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 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.
Our top-notch dedicated system is used to design specialised libraries.
Fig. 1. The sreening workflow of Receptor.AI
Utilising molecular simulations, our approach thoroughly examines a wide array of proteins, tracking their conformational changes individually and within complexes. Ensemble virtual screening enables us to address conformational flexibility, revealing essential binding sites at functional regions and allosteric locations. Our rigorous analysis guarantees that no potential mechanism of action is overlooked, aiming to uncover new therapeutic targets and lead compounds across diverse biological functions.
Our library stands out due to several important features:
partner
Reaxense
upacc
P01160
UPID:
ANF_HUMAN
Alternative names:
Atrial natriuretic factor prohormone; Atrial natriuretic peptide prohormone; Atriopeptigen; Cardiodilatin; preproCDD-ANF
Alternative UPACC:
P01160; Q13766; Q5JZE1
Background:
Natriuretic peptides A, known by various names such as Atrial natriuretic factor prohormone and Cardiodilatin, plays a pivotal role in cardio-renal homeostasis. It regulates blood pressure, fluid-electrolyte balance, and inhibits aldosterone synthesis through its actions on vasodilation, natriuresis, and diuresis. Its ability to bind and stimulate NPR1 to produce cGMP, activating effector proteins like PRKG1, underscores its significance in vascular remodeling and energy metabolism.
Therapeutic significance:
Linked to diseases such as Atrial standstill 2 and Familial atrial fibrillation, Natriuretic peptides A's involvement in arrhythmias and cardiac rhythm disturbances highlights its potential as a target for therapeutic intervention. Understanding the role of Natriuretic peptides A could open doors to potential therapeutic strategies, especially in cardiovascular disorders.