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.
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.
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.
Our high-tech, dedicated method is applied to construct targeted libraries for enzymes.
Fig. 1. The sreening workflow of Receptor.AI
The method includes detailed molecular simulations of the catalytic and allosteric binding pockets, along with ensemble virtual screening that considers their conformational flexibility. In the design of modulators, structural changes induced by reaction intermediates are taken into account to enhance activity and selectivity.
Our library stands out due to several important features:
partner
Reaxense
upacc
Q9Y227
UPID:
ENTP4_HUMAN
Alternative names:
Golgi UDPase; Lysosomal apyrase-like protein of 70 kDa; Uridine-diphosphatase
Alternative UPACC:
Q9Y227; D3DSS3; O15092
Background:
Ectonucleoside triphosphate diphosphohydrolase 4, known by alternative names such as Golgi UDPase, Lysosomal apyrase-like protein of 70 kDa, and Uridine-diphosphatase, plays a crucial role in cellular processes. It catalyzes the hydrolysis of nucleoside triphosphates and diphosphates in a calcium- or magnesium-dependent manner, showing a preference for pyrimidines and specifically hydrolyzing UTP and TTP. This enzyme is preferentially activated by Ca(2+) over Mg(2+), highlighting its unique substrate specificity and activation requirements.
Therapeutic significance:
Understanding the role of Ectonucleoside triphosphate diphosphohydrolase 4 could open doors to potential therapeutic strategies.