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Two triterpenoids from Rubus fraxinifolius leaves and their tyrosinase and elastase inhibitory activities

Numerous therapeutic compounds have been isolated from naturally abundant organic resources, which may offer economical and sustainable sources of compounds with safe and efficacious biological activities. In the cosmetics industry, natural compounds with anti-aging activities are eagerly sought. Th...

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Autores principales: Desmiaty, Yesi, Hanafi, Muhammad, Saputri, Fadlina Chany, Elya, Berna, Rifai, Eko Aditya, Syahdi, Rezi Riadhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8516952/
https://www.ncbi.nlm.nih.gov/pubmed/34650166
http://dx.doi.org/10.1038/s41598-021-99970-x
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author Desmiaty, Yesi
Hanafi, Muhammad
Saputri, Fadlina Chany
Elya, Berna
Rifai, Eko Aditya
Syahdi, Rezi Riadhi
author_facet Desmiaty, Yesi
Hanafi, Muhammad
Saputri, Fadlina Chany
Elya, Berna
Rifai, Eko Aditya
Syahdi, Rezi Riadhi
author_sort Desmiaty, Yesi
collection PubMed
description Numerous therapeutic compounds have been isolated from naturally abundant organic resources, which may offer economical and sustainable sources of compounds with safe and efficacious biological activities. In the cosmetics industry, natural compounds with anti-aging activities are eagerly sought. Thus, we prepared various extracts from Rubus fraxinifolius leaves and used enzyme inhibition assays to isolate compounds with protective effects against skin aging. Two triterpenoids were isolated from Rubus fraxinifolius Poir. leaves. The structures were characterized by spectroscopic analyses (LC-ESI-MS, 1D/2D NMR) and comparison to reported data. Compound 1 and 2 were determined as 2,3-O-ethyleneglycol, 19-hydroxyurs-12-en-23,28-dioic acid and 2,3-O-propanediol,19-hydroxyurs-12-en-28-oic acid. Methanol extract and isolates were assessed for their inhibitory effects on elastase and tyrosinase. Compounds 1 and 2 inhibited elastase with IC(50) 122.199 µg/mL and 98.22 µg/mL, and also inhibited tyrosinase with IC(50) 207.79 µg/mL and 221.51 µg/mL, respectively. The molecular docking proved that both compounds have affinities toward the enzymes.
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spelling pubmed-85169522021-10-15 Two triterpenoids from Rubus fraxinifolius leaves and their tyrosinase and elastase inhibitory activities Desmiaty, Yesi Hanafi, Muhammad Saputri, Fadlina Chany Elya, Berna Rifai, Eko Aditya Syahdi, Rezi Riadhi Sci Rep Article Numerous therapeutic compounds have been isolated from naturally abundant organic resources, which may offer economical and sustainable sources of compounds with safe and efficacious biological activities. In the cosmetics industry, natural compounds with anti-aging activities are eagerly sought. Thus, we prepared various extracts from Rubus fraxinifolius leaves and used enzyme inhibition assays to isolate compounds with protective effects against skin aging. Two triterpenoids were isolated from Rubus fraxinifolius Poir. leaves. The structures were characterized by spectroscopic analyses (LC-ESI-MS, 1D/2D NMR) and comparison to reported data. Compound 1 and 2 were determined as 2,3-O-ethyleneglycol, 19-hydroxyurs-12-en-23,28-dioic acid and 2,3-O-propanediol,19-hydroxyurs-12-en-28-oic acid. Methanol extract and isolates were assessed for their inhibitory effects on elastase and tyrosinase. Compounds 1 and 2 inhibited elastase with IC(50) 122.199 µg/mL and 98.22 µg/mL, and also inhibited tyrosinase with IC(50) 207.79 µg/mL and 221.51 µg/mL, respectively. The molecular docking proved that both compounds have affinities toward the enzymes. Nature Publishing Group UK 2021-10-14 /pmc/articles/PMC8516952/ /pubmed/34650166 http://dx.doi.org/10.1038/s41598-021-99970-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Desmiaty, Yesi
Hanafi, Muhammad
Saputri, Fadlina Chany
Elya, Berna
Rifai, Eko Aditya
Syahdi, Rezi Riadhi
Two triterpenoids from Rubus fraxinifolius leaves and their tyrosinase and elastase inhibitory activities
title Two triterpenoids from Rubus fraxinifolius leaves and their tyrosinase and elastase inhibitory activities
title_full Two triterpenoids from Rubus fraxinifolius leaves and their tyrosinase and elastase inhibitory activities
title_fullStr Two triterpenoids from Rubus fraxinifolius leaves and their tyrosinase and elastase inhibitory activities
title_full_unstemmed Two triterpenoids from Rubus fraxinifolius leaves and their tyrosinase and elastase inhibitory activities
title_short Two triterpenoids from Rubus fraxinifolius leaves and their tyrosinase and elastase inhibitory activities
title_sort two triterpenoids from rubus fraxinifolius leaves and their tyrosinase and elastase inhibitory activities
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8516952/
https://www.ncbi.nlm.nih.gov/pubmed/34650166
http://dx.doi.org/10.1038/s41598-021-99970-x
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