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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
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