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 pick out particular compounds from an extensive virtual database of more than 60 billion molecules. The preparation and shipment of these compounds are facilitated by our associate Reaxense.
The library features a range of promising modulators, each detailed with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Plus, each compound is presented with its ideal docking poses, affinity scores, and activity scores, ensuring a thorough insight.
We utilise our cutting-edge, exclusive workflow to develop 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.
Our library is unique due to several crucial aspects:
partner
Reaxense
upacc
Q687X5
UPID:
STEA4_HUMAN
Alternative names:
Six-transmembrane epithelial antigen of prostate 4; SixTransMembrane protein of prostate 2; Tumor necrosis factor, alpha-induced protein 9
Alternative UPACC:
Q687X5; Q658Q9; Q687X4; Q8WWB0; Q9H5R1
Background:
Metalloreductase STEAP4, also known as Six-transmembrane epithelial antigen of prostate 4, plays a crucial role in iron and copper homeostasis. It functions as an NADPH-dependent ferric-chelate reductase, facilitating the reduction of Fe(3+) to Fe(2+) and Cu(2+) to Cu(1+). This protein is integral in systemic metabolic homeostasis, linking inflammatory responses with metabolism.
Therapeutic significance:
Given its association with obesity, insulin resistance, and inflammatory arthritis, Metalloreductase STEAP4 emerges as a promising target for therapeutic intervention. Understanding the role of Metalloreductase STEAP4 could open doors to potential therapeutic strategies, particularly in the management of metabolic disorders and inflammatory conditions.