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1.
Fitoterapia ; 142: 104516, 2020 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-32081701

RESUMEN

A new bilobalide isomer (1), together with two flavonol glycosides (2, 3), have been isolated and elucidated from the extract of Ginkgo biloba leaves. Significantly, 1 was a new sesquiterpene lactone with two lactone ring groups, both 2 and 3 were two flavonol glycosides with a same cis-coumaroylated fragment. Their chemical structures were elucidated by NMR and MS spectroscopic date and the absolute configuration of 1 was specific established by Cu-Kα X-ray crystallographic analyses. However, 1-3 showed no obvious anti-platelet aggregation activity.


Asunto(s)
Bilobálidos/aislamiento & purificación , Flavonoles/aislamiento & purificación , Ginkgo biloba/química , Glicósidos/aislamiento & purificación , Bilobálidos/química , Ciclopentanos/química , Ciclopentanos/aislamiento & purificación , Flavonoles/química , Furanos/química , Furanos/aislamiento & purificación , Ginkgólidos/química , Ginkgólidos/aislamiento & purificación , Glicósidos/química , Hojas de la Planta/química
2.
Fitoterapia ; 141: 104454, 2020 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-31857181

RESUMEN

Three rare squiterpene lactone dimers lineariifolianoids M-O (1-3) were isolated from Inula lineariifolia for the first time. Their structures and absolute configuration were established on the basis of by NMR and MS spectroscopic data and X-ray crystallography. Furthermore, those three compounds exhibited significant inhibitory activity against LPS-induced NO production in RAW 264.7 macrophages with IC50 values of 1.421, 1.087 and 1.243 µM, respectively.


Asunto(s)
Inula/química , Lactonas/química , Óxido Nítrico/biosíntesis , Sesquiterpenos/química , Animales , Biología Computacional , Ratones , Modelos Moleculares , Estructura Molecular , Células RAW 264.7
3.
Plant Physiol ; 146(3): 1322-32, 2008 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-18218968

RESUMEN

Sphingolipids are important signaling molecules involved in various cellular activities. De novo sphingolipid synthesis is initiated by a rate-limiting enzyme, serine palmitoyltransferase (SPT), a heterodimer consisting of LONG-CHAIN BASE1 (LCB1) and LCB2 subunits. A mutation in the Arabidopsis thaliana LCB1 gene, lcb1-1, was found to cause embryo lethality. However, the underpinning molecular and cellular mechanisms remain largely unclear. Here, we report the identification of the fumonisin B(1) resistant11-2 (fbr11-2) mutant, an allele of lcb1-1. The fbr11-2 mutation, most likely an allele stronger than lcb1-1, was transmitted only through female gametophytes and caused the formation of abortive microspores. During the second pollen mitosis, fbr11-2 initiated apoptotic cell death in binucleated microspores characteristic of nuclear DNA fragmentation, followed by cytoplasm shrinkage and organelle degeneration at the trinucleated stage. In addition, a double mutant with T-DNA insertions in two homologous LCB2 genes showed a phenotype similar to fbr11-2. Consistent with these observations, the FBR11/LCB1 expression was confined in microspores during microgametogenesis. These results suggest that SPT-modulated programmed cell death plays an important role in the regulation of male gametophyte development.


Asunto(s)
Proteínas de Arabidopsis/metabolismo , Arabidopsis/metabolismo , Muerte Celular/fisiología , Polen/crecimiento & desarrollo , Serina C-Palmitoiltransferasa/metabolismo , Arabidopsis/crecimiento & desarrollo , Arabidopsis/ultraestructura , Proteínas de Arabidopsis/genética , Expresión Génica , Prueba de Complementación Genética , Mitosis/fisiología , Mutagénesis Insercional , Fenotipo , Polen/ultraestructura , Serina C-Palmitoiltransferasa/genética , Esfingolípidos/biosíntesis , Transgenes
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