BridGene’s pursuit of undruggable targets is enabled ...

Earlier this year, they released that data as training fodder in a competition aimed at determining whether any AI models for predicting small molecule interactions with proteins were really ...

Experts from the University of of Dundee's Centre for Targeted Protein Degradation (CeTPD), working with Boehringer Ingelheim scientists, have developed a breakthrough small-molecule drug ...

A team led by UNC School of Medicine researchers is the first to confirm that a small molecule called miR-29 plays a role in driving aging. Their new findings are published in Communications Biology.

New small molecule could treat sickle cell disease in adults that don't respond to hydroxyurea, alone. ScienceDaily . Retrieved June 1, 2025 from www.sciencedaily.com / releases / 2024 / 07 ...

Angelman syndrome (AS) is a rare genetic disorder characterized by poor muscle control, limited speech, epilepsy, and intellectual disabilities. There is no cure for the disorder, named after ...