Explore the Potential with AI-Driven Innovation
The focused library is created on demand with the latest virtual screening and parameter assessment technology, supported by the Receptor.AI drug discovery platform. This method is more effective than traditional methods and results in higher-quality compounds with better 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 effective modulators, each annotated with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Furthermore, each compound is shown with its optimal docking poses, affinity scores, and activity scores, offering a detailed summary.
Our high-tech, dedicated method is applied to construct targeted 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.
Our library is unique due to several crucial aspects:
partner
Reaxense
upacc
P10745
UPID:
RET3_HUMAN
Alternative names:
Interphotoreceptor retinoid-binding protein; Interstitial retinol-binding protein
Alternative UPACC:
P10745; Q0QD34; Q5VSR0; Q8IXN0
Background:
Retinol-binding protein 3, also known as Interphotoreceptor retinoid-binding protein or Interstitial retinol-binding protein, plays a crucial role in the visual cycle. It is responsible for the transport of 11-cis and all-trans retinoids between the retinol isomerase in the pigment epithelium and the visual pigments in the photoreceptor cells of the retina, facilitating the conversion of light into visual signals.
Therapeutic significance:
Retinol-binding protein 3 is directly associated with Retinitis pigmentosa 66, a retinal dystrophy characterized by loss of vision and pigment deposits in the retina. Understanding the role of this protein could lead to novel therapeutic strategies for treating this debilitating disease.