id todo:paper_01633864_v77_n7_p1579_Fernandez
record_format dspace
spelling todo:paper_01633864_v77_n7_p1579_Fernandez2023-10-03T15:02:18Z Antifungal terpenoids from Hyalis argentea var. latisquama Fernández, L.R. Butassi, E. Svetaz, L. Zacchino, S.A. Palermo, J.A. Sánchez, M. 8alpha,9alpha exposyonoseriolide acetate amphotericin B ent 7alpha hydroxy 15 oxokauran 19 beta dextro glucopyranosyl ester ent 7alpha,15beta dihydroxykaur 16 ene 19 beta dextro glucopyranosyl ester hyalic acid beta dextro glucopyranosyl ester terpenoid derivative unclassified drug antifungal activity article Candida albicans controlled study Cryptococcus neoformans drug identification drug isolation fungus growth growth inhibition Hyalis latisquama medicinal plant nonhuman rhizome Antifungal Agents Asteraceae Candida albicans Cryptococcus neoformans Diterpenes, Kaurane Molecular Structure Sesquiterpenes Sesquiterpenes, Guaiane A detailed chemical study of the aerial parts and rhizomes of Hyalis argentea var. latisquama yielded a variety of sesqui- and diterpenes. In total, 26 compounds were isolated and identified, of which four are new, namely, two ent-kaurenes (1 and 2), a diterpene lactone (3), and a lindenanolide (4). The previously reported compounds included a series of lindenanolides, guaianolides, elemanolides, and additional diterpenes. The antifungal activity of the isolated compounds was tested against Cryptococcus neoformans and Candida albicans. Among the isolated compounds, the lindenanolides were the only structural class that showed strong antifungal activity, and onoseriolide acetate (5) was the most active. On the other hand, the isolated guaianolides were only moderately active, while the diterpenes did not show significant antifungal activity. © 2014 The American Chemical Society and American Society of Pharmacognosy. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_01633864_v77_n7_p1579_Fernandez
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic 8alpha,9alpha exposyonoseriolide acetate
amphotericin B
ent 7alpha hydroxy 15 oxokauran 19 beta dextro glucopyranosyl ester
ent 7alpha,15beta dihydroxykaur 16 ene 19 beta dextro glucopyranosyl ester
hyalic acid beta dextro glucopyranosyl ester
terpenoid derivative
unclassified drug
antifungal activity
article
Candida albicans
controlled study
Cryptococcus neoformans
drug identification
drug isolation
fungus growth
growth inhibition
Hyalis latisquama
medicinal plant
nonhuman
rhizome
Antifungal Agents
Asteraceae
Candida albicans
Cryptococcus neoformans
Diterpenes, Kaurane
Molecular Structure
Sesquiterpenes
Sesquiterpenes, Guaiane
spellingShingle 8alpha,9alpha exposyonoseriolide acetate
amphotericin B
ent 7alpha hydroxy 15 oxokauran 19 beta dextro glucopyranosyl ester
ent 7alpha,15beta dihydroxykaur 16 ene 19 beta dextro glucopyranosyl ester
hyalic acid beta dextro glucopyranosyl ester
terpenoid derivative
unclassified drug
antifungal activity
article
Candida albicans
controlled study
Cryptococcus neoformans
drug identification
drug isolation
fungus growth
growth inhibition
Hyalis latisquama
medicinal plant
nonhuman
rhizome
Antifungal Agents
Asteraceae
Candida albicans
Cryptococcus neoformans
Diterpenes, Kaurane
Molecular Structure
Sesquiterpenes
Sesquiterpenes, Guaiane
Fernández, L.R.
Butassi, E.
Svetaz, L.
Zacchino, S.A.
Palermo, J.A.
Sánchez, M.
Antifungal terpenoids from Hyalis argentea var. latisquama
topic_facet 8alpha,9alpha exposyonoseriolide acetate
amphotericin B
ent 7alpha hydroxy 15 oxokauran 19 beta dextro glucopyranosyl ester
ent 7alpha,15beta dihydroxykaur 16 ene 19 beta dextro glucopyranosyl ester
hyalic acid beta dextro glucopyranosyl ester
terpenoid derivative
unclassified drug
antifungal activity
article
Candida albicans
controlled study
Cryptococcus neoformans
drug identification
drug isolation
fungus growth
growth inhibition
Hyalis latisquama
medicinal plant
nonhuman
rhizome
Antifungal Agents
Asteraceae
Candida albicans
Cryptococcus neoformans
Diterpenes, Kaurane
Molecular Structure
Sesquiterpenes
Sesquiterpenes, Guaiane
description A detailed chemical study of the aerial parts and rhizomes of Hyalis argentea var. latisquama yielded a variety of sesqui- and diterpenes. In total, 26 compounds were isolated and identified, of which four are new, namely, two ent-kaurenes (1 and 2), a diterpene lactone (3), and a lindenanolide (4). The previously reported compounds included a series of lindenanolides, guaianolides, elemanolides, and additional diterpenes. The antifungal activity of the isolated compounds was tested against Cryptococcus neoformans and Candida albicans. Among the isolated compounds, the lindenanolides were the only structural class that showed strong antifungal activity, and onoseriolide acetate (5) was the most active. On the other hand, the isolated guaianolides were only moderately active, while the diterpenes did not show significant antifungal activity. © 2014 The American Chemical Society and American Society of Pharmacognosy.
format JOUR
author Fernández, L.R.
Butassi, E.
Svetaz, L.
Zacchino, S.A.
Palermo, J.A.
Sánchez, M.
author_facet Fernández, L.R.
Butassi, E.
Svetaz, L.
Zacchino, S.A.
Palermo, J.A.
Sánchez, M.
author_sort Fernández, L.R.
title Antifungal terpenoids from Hyalis argentea var. latisquama
title_short Antifungal terpenoids from Hyalis argentea var. latisquama
title_full Antifungal terpenoids from Hyalis argentea var. latisquama
title_fullStr Antifungal terpenoids from Hyalis argentea var. latisquama
title_full_unstemmed Antifungal terpenoids from Hyalis argentea var. latisquama
title_sort antifungal terpenoids from hyalis argentea var. latisquama
url http://hdl.handle.net/20.500.12110/paper_01633864_v77_n7_p1579_Fernandez
work_keys_str_mv AT fernandezlr antifungalterpenoidsfromhyalisargenteavarlatisquama
AT butassie antifungalterpenoidsfromhyalisargenteavarlatisquama
AT svetazl antifungalterpenoidsfromhyalisargenteavarlatisquama
AT zacchinosa antifungalterpenoidsfromhyalisargenteavarlatisquama
AT palermoja antifungalterpenoidsfromhyalisargenteavarlatisquama
AT sanchezm antifungalterpenoidsfromhyalisargenteavarlatisquama
_version_ 1807320904137441280