• Korean Journal of Pharmacognosy
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• v.29 no.4
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• pp.357-359
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• 1998

From the n-butanol fraction of the water extract of the seeds of Phaseolus radiatus, two flavonoid C-glycosides were isolated and identified as iso-vitexin (1) and vitexin (2) by spectroscopic methods.

• Korean Journal of Pharmacognosy
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• v.19 no.2
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• pp.93-96
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• 1988

Three flavonoids were isolated from Epimedium koreanum and identified as quercetin(1), $anhydroicaritin-3-O-{\alpha}-rhamnoside(2)$ and icariin(3) by spectroscopic methods. The former two compounds are the first isolation from this plant.

• Archives of Pharmacal Research
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• v.5 no.1
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• pp.1-5
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• 1982

From the seeds of Phytolacca americana, acentonylidene americanin. A was isolated and its structure elucidated mainly by spectroscopic methods. This compound is not a genuine constituent but formed in the tissue on heating with acetone.

• Archives of Pharmacal Research
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• v.20 no.4
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• pp.338-341
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• 1997

Six substituted phenacyl derivatives of 4-hydroxypiperidine were prepared and their structures were confirmed through spectroscopic techniques. These newly synthesized derivatives were also screened for analgesic activity by chemical and thermal methods. Only halogenated phenacyl derivatives demonstrated more or less protection against acetic acid induced writhing in mice where as rest of three derivatives were found inactive when screened by this chemical method. Similarly all the six derivatives were proved inactive by tail flick test.

• Archives of Pharmacal Research
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• v.14 no.2
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• pp.103-104
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• 1991

The ionophore activity of frangufoline (1), a sedative cyclopeptide alkaloid isolated from Zizyphus jujuba, was investigated by UV and CD spectroscopic methods. Frangufoline (1) showed ion binding activity to calcium and magnesium ions.

• 한국정보디스플레이학회:학술대회논문집
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• 2008.10a
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• pp.57-60
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• 2008

Over 5lm/W white luminous efficacy was obtained by 11" color test panel with narrowed discharge electrodes combined with high Xe partial pressure. By using optical spectroscopic methods, it was suggested that the electron heating efficiency is the most significant to improve the plasma efficiency in our experimental conditions.

• Journal of Environmental Science International
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• v.5 no.6
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• pp.757-762
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• 1996

The removal effectiveness of various heavy metal ions in boron-rich containing plants has been studied by means of spectroscopic and pH methods. Treatment of the boron-rich containing sample which was collected from cherry and root of cabbage to heavy metal ions is resulted in that an excellent removal effect shows in the case of large ionic size of heavy metal. Stability constants are depended on the variation of pH.

• Natural Product Sciences
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• v.7 no.2
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• pp.27-32
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• 2001

In addition to known cucurbitacins, a glucosphingosine type cerebroside and amino acids were isolated from the roots of Trichosanthes kirilowii. The structure of cerebroside was determined as soya-cerebroside I by means of spectroscopic methods. Fifteen amino acids were identified as aspartic acid, glutamic acid, serine, glycine, histidine, citrulline, threonine, alanine, proline, tyrosine, valine, isoleucine, leucine, phenylalanine and tryptophan, among which the major components such as citrulline, phenylalanine, leucine/isoleucine and valine were isolated.

• Natural Product Sciences
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• v.10 no.1
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• pp.32-34
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• 2004

Two 2-phenoxychromones; a rare group of natural products, were isolated from the combined ethylacetate and chloroform fractions of the ethanolic extract of Ononis serrata frossk (Leguminosae) growing in Egypt. Structures were elucidated by chemical, spectroscopic methods as well as single X-ray diffraction analyses. The cytotoxic and antimicrobial effects of the two compounds were examined. It is worth to mention that this is the first report on the isolation of 2-phenoxychromones from the family Leguminosae.

• Natural Product Sciences
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• v.24 no.2
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• pp.79-81
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• 2018

Norcolensoic acid (1) was isolated from both the fruiting bodies and the liquid culture of Lachnum virgineum. The structures of 1 was determined using spectroscopic methods. Compound 1 was isolated for the first time from this fungus. Compound 1 showed moderate antibacterial and phytotoxic activities.