Explore the Potential with AI-Driven Innovation
This comprehensive focused library is produced on demand with state-of-the-art virtual screening and parameter assessment technology driven by Receptor.AI drug discovery platform. This approach outperforms traditional methods and provides higher-quality compounds with superior 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.
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 employ our advanced, specialised process to create targeted libraries for enzymes.
Fig. 1. The sreening workflow of Receptor.AI
It includes in-depth molecular simulations of both the catalytic and allosteric binding pockets, with ensemble virtual screening focusing on their conformational flexibility. For modulators, the process includes considering the structural shifts due to reaction intermediates to boost activity and selectivity.
Key features that set our library apart include:
partner
Reaxense
upacc
Q99487
UPID:
PAFA2_HUMAN
Alternative names:
PAF:lysophospholipid transacetylase; PAF:sphingosine transacetylase; Platelet-activating factor acetyltransferase PAFAH2; Serine-dependent phospholipase A2
Alternative UPACC:
Q99487; D3DPK1; O15458; Q5SY02
Background:
Platelet-activating factor acetylhydrolase 2, cytoplasmic (PAFAH2) plays a pivotal role in lipid metabolism by hydrolyzing the acetyl group at the sn-2 position of platelet-activating factor (PAF) and its analogs. This enzymatic action leads to the inactivation of PAF, a potent phospholipid activator involved in various biological processes. PAFAH2 exhibits specificity for phospholipids with short acyl chains and is capable of catalyzing transacetylation reactions, producing plasmalogen analogs of PAF and N-acetylsphingosine.
Therapeutic significance:
Understanding the role of Platelet-activating factor acetylhydrolase 2, cytoplasmic could open doors to potential therapeutic strategies. Its involvement in lipid metabolism and the regulation of bioactive lipids highlights its potential as a target for modulating inflammatory responses and other PAF-related pathologies.