Three new dihydrochalcones from the leaves of Artocarpus sericicarpus Jarrett and their activity against Plasmodium falciparum
Three new dihydrochalcones: artoserichalcone A-C (1-3), were isolated from the leaves of Artocarpus sericicarpus. The structures of compounds were determined based on NMR spectrum (1H, 13C, and 2D) and HRESIMS spectroscopic analysis. Compounds (1) and (3) showed active antimalarial activity with IC5...
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Taylor and Francis Ltd.
2024
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2-s2.0-85183871546 Tumewu L.; Ilmi H.; Kartika Sari D.; Permanasari A.A.; Khairun Nisa H.; Saputri R.D.; Tjahjandarie T.S.; Tanjung M.; Osman C.P.; Ismail N.H.; Suciati; Widyawaruyanti A.; Hafid A.F. Three new dihydrochalcones from the leaves of Artocarpus sericicarpus Jarrett and their activity against Plasmodium falciparum 2024 Natural Product Research 10.1080/14786419.2024.2308726 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85183871546&doi=10.1080%2f14786419.2024.2308726&partnerID=40&md5=de91f3a0dbb28c2baf149d2b65df4f9c Three new dihydrochalcones: artoserichalcone A-C (1-3), were isolated from the leaves of Artocarpus sericicarpus. The structures of compounds were determined based on NMR spectrum (1H, 13C, and 2D) and HRESIMS spectroscopic analysis. Compounds (1) and (3) showed active antimalarial activity with IC50 values of 16.90 and 13.56 µM, respectively. Meanwhile, compound (2) with an IC50 value of 63.01 µM was categorised as a moderate antimalarial substance. The cytotoxicity against Huh7, HepG2, BHK-21, and Vero cells showed that compounds (1-3) with CC50 values > 20 µg/mL could be considered non-cytotoxic. Compounds (1-3) exhibited antimalarial activity against Plasmodium falciparum and non-toxic as an antimalarial agent. © 2024 Informa UK Limited, trading as Taylor & Francis Group. Taylor and Francis Ltd. 14786419 English Article All Open Access; Green Open Access |
author |
Tumewu L.; Ilmi H.; Kartika Sari D.; Permanasari A.A.; Khairun Nisa H.; Saputri R.D.; Tjahjandarie T.S.; Tanjung M.; Osman C.P.; Ismail N.H.; Suciati; Widyawaruyanti A.; Hafid A.F. |
spellingShingle |
Tumewu L.; Ilmi H.; Kartika Sari D.; Permanasari A.A.; Khairun Nisa H.; Saputri R.D.; Tjahjandarie T.S.; Tanjung M.; Osman C.P.; Ismail N.H.; Suciati; Widyawaruyanti A.; Hafid A.F. Three new dihydrochalcones from the leaves of Artocarpus sericicarpus Jarrett and their activity against Plasmodium falciparum |
author_facet |
Tumewu L.; Ilmi H.; Kartika Sari D.; Permanasari A.A.; Khairun Nisa H.; Saputri R.D.; Tjahjandarie T.S.; Tanjung M.; Osman C.P.; Ismail N.H.; Suciati; Widyawaruyanti A.; Hafid A.F. |
author_sort |
Tumewu L.; Ilmi H.; Kartika Sari D.; Permanasari A.A.; Khairun Nisa H.; Saputri R.D.; Tjahjandarie T.S.; Tanjung M.; Osman C.P.; Ismail N.H.; Suciati; Widyawaruyanti A.; Hafid A.F. |
title |
Three new dihydrochalcones from the leaves of Artocarpus sericicarpus Jarrett and their activity against Plasmodium falciparum |
title_short |
Three new dihydrochalcones from the leaves of Artocarpus sericicarpus Jarrett and their activity against Plasmodium falciparum |
title_full |
Three new dihydrochalcones from the leaves of Artocarpus sericicarpus Jarrett and their activity against Plasmodium falciparum |
title_fullStr |
Three new dihydrochalcones from the leaves of Artocarpus sericicarpus Jarrett and their activity against Plasmodium falciparum |
title_full_unstemmed |
Three new dihydrochalcones from the leaves of Artocarpus sericicarpus Jarrett and their activity against Plasmodium falciparum |
title_sort |
Three new dihydrochalcones from the leaves of Artocarpus sericicarpus Jarrett and their activity against Plasmodium falciparum |
publishDate |
2024 |
container_title |
Natural Product Research |
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container_issue |
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doi_str_mv |
10.1080/14786419.2024.2308726 |
url |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85183871546&doi=10.1080%2f14786419.2024.2308726&partnerID=40&md5=de91f3a0dbb28c2baf149d2b65df4f9c |
description |
Three new dihydrochalcones: artoserichalcone A-C (1-3), were isolated from the leaves of Artocarpus sericicarpus. The structures of compounds were determined based on NMR spectrum (1H, 13C, and 2D) and HRESIMS spectroscopic analysis. Compounds (1) and (3) showed active antimalarial activity with IC50 values of 16.90 and 13.56 µM, respectively. Meanwhile, compound (2) with an IC50 value of 63.01 µM was categorised as a moderate antimalarial substance. The cytotoxicity against Huh7, HepG2, BHK-21, and Vero cells showed that compounds (1-3) with CC50 values > 20 µg/mL could be considered non-cytotoxic. Compounds (1-3) exhibited antimalarial activity against Plasmodium falciparum and non-toxic as an antimalarial agent. © 2024 Informa UK Limited, trading as Taylor & Francis Group. |
publisher |
Taylor and Francis Ltd. |
issn |
14786419 |
language |
English |
format |
Article |
accesstype |
All Open Access; Green Open Access |
record_format |
scopus |
collection |
Scopus |
_version_ |
1809678014988943360 |