• Korean Journal of Pharmacognosy
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• v.29 no.2
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• pp.75-78
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• 1998

In the course of phytochemical studies for the aerial parts of Ajuga multiflora, one flavonoid and two iridoid glycosides were isolated and identified as apigenin (1), 8-O-acetylharpagide (2) and harpagide (3) on the basis of spectroscopic evidence.

• Natural Product Sciences
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• v.9 no.2
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• pp.52-55
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• 2003

The aerial parts of Ephedra aphylla afforded two alkaloids belonging to two different classes. The first alkaloid, ephedradine C, belonging to the spermine alkaloid, a group characterized by its hypotensive effect. The other alkaloid, hordenine is a phenylalkylamine alkaloid isolated for the first time from Ephedra Species. The structures were elucidated by spectroscopic methods and the assignment of some carbons in ephedradine C was achieved based on 2 D-NMR experiments.

• Korean Journal of Pharmacognosy
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• v.48 no.4
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• pp.285-288
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• 2017

A lignan and four flavonoid derivatives were isolated from the aerial parts of Panicum dichotomiflorum Michaux (Gramineae) through repeated column chromatography. Their chemical structures were identified as (-)-pinoresinol (1), tricin (2), luteolin (3), luteolin-4'-O-${\beta}$-D-glucopyranosde (4) and luteolin-7-O-${\beta}$-D-glucopyranosde (5), respectively, by spectroscopic analysis. These compounds were isolated for the first time from this plant.

• Bulletin of the Korean Chemical Society
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• v.31 no.4
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• pp.1070-1072
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• 2010

• Archives of Pharmacal Research
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• v.21 no.5
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• pp.618-620
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• 1998

Four thymol derivatives, 2,5-dimethoxythymol (1), 2-methoxythymol isobutyrate (2), 10-isobutyloxy-8,9-epoxythymolisobutyrate (3) and 10-(2-methylbutyloxy)-8,9-eposythymolisobutyrate (4) were isolated from the aerial parts of Carpesium divaricatum. the structures were elucidated by high field 1D and 2D NMR techniques.

• Proceedings of the Plant Resources Society of Korea Conference
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• 2007.11a
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• pp.347.2-347.2
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• 2007

• Archives of Pharmacal Research
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• v.24 no.3
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• pp.194-197
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• 2001

The phytochemical study of the aerial parts of Artemisia japonica ssp. littoricola (Asteraceae) led to the isolation of two acetylenic compounds, (3R)-dehydrofalcarinol (2) and (3R)-dehydrofalcarindiol (6), two sesquiterpenes, $1{\beta}$, $6{\alpha}$-dihydroxy-4(15)-eudesmene (5) and oplodiol (8), and four phenolic compounds, eugenol (1), vanillin (3), 3'-methoxy-4'- hydroxy-trrans-cinnamaldehyde (4) and p-hydroxyacetophenone (7). Their structures were determined by chemical and spectroscopic methods.

• 한국약용작물학회:학술대회논문집
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• 2012.05a
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• pp.289-290
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• 2012

• 한국약용작물학회:학술대회논문집
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• 2012.05a
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• pp.133-134
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• 2012

• Proceedings of the PSK Conference
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• 2000.04a
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• pp.183.2-183.2
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• 2000