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 pick out particular compounds from an extensive virtual database of more than 60 billion molecules. The preparation and shipment of these compounds are facilitated by our associate 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
It includes comprehensive molecular simulations of the catalytic and allosteric binding pockets and the ensemble virtual screening accounting for their conformational mobility. In the case of designing modulators, the structural changes induced by reaction intermediates are taken into account to leverage activity and selectivity.
Our library distinguishes itself through several key aspects:
partner
Reaxense
upacc
Q9H6V9
UPID:
LDAH_HUMAN
Alternative names:
Lipid droplet-associated serine hydrolase
Alternative UPACC:
Q9H6V9; B7ZA47; B7ZAJ5; D6W530; E7ESN0; Q53T37; Q53T58
Background:
The Lipid droplet-associated hydrolase, alternatively known as Lipid droplet-associated serine hydrolase, is identified by its probable function as a serine lipid hydrolase associated with lipid droplets. Despite lacking cholesterol esterase and triglyceride lipase activities, its high expression in macrophage-rich areas of atherosclerotic lesions highlights its potential role in cholesterol ester turnover in macrophages.
Therapeutic significance:
Understanding the role of Lipid droplet-associated hydrolase could open doors to potential therapeutic strategies, particularly in the context of atherosclerosis where its expression is notably high.