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Synthesis of a Cholesteryl-HEG Phosphoramidite Derivative and Its Application to Lipid-conjugates of the Anti-HIV (5')TGGGAG(3') Hotoda’s Sequence
A novel phosphoramidite derivative of cholesterol, with an ether-linked hexaethylene glycol (HEG) spacer arm, has been obtained through simple and reproducible solid phase modified oligonucleotide synthesis manipulations. This building block and the known phosphoramidite derivative of 3β-(2-hydroxye...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268758/ https://www.ncbi.nlm.nih.gov/pubmed/23090019 http://dx.doi.org/10.3390/molecules171012378 |
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author | Musumeci, Domenica Montesarchio, Daniela |
author_facet | Musumeci, Domenica Montesarchio, Daniela |
author_sort | Musumeci, Domenica |
collection | PubMed |
description | A novel phosphoramidite derivative of cholesterol, with an ether-linked hexaethylene glycol (HEG) spacer arm, has been obtained through simple and reproducible solid phase modified oligonucleotide synthesis manipulations. This building block and the known phosphoramidite derivative of 3β-(2-hydroxyethoxy)cholesterol have been exploited in standard oligonucleotide synthesis protocols for the preparation of 5'- conjugates of the G-quadruplex-forming (5)(')TGGGAG(3)(') oligomer, known as the Hotoda’s sequence, to produce new potential anti-HIV agents. |
format | Online Article Text |
id | pubmed-6268758 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62687582018-12-12 Synthesis of a Cholesteryl-HEG Phosphoramidite Derivative and Its Application to Lipid-conjugates of the Anti-HIV (5')TGGGAG(3') Hotoda’s Sequence Musumeci, Domenica Montesarchio, Daniela Molecules Article A novel phosphoramidite derivative of cholesterol, with an ether-linked hexaethylene glycol (HEG) spacer arm, has been obtained through simple and reproducible solid phase modified oligonucleotide synthesis manipulations. This building block and the known phosphoramidite derivative of 3β-(2-hydroxyethoxy)cholesterol have been exploited in standard oligonucleotide synthesis protocols for the preparation of 5'- conjugates of the G-quadruplex-forming (5)(')TGGGAG(3)(') oligomer, known as the Hotoda’s sequence, to produce new potential anti-HIV agents. MDPI 2012-10-22 /pmc/articles/PMC6268758/ /pubmed/23090019 http://dx.doi.org/10.3390/molecules171012378 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Musumeci, Domenica Montesarchio, Daniela Synthesis of a Cholesteryl-HEG Phosphoramidite Derivative and Its Application to Lipid-conjugates of the Anti-HIV (5')TGGGAG(3') Hotoda’s Sequence |
title | Synthesis of a Cholesteryl-HEG Phosphoramidite Derivative and Its Application to Lipid-conjugates of the Anti-HIV (5')TGGGAG(3') Hotoda’s Sequence |
title_full | Synthesis of a Cholesteryl-HEG Phosphoramidite Derivative and Its Application to Lipid-conjugates of the Anti-HIV (5')TGGGAG(3') Hotoda’s Sequence |
title_fullStr | Synthesis of a Cholesteryl-HEG Phosphoramidite Derivative and Its Application to Lipid-conjugates of the Anti-HIV (5')TGGGAG(3') Hotoda’s Sequence |
title_full_unstemmed | Synthesis of a Cholesteryl-HEG Phosphoramidite Derivative and Its Application to Lipid-conjugates of the Anti-HIV (5')TGGGAG(3') Hotoda’s Sequence |
title_short | Synthesis of a Cholesteryl-HEG Phosphoramidite Derivative and Its Application to Lipid-conjugates of the Anti-HIV (5')TGGGAG(3') Hotoda’s Sequence |
title_sort | synthesis of a cholesteryl-heg phosphoramidite derivative and its application to lipid-conjugates of the anti-hiv (5')tgggag(3') hotoda’s sequence |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268758/ https://www.ncbi.nlm.nih.gov/pubmed/23090019 http://dx.doi.org/10.3390/molecules171012378 |
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