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1.
Food Sci Biotechnol ; 28(2): 355-364, 2019 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-30956847

RESUMEN

The red stigmas of saffron are one of the most expensive spices in the world and serve as a traditional Chinese medicine. More saffron has been cultivated in China, and different drying technologies have been studied. However, a comprehensive and comparative analysis of different drying approaches has not been well studied. In this study, we compared electric oven and vacuum oven drying approaches on saffron. We found saffron was dried quicker under high vacuum drying mode with high temperature and the quicker drying rate provided, the more open microstructural interstices on the saffron surface. Both methods were best fit to Midilli and Kucuk model. Besides, the coloring, aroma and bitterness strength after drying showed the similar results. In sum, our data suggested the optimal drying temperature was 100 °C for 20 min for two evaluated methods, however considering the machine cost, the electric oven drying would be the first choice.

2.
Fitoterapia ; 102: 177-81, 2015 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-25771123

RESUMEN

An unprecedented trinorcassane diterpenoid and a cassane furanoditerpenoid were isolated from the seeds of Caesalpinia minax. It is the first example of dicylic cassane-type trinorditerpenoid, which is different from reported 16- or 17-norcassane diterpenoids. The structure of the compounds was elucidated on the basis of 1D and 2D NMR analysis. Biosynthesis pathways are postulated, and this pathway was supported by semi-synthesis.


Asunto(s)
Caesalpinia/química , Diterpenos/química , Semillas/química , Vías Biosintéticas , Diterpenos/aislamiento & purificación , Espectroscopía de Resonancia Magnética , Estructura Molecular , Extractos Vegetales/química
3.
J Nat Prod ; 77(5): 1201-9, 2014 May 23.
Artículo en Inglés | MEDLINE | ID: mdl-24806310

RESUMEN

Thirteen new dammarane-type triterpenoids (1-13) and four known analogues, gentirigenic acid (14) and the gentirigeosides A, B, and E (15-17), were isolated from Gentianella azurea. Their structures were elucidated by detailed analysis of the NMR, MS, and X-ray crystallographic data. This is the first report of dammarane-type triterpenoids in the Gentianella genus. In addition, the known structures of gentirigenic acid (14) and the gentirigeosides A, B, and E (15-17) were revised based on the X-ray diffraction analysis. Gentirigeoside A (15) was found to inhibit nitric oxide production in RAW 264.7 macrophages with an IC50 value of 6.6 ± 2.1 µM.


Asunto(s)
Medicamentos Herbarios Chinos/aislamiento & purificación , Gentianella/química , Triterpenos/aislamiento & purificación , Animales , Medicamentos Herbarios Chinos/química , Medicamentos Herbarios Chinos/farmacología , Lipopolisacáridos/farmacología , Macrófagos/efectos de los fármacos , Ratones , Estructura Molecular , Óxido Nítrico/biosíntesis , Resonancia Magnética Nuclear Biomolecular , Triterpenos/química , Triterpenos/farmacología , Damaranos
4.
J Nat Prod ; 76(12): 2210-8, 2013 Dec 27.
Artículo en Inglés | MEDLINE | ID: mdl-24303808

RESUMEN

Fourteen new cassane diterpenoids, caesalminaxins A-L (1-14), and three known compounds were isolated from the seeds of Caesalpinia minax. Among the new diterpenoids, compounds 3 and 4 possess a rare spiro C/D ring system. The C-16 epimeric mixture 1/2 has an unprecedented carbon skeleton, presumably derived from 3 by cleavage of the C-13-C-14 bond. Compound 5 is the first example of a cassane diterpenoid with a spiro A/B ring system. The structures of the compounds were elucidated on the basis of 1D and 2D NMR analysis, and the absolute configurations of 3, 4, 9, and 11 were determined by single-crystal X-ray crystallography. Biosynthesis pathways for 1/2, 3, and 5 are postulated. Compounds 4, 8, and the known bonducellpin D exhibited moderate activity against four tested human cancer cell lines, HepG-2, K562, HeLa, and Du145.


Asunto(s)
Antineoplásicos Fitogénicos/aislamiento & purificación , Caesalpinia/química , Diterpenos/aislamiento & purificación , Medicamentos Herbarios Chinos/aislamiento & purificación , Antineoplásicos Fitogénicos/química , Antineoplásicos Fitogénicos/farmacología , Cristalografía por Rayos X , Diterpenos/química , Diterpenos/farmacología , Ensayos de Selección de Medicamentos Antitumorales , Medicamentos Herbarios Chinos/química , Medicamentos Herbarios Chinos/farmacología , Células HeLa , Células Hep G2 , Humanos , Células K562 , Estructura Molecular , Resonancia Magnética Nuclear Biomolecular , Semillas/química
5.
J Nat Prod ; 76(7): 1351-7, 2013 Jul 26.
Artículo en Inglés | MEDLINE | ID: mdl-23848163

RESUMEN

Eleven new guanidine alkaloids, plumbagines A-G (2-8) and plumbagosides A-D (9-12), as well as two known analogues (1, 13), were isolated from the aerial parts of Plumbago zeylanica. Their structures were elucidated by spectroscopic analyses including 1D and 2D NMR, MS, IR, and CD methods. The absolute configuration of 1 was determined by single-crystal X-ray diffraction of its derivative (1a).


