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 use our state-of-the-art dedicated workflow for designing focused 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.
Key features that set our library apart include:
partner
Reaxense
upacc
Q96JB6
UPID:
LOXL4_HUMAN
Alternative names:
Lysyl oxidase-like protein 4; Lysyl oxidase-related protein C
Alternative UPACC:
Q96JB6; Q5W0B3; Q96DY1; Q96PC0; Q9H6T5
Background:
Lysyl oxidase homolog 4, also known as Lysyl oxidase-like protein 4 and Lysyl oxidase-related protein C, plays a crucial role in the modulation of collagenous extracellular matrix formation. This protein, identified by the accession number Q96JB6, is pivotal in maintaining the structural integrity and function of various tissues.
Therapeutic significance:
Understanding the role of Lysyl oxidase homolog 4 could open doors to potential therapeutic strategies. Its involvement in the extracellular matrix formation suggests its significance in tissue repair and fibrosis, highlighting its potential as a therapeutic target.