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.
We carefully select specific compounds from a vast collection of over 60 billion molecules in virtual chemical space. Our partner Reaxense helps in synthesizing and delivering these compounds.
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 use our state-of-the-art dedicated workflow for designing 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.
Several key aspects differentiate our library:
partner
Reaxense
upacc
Q8N1G0
UPID:
ZN687_HUMAN
Alternative names:
-
Alternative UPACC:
Q8N1G0; D3DV17; Q68DQ8; Q9H937; Q9P2A7
Background:
Zinc finger protein 687, encoded by the gene with accession number Q8N1G0, plays a crucial role in the cellular machinery, potentially involved in transcriptional regulation. Its unique structure, characterized by zinc finger motifs, suggests a specific interaction with DNA, guiding the expression of genes critical for cellular function.
Therapeutic significance:
The protein's association with Paget disease of bone 6, a condition marked by abnormal bone remodeling and susceptibility to fractures, underscores its clinical importance. Understanding the role of Zinc finger protein 687 could open doors to potential therapeutic strategies, especially considering its link to osteosarcoma in disease progression.