Focused On-demand Library for CCR4-NOT transcription complex subunit 3

Focused On-demand Libraries - Receptor.AI Collaboration


Explore the Potential with AI-Driven Innovation

This comprehensive focused library is produced on demand with state-of-the-art virtual screening and parameter assessment technology driven by Receptor.AI drug discovery platform. This approach outperforms traditional methods and provides higher-quality compounds with superior 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.


In the library, a selection of top modulators is provided, each marked with 38 ADME-Tox and 32 parameters related to physicochemical properties and drug-likeness. Also, every compound comes with its best docking poses, affinity scores, and activity scores, providing a comprehensive overview.


We utilise our cutting-edge, exclusive workflow to develop focused libraries.


 

Fig. 1. The screening workflow of Receptor.AI

Our methodology leverages molecular simulations to examine a vast array of proteins, capturing their dynamics in both isolated forms and in complexes with other proteins. Through ensemble virtual screening, we thoroughly account for the protein's conformational mobility, identifying critical binding sites within functional regions and distant allosteric locations. This detailed exploration ensures that we comprehensively assess every possible mechanism of action, with the objective of identifying novel therapeutic targets and lead compounds that span a wide spectrum of biological functions.


Several key aspects differentiate our library:


  • Receptor.AI compiles an all-encompassing dataset on the target protein, including historical experiments, literature data, known ligands, and structural insights, maximising the chances of prioritising the most pertinent compounds.

  • The platform employs state-of-the-art molecular simulations to identify potential binding sites, ensuring the focused library is primed for discovering allosteric inhibitors and binders of concealed pockets.

  • Over 50 customisable AI models, thoroughly evaluated in various drug discovery endeavours and research projects, make Receptor.AI both efficient and accurate. This technology is integral to the development of our focused libraries.

  • In addition to generating focused libraries, Receptor.AI offers a full range of services and solutions for every step of preclinical drug discovery, with a pricing model based on success, thereby reducing risk and promoting joint project success.


PARTNER
Receptor.AI
 
UPACC
O75175

UPID:
CNOT3_HUMAN

ALTERNATIVE NAMES:
CCR4-associated factor 3; Leukocyte receptor cluster member 2

ALTERNATIVE UPACC:
O75175; Q9NZN7; Q9UF76

BACKGROUND:
Known alternatively as Leukocyte receptor cluster member 2, CCR4-NOT transcription complex subunit 3 is integral to the CCR4-NOT complex, affecting bulk mRNA degradation, translational repression, and transcriptional regulation. It plays a role in energy metabolism, spindle assembly checkpoint regulation, and embryonic stem cell identity maintenance.

THERAPEUTIC SIGNIFICANCE:
Given its association with Intellectual developmental disorder with speech delay, autism, and dysmorphic facies, exploring the functions of CCR4-NOT transcription complex subunit 3 may lead to groundbreaking therapeutic approaches.

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