Explore the Potential with AI-Driven Innovation
This comprehensive focused library is produced on demand with state-of-the-art virtual screening and parameter assessment technology driven by Receptor.AI drug discovery platform. This approach outperforms traditional methods and provides higher-quality compounds with superior 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 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 strategy employs molecular simulations to explore an extensive range of proteins, capturing their dynamics both individually and within complexes with other proteins. Through ensemble virtual screening, we address proteins' conformational mobility, uncovering key binding sites at both functional regions and remote allosteric locations. This comprehensive investigation ensures a thorough assessment of all potential mechanisms of action, with the goal of discovering innovative therapeutic targets and lead molecules across across diverse biological functions.
Several key aspects differentiate our library:
partner
Reaxense
upacc
Q6DKI2
UPID:
LEG9C_HUMAN
Alternative names:
Galectin-9-like protein B
Alternative UPACC:
Q6DKI2; B0AZM7
Background:
Galectin-9C, alternatively known as Galectin-9-like protein B, is a pivotal protein that binds galactosides. This specific interaction suggests a significant role in cellular processes, including cell-cell and cell-matrix interactions, signaling pathways, and immune responses. The unique binding capability of Galectin-9C to galactosides positions it as a crucial mediator in physiological and potentially pathological contexts.
Therapeutic significance:
Understanding the role of Galectin-9C could open doors to potential therapeutic strategies. Its ability to bind galactosides hints at a profound impact on cellular communication and immune system modulation. This insight lays the groundwork for exploring Galectin-9C as a target in therapeutic interventions, aiming to harness its functions for beneficial outcomes in disease management and treatment.