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 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.
Several key aspects differentiate our library:
partner
Reaxense
upacc
Q16363
UPID:
LAMA4_HUMAN
Alternative names:
Laminin-14 subunit alpha; Laminin-8 subunit alpha; Laminin-9 subunit alpha
Alternative UPACC:
Q16363; Q14731; Q14735; Q15335; Q4LE44; Q5SZG8; Q9BTB8; Q9UE18; Q9UJN9
Background:
Laminin subunit alpha-4, known by alternative names such as Laminin-14 subunit alpha, Laminin-8 subunit alpha, and Laminin-9 subunit alpha, plays a crucial role in the attachment, migration, and organization of cells into tissues during embryonic development. It achieves this by binding to cells via a high-affinity receptor and interacting with other extracellular matrix components.
Therapeutic significance:
The protein's involvement in Cardiomyopathy, dilated, 1JJ, a disorder characterized by ventricular dilation and impaired systolic function leading to congestive heart failure and arrhythmia, highlights its potential as a target for therapeutic intervention. Understanding the role of Laminin subunit alpha-4 could open doors to potential therapeutic strategies.