Explore the Potential with AI-Driven Innovation
Our detailed focused library is generated on demand with advanced virtual screening and parameter assessment technology powered by the Receptor.AI drug discovery platform. This method surpasses traditional approaches, delivering compounds of better quality with enhanced activity, selectivity, and safety.
We pick out particular compounds from an extensive virtual database of more than 60 billion molecules. The preparation and shipment of these compounds are facilitated by our associate Reaxense.
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.
Our high-tech, dedicated method is applied to construct targeted libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our methodology employs molecular simulations to explore a wide array of proteins, capturing their dynamic states both individually and within complexes. Through ensemble virtual screening, we address conformational mobility, uncovering binding sites within functional regions and remote allosteric locations. This thorough exploration ensures no potential mechanism of action is overlooked, aiming to discover novel therapeutic targets and lead compounds across an extensive spectrum of biological functions.
Several key aspects differentiate our library:
partner
Reaxense
upacc
P52926
UPID:
HMGA2_HUMAN
Alternative names:
High mobility group AT-hook protein 2
Alternative UPACC:
P52926; E7EP85; E7EWA2; Q1M182; Q1M185; Q1M186; Q1M187; Q1M188
Background:
High mobility group protein HMGI-C, also known as High mobility group AT-hook protein 2, plays a pivotal role in transcriptional regulation, cell cycle control, and chromosome condensation during spermatocyte meiosis. It is crucial for postnatal muscle development and satellite cell activation, suggesting its broad impact on cellular functions.
Therapeutic significance:
Linked to Silver-Russell syndrome 5, a condition marked by growth retardation and craniofacial abnormalities, HMGI-C's involvement in this autosomal dominant disorder highlights its potential as a therapeutic target. Understanding the role of High mobility group protein HMGI-C could open doors to potential therapeutic strategies.