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.
Our selection of compounds is from a large virtual library of over 60 billion molecules. The production and distribution of these compounds are managed by our partner Reaxense.
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 use our state-of-the-art dedicated workflow for designing focused 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
Q9H2I8
UPID:
LRMDA_HUMAN
Alternative names:
-
Alternative UPACC:
Q9H2I8; B1AVW6
Background:
The Leucine-rich melanocyte differentiation-associated protein plays a pivotal role in melanocyte differentiation, a critical process in the development of skin, hair, and eye pigmentation. This protein's unique structure and function underscore its importance in the biosynthesis of melanin, the pigment responsible for coloration in these tissues.
Therapeutic significance:
Given its crucial role in melanin production, mutations affecting this protein lead to Albinism, oculocutaneous, 7, a disorder characterized by reduced pigmentation and ocular abnormalities. Understanding the role of Leucine-rich melanocyte differentiation-associated protein could open doors to potential therapeutic strategies for albinism and related pigmentary disorders.