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.
From a virtual chemical space containing more than 60 billion molecules, we precisely choose certain compounds. Our collaborator, Reaxense, aids in their synthesis and provision.
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.
Our top-notch dedicated system is used to design specialised libraries for receptors.
Fig. 1. The sreening workflow of Receptor.AI
The method involves detailed molecular simulations of the receptor in its native membrane environment, with ensemble virtual screening focusing on its conformational mobility. When dealing with dimeric or oligomeric receptors, the whole functional complex is modelled, and the tentative binding pockets on and between the subunits are established to address all possible mechanisms of action.
Our library is unique due to several crucial aspects:
partner
Reaxense
upacc
Q01344
UPID:
IL5RA_HUMAN
Alternative names:
CDw125
Alternative UPACC:
Q01344; B3IU77; B4E2G0; Q14633; Q15469; Q6ISX9
Background:
Interleukin-5 receptor subunit alpha, also known as CDw125, plays a pivotal role in eosinophil survival, differentiation, and chemotaxis. This protein operates by forming a heterodimeric receptor with the CSF2RB subunit, which binds to interleukin-5, activating the JAK-STAT pathway through JAK2 stimulation. Its interaction with JAK2 in unstimulated conditions highlights its regulatory complexity.
Therapeutic significance:
Understanding the role of Interleukin-5 receptor subunit alpha could open doors to potential therapeutic strategies. Its involvement in eosinophil function suggests its potential as a target in diseases where eosinophils play a critical role.