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.
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 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
Q8IYY4
UPID:
DZI1L_HUMAN
Alternative names:
DAZ-interacting zinc finger protein 1-like
Alternative UPACC:
Q8IYY4; C9JUG5; Q96M38
Background:
Cilium assembly protein DZIP1L, also known as DAZ-interacting zinc finger protein 1-like, plays a crucial role in primary cilium formation. It is pivotal for the localization of PKD1/PC1 and PKD2/PC2 to the ciliary membrane, acting as a transition zone protein. This function is essential for the proper structural and functional assembly of cilia.
Therapeutic significance:
DZIP1L is directly associated with Polycystic Kidney Disease 5, an autosomal recessive disorder leading to end-stage renal disease. Understanding the role of DZIP1L could open doors to potential therapeutic strategies for treating or managing this debilitating condition.