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Multicomponent synthesis of artificial nucleases and their RNase and DNase activity
The synthesis of new, artificial ribonucleases containing two amino acid residues connected by an aliphatic linker has been developed. Target molecules were synthesized via a catalytic three-component Ugi reaction from aliphatic diisocyanides. Preliminary investigations proved unspecific nuclease ac...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170195/ https://www.ncbi.nlm.nih.gov/pubmed/21915218 http://dx.doi.org/10.3762/bjoc.7.131 |
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author | Gulevich, Anton V Koroleva, Lyudmila S Morozova, Olga V Bakhvalova, Valentina N Silnikov, Vladimir N Nenajdenko, Valentine G |
author_facet | Gulevich, Anton V Koroleva, Lyudmila S Morozova, Olga V Bakhvalova, Valentina N Silnikov, Vladimir N Nenajdenko, Valentine G |
author_sort | Gulevich, Anton V |
collection | PubMed |
description | The synthesis of new, artificial ribonucleases containing two amino acid residues connected by an aliphatic linker has been developed. Target molecules were synthesized via a catalytic three-component Ugi reaction from aliphatic diisocyanides. Preliminary investigations proved unspecific nuclease activity of the new compounds towards single-stranded RNA and double-stranded circular DNA. |
format | Online Article Text |
id | pubmed-3170195 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-31701952011-09-13 Multicomponent synthesis of artificial nucleases and their RNase and DNase activity Gulevich, Anton V Koroleva, Lyudmila S Morozova, Olga V Bakhvalova, Valentina N Silnikov, Vladimir N Nenajdenko, Valentine G Beilstein J Org Chem Full Research Paper The synthesis of new, artificial ribonucleases containing two amino acid residues connected by an aliphatic linker has been developed. Target molecules were synthesized via a catalytic three-component Ugi reaction from aliphatic diisocyanides. Preliminary investigations proved unspecific nuclease activity of the new compounds towards single-stranded RNA and double-stranded circular DNA. Beilstein-Institut 2011-08-19 /pmc/articles/PMC3170195/ /pubmed/21915218 http://dx.doi.org/10.3762/bjoc.7.131 Text en Copyright © 2011, Gulevich et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Gulevich, Anton V Koroleva, Lyudmila S Morozova, Olga V Bakhvalova, Valentina N Silnikov, Vladimir N Nenajdenko, Valentine G Multicomponent synthesis of artificial nucleases and their RNase and DNase activity |
title | Multicomponent synthesis of artificial nucleases and their RNase and DNase activity |
title_full | Multicomponent synthesis of artificial nucleases and their RNase and DNase activity |
title_fullStr | Multicomponent synthesis of artificial nucleases and their RNase and DNase activity |
title_full_unstemmed | Multicomponent synthesis of artificial nucleases and their RNase and DNase activity |
title_short | Multicomponent synthesis of artificial nucleases and their RNase and DNase activity |
title_sort | multicomponent synthesis of artificial nucleases and their rnase and dnase activity |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170195/ https://www.ncbi.nlm.nih.gov/pubmed/21915218 http://dx.doi.org/10.3762/bjoc.7.131 |
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