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.
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.
In the library, a selection of top modulators is provided, each marked with 38 ADME-Tox and 32 parameters related to physicochemical properties and drug-likeness. Also, every compound comes with its best 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.
Our library stands out due to several important features:
partner
Reaxense
upacc
Q00610
UPID:
CLH1_HUMAN
Alternative names:
Clathrin heavy chain on chromosome 17
Alternative UPACC:
Q00610; D3DU00; Q6N0A0; Q86TF2
Background:
Clathrin heavy chain 1, located on chromosome 17, is pivotal in cellular processes such as the formation of coated pits and vesicles. It links clathrin lattices to the plasma membrane or the trans-Golgi network. This protein is a key component of the TACC3/ch-TOG/clathrin complex, enhancing the stability of kinetochore fibers in the mitotic spindle and playing a crucial role in autophagosome formation.
Therapeutic significance:
Clathrin heavy chain 1 is implicated in Intellectual developmental disorder, autosomal dominant 56, highlighting its genetic significance. Understanding the role of Clathrin heavy chain 1 could open doors to potential therapeutic strategies.