Explore the Potential with AI-Driven Innovation
The specialised, focused library is developed on demand with the most recent virtual screening and parameter assessment technology, guided by the Receptor.AI drug discovery platform. This approach exceeds the capabilities of traditional methods and offers compounds with higher activity, selectivity, and safety.
Our selection of compounds is from a large virtual library of over 60 billion molecules. The production and distribution of these compounds are managed by our partner Reaxense.
The library includes a list of the most promising modulators annotated with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Also, each compound is presented with its optimal docking poses, affinity scores, and activity scores, providing a comprehensive overview.
Our top-notch dedicated system is used to design specialised libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our methodology leverages molecular simulations to examine a vast array of proteins, capturing their dynamics in both isolated forms and in complexes with other proteins. Through ensemble virtual screening, we thoroughly account for the protein's conformational mobility, identifying critical binding sites within functional regions and distant allosteric locations. This detailed exploration ensures that we comprehensively assess every possible mechanism of action, with the objective of identifying novel therapeutic targets and lead compounds that span a wide spectrum of biological functions.
Our library distinguishes itself through several key aspects:
partner
Reaxense
upacc
P04156
UPID:
PRIO_HUMAN
Alternative names:
ASCR; PrP27-30; PrP33-35C
Alternative UPACC:
P04156; O60489; P78446; Q15216; Q15221; Q27H91; Q5QPB4; Q8TBG0; Q96E70; Q9UP19
Background:
The Major prion protein, known by its alternative names ASCR, PrP27-30, and PrP33-35C, plays a pivotal role in neuronal development and synaptic plasticity. It is essential for the maintenance of neuronal myelin sheath and may contribute to myelin homeostasis through its action as an agonist for the ADGRG6 receptor. Its involvement in iron uptake and homeostasis underscores its significance in neural function.
Therapeutic significance:
Linked to a spectrum of neurodegenerative disorders, including Creutzfeldt-Jakob disease and Fatal Familial Insomnia, the Major prion protein's pathological variants underscore its therapeutic significance. Understanding its role could lead to groundbreaking treatments for these devastating conditions.