Explore the Potential with AI-Driven Innovation
The specialised, focused library is developed on demand with the most recent virtual screening and parameter assessment technology, guided by the Receptor.AI drug discovery platform. This approach exceeds the capabilities of traditional methods and offers compounds with higher 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 utilise our cutting-edge, exclusive workflow to develop 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 distinguishes itself through several key aspects:
partner
Reaxense
upacc
P15814
UPID:
IGLL1_HUMAN
Alternative names:
CD179 antigen-like family member B; Ig lambda-5; Immunoglobulin omega polypeptide; Immunoglobulin-related protein 14.1
Alternative UPACC:
P15814; Q0P681
Background:
Immunoglobulin lambda-like polypeptide 1, also known as CD179 antigen-like family member B, Ig lambda-5, Immunoglobulin omega polypeptide, and Immunoglobulin-related protein 14.1, plays a pivotal role in B-cell development. This protein's critical function underscores its importance in the immune system's ability to produce antibodies.
Therapeutic significance:
Agammaglobulinemia 2, an autosomal recessive condition, is directly linked to mutations affecting this protein, leading to severe infections early in life due to low or absent serum antibodies and B cells. Understanding the role of Immunoglobulin lambda-like polypeptide 1 could open doors to potential therapeutic strategies for this primary immunodeficiency.