Focused On-demand Libraries - Receptor.AI 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.


From a virtual chemical space containing more than 60 billion molecules, we precisely choose certain compounds. Reaxense aids in their synthesis and provision.


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 employ our advanced, specialised process to create targeted libraries for enzymes.


 

Fig. 1. The screening workflow of Receptor.AI

It includes comprehensive molecular simulations of the catalytic and allosteric binding pockets and the ensemble virtual screening accounting for their conformational mobility. In the case of designing modulators, the structural changes induced by reaction intermediates are taken into account to leverage activity and selectivity.


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
Receptor.AI
 
UPACC
Q9Y6F7

UPID:
CDY2_HUMAN

ALTERNATIVE NAMES:
-

ALTERNATIVE UPACC:
Q9Y6F7; A8K868

BACKGROUND:
The protein known as Testis-specific chromodomain protein Y 2, with the unique identifier Q9Y6F7, is implicated in having histone acetyltransferase activity. This function is pivotal for the epigenetic regulation of gene expression, which involves the acetylation of histones to facilitate transcriptional activation. The specificity of this protein to the testis indicates its importance in the processes of spermatogenesis, possibly affecting the epigenetic landscape during male germ cell development.

THERAPEUTIC SIGNIFICANCE:
Understanding the role of Testis-specific chromodomain protein Y 2 could open doors to potential therapeutic strategies. By elucidating its function in spermatogenesis and chromatin remodeling, new avenues for treating male infertility could emerge. This protein's unique activity offers a promising target for developing novel therapeutic interventions aimed at restoring or enhancing male reproductive health.

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