Please join us for a webinar "Hit Discovery for GPCRs: HTS or Virtual Screens?” presented by Guest Speaker, Carleton Sage, Ph.D., Vice President of Computational Sciences at Eurofins, Beacon Discovery on Thursday, June 24, 2021, at the following times:
- 4 - 5 p.m. | Central European Summer Time (CET)
- 3 - 4 p.m. | British Summer Time (BST)
- 10 – 11 a.m. | U.S. Eastern Daylight Time (EDT)
- 9 – 10 a.m. | U.S. Central Daylight Time (CDT)
- 8 – 9 a.m. | U.S. Mountain Daylight Time (MDT)
- 7 – 8 a.m. | U.S. Pacific Daylight Time (PDT)
G protein-coupled receptors (GPCRs) constitute the largest class of transmembrane proteins in the human genome and play important roles in disease pathogenesis, and therefore are one of the largest classes of drug targets including blockbuster drugs such as Cimetidine, Olanzapine and Clopidogrel. Over 100 GPCRs in the human genome are classified as orphans: receptors whose endogenous ligands and biological function remain unknown, thus these targets represent promising, yet challenging targets for drug discovery.
We will present examples of diverse and complementary approaches to hit discovery performed in two ongoing drug discovery projects: We will discuss both our HTS campaign for the orphan receptor GPCR174 including target rationale, assay development requirements and challenges, hit identification, and hit confirmation and validation. In addition, we will address how we approached the Serotonin 2B receptor, discussing the target selection rationale, a massive virtual screening approach including validation of docking approaches as well as shape and chemical features for hit identification, assay development for hit validation, and early lead series identification.
Please register for the webinar, which will be hosted through GoToWebinar.
For those who are unable to attend the “live” webinar, a recording of the webinar also will be available. To receive the link to the recorded webinar, please register for the webinar.
We hope you can attend.