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 pick out particular compounds from an extensive virtual database of more than 60 billion molecules. The preparation and shipment of these compounds are facilitated by our associate Reaxense.
Contained in the library are leading modulators, each labelled with 38 ADME-Tox and 32 physicochemical and drug-likeness qualities. In addition, each compound is illustrated with its optimal docking poses, affinity scores, and activity scores, giving a complete picture.
We use our state-of-the-art dedicated workflow for designing focused libraries for enzymes.
Fig. 1. The sreening workflow of Receptor.AI
It includes in-depth molecular simulations of both the catalytic and allosteric binding pockets, with ensemble virtual screening focusing on their conformational flexibility. For modulators, the process includes considering the structural shifts due to reaction intermediates to boost activity and selectivity.
Several key aspects differentiate our library:
partner
Reaxense
upacc
P05230
UPID:
FGF1_HUMAN
Alternative names:
Acidic fibroblast growth factor; Endothelial cell growth factor; Heparin-binding growth factor 1
Alternative UPACC:
P05230; B2R5T0; D3DQF2; P07502; Q16588
Background:
Fibroblast growth factor 1 (FGF1), also known as acidic fibroblast growth factor, plays a pivotal role in cell survival, division, angiogenesis, differentiation, and migration. It acts as a potent mitogen and ligand for FGFR1 and integrins, initiating signaling cascades essential for cellular processes. Its interaction with FGFR1 and integrins is crucial for its biological functions, including angiogenesis.
Therapeutic significance:
Understanding the role of Fibroblast growth factor 1 could open doors to potential therapeutic strategies. Its involvement in critical cellular processes and angiogenesis highlights its potential as a target for therapeutic intervention in diseases where these processes are dysregulated.