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Synthesis of the Nakanishi Ring-Locked Retinoid

An optimized synthetic route to prepare ring-locked retinoid 1a has been developed. We fully describe a purification protocol that provides isomerically pure 1a in support of on-going proof of concept studies for the development of therapeutic agents to treat human ADRP. Additionally, we have found...

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Detalles Bibliográficos
Autores principales: Côté, Jamie B., Quach, Tan D., Demenev, Andrey P., Garvey, David S., Berman, Judd M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4411895/
https://www.ncbi.nlm.nih.gov/pubmed/25954523
http://dx.doi.org/10.1155/2011/826792
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author Côté, Jamie B.
Quach, Tan D.
Demenev, Andrey P.
Garvey, David S.
Berman, Judd M.
author_facet Côté, Jamie B.
Quach, Tan D.
Demenev, Andrey P.
Garvey, David S.
Berman, Judd M.
author_sort Côté, Jamie B.
collection PubMed
description An optimized synthetic route to prepare ring-locked retinoid 1a has been developed. We fully describe a purification protocol that provides isomerically pure 1a in support of on-going proof of concept studies for the development of therapeutic agents to treat human ADRP. Additionally, we have found that isomerically pure 1a can be stored in amber vials under argon at −20°C for use over time (up to six months) without degradation. Thus, enabling 1a to be an accessible and valuable biological tool.
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spelling pubmed-44118952015-05-07 Synthesis of the Nakanishi Ring-Locked Retinoid Côté, Jamie B. Quach, Tan D. Demenev, Andrey P. Garvey, David S. Berman, Judd M. Int J Med Chem Research Article An optimized synthetic route to prepare ring-locked retinoid 1a has been developed. We fully describe a purification protocol that provides isomerically pure 1a in support of on-going proof of concept studies for the development of therapeutic agents to treat human ADRP. Additionally, we have found that isomerically pure 1a can be stored in amber vials under argon at −20°C for use over time (up to six months) without degradation. Thus, enabling 1a to be an accessible and valuable biological tool. Hindawi Publishing Corporation 2011 2011-10-05 /pmc/articles/PMC4411895/ /pubmed/25954523 http://dx.doi.org/10.1155/2011/826792 Text en Copyright © 2011 Jamie B. Côté et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Côté, Jamie B.
Quach, Tan D.
Demenev, Andrey P.
Garvey, David S.
Berman, Judd M.
Synthesis of the Nakanishi Ring-Locked Retinoid
title Synthesis of the Nakanishi Ring-Locked Retinoid
title_full Synthesis of the Nakanishi Ring-Locked Retinoid
title_fullStr Synthesis of the Nakanishi Ring-Locked Retinoid
title_full_unstemmed Synthesis of the Nakanishi Ring-Locked Retinoid
title_short Synthesis of the Nakanishi Ring-Locked Retinoid
title_sort synthesis of the nakanishi ring-locked retinoid
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4411895/
https://www.ncbi.nlm.nih.gov/pubmed/25954523
http://dx.doi.org/10.1155/2011/826792
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