Explore the Potential with AI-Driven Innovation
Our detailed focused library is generated on demand with advanced virtual screening and parameter assessment technology powered by the Receptor.AI drug discovery platform. This method surpasses traditional approaches, delivering compounds of better quality with enhanced activity, selectivity, and safety.
From a virtual chemical space containing more than 60 billion molecules, we precisely choose certain compounds. Our collaborator, Reaxense, aids in their synthesis and provision.
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.
We use our state-of-the-art dedicated workflow for designing focused libraries.
Fig. 1. The sreening 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.
Our library distinguishes itself through several key aspects:
partner
Reaxense
upacc
Q04724
UPID:
TLE1_HUMAN
Alternative names:
E(Sp1) homolog; Enhancer of split groucho-like protein 1
Alternative UPACC:
Q04724; A8K495; Q5T3G4; Q969V9
Background:
Transducin-like enhancer protein 1, known as E(Sp1) homolog or Enhancer of split groucho-like protein 1, plays a pivotal role in gene expression regulation. It acts as a transcriptional corepressor, binding to various transcription factors, notably inhibiting NF-kappa-B-regulated gene expression and Wnt signaling. Additionally, it enhances transcriptional repression mediated by FOXG1/BF-1 and HES1, showcasing its versatile regulatory capabilities.
Therapeutic significance:
Understanding the role of Transducin-like enhancer protein 1 could open doors to potential therapeutic strategies. Its regulatory influence on key signaling pathways underscores its potential as a target in modulating gene expression related to various diseases.