Explore the Potential with AI-Driven Innovation
This extensive focused library is tailor-made using the latest virtual screening and parameter assessment technology, operated by the Receptor.AI drug discovery platform. This technique is more effective than traditional methods, offering compounds with improved 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 for enzymes.
Fig. 1. The sreening workflow of Receptor.AI
This approach involves comprehensive molecular simulations of the catalytic and allosteric binding pockets and ensemble virtual screening that accounts for their conformational flexibility. In the case of designing modulators, the structural adjustments caused by reaction intermediates are considered to improve activity and selectivity.
Our library distinguishes itself through several key aspects:
partner
Reaxense
upacc
Q9HD43
UPID:
PTPRH_HUMAN
Alternative names:
Stomach cancer-associated protein tyrosine phosphatase 1; Transmembrane-type protein-tyrosine phosphatase type H
Alternative UPACC:
Q9HD43; C9JCH2; Q15426; Q2NKN9; Q2NKP0
Background:
Receptor-type tyrosine-protein phosphatase H, also known as Stomach cancer-associated protein tyrosine phosphatase 1 and Transmembrane-type protein-tyrosine phosphatase type H, plays a crucial role in cell growth, motility, and apoptotic cell death. It mediates dephosphorylation of focal adhesion-associated substrates, negatively regulating integrin-promoted signaling processes. This protein is pivotal in inhibiting cell survival signaling pathways and activating caspase-dependent proapoptotic pathways.
Therapeutic significance:
Understanding the role of Receptor-type tyrosine-protein phosphatase H could open doors to potential therapeutic strategies. Its involvement in cell survival signaling and apoptotic pathways makes it a promising target for developing treatments for diseases where these processes are dysregulated.