AI-ACCELERATED DRUG DISCOVERY

Focused On-demand Library for Glutaredoxin-1

Available from Reaxense
Predicted by Alphafold

Focused On-demand Libraries - Reaxense Collaboration

Explore the Potential with AI-Driven Innovation

This extensive focused library is tailor-made using the latest virtual screening and parameter assessment technology, operated by the Receptor.AI drug discovery platform. This technique is more effective than traditional methods, offering compounds with improved activity, selectivity, and safety.

We carefully select specific compounds from a vast collection of over 60 billion molecules in virtual chemical space. Our partner Reaxense helps in synthesizing and delivering these compounds.

The library includes a list of the most effective modulators, each annotated with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Furthermore, each compound is shown with its optimal docking poses, affinity scores, and activity scores, offering a detailed summary.

We use our state-of-the-art dedicated workflow for designing focused libraries.

 Fig. 1. The sreening workflow of Receptor.AI

Our methodology employs molecular simulations to explore a wide array of proteins, capturing their dynamic states both individually and within complexes. Through ensemble virtual screening, we address conformational mobility, uncovering binding sites within functional regions and remote allosteric locations. This thorough exploration ensures no potential mechanism of action is overlooked, aiming to discover novel therapeutic targets and lead compounds across an extensive spectrum of biological functions.

Our library stands out due to several important features:

  • The Receptor.AI platform compiles comprehensive data on the target protein, encompassing previous experiments, literature, known ligands, structural details, and more, leading to a higher chance of selecting the most relevant compounds.
  • Advanced molecular simulations on the platform help pinpoint potential binding sites, making the compounds in our focused library ideal for finding allosteric inhibitors and targeting cryptic pockets.
  • Receptor.AI boasts over 50 tailor-made AI models, rigorously tested and proven in various drug discovery projects and research initiatives. They are crafted for efficacy, dependability, and precision, all of which are key in creating our focused libraries.
  • Beyond creating focused libraries, Receptor.AI offers comprehensive services and complete solutions throughout the preclinical drug discovery phase. Our success-based pricing model minimises risk and maximises the mutual benefits of the project's success.

partner

Reaxense

upacc

P35754

UPID:

GLRX1_HUMAN

Alternative names:

Thioltransferase-1

Alternative UPACC:

P35754; B2R4L2; Q3KQS1; Q6ICT1

Background:

Glutaredoxin-1, also known as Thioltransferase-1, is a pivotal enzyme in cellular redox regulation. It exhibits glutathione-disulfide oxidoreductase activity, leveraging NADPH and glutathione reductase to reduce disulfides in low molecular weight proteins. This protein plays a crucial role in maintaining cellular redox homeostasis by facilitating the reversible protein S-glutathionylation.

Therapeutic significance:

Understanding the role of Glutaredoxin-1 could open doors to potential therapeutic strategies. Its critical function in redox regulation suggests its involvement in oxidative stress-related conditions, making it a target for therapeutic intervention in diseases where oxidative stress is a contributing factor.

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