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1.
Article | IMSEAR | ID: sea-215771

ABSTRACT

For drug discovery it takes approximately 6 years to expose in the market and for commercial uses. There are different procedure to get success in the drug discovery like preliminary phytochemical analysis, structural elucidation of the bioactive compound, preclinical test and clinical test etc. So to optimize the time for invention of new drug molecule, computer aided drug designing and molecular docking analysis is being used as one of the highly effective methodology. The phytochemical extraction of Hydnora africana plant was reported to inhibit the growth of Aeromonas hydrophilawhich cause Septicemia.“Biovia Discovery Studio” molecular docking methods give us opportunity to identify the effective molecule against the microbes. “High positive values of -CDOCKER energy and -CDOCKER interaction energy” recommended that flavone can effectively deactivate the acetaldehyde dehydrogenase enzyme thereby interrupting the life cycle of the organism

2.
Rev. bras. farmacogn ; 27(5): 576-579, Sept.-Oct. 2017. tab, graf
Article in English | LILACS | ID: biblio-898709

ABSTRACT

Abstract Myricaria bracteata Royle, Tamaricaceae, is a species with a wide geographic range that encompasses Eastern Europe, Western and Central Siberia, Central Asia, and the Himalayas. This plant is used in traditional folk medicine in Russia (Siberia) and in China typically as an analgesic and for the treatment of some infections and certain types of intoxication. The aim of this study was to identify phenolic constituents of the leaves of M. bracteata from two considerably distant populations. Chromatographic profiles of the leaves of M. bracteata were analyzed for the first time. Seventeen compounds, mainly methyl ethers of quercetin (isorhamnetin, rhamnazin), kaempferol (kaempferide, rhamnocitrin), and ellagic acid as well as quercetin, quercetin 3-glucoside, kaempferol, luteolin, chrysoeriol, citric acid, gallic acid, methyl gallate, ethyl gallate, and ferulic acid were identified in hydrolyzed aqueous ethanol extracts of the leaves. Flavonols and ellagic acid were the major compounds in both samples. Isorhamnetin was the main flavonoid constituent. Kaempferide and rhamnazin were also abundant in the flavonoid complex of the leaves of M. bracteata from the Altai. This study shows that M. bracteata leaves are a source of flavonoids with possible biological activities.

3.
Orthopedic Journal of China ; (24)2006.
Article in Chinese | WPRIM | ID: wpr-542500

ABSTRACT

[Objective]To study the relationship between ossification of ligamentum nuchae(LN) and degeneration of ligamentum flavon(LF) of cervical spondylotic myelopathy(CSM).[Method]Fifty-six cervical LF samples from CSM patient of C_(3~7) in relation to the stage of ossification of LN samples(experimental group,EG) and 38 samples of corresponding ligament from patient with cervical vertebral trauma(CVT)(control group,CG) were obtained.Thickness of LF was measured,their pathological change was examined by microscopy,content of collagen and kydrolyproline and the ratio of type Ⅰ/ type Ⅱ collagen were determined by Woessners method and setting Salting out method.The correlation among the thickness of degenerative LF,the ratio of type Ⅰ/ type Ⅱ collagen,the content of collagen and hydrokyproline,and arrangement disorder of LF in relation to the ossification stage of LN were analyzed.[Result]In EG,as compared with in CG,there showed a decrease of elastic fibre,decrease of ratio type Ⅰ/ type Ⅱ collagen due to significant increase of type Ⅱ collagen,increase collagen content and disorder arrangement of LF.In relation to the ossification of LN,above changes were more marked in LF of C_(4、5),C_(5、6),than that of C_(3、4),C_(6、7)(P

4.
Korean Journal of Pediatrics ; : 677-684, 2004.
Article in English | WPRIM | ID: wpr-203173

ABSTRACT

PURPOSE: In this study, a possible suppressive effect of a flavon extracted from Artemisia absinthium on a mouse collagen-induced arthritis (CIA) model was investigated. METHODS: DBA/1 mice were injected intradermally with emulsified chicken type II collagen. Three weeks after immunization, a flavon was introduced p.o. everyday. Clinical incidences of arthritis and arthritis index were measured. Measurement of anti-collagen antibodies and a stimulation index of the splenocytes of the mice were measured. IL-10 and TNF-alpha in the supernatants of the mice sera were measured by ELISA. mRNA expression for IL-10 and TNF-alpha in the splenocytes were tested. RESULTS: Flavon extracted from Artemisia absinthium appears to be an effective suppressor of CIA in mice. The serum anti-collagen antibody level and stimulation index of the cultured splenocytes showed no significant differences among the three experimental groups. Also serum IL-10 and TNF-alpha levels did not show any significant differences among the three experimental groups. An increased expression of mRNA for IL-10 was observed in the splenocytes treated with flavon. CONCLUSION: With these results, flavon extracted from Artemisia absinthium appears to have a suppressive effect of CIA. The mechanism of the suppressive effect of flavon extracted from Artemisia absinthium may be from a stimulation of IL-10 production.


Subject(s)
Animals , Mice , Antibodies , Artemisia absinthium , Artemisia , Arthritis , Arthritis, Experimental , Chickens , Collagen Type II , Collagen , Enzyme-Linked Immunosorbent Assay , Immunization , Incidence , Interleukin-10 , RNA, Messenger , Tumor Necrosis Factor-alpha
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