نتایج جستجو برای: a millefolium l

تعداد نتایج: 13618236  

2011
HINA FAZAL NISAR AHMAD AJAB KHAN

The active parts of 11 medicinal plants were analyzed for physico-chemical evaluation, phytochemical determination and antioxidant activity. The physico-chemical evaluation revealed that highest water soluble extractive was from Origanum vulgare (38%), highest chloroform extractive was from Psoralea corylifolia (21%); highest ethanolic extractive was that of Acorus calamus (11%) and the highest...

Journal: :Journal of Ethnobiology and Ethnomedicine 2007
Cheryl Lans Nancy Turner Tonya Khan Gerhard Brauer Willi Boepple

BACKGROUND The use of medicinal plants is an option for livestock farmers who are not allowed to use allopathic drugs under certified organic programs or cannot afford to use allopathic drugs for minor health problems of livestock. METHODS In 2003 we conducted semi-structured interviews with 60 participants obtained using a purposive sample. Medicinal plants are used to treat a range of condi...

Journal: :Chemistry of Natural Compounds 1973

In many field observation, ecological equipment, phenology and ethnopharmacological data of Achillea millefolium L. and A. micrantha Wild. were studied. The inflorescences of plants were collected in different locations of Golestan province: Chaharbagh (2000 m) and Dozan (2200 m) respectively. Essential oils were obtained by steam distillation (Clevenger) and analyzed by gas chromatography-mass...

2011
Anat Elmann Sharon Mordechay Hilla Erlank Miriam Rindner

Statistical review: Yes, but I do not feel adequately qualified to assess the statistics.

Journal: :Bioscience, biotechnology, and biochemistry 2011
Yong Li Man-Li Zhang Bin Cong Si-Ming Wang Mei Dong Françoise Sauriol Chang-Hong Huo Qing-Wen Shi Yu-Cheng Gu Hiromasa Kiyota

Achillinin A (2β,3β-epoxy-1α,4β,10α-trihydroxyguai-11(13)-en-12,6α-olide, 1), a new guaianolide isolated from the flower of Achillea millefolium, exhibited potential antiproliferative activity to A549, RERF-LC-kj and QG-90 cells with 50% inhibitory concentration (IC(50)) values of 5.8, 10 and 0.31 µM, respectively.

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