Explore the Potential with AI-Driven Innovation
This extensive focused library is tailor-made using the latest virtual screening and parameter assessment technology, operated by the Receptor.AI drug discovery platform. This technique is more effective than traditional methods, offering compounds with improved 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 promising modulators annotated with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Also, each compound is presented with its optimal docking poses, affinity scores, and activity scores, providing a comprehensive overview.
We employ our advanced, specialised process to create targeted 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
Q6SZW1
UPID:
SARM1_HUMAN
Alternative names:
NADP(+) hydrolase SARM1; Sterile alpha and Armadillo repeat protein; Sterile alpha and TIR motif-containing protein 1; Sterile alpha motif domain-containing protein 2; Tir-1 homolog
Alternative UPACC:
Q6SZW1; O60277; Q7LGG3; Q9NXY5
Background:
NAD(+) hydrolase SARM1, also known as Sterile alpha and TIR motif-containing protein 1, plays a pivotal role in axonal degeneration by regulating NAD(+) metabolism. It acts as a negative regulator of toll-like receptor signaling pathway, promoting Wallerian degeneration, a form of programmed axon destruction following injury. This process is triggered by NAD(+) depletion, leading to cytoskeletal degradation.
Therapeutic significance:
Understanding the role of NAD(+) hydrolase SARM1 could open doors to potential therapeutic strategies. Its involvement in axonal degeneration and neuronal cell death highlights its significance in neurodegenerative diseases and injury recovery processes.