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 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.
The library features a range of promising modulators, each detailed with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Plus, each compound is presented with its ideal docking poses, affinity scores, and activity scores, ensuring a thorough insight.
We utilise our cutting-edge, exclusive workflow to develop focused libraries for enzymes.
Fig. 1. The sreening workflow of Receptor.AI
This approach involves comprehensive molecular simulations of the catalytic and allosteric binding pockets and ensemble virtual screening that accounts for their conformational flexibility. In the case of designing modulators, the structural adjustments caused by reaction intermediates are considered to improve activity and selectivity.
Our library distinguishes itself through several key aspects:
partner
Reaxense
upacc
Q02083
UPID:
NAAA_HUMAN
Alternative names:
Acid ceramidase-like protein; Acylsphingosine deacylase NAAA; N-acylsphingosine amidohydrolase-like
Alternative UPACC:
Q02083; Q5KTF2; Q96EY2; Q9BRA8
Background:
N-acylethanolamine-hydrolyzing acid amidase, also known as Acid ceramidase-like protein, Acylsphingosine deacylase NAAA, and N-acylsphingosine amidohydrolase-like, plays a crucial role in the degradation of bioactive fatty acid amides. It preferentially targets N-palmitoylethanolamine among others, and exhibits activity against certain ceramides, highlighting its importance in lipid metabolism.
Therapeutic significance:
Understanding the role of N-acylethanolamine-hydrolyzing acid amidase could open doors to potential therapeutic strategies. Its involvement in lipid metabolism suggests a pivotal function that could be leveraged in disease management and treatment innovation.