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.
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.
Contained in the library are leading modulators, each labelled with 38 ADME-Tox and 32 physicochemical and drug-likeness qualities. In addition, each compound is illustrated with its optimal docking poses, affinity scores, and activity scores, giving a complete picture.
We employ our advanced, specialised process to create targeted 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
Q8WZ75
UPID:
ROBO4_HUMAN
Alternative names:
Magic roundabout
Alternative UPACC:
Q8WZ75; A8K154; Q14DU7; Q8TEG1; Q96JV6; Q9H718; Q9NWJ8
Background:
Roundabout homolog 4, also known as 'Magic roundabout', plays a pivotal role in angiogenesis and vascular patterning. It acts as a receptor for Slit proteins, particularly SLIT2, influencing endothelial cell migration and vascular development. Additionally, it contributes to the maintenance of endothelial barrier organization and function.
Therapeutic significance:
Roundabout homolog 4's involvement in Aortic valve disease 3, characterized by bicuspid aortic valve, aortic valve stenosis, and ascending aortic aneurysm, highlights its potential as a therapeutic target. Understanding the role of Roundabout homolog 4 could open doors to potential therapeutic strategies for cardiovascular diseases.