Cargando…
Antiplatelet Aggregation Coumarins from the Leaves of Murraya omphalocarpa
Using a bioactivity-guided fractionation method, two coumarins: minumicroline acetonide (1) and epimurpaniculol senecioate (2), were isolated from the leaves of Murraya omphalocarpa Hayata (Rutaceae). Compound 1 had been previously synthesized and was now isolated from natural sources for the first...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2008
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245345/ https://www.ncbi.nlm.nih.gov/pubmed/18259135 http://dx.doi.org/10.3390/molecules13010122 |
_version_ | 1783372217721028608 |
---|---|
author | Chia, Yi-Chen Chang, Fang-Rong Wang, Jinn-Chyi Wu, Chin-Chung Chiang, Michael Y.-N. Lan, Yu-Hsuan Chen, Keh-Shaw Wu, Yang-Chang |
author_facet | Chia, Yi-Chen Chang, Fang-Rong Wang, Jinn-Chyi Wu, Chin-Chung Chiang, Michael Y.-N. Lan, Yu-Hsuan Chen, Keh-Shaw Wu, Yang-Chang |
author_sort | Chia, Yi-Chen |
collection | PubMed |
description | Using a bioactivity-guided fractionation method, two coumarins: minumicroline acetonide (1) and epimurpaniculol senecioate (2), were isolated from the leaves of Murraya omphalocarpa Hayata (Rutaceae). Compound 1 had been previously synthesized and was now isolated from natural sources for the first time, and compound 2, possessing a negative optical rotation value, is new. The structures and their stereochemistry were fully elucidated on the basis of spectroscopic and X-ray crystallographic techniques. Both compounds 1 and 2 are active in the antiplatelet aggregation assay. Interestingly, the possible acetonide artifact 1 displayed significant antiplatelet aggregation induced not only by AA and collagen but also by platelet activating factor (PAF). |
format | Online Article Text |
id | pubmed-6245345 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62453452018-11-26 Antiplatelet Aggregation Coumarins from the Leaves of Murraya omphalocarpa Chia, Yi-Chen Chang, Fang-Rong Wang, Jinn-Chyi Wu, Chin-Chung Chiang, Michael Y.-N. Lan, Yu-Hsuan Chen, Keh-Shaw Wu, Yang-Chang Molecules Article Using a bioactivity-guided fractionation method, two coumarins: minumicroline acetonide (1) and epimurpaniculol senecioate (2), were isolated from the leaves of Murraya omphalocarpa Hayata (Rutaceae). Compound 1 had been previously synthesized and was now isolated from natural sources for the first time, and compound 2, possessing a negative optical rotation value, is new. The structures and their stereochemistry were fully elucidated on the basis of spectroscopic and X-ray crystallographic techniques. Both compounds 1 and 2 are active in the antiplatelet aggregation assay. Interestingly, the possible acetonide artifact 1 displayed significant antiplatelet aggregation induced not only by AA and collagen but also by platelet activating factor (PAF). MDPI 2008-01-21 /pmc/articles/PMC6245345/ /pubmed/18259135 http://dx.doi.org/10.3390/molecules13010122 Text en © 2008 by MDPI (http://www.mdpi.org). Reproduction is permitted for noncommercial purposes. |
spellingShingle | Article Chia, Yi-Chen Chang, Fang-Rong Wang, Jinn-Chyi Wu, Chin-Chung Chiang, Michael Y.-N. Lan, Yu-Hsuan Chen, Keh-Shaw Wu, Yang-Chang Antiplatelet Aggregation Coumarins from the Leaves of Murraya omphalocarpa |
title | Antiplatelet Aggregation Coumarins from the Leaves of Murraya omphalocarpa |
title_full | Antiplatelet Aggregation Coumarins from the Leaves of Murraya omphalocarpa |
title_fullStr | Antiplatelet Aggregation Coumarins from the Leaves of Murraya omphalocarpa |
title_full_unstemmed | Antiplatelet Aggregation Coumarins from the Leaves of Murraya omphalocarpa |
title_short | Antiplatelet Aggregation Coumarins from the Leaves of Murraya omphalocarpa |
title_sort | antiplatelet aggregation coumarins from the leaves of murraya omphalocarpa |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245345/ https://www.ncbi.nlm.nih.gov/pubmed/18259135 http://dx.doi.org/10.3390/molecules13010122 |
work_keys_str_mv | AT chiayichen antiplateletaggregationcoumarinsfromtheleavesofmurrayaomphalocarpa AT changfangrong antiplateletaggregationcoumarinsfromtheleavesofmurrayaomphalocarpa AT wangjinnchyi antiplateletaggregationcoumarinsfromtheleavesofmurrayaomphalocarpa AT wuchinchung antiplateletaggregationcoumarinsfromtheleavesofmurrayaomphalocarpa AT chiangmichaelyn antiplateletaggregationcoumarinsfromtheleavesofmurrayaomphalocarpa AT lanyuhsuan antiplateletaggregationcoumarinsfromtheleavesofmurrayaomphalocarpa AT chenkehshaw antiplateletaggregationcoumarinsfromtheleavesofmurrayaomphalocarpa AT wuyangchang antiplateletaggregationcoumarinsfromtheleavesofmurrayaomphalocarpa |