Explore the Potential with AI-Driven Innovation
Our detailed focused library is generated on demand with advanced virtual screening and parameter assessment technology powered by the Receptor.AI drug discovery platform. This method surpasses traditional approaches, delivering compounds of better quality with enhanced 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 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 top-notch dedicated system is used to design specialised 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
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.