Explore the Potential with AI-Driven Innovation
The specialised, focused library is developed on demand with the most recent virtual screening and parameter assessment technology, guided by the Receptor.AI drug discovery platform. This approach exceeds the capabilities of traditional methods and offers compounds with higher 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.
Contained in the library are leading modulators, each labelled with 38 ADME-Tox and 32 physicochemical and drug-likeness qualities. In addition, each compound is illustrated with its optimal docking poses, affinity scores, and activity scores, giving a complete picture.
Our top-notch dedicated system is used to design specialised libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our strategy employs molecular simulations to explore an extensive range of proteins, capturing their dynamics both individually and within complexes with other proteins. Through ensemble virtual screening, we address proteins' conformational mobility, uncovering key binding sites at both functional regions and remote allosteric locations. This comprehensive investigation ensures a thorough assessment of all potential mechanisms of action, with the goal of discovering innovative therapeutic targets and lead molecules across across diverse biological functions.
Several key aspects differentiate our library:
partner
Reaxense
upacc
P12110
UPID:
CO6A2_HUMAN
Alternative names:
-
Alternative UPACC:
P12110; Q13909; Q13910; Q13911; Q14048; Q14049; Q16259; Q16597; Q6P0Q1; Q9UML3; Q9Y4S8
Background:
Collagen alpha-2(VI) chain, encoded by the gene with accession number P12110, plays a pivotal role as a cell-binding protein. This protein is integral to the structural integrity and function of connective tissues.
Therapeutic significance:
Linked to Bethlem myopathy 1, Ullrich congenital muscular dystrophy 1, and Myosclerosis autosomal recessive, Collagen alpha-2(VI) chain's dysfunction underscores its therapeutic potential. Targeting the pathways involving this protein could lead to innovative treatments for these connective tissue disorders.