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Updated: Jun 24, 2026

Methods for the Discovery of Novel Compounds Modulating a Gamma-Aminobutyric Acid Receptor Type A Neurotransmission
Published on: August 16, 2018
Exploring the PI3K alpha and gamma binding sites with 2,6-disubstituted isonicotinic derivatives
Philip T Cherian1, Leonid N Koikov, Matthew D Wortman
1The James L. Winkle College of Pharmacy, University of Cincinnati, Cincinnati, OH 45267, USA.
Abstract:
A homology model of the p110alpha catalytic subunit of PI3Kalpha was generated from the p110gamma crystal structure. Using this model, an isonicotinic scaffold was designed for chemically exploring the PI3Kalpha and gamma binding sites. A focused library of derivatives was synthesized and tested. The morpholine acids 5a and 5b proved to be the most potent analogs.
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