AI-ACCELERATED DRUG DISCOVERY

Focused On-demand Library for Epsin-1

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.

Contained in the library are leading modulators, each labelled with 38 ADME-Tox and 32 physicochemical and drug-likeness qualities. In addition, each compound is illustrated with its optimal docking poses, affinity scores, and activity scores, giving a complete picture.

We use our state-of-the-art dedicated workflow for designing focused 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.

Our library is unique due to several crucial aspects:

  • Receptor.AI compiles all relevant data on the target protein, such as past experimental results, literature findings, known ligands, and structural data, thereby enhancing the likelihood of focusing on the most significant compounds.
  • By utilizing advanced molecular simulations, the platform is adept at locating potential binding sites, rendering the compounds in the focused library well-suited for unearthing allosteric inhibitors and binders for hidden pockets.
  • The platform is supported by more than 50 highly specialized AI models, all of which have been rigorously tested and validated in diverse drug discovery and research programs. Its design emphasizes efficiency, reliability, and accuracy, crucial for producing focused libraries.
  • Receptor.AI extends beyond just creating focused libraries; it offers a complete spectrum of services and solutions during the preclinical drug discovery phase, with a success-dependent pricing strategy that reduces risk and fosters shared success in the project.

partner

Reaxense

upacc

Q9Y6I3

UPID:

EPN1_HUMAN

Alternative names:

EH domain-binding mitotic phosphoprotein; EPS-15-interacting protein 1

Alternative UPACC:

Q9Y6I3; Q86ST3; Q9HA18

Background:

Epsin-1, also known as EH domain-binding mitotic phosphoprotein and EPS-15-interacting protein 1, plays a crucial role in cellular processes. It binds to membranes enriched in phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2), modifying membrane curvature and facilitating the formation of clathrin-coated invaginations. This protein is instrumental in regulating receptor-mediated endocytosis, a process vital for cellular signaling and nutrient uptake.

Therapeutic significance:

Understanding the role of Epsin-1 could open doors to potential therapeutic strategies. Its involvement in receptor-mediated endocytosis highlights its potential as a target in diseases where this process is dysregulated.

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