Remove Drugs Remove Fragment Screening Remove Small Molecule
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Reinventing the small molecule toolbox: from proteins to RNA

Dark Matter Blog

The bulk of my nearly three decades of experience up to that point was with drugging protein targets using a variety of modalities, but principally small molecules. It’s all well and good to say, “we should drug RNA,” but which RNA? Prior to 2015, I had a casual relationship, at best, with targeting RNA.

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Target-directed cancer: protein-ligand interactions  

Drug Target Review

Could you provide an overview of your research on target directed cancer drug discovery, particularly your focus on protein lagging interactions. I work in the Centre for Cancer Drug Discovery (CCDD) at The Institute of Cancer Research in London, which is an academic drug discovery centre. 2013) 56, 2059-2073.

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Silly Things Large Language Models Do With Molecules

Practical Cheminformatics

While there was a slight chance that my roommates, with no chemistry knowledge, could have accidentally created the structure of a blockbuster drug, it was highly improbable. Examining molecules produced by LLMs gives me a similar impression. It's like someone with no chemistry background is trying to generate a molecule.

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Biophysical Technologies

Sygnature Discovery

At Sygnature Discovery, we utilise various biophysical technologies to create assays for diverse targets, integral to every stage of the drug discovery process, from hit identification to candidate selection. Covalent drugs may have advantages over non-covalent molecules, such as greater potency and duration of action.

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Biophysics

Sygnature Discovery

At Sygnature Discovery, we see biophysics as a core component of drug discovery projects, which can generate data throughout the pipeline. Comprehensive Assay Development for Diverse Applications Our team here at Sygnature Discovery, comprised of expert biophysicists, is highly experienced in a variety of target classes and drug modalities.

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Open-source Electrophilic Fragment Screening Platform to Identify Chemical Starting Points for UCHL1 Covalent Inhibitors

Covalent Modifiers

Marto SLAS Discovery, 2024 [link] Target-based screening of covalent fragment libraries with mass spectrometry has emerged as a powerful strategy to identify chemical starting points for small molecule inhibitors or find new binding pockets on proteins of interest.