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.
The compounds are cherry-picked from the vast virtual chemical space of over 60B molecules. The synthesis and delivery of compounds is facilitated by our partner Reaxense.
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 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.
Several key aspects differentiate our library:
partner
Reaxense
upacc
P78536
UPID:
ADA17_HUMAN
Alternative names:
Snake venom-like protease; TNF-alpha convertase; TNF-alpha-converting enzyme
Alternative UPACC:
P78536; O60226
Background:
Disintegrin and metalloproteinase domain-containing protein 17, also known as TNF-alpha convertase, plays a pivotal role in the cleavage of membrane-bound precursors to their mature soluble forms. It is involved in the release of several cell-surface proteins, including TNF-receptor, interleukin 1 receptor type II, and the amyloid precursor protein. This enzyme is also an activator of the Notch pathway, crucial for cell differentiation.
Therapeutic significance:
The protein's involvement in Inflammatory skin and bowel disease, neonatal, 1, underscores its potential as a therapeutic target. Understanding the role of Disintegrin and metalloproteinase domain-containing protein 17 could open doors to potential therapeutic strategies for managing this disorder.