Explore the Potential with AI-Driven Innovation
This comprehensive focused library is produced on demand with state-of-the-art virtual screening and parameter assessment technology driven by Receptor.AI drug discovery platform. This approach outperforms traditional methods and provides higher-quality compounds with superior 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 features a range of promising modulators, each detailed with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Plus, each compound is presented with its ideal docking poses, affinity scores, and activity scores, ensuring a thorough insight.
We use our state-of-the-art dedicated workflow for designing focused 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 is unique due to several crucial aspects:
partner
Reaxense
upacc
O75369
UPID:
FLNB_HUMAN
Alternative names:
ABP-278; ABP-280 homolog; Actin-binding-like protein; Beta-filamin; Filamin homolog 1; Filamin-3; Thyroid autoantigen; Truncated actin-binding protein
Alternative UPACC:
O75369; B2ZZ83; B2ZZ84; B2ZZ85; C9JKE6; C9JMC4; Q13706; Q59EC2; Q60FE7; Q6MZJ1; Q8WXS9; Q8WXT0; Q8WXT1; Q8WXT2; Q8WXT3; Q9NRB5; Q9NT26; Q9UEV9
Background:
Filamin-B, known by alternative names such as ABP-278 and Filamin-3, plays a crucial role in connecting cell membrane constituents to the actin cytoskeleton. It promotes orthogonal branching of actin filaments and anchors various transmembrane proteins to the actin cytoskeleton. Its interaction with FLNA is vital for neuroblast migration, affecting myotube morphology and myogenesis.
Therapeutic significance:
Filamin-B is implicated in a range of skeletal dysplasias, including Atelosteogenesis 1 and 3, Boomerang dysplasia, Larsen syndrome, and Spondylocarpotarsal synostosis syndrome. These associations highlight its potential as a target for therapeutic strategies aimed at treating these debilitating conditions.