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.
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 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.
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.
Several key aspects differentiate our library:
partner
Reaxense
upacc
O95971
UPID:
BY55_HUMAN
Alternative names:
Natural killer cell receptor BY55
Alternative UPACC:
O95971; A0A0B4J2A1; B8PRF2; Q5T2V6
Background:
The CD160 antigen, also known as Natural killer cell receptor BY55, plays a pivotal role in immune regulation. It exists in both GPI-anchored and transmembrane forms, initiating distinct signaling pathways in activated NK and T cells. This receptor interacts with classical and non-classical MHC class I molecules, contributing to immune responses against viral infections and controlling angiogenesis in immune privileged sites. Its interaction with TNFRSF14 influences bidirectional signaling between antigen-presenting cells and lymphocytes.
Therapeutic significance:
Understanding the role of CD160 antigen could open doors to potential therapeutic strategies. Its involvement in immune cell regulation, anti-viral responses, and angiogenesis highlights its potential as a target in designing treatments for immune-related disorders and cancer.