Flavonoids with antiplasmodial and cytotoxic activities of Macaranga triloba

A new flavanone derivative, malaysianone A (1), four prenylated flavanones, 6-prenyl-3′-methoxyeriodictyol (2), nymphaeol B (3), nymphaeol C (4) and 6-farnesyl-3′,4′,5,7-tetrahydroxyflavanone (5), and two coumarins, 5,7-dihydroxycoumarin (6) and scopoletin (7), were isolated from the dichloromethane...

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Published in:Fitoterapia
Main Author: Zakaria I.; Ahmat N.; Jaafar F.M.; Widyawaruyanti A.
Format: Article
Language:English
Published: 2012
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84861650633&doi=10.1016%2fj.fitote.2012.04.020&partnerID=40&md5=89a8cb48cc56d5411eae7e1aff680bf2
id 2-s2.0-84861650633
spelling 2-s2.0-84861650633
Zakaria I.; Ahmat N.; Jaafar F.M.; Widyawaruyanti A.
Flavonoids with antiplasmodial and cytotoxic activities of Macaranga triloba
2012
Fitoterapia
83
5
10.1016/j.fitote.2012.04.020
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84861650633&doi=10.1016%2fj.fitote.2012.04.020&partnerID=40&md5=89a8cb48cc56d5411eae7e1aff680bf2
A new flavanone derivative, malaysianone A (1), four prenylated flavanones, 6-prenyl-3′-methoxyeriodictyol (2), nymphaeol B (3), nymphaeol C (4) and 6-farnesyl-3′,4′,5,7-tetrahydroxyflavanone (5), and two coumarins, 5,7-dihydroxycoumarin (6) and scopoletin (7), were isolated from the dichloromethane extract of the inflorescences of Macaranga triloba. The structures of these compounds were elucidated based on spectroscopic methods including nuclear magnetic resonance (NMR-1D and 2D), UV, IR and mass spectrometry. The cytotoxic activity of the compounds was tested against several cell lines, with 5 inhibiting very strongly the growth of HeLa and HL-60 cells (IC 50: 1.3 μg/ml and 3.3 μg/ml, respectively). Compound 5 also showed strong antiplasmodial activity (IC 50: 0.06 μM). © 2012 Elsevier B.V. All rights reserved.

18736971
English
Article
All Open Access; Green Open Access
author Zakaria I.; Ahmat N.; Jaafar F.M.; Widyawaruyanti A.
spellingShingle Zakaria I.; Ahmat N.; Jaafar F.M.; Widyawaruyanti A.
Flavonoids with antiplasmodial and cytotoxic activities of Macaranga triloba
author_facet Zakaria I.; Ahmat N.; Jaafar F.M.; Widyawaruyanti A.
author_sort Zakaria I.; Ahmat N.; Jaafar F.M.; Widyawaruyanti A.
title Flavonoids with antiplasmodial and cytotoxic activities of Macaranga triloba
title_short Flavonoids with antiplasmodial and cytotoxic activities of Macaranga triloba
title_full Flavonoids with antiplasmodial and cytotoxic activities of Macaranga triloba
title_fullStr Flavonoids with antiplasmodial and cytotoxic activities of Macaranga triloba
title_full_unstemmed Flavonoids with antiplasmodial and cytotoxic activities of Macaranga triloba
title_sort Flavonoids with antiplasmodial and cytotoxic activities of Macaranga triloba
publishDate 2012
container_title Fitoterapia
container_volume 83
container_issue 5
doi_str_mv 10.1016/j.fitote.2012.04.020
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-84861650633&doi=10.1016%2fj.fitote.2012.04.020&partnerID=40&md5=89a8cb48cc56d5411eae7e1aff680bf2
description A new flavanone derivative, malaysianone A (1), four prenylated flavanones, 6-prenyl-3′-methoxyeriodictyol (2), nymphaeol B (3), nymphaeol C (4) and 6-farnesyl-3′,4′,5,7-tetrahydroxyflavanone (5), and two coumarins, 5,7-dihydroxycoumarin (6) and scopoletin (7), were isolated from the dichloromethane extract of the inflorescences of Macaranga triloba. The structures of these compounds were elucidated based on spectroscopic methods including nuclear magnetic resonance (NMR-1D and 2D), UV, IR and mass spectrometry. The cytotoxic activity of the compounds was tested against several cell lines, with 5 inhibiting very strongly the growth of HeLa and HL-60 cells (IC 50: 1.3 μg/ml and 3.3 μg/ml, respectively). Compound 5 also showed strong antiplasmodial activity (IC 50: 0.06 μM). © 2012 Elsevier B.V. All rights reserved.
publisher
issn 18736971
language English
format Article
accesstype All Open Access; Green Open Access
record_format scopus
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