Natural Product-Derived Drugs Based on β-Adrenergic Agents and Nucleosides
Autor(a) principal: | |
---|---|
Data de Publicação: | 2016 |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Journal of the Brazilian Chemical Society (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532016000801320 |
Resumo: | This relatively short review demonstrates the very important role of the structures of the natural products adrenaline and relatives, in the design and subsequent approval of β-agonists and antagonists, and of modified nucleosides as anticancer, and in particular, antiviral agents against herpes (HSV), human immunodeficiency virus (HIV) and hepatitis C virus (HCV) that would not have been synthesized in the absence of knowledge of bioactive arabinose nucleosides. |
id |
SBQ-2_3a7a02a5d3813967db2416fe4aa2aa9c |
---|---|
oai_identifier_str |
oai:scielo:S0103-50532016000801320 |
network_acronym_str |
SBQ-2 |
network_name_str |
Journal of the Brazilian Chemical Society (Online) |
repository_id_str |
|
spelling |
Natural Product-Derived Drugs Based on β-Adrenergic Agents and Nucleosidesβ-agonistβ-antagonistnucleosidenatural product-based drugThis relatively short review demonstrates the very important role of the structures of the natural products adrenaline and relatives, in the design and subsequent approval of β-agonists and antagonists, and of modified nucleosides as anticancer, and in particular, antiviral agents against herpes (HSV), human immunodeficiency virus (HIV) and hepatitis C virus (HCV) that would not have been synthesized in the absence of knowledge of bioactive arabinose nucleosides.Sociedade Brasileira de Química2016-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532016000801320Journal of the Brazilian Chemical Society v.27 n.8 2016reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.5935/0103-5053.20160070info:eu-repo/semantics/openAccessNewman,David J.eng2016-08-19T00:00:00Zoai:scielo:S0103-50532016000801320Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2016-08-19T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Natural Product-Derived Drugs Based on β-Adrenergic Agents and Nucleosides |
title |
Natural Product-Derived Drugs Based on β-Adrenergic Agents and Nucleosides |
spellingShingle |
Natural Product-Derived Drugs Based on β-Adrenergic Agents and Nucleosides Newman,David J. β-agonist β-antagonist nucleoside natural product-based drug |
title_short |
Natural Product-Derived Drugs Based on β-Adrenergic Agents and Nucleosides |
title_full |
Natural Product-Derived Drugs Based on β-Adrenergic Agents and Nucleosides |
title_fullStr |
Natural Product-Derived Drugs Based on β-Adrenergic Agents and Nucleosides |
title_full_unstemmed |
Natural Product-Derived Drugs Based on β-Adrenergic Agents and Nucleosides |
title_sort |
Natural Product-Derived Drugs Based on β-Adrenergic Agents and Nucleosides |
author |
Newman,David J. |
author_facet |
Newman,David J. |
author_role |
author |
dc.contributor.author.fl_str_mv |
Newman,David J. |
dc.subject.por.fl_str_mv |
β-agonist β-antagonist nucleoside natural product-based drug |
topic |
β-agonist β-antagonist nucleoside natural product-based drug |
description |
This relatively short review demonstrates the very important role of the structures of the natural products adrenaline and relatives, in the design and subsequent approval of β-agonists and antagonists, and of modified nucleosides as anticancer, and in particular, antiviral agents against herpes (HSV), human immunodeficiency virus (HIV) and hepatitis C virus (HCV) that would not have been synthesized in the absence of knowledge of bioactive arabinose nucleosides. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016-08-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532016000801320 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532016000801320 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.5935/0103-5053.20160070 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Sociedade Brasileira de Química |
publisher.none.fl_str_mv |
Sociedade Brasileira de Química |
dc.source.none.fl_str_mv |
Journal of the Brazilian Chemical Society v.27 n.8 2016 reponame:Journal of the Brazilian Chemical Society (Online) instname:Sociedade Brasileira de Química (SBQ) instacron:SBQ |
instname_str |
Sociedade Brasileira de Química (SBQ) |
instacron_str |
SBQ |
institution |
SBQ |
reponame_str |
Journal of the Brazilian Chemical Society (Online) |
collection |
Journal of the Brazilian Chemical Society (Online) |
repository.name.fl_str_mv |
Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ) |
repository.mail.fl_str_mv |
||office@jbcs.sbq.org.br |
_version_ |
1750318178673623040 |