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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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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. |
format | Online Article Text |
id | pubmed-8516952 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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