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.
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.
Our library stands out due to several important features:
partner
Reaxense
upacc
P55795
UPID:
HNRH2_HUMAN
Alternative names:
FTP-3; Heterogeneous nuclear ribonucleoprotein H'
Alternative UPACC:
P55795; A1L400; Q9HHA7
Background:
Heterogeneous nuclear ribonucleoprotein H2 (hnRNP H2), also known as FTP-3, plays a crucial role in the processing of pre-mRNAs into functional mRNAs, a fundamental step in gene expression. It binds specifically to poly(RG) sequences, indicating its involvement in the regulation of RNA metabolism.
Therapeutic significance:
The protein is linked to Intellectual developmental disorder, X-linked, syndromic, Bain type, characterized by developmental delay, intellectual disability, and seizures, among other symptoms. Targeting hnRNP H2 could offer new avenues for therapeutic interventions in treating this disorder.