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 employ our advanced, specialised process to create 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.
Key features that set our library apart include:
partner
Reaxense
upacc
O14926
UPID:
FSCN2_HUMAN
Alternative names:
Retinal fascin
Alternative UPACC:
O14926; A0AVC4; A8MRA6
Background:
Fascin-2, also known as Retinal fascin, plays a crucial role in the human body as an actin bundling protein. It is instrumental in photoreceptor cell-specific events, including disk morphogenesis, which is vital for vision.
Therapeutic significance:
Fascin-2 is directly linked to Retinitis pigmentosa 30, a retinal dystrophy characterized by night vision blindness and progressive loss of visual field. Understanding the role of Fascin-2 could lead to groundbreaking therapeutic strategies for this debilitating condition.