Abstract

We previously identified TRAIL-inducing compound 10 (TIC10), also known as NSC350625 or ONC201, from a NCI chemical library screen as a small molecule that has potent anti-tumor efficacy and a benign safety profile in preclinical cancer models. The chemical structure that was originally published by Stahle, et. al. in the patent literature was described as an imidazo[1,2-a]pyrido[4,3-d]pyrimidine derivative. The NCI and others generally accepted this as the correct structure, which was consistent with the mass spectrometry analysis outlined in the publication by Allen et. al. that first reported the molecule's anticancer properties. A recent publication demonstrated that the chemical structure of ONC201 material from the NCI is an angular [3,4-e] isomer of the originally disclosed, linear [4,3-d] structure. Here we confirm by NMR and X-ray structural analysis of the dihydrochloride salt form that the ONC201 material produced by Oncoceutics is the angular [3,4-e] structure and not the linear structure originally depicted in the patent literature and by the NCI. Similarly, in accordance with our biological evaluation, the previously disclosed anti-cancer activity is associated with the angular structure and not the linear isomer. Together these studies confirm that ONC201, produced by Oncoceutics or obtained from the NCI, possesses an angular [3,4-e] structure that represents the highly active anti-cancer compound utilized in prior preclinical studies and now entering clinical trials in advanced cancers.

Highlights

  • IntroductionThe endogenous anti-tumor protein TRAIL (tumor necrosis factor-related apoptosis-inducing ligand) was previously investigated as a therapeutic target in oncology due to its ability to activate death receptors in tumor cells, leading to apoptosis [1, 2]

  • The endogenous anti-tumor protein TRAIL was previously investigated as a therapeutic target in oncology due to its ability to activate death receptors in tumor cells, leading to apoptosis [1, 2]

  • After the preclinical studies of ONC201/ NSC350625 revealed its robust anti-tumor effects by activating the TRAIL pathway, we began to observe a disparity between the Oncoceutics and National Cancer Institute (NCI) obtained ONC201 material and material obtained from an alternatively synthesized commercial source

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Summary

Introduction

The endogenous anti-tumor protein TRAIL (tumor necrosis factor-related apoptosis-inducing ligand) was previously investigated as a therapeutic target in oncology due to its ability to activate death receptors in tumor cells, leading to apoptosis [1, 2]. Based on its ability to induce the TRAIL gene, we previously obtained and studied the compound NSC-350625 from the National Cancer Institute (NCI) Diversity Set II, which the NCI depicted as 7-benzyl10-(2-methylbenzyl)-2,6,7,8,9,10-hexahydroimidazo[1,2-a] pyrido[4,3-d]pyrimidin-5(3H)-one [4]. This compound, which is referred to as ONC201 by Oncoceutics, Inc. that is developing the molecule as an anticancer drug, was originally synthesized and described in a patent application published in 1973 without disclosure of biological data [5]. ONC201 possesses numerous ideal www.impactjournals.com/oncotarget drug properties, including a broad spectrum of activity, wide safety margin, robust stability, aqueous solubility, favorable pharmacokinetics, and oral activity; all of which are superior to TRAIL-based therapies and have prompted clinical development of the compound [4]

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