Explore the Potential with AI-Driven Innovation
This extensive focused library is tailor-made using the latest virtual screening and parameter assessment technology, operated by the Receptor.AI drug discovery platform. This technique is more effective than traditional methods, offering compounds with improved activity, selectivity, and safety.
The compounds are cherry-picked from the vast virtual chemical space of over 60B molecules. The synthesis and delivery of compounds is facilitated by our partner Reaxense.
The library includes a list of the most promising modulators annotated with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Also, each compound is presented with its optimal docking poses, affinity scores, and activity scores, providing a comprehensive overview.
We utilise our cutting-edge, exclusive workflow to develop focused 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.
Key features that set our library apart include:
partner
Reaxense
upacc
Q8WY41
UPID:
NANO1_HUMAN
Alternative names:
EC_Rep1a
Alternative UPACC:
Q8WY41
Background:
Nanos homolog 1, also known as EC_Rep1a, plays a crucial role in post-transcriptional gene regulation by acting as a translational repressor. It forms a complex with PUM2, targeting the 3'-UTR of specific mRNAs, thereby regulating their translation. Additionally, it influences cell adhesion and invasion processes by modulating E-cadherin functions and up-regulating MMP14 production, facilitating tumor cell invasion.
Therapeutic significance:
The involvement of Nanos homolog 1 in Spermatogenic failure 12, characterized by defects in spermatogenesis leading to reduced sperm motility and concentration, highlights its potential as a target for therapeutic intervention. Understanding the role of Nanos homolog 1 could open doors to potential therapeutic strategies for treating infertility disorders and possibly certain cancers.