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.
The compounds are cherry-picked from the vast virtual chemical space of over 60B molecules. The synthesis and delivery of compounds is facilitated by our partner Reaxense.
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.
Fig. 1. The sreening workflow of Receptor.AI
By deploying molecular simulations, our approach comprehensively covers a broad array of proteins, tracking their flexibility and dynamics individually and within complexes. Ensemble virtual screening is utilised to take into account conformational dynamics, identifying pivotal binding sites located within functional regions and at allosteric locations. This thorough exploration ensures that every conceivable mechanism of action is considered, aiming to identify new therapeutic targets and advance lead compounds throughout a vast spectrum of biological functions.
Our library stands out due to several important features:
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.