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.
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 utilise our cutting-edge, exclusive workflow to develop 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.
Our library stands out due to several important features:
partner
Reaxense
upacc
P24385
UPID:
CCND1_HUMAN
Alternative names:
B-cell lymphoma 1 protein; BCL-1 oncogene; PRAD1 oncogene
Alternative UPACC:
P24385; Q6LEF0
Background:
G1/S-specific cyclin-D1, also known as B-cell lymphoma 1 protein, BCL-1 oncogene, and PRAD1 oncogene, plays a pivotal role in cell cycle regulation. It forms a complex with CDK4, phosphorylating and inhibiting the retinoblastoma protein family, thus regulating the G(1)/S transition. This protein is also involved in the nuclear translocation and activity of the cyclin D-CDK4 complex.
Therapeutic significance:
G1/S-specific cyclin-D1's aberration is linked to multiple myeloma, characterized by a malignant tumor of plasma cells. Understanding the role of G1/S-specific cyclin-D1 could open doors to potential therapeutic strategies targeting its pathway to treat multiple myeloma.