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The angular structure of ONC201, a TRAIL pathway-inducing compound, determines its potent anti-cancer activity
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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4350349/ https://www.ncbi.nlm.nih.gov/pubmed/25587031 |
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author | Wagner, Jessica Kline, Christina Leah Pottorf, Richard S. Nallaganchu, Bhaskara Rao Olson, Gary L. Dicker, David T. Allen, Joshua E. El-Deiry, Wafik S. |
author_facet | Wagner, Jessica Kline, Christina Leah Pottorf, Richard S. Nallaganchu, Bhaskara Rao Olson, Gary L. Dicker, David T. Allen, Joshua E. El-Deiry, Wafik S. |
author_sort | Wagner, Jessica |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-4350349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-43503492015-03-06 The angular structure of ONC201, a TRAIL pathway-inducing compound, determines its potent anti-cancer activity Wagner, Jessica Kline, Christina Leah Pottorf, Richard S. Nallaganchu, Bhaskara Rao Olson, Gary L. Dicker, David T. Allen, Joshua E. El-Deiry, Wafik S. Oncotarget Research Paper 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. Impact Journals LLC 2015-01-13 /pmc/articles/PMC4350349/ /pubmed/25587031 Text en Copyright: © 2014 Wagner et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited |
spellingShingle | Research Paper Wagner, Jessica Kline, Christina Leah Pottorf, Richard S. Nallaganchu, Bhaskara Rao Olson, Gary L. Dicker, David T. Allen, Joshua E. El-Deiry, Wafik S. The angular structure of ONC201, a TRAIL pathway-inducing compound, determines its potent anti-cancer activity |
title | The angular structure of ONC201, a TRAIL pathway-inducing compound, determines its potent anti-cancer activity |
title_full | The angular structure of ONC201, a TRAIL pathway-inducing compound, determines its potent anti-cancer activity |
title_fullStr | The angular structure of ONC201, a TRAIL pathway-inducing compound, determines its potent anti-cancer activity |
title_full_unstemmed | The angular structure of ONC201, a TRAIL pathway-inducing compound, determines its potent anti-cancer activity |
title_short | The angular structure of ONC201, a TRAIL pathway-inducing compound, determines its potent anti-cancer activity |
title_sort | angular structure of onc201, a trail pathway-inducing compound, determines its potent anti-cancer activity |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4350349/ https://www.ncbi.nlm.nih.gov/pubmed/25587031 |
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