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spelling paper:paper_01633864_v67_n5_p778_Viturro2023-06-08T15:14:16Z 5-Methylcoumaranones from Mutisia friesiana and their bioactivity Maier, Marta Silvia 5 methylcoumaranone 5 methylcoumaranone a 5 methylcoumaranone b 5 methylcoumaranone c 5 methylcoumaranone d mutisicoumaranone a mutisicoumaranone b mutisicoumaranone c mutisicoumaranone d plant extract unclassified drug antifungal activity article bactericidal activity carbon nuclear magnetic resonance chemical structure Cladosporium cucumerinum drug activity Mutisia friesiana plant proton nuclear magnetic resonance spectroscopy Staphylococcus aureus structure analysis woody stem Antibiotics, Antifungal Antifungal Agents Argentina Asteraceae Benzofurans Cladosporium Microbial Sensitivity Tests Molecular Structure Nuclear Magnetic Resonance, Biomolecular Plants, Medicinal Staphylococcus aureus Cladosporium Cladosporium cucumerinum Fungi Mutisia Staphylococcus Staphylococcus aureus In addition to the known mutisicoumaranones A (1) and B (2), the methanolic extract of the aerial parts of the shrub Mutisia friesiana afforded two new 5-methylcoumaranones, mutisicoumaranones C (3) and D (4). Their structures were elucidated by spectroscopic methods. 13C NMR data for mutisicoumaranones A and B are reported for the first time. All compounds showed antifungal activity against the phytopathogenic fungus Cladosporium cucumerinum and bactericidal activity against Staphylococcus aureus. The presence of 5-methylcoumaranones A-D is biosynthetically related to 5-methylcoumarins and phenolic derivatives previously isolated from M. friesiana. Fil:Maier, M.S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2004 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01633864_v67_n5_p778_Viturro http://hdl.handle.net/20.500.12110/paper_01633864_v67_n5_p778_Viturro
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic 5 methylcoumaranone
5 methylcoumaranone a
5 methylcoumaranone b
5 methylcoumaranone c
5 methylcoumaranone d
mutisicoumaranone a
mutisicoumaranone b
mutisicoumaranone c
mutisicoumaranone d
plant extract
unclassified drug
antifungal activity
article
bactericidal activity
carbon nuclear magnetic resonance
chemical structure
Cladosporium cucumerinum
drug activity
Mutisia friesiana
plant
proton nuclear magnetic resonance
spectroscopy
Staphylococcus aureus
structure analysis
woody stem
Antibiotics, Antifungal
Antifungal Agents
Argentina
Asteraceae
Benzofurans
Cladosporium
Microbial Sensitivity Tests
Molecular Structure
Nuclear Magnetic Resonance, Biomolecular
Plants, Medicinal
Staphylococcus aureus
Cladosporium
Cladosporium cucumerinum
Fungi
Mutisia
Staphylococcus
Staphylococcus aureus
spellingShingle 5 methylcoumaranone
5 methylcoumaranone a
5 methylcoumaranone b
5 methylcoumaranone c
5 methylcoumaranone d
mutisicoumaranone a
mutisicoumaranone b
mutisicoumaranone c
mutisicoumaranone d
plant extract
unclassified drug
antifungal activity
article
bactericidal activity
carbon nuclear magnetic resonance
chemical structure
Cladosporium cucumerinum
drug activity
Mutisia friesiana
plant
proton nuclear magnetic resonance
spectroscopy
Staphylococcus aureus
structure analysis
woody stem
Antibiotics, Antifungal
Antifungal Agents
Argentina
Asteraceae
Benzofurans
Cladosporium
Microbial Sensitivity Tests
Molecular Structure
Nuclear Magnetic Resonance, Biomolecular
Plants, Medicinal
Staphylococcus aureus
Cladosporium
Cladosporium cucumerinum
Fungi
Mutisia
Staphylococcus
Staphylococcus aureus
Maier, Marta Silvia
5-Methylcoumaranones from Mutisia friesiana and their bioactivity
topic_facet 5 methylcoumaranone
5 methylcoumaranone a
5 methylcoumaranone b
5 methylcoumaranone c
5 methylcoumaranone d
mutisicoumaranone a
mutisicoumaranone b
mutisicoumaranone c
mutisicoumaranone d
plant extract
unclassified drug
antifungal activity
article
bactericidal activity
carbon nuclear magnetic resonance
chemical structure
Cladosporium cucumerinum
drug activity
Mutisia friesiana
plant
proton nuclear magnetic resonance
spectroscopy
Staphylococcus aureus
structure analysis
woody stem
Antibiotics, Antifungal
Antifungal Agents
Argentina
Asteraceae
Benzofurans
Cladosporium
Microbial Sensitivity Tests
Molecular Structure
Nuclear Magnetic Resonance, Biomolecular
Plants, Medicinal
Staphylococcus aureus
Cladosporium
Cladosporium cucumerinum
Fungi
Mutisia
Staphylococcus
Staphylococcus aureus
description In addition to the known mutisicoumaranones A (1) and B (2), the methanolic extract of the aerial parts of the shrub Mutisia friesiana afforded two new 5-methylcoumaranones, mutisicoumaranones C (3) and D (4). Their structures were elucidated by spectroscopic methods. 13C NMR data for mutisicoumaranones A and B are reported for the first time. All compounds showed antifungal activity against the phytopathogenic fungus Cladosporium cucumerinum and bactericidal activity against Staphylococcus aureus. The presence of 5-methylcoumaranones A-D is biosynthetically related to 5-methylcoumarins and phenolic derivatives previously isolated from M. friesiana.
author Maier, Marta Silvia
author_facet Maier, Marta Silvia
author_sort Maier, Marta Silvia
title 5-Methylcoumaranones from Mutisia friesiana and their bioactivity
title_short 5-Methylcoumaranones from Mutisia friesiana and their bioactivity
title_full 5-Methylcoumaranones from Mutisia friesiana and their bioactivity
title_fullStr 5-Methylcoumaranones from Mutisia friesiana and their bioactivity
title_full_unstemmed 5-Methylcoumaranones from Mutisia friesiana and their bioactivity
title_sort 5-methylcoumaranones from mutisia friesiana and their bioactivity
publishDate 2004
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01633864_v67_n5_p778_Viturro
http://hdl.handle.net/20.500.12110/paper_01633864_v67_n5_p778_Viturro
work_keys_str_mv AT maiermartasilvia 5methylcoumaranonesfrommutisiafriesianaandtheirbioactivity
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