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.
We utilise our cutting-edge, exclusive workflow to develop focused libraries for enzymes.
Fig. 1. The sreening workflow of Receptor.AI
The procedure entails thorough molecular simulations of the catalytic and allosteric binding pockets, accompanied by ensemble virtual screening that factors in their conformational flexibility. When developing modulators, the structural modifications brought about by reaction intermediates are factored in to optimize activity and selectivity.
Key features that set our library apart include:
partner
Reaxense
upacc
Q8N6T7
UPID:
SIR6_HUMAN
Alternative names:
NAD-dependent protein deacetylase sirtuin-6; Protein mono-ADP-ribosyltransferase sirtuin-6; Regulatory protein SIR2 homolog 6; SIR2-like protein 6
Alternative UPACC:
Q8N6T7; B2RCD0; O75291; Q6IAF5; Q6PK99; Q8NCD2; Q9BSI5; Q9BWP3; Q9NRC7; Q9UQD1
Background:
NAD-dependent protein deacylase sirtuin-6, known as SIRT6, is pivotal in DNA repair, metabolic regulation, and aging. It exhibits deacetylase, deacylase, and mono-ADP-ribosyltransferase activities, influencing gene expression, inflammation, and tumorigenesis. SIRT6 modulates histone deacetylation, crucial for DNA damage repair and telomere maintenance, and plays a significant role in metabolic processes.
Therapeutic significance:
Understanding the role of NAD-dependent protein deacylase sirtuin-6 could open doors to potential therapeutic strategies.