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.
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.
Our high-tech, dedicated method is applied to construct targeted libraries for enzymes.
Fig. 1. The sreening workflow of Receptor.AI
The procedure entails thorough molecular simulations of the catalytic and allosteric binding pockets, accompanied by ensemble virtual screening that factors in their conformational flexibility. When developing modulators, the structural modifications brought about by reaction intermediates are factored in to optimize activity and selectivity.
Our library is unique due to several crucial aspects:
partner
Reaxense
upacc
Q8IW92
UPID:
GLBL2_HUMAN
Alternative names:
-
Alternative UPACC:
Q8IW92; A6NCE6; Q6UX60; Q8NC62; Q8NCB3; Q8NCJ1; Q96HP3
Background:
Beta-galactosidase-1-like protein 2, encoded by the gene with the accession number Q8IW92, plays a crucial role in the breakdown of complex sugars into simpler molecules. This process is vital for the proper digestion and absorption of nutrients, highlighting the protein's importance in metabolic pathways.
Therapeutic significance:
Understanding the role of Beta-galactosidase-1-like protein 2 could open doors to potential therapeutic strategies. Its involvement in metabolic processes suggests that targeting this protein could lead to novel treatments for metabolic disorders.