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.
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.
Our top-notch dedicated system is used to design specialised libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our methodology leverages molecular simulations to examine a vast array of proteins, capturing their dynamics in both isolated forms and in complexes with other proteins. Through ensemble virtual screening, we thoroughly account for the protein's conformational mobility, identifying critical binding sites within functional regions and distant allosteric locations. This detailed exploration ensures that we comprehensively assess every possible mechanism of action, with the objective of identifying novel therapeutic targets and lead compounds that span a wide spectrum of biological functions.
Our library distinguishes itself through several key aspects:
partner
Reaxense
upacc
Q9NTN3
UPID:
S35D1_HUMAN
Alternative names:
Solute carrier family 35 member D1; UDP-galactose transporter-related protein 7; UDP-glucuronic acid/UDP-N-acetylgalactosamine transporter
Alternative UPACC:
Q9NTN3; A8K185; B7Z3X2; Q52LU5; Q92548
Background:
The Nucleotide sugar transporter SLC35D1, also known as Solute carrier family 35 member D1, UDP-galactose transporter-related protein 7, and UDP-glucuronic acid/UDP-N-acetylgalactosamine transporter, plays a crucial role in the transport of nucleotide sugars across the endoplasmic reticulum membrane. This process is vital for the synthesis of glycoproteins, glycolipids, and oligosaccharides, contributing to the formation of cartilage extracellular matrix and normal skeletal development.
Therapeutic significance:
SLC35D1's involvement in Schneckenbecken dysplasia, a rare skeletal dysplasia, underscores its potential as a target for therapeutic intervention. Understanding the role of SLC35D1 could open doors to potential therapeutic strategies for skeletal dysplasias and related disorders.