Asunto(s)
Alcaloides/aislamiento & purificación , Medicamentos Herbarios Chinos/aislamiento & purificación , Guanidinas/aislamiento & purificación , Plumbaginaceae/química , Alcaloides/química , Alcaloides/farmacología , Cristalografía por Rayos X , Ensayos de Selección de Medicamentos Antitumorales , Medicamentos Herbarios Chinos/química , Femenino , Guanidinas/química , Guanidinas/farmacología , Humanos , Estructura Molecular , Resonancia Magnética Nuclear Biomolecular
6.
Sex Plant Reprod ; 25(4): 337-45, 2012 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-23114638

RESUMEN

Seedlessness is an important economic trait of lemon. Understanding the cellular and molecular mechanisms of seedlessness in 'Xiangshui' lemon requires detailed data on pollen and embryo sac fertility, embryo development and compatibility mechanisms governing self- and cross-pollination. The results of the current study indicate that the fertility of pollen and mature embryo sac remains normal. When flowers were self- or cross-pollinated, pollen grains of 'Xiangshui' were able to germinate on the stigma. In the case of self-pollination, pollen tubes became twisted, tube tips enlarged and tubes ruptured in the bottom of stigma. Following cross-pollination, tubes were able to grow normally in the style and ovary and enter the embryo sac, where double fertilization took place. Embryonic development resulting from cross-pollination was normal. After cross-pollination, the zygote began to divide at 2 weeks post-pollination, with early globular embryos observed after 3 weeks, globular and heart-shaped embryos at 4 weeks, torpedo-shaped embryos at 5 weeks, cotyledonary embryos at 6 weeks and thereafter germinable seeds. After self-pollination, however, ovules began to abort at 2 weeks post-pollination, with ovules disappearing at 5 weeks, ultimately producing seedless fruits. Emasculated unpollinated flowers also developed into seedless fruits, indicating that seedlessness contributes to parthenocarpy. However, gametophytic self-incompatibility has a major role in seedlessness in 'Xiangshui' lemon by blocking fertilization at the bottom of the stigma.


Asunto(s)
Citrus/fisiología , Polen/fisiología , Polinización/fisiología , Autoincompatibilidad en las Plantas con Flores/fisiología , Supervivencia Celular , Citrus/citología , Citrus/embriología , Citrus/genética , Cruzamientos Genéticos , Flores/citología , Flores/embriología , Flores/genética , Flores/fisiología , Frutas/citología , Frutas/embriología , Frutas/genética , Frutas/fisiología , Meiosis , Óvulo Vegetal/citología , Óvulo Vegetal/embriología , Óvulo Vegetal/genética , Óvulo Vegetal/fisiología , Polen/citología , Polen/embriología , Polen/genética , Semillas/citología , Semillas/embriología , Semillas/genética , Semillas/fisiología , Autofecundación
7.
Planta Med ; 77(5): 477-81, 2011 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-20979022

RESUMEN

Five new phenylpropanoids, named balajaponins A-E (1-5), were isolated from Balanophora japonica, along with 24 known compounds. Among them, three hydrolysable tannins (6-8) showed specific in vitro α-glucosidase inhibition, with IC50 values in the range of 1-4 µM. Kinetic analysis revealed that they all acted in a noncompetitive mode.


Asunto(s)
Balanophoraceae/química , Inhibidores de Glicósido Hidrolasas , Taninos Hidrolizables/farmacología , Fenilpropionatos/farmacología , Inhibidores Enzimáticos/química , Inhibidores Enzimáticos/farmacología , Taninos Hidrolizables/química , Concentración 50 Inhibidora , Cinética , Espectroscopía de Resonancia Magnética , Estructura Molecular , Fenilpropionatos/química , Extractos Vegetales/química , Extractos Vegetales/farmacología , alfa-Glucosidasas/metabolismo
8.
Planta Med ; 75(4): 367-70, 2009 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-19156599

RESUMEN

Two new labdane-type diterpenoids vitetrifolin H (1) and vitetrifolin I (2), and one new monoterpenoid vitexoid (3), were isolated from the fruits of Vitex trifolia L., together with seven known diterpenoids. Structures of all compounds were elucidated by extensive spectroscopic methods. All these compounds exhibited inhibition of Hela cell proliferation, with IC50 values in the range of 4-28 microM. In addition, vitetrifolin I (2) induced cell cycle G0/G1 phase arrest and apoptosis of Hela cells.


Asunto(s)
Antineoplásicos Fitogénicos/farmacología , Frutas/química , Terpenos/química , Terpenos/farmacología , Vitex/química , Antineoplásicos Fitogénicos/química , Células HeLa , Humanos , Estructura Molecular
9.
J Asian Nat Prod Res ; 10(1-2): 205-10, 2008.
Artículo en Inglés | MEDLINE | ID: mdl-18253890

RESUMEN

Chemical studies on the roots of Fraxinus rhynchophylla led to the isolation of fraxisecoside (1), a novel coumarin-secoiridoid hybrid glycoside, namely, fraxetin-8-O-[11'-methyl-oleosidyl-(7'-->6'')]-beta-D-glucopyranoside and 14 known compounds. Their structures were elucidated based on chemical evidence and spectroscopic analysis, including extensive 2D NMR methods. Compound 2 was first isolated as a pure compound. Compound 1 exhibited moderate PTP1B inhibition activity. Compounds 1 and 2 showed inhibition activity against B- and T-cell proliferation, without cytotoxicity.


Asunto(s)
Medicamentos Herbarios Chinos/química , Fraxinus/química , Corteza de la Planta/química , Raíces de Plantas/química , Agua/química , Cumarinas/química , Iridoides/química , Estructura Molecular , Solubilidad
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