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.
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
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
Q86SQ7
UPID:
SDCG8_HUMAN
Alternative names:
Antigen NY-CO-8; Centrosomal colon cancer autoantigen protein
Alternative UPACC:
Q86SQ7; O60527; Q3ZCR6; Q8N5F2; Q9P0F1
Background:
Serologically defined colon cancer antigen 8, also known as Antigen NY-CO-8, plays a pivotal role in cell polarity, epithelial lumen formation, and ciliogenesis. Its interaction with RABEP2 is crucial for centrosomal localization, essential for the formation of primary cilia and activation of the Hedgehog signaling pathway.
Therapeutic significance:
The protein's involvement in Senior-Loken syndrome 7 and Bardet-Biedl syndrome 16, through its role in ciliogenesis and Hedgehog signaling, highlights its potential as a target for therapeutic intervention in renal-retinal disorders and syndromes with complex phenotypes.