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Lignans, Amides, and Saponins from Haplophyllum tuberculatum and Their Antiprotozoal Activity

A screening of Sudanese medicinal plants for antiprotozoal activities revealed that the chloroform and water fractions of the ethanolic root extract of Haplophyllum tuberculatum exhibited appreciable bioactivity against Leishmania donovani. The antileishmanial activity was tracked by HPLC-based acti...

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Autores principales: Mahmoud, Abdelhalim Babiker, Danton, Ombeline, Kaiser, Marcel, Han, Sohee, Moreno, Aitor, Abd Algaffar, Shereen, Khalid, Sami, Oh, Won Keun, Hamburger, Matthias, Mäser, Pascal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7355546/
https://www.ncbi.nlm.nih.gov/pubmed/32575379
http://dx.doi.org/10.3390/molecules25122825
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author Mahmoud, Abdelhalim Babiker
Danton, Ombeline
Kaiser, Marcel
Han, Sohee
Moreno, Aitor
Abd Algaffar, Shereen
Khalid, Sami
Oh, Won Keun
Hamburger, Matthias
Mäser, Pascal
author_facet Mahmoud, Abdelhalim Babiker
Danton, Ombeline
Kaiser, Marcel
Han, Sohee
Moreno, Aitor
Abd Algaffar, Shereen
Khalid, Sami
Oh, Won Keun
Hamburger, Matthias
Mäser, Pascal
author_sort Mahmoud, Abdelhalim Babiker
collection PubMed
description A screening of Sudanese medicinal plants for antiprotozoal activities revealed that the chloroform and water fractions of the ethanolic root extract of Haplophyllum tuberculatum exhibited appreciable bioactivity against Leishmania donovani. The antileishmanial activity was tracked by HPLC-based activity profiling, and eight compounds were isolated from the chloroform fraction. These included lignans tetrahydrofuroguaiacin B (1), nectandrin B (2), furoguaiaoxidin (7), and 3,3′-dimethoxy-4,4′-dihydroxylignan-9-ol (10), and four cinnamoylphenethyl amides, namely dihydro-feruloyltyramine (5), (E)-N-feruloyltyramine (6), N,N′-diferuloylputrescine (8), and 7′-ethoxy-feruloyltyramine (9). The water fraction yielded steroid saponins 11–13. Compounds 1, 2, and 5–13 are reported for the first time from Haplophyllum species and the family Rutaceae. The antiprotozoal activity of the compounds plus two stereoisomeric tetrahydrofuran lignans—fragransin B(2) (3) and fragransin B(1) (4)—was determined against Leishmania donovani amastigotes, Plasmodium falciparum, and Trypanosoma brucei rhodesiense bloodstream forms, along with their cytotoxicity to rat myoblast L6 cells. Nectandrin B (2) exhibited the highest activity against L. donovani (IC(50) 4.5 µM) and the highest selectivity index (25.5).
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spelling pubmed-73555462020-07-23 Lignans, Amides, and Saponins from Haplophyllum tuberculatum and Their Antiprotozoal Activity Mahmoud, Abdelhalim Babiker Danton, Ombeline Kaiser, Marcel Han, Sohee Moreno, Aitor Abd Algaffar, Shereen Khalid, Sami Oh, Won Keun Hamburger, Matthias Mäser, Pascal Molecules Article A screening of Sudanese medicinal plants for antiprotozoal activities revealed that the chloroform and water fractions of the ethanolic root extract of Haplophyllum tuberculatum exhibited appreciable bioactivity against Leishmania donovani. The antileishmanial activity was tracked by HPLC-based activity profiling, and eight compounds were isolated from the chloroform fraction. These included lignans tetrahydrofuroguaiacin B (1), nectandrin B (2), furoguaiaoxidin (7), and 3,3′-dimethoxy-4,4′-dihydroxylignan-9-ol (10), and four cinnamoylphenethyl amides, namely dihydro-feruloyltyramine (5), (E)-N-feruloyltyramine (6), N,N′-diferuloylputrescine (8), and 7′-ethoxy-feruloyltyramine (9). The water fraction yielded steroid saponins 11–13. Compounds 1, 2, and 5–13 are reported for the first time from Haplophyllum species and the family Rutaceae. The antiprotozoal activity of the compounds plus two stereoisomeric tetrahydrofuran lignans—fragransin B(2) (3) and fragransin B(1) (4)—was determined against Leishmania donovani amastigotes, Plasmodium falciparum, and Trypanosoma brucei rhodesiense bloodstream forms, along with their cytotoxicity to rat myoblast L6 cells. Nectandrin B (2) exhibited the highest activity against L. donovani (IC(50) 4.5 µM) and the highest selectivity index (25.5). MDPI 2020-06-19 /pmc/articles/PMC7355546/ /pubmed/32575379 http://dx.doi.org/10.3390/molecules25122825 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mahmoud, Abdelhalim Babiker
Danton, Ombeline
Kaiser, Marcel
Han, Sohee
Moreno, Aitor
Abd Algaffar, Shereen
Khalid, Sami
Oh, Won Keun
Hamburger, Matthias
Mäser, Pascal
Lignans, Amides, and Saponins from Haplophyllum tuberculatum and Their Antiprotozoal Activity
title Lignans, Amides, and Saponins from Haplophyllum tuberculatum and Their Antiprotozoal Activity
title_full Lignans, Amides, and Saponins from Haplophyllum tuberculatum and Their Antiprotozoal Activity
title_fullStr Lignans, Amides, and Saponins from Haplophyllum tuberculatum and Their Antiprotozoal Activity
title_full_unstemmed Lignans, Amides, and Saponins from Haplophyllum tuberculatum and Their Antiprotozoal Activity
title_short Lignans, Amides, and Saponins from Haplophyllum tuberculatum and Their Antiprotozoal Activity
title_sort lignans, amides, and saponins from haplophyllum tuberculatum and their antiprotozoal activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7355546/
https://www.ncbi.nlm.nih.gov/pubmed/32575379
http://dx.doi.org/10.3390/molecules25122825
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