Explore the Potential with AI-Driven Innovation
This extensive focused library is tailor-made using the latest virtual screening and parameter assessment technology, operated by the Receptor.AI drug discovery platform. This technique is more effective than traditional methods, offering compounds with improved 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
Our methodology employs molecular simulations to explore a wide array of proteins, capturing their dynamic states both individually and within complexes. Through ensemble virtual screening, we address conformational mobility, uncovering binding sites within functional regions and remote allosteric locations. This thorough exploration ensures no potential mechanism of action is overlooked, aiming to discover novel therapeutic targets and lead compounds across an extensive spectrum of biological functions.
Our library stands out due to several important features:
partner
Reaxense
upacc
O60609
UPID:
GFRA3_HUMAN
Alternative names:
-
Alternative UPACC:
O60609; B2RA36; B4DMY9; Q6UW20; Q8IUZ2
Background:
The GDNF family receptor alpha-3 (GFRα-3) plays a pivotal role as the receptor for the glial cell line-derived neurotrophic factor, ARTN (artemin). It is instrumental in the artemin-induced autophosphorylation and activation of the RET receptor tyrosine kinase, highlighting its critical function in neural cell signaling pathways.
Therapeutic significance:
Understanding the role of GDNF family receptor alpha-3 could open doors to potential therapeutic strategies. Its involvement in neural cell signaling pathways underscores its potential as a target for developing treatments for neurological disorders.