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.
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.
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 employ our advanced, specialised process to create targeted libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our strategy employs molecular simulations to explore an extensive range of proteins, capturing their dynamics both individually and within complexes with other proteins. Through ensemble virtual screening, we address proteins' conformational mobility, uncovering key binding sites at both functional regions and remote allosteric locations. This comprehensive investigation ensures a thorough assessment of all potential mechanisms of action, with the goal of discovering innovative therapeutic targets and lead molecules across across diverse biological functions.
Our library distinguishes itself through several key aspects:
partner
Reaxense
upacc
Q9BY79
UPID:
MFRP_HUMAN
Alternative names:
Membrane-type frizzled-related protein
Alternative UPACC:
Q9BY79; B0YJ36; B0YJ37; B4DHN8; Q335M3; Q96DQ9
Background:
The Membrane frizzled-related protein, alternatively known as Membrane-type frizzled-related protein, plays a pivotal role in eye development. This protein, encoded by the gene with the accession number Q9BY79, is crucial for the proper formation and function of the eyes.
Therapeutic significance:
Linked to rare eye disorders such as Nanophthalmos 2 and Microphthalmia, isolated, 5, the Membrane frizzled-related protein's involvement in these conditions underscores its potential as a target for therapeutic intervention. Understanding the role of Membrane frizzled-related protein could open doors to potential therapeutic strategies.