AI-ACCELERATED DRUG DISCOVERY

Focused On-demand Library for Pendrin

Available from Reaxense
Predicted by Alphafold

Focused On-demand Libraries - Reaxense Collaboration

Explore the Potential with AI-Driven Innovation

The focused library is created on demand with the latest virtual screening and parameter assessment technology, supported by the Receptor.AI drug discovery platform. This method is more effective than traditional methods and results in higher-quality compounds with better activity, selectivity, and safety.

We pick out particular compounds from an extensive virtual database of more than 60 billion molecules. The preparation and shipment of these compounds are facilitated by our associate Reaxense.

The library includes a list of the most promising modulators annotated with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Also, each compound is presented with its optimal docking poses, affinity scores, and activity scores, providing a comprehensive overview.

Our high-tech, dedicated method is applied to construct targeted libraries.

 Fig. 1. The sreening workflow of Receptor.AI

Utilising molecular simulations, our approach thoroughly examines a wide array of proteins, tracking their conformational changes individually and within complexes. Ensemble virtual screening enables us to address conformational flexibility, revealing essential binding sites at functional regions and allosteric locations. Our rigorous analysis guarantees that no potential mechanism of action is overlooked, aiming to uncover new therapeutic targets and lead compounds across diverse biological functions.

Key features that set our library apart include:

  • The Receptor.AI platform integrates extensive information about the target protein, such as historical experiments, academic research, known ligands, and structural insights, thereby increasing the likelihood of identifying highly relevant compounds.
  • The platform’s sophisticated molecular simulations are designed to discover potential binding sites, ensuring that our focused library is optimal for the discovery of allosteric inhibitors and binders for cryptic pockets.
  • With over 50 customisable AI models, verified through extensive testing in commercial drug discovery and research, Receptor.AI is efficient, reliable, and precise. These models are essential in the production of our focused libraries.
  • Receptor.AI not only produces focused libraries but also provides full services and solutions at every stage of preclinical drug discovery, with a success-based pricing structure that aligns our interests with the success of your project.

partner

Reaxense

upacc

O43511

UPID:

S26A4_HUMAN

Alternative names:

Sodium-independent chloride/iodide transporter; Solute carrier family 26 member 4

Alternative UPACC:

O43511; B7Z266; O43170

Background:

Pendrin, identified by the gene symbol SLC26A4, functions as a sodium-independent transporter of chloride and iodide. It plays a crucial role in mediating electroneutral exchange of chloride-bicarbonate, chloride-iodide, and chloride-formate, as well as iodide-bicarbonate exchange. This protein's alternative names include Sodium-independent chloride/iodide transporter and Solute carrier family 26 member 4.

Therapeutic significance:

Pendrin is implicated in Pendred syndrome, a disorder characterized by congenital sensorineural hearing loss and thyroid goiter, and in non-syndromic sensorineural deafness associated with an enlarged vestibular aqueduct. Understanding the role of Pendrin could open doors to potential therapeutic strategies for these conditions.

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