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.
In the library, a selection of top modulators is provided, each marked with 38 ADME-Tox and 32 parameters related to physicochemical properties and drug-likeness. Also, every compound comes with its best docking poses, affinity scores, and activity scores, providing a comprehensive overview.
We employ our advanced, specialised process to create targeted libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our methodology employs molecular simulations to explore a wide array of proteins, capturing their dynamic states both individually and within complexes. Through ensemble virtual screening, we address conformational mobility, uncovering binding sites within functional regions and remote allosteric locations. This thorough exploration ensures no potential mechanism of action is overlooked, aiming to discover novel therapeutic targets and lead compounds across an extensive spectrum of biological functions.
Several key aspects differentiate our library:
partner
Reaxense
upacc
P55011
UPID:
S12A2_HUMAN
Alternative names:
Basolateral Na-K-Cl symporter; Bumetanide-sensitive sodium-(potassium)-chloride cotransporter 2
Alternative UPACC:
P55011; Q8N713; Q8WWH7
Background:
Solute carrier family 12 member 2, also known as the Basolateral Na-K-Cl symporter or Bumetanide-sensitive sodium-(potassium)-chloride cotransporter 2, plays a crucial role in the electroneutral transport of chloride, potassium, and/or sodium ions across the membrane. This protein is pivotal in maintaining ionic balance and cell volume, showcasing its fundamental role in cellular physiology.
Therapeutic significance:
Linked to diseases such as Deafness, autosomal dominant, 78, Delpire-McNeill syndrome, and Kilquist syndrome, this protein's dysfunction underscores its importance in neurodevelopmental disorders and sensorineural hearing loss. Understanding the role of Solute carrier family 12 member 2 could pave the way for innovative therapeutic strategies targeting these conditions.