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.
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 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.
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.
Key features that set our library apart include:
partner
Reaxense
upacc
Q07890
UPID:
SOS2_HUMAN
Alternative names:
-
Alternative UPACC:
Q07890; B7ZKT6; D3DSB4; Q15503; Q17RN1
Background:
Son of sevenless homolog 2 (SOS2) is a crucial protein that promotes the exchange of Ras-bound GDP by GTP, playing a pivotal role in the Ras signaling pathway. This pathway is essential for the regulation of cell division, survival, and differentiation. The protein's name is derived from its function in the signal transduction process, acting as a molecular switch that activates Ras by facilitating the exchange of GDP for GTP.
Therapeutic significance:
SOS2 is linked to Noonan syndrome 9, a condition marked by congenital heart defects, facial dysmorphisms, and developmental challenges. Given its critical role in cell signaling pathways, targeting SOS2 could offer novel therapeutic avenues for managing Noonan syndrome 9 and potentially other Ras pathway-related disorders.