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.
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.
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.
We utilise our cutting-edge, exclusive workflow to develop focused libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our methodology leverages molecular simulations to examine a vast array of proteins, capturing their dynamics in both isolated forms and in complexes with other proteins. Through ensemble virtual screening, we thoroughly account for the protein's conformational mobility, identifying critical binding sites within functional regions and distant allosteric locations. This detailed exploration ensures that we comprehensively assess every possible mechanism of action, with the objective of identifying novel therapeutic targets and lead compounds that span a wide spectrum of biological functions.
Key features that set our library apart include:
partner
Reaxense
upacc
Q9H3U7
UPID:
SMOC2_HUMAN
Alternative names:
Secreted modular calcium-binding protein 2; Smooth muscle-associated protein 2
Alternative UPACC:
Q9H3U7; B3KPS7; Q4G169; Q5TAT7; Q5TAT8; Q86VV9; Q96SF3; Q9H1L3; Q9H1L4; Q9H3U0; Q9H4F7; Q9HCV2
Background:
SPARC-related modular calcium-binding protein 2, also known as Secreted modular calcium-binding protein 2 or Smooth muscle-associated protein 2, plays a crucial role in matrix assembly and cell adhesiveness. This protein, by similarity, is known to stimulate endothelial cell proliferation, migration, and angiogenesis, showcasing its vital role in vascular biology.
Therapeutic significance:
Linked to Dentin dysplasia 1, a dental defect characterized by inadequate root formation and potential tooth exfoliation, this protein's gene variants highlight its clinical importance. Understanding the role of SPARC-related modular calcium-binding protein 2 could open doors to potential therapeutic strategies for dental and bone diseases.