• Archives of Plastic Surgery
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• v.42 no.5
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• pp.642-645
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• 2015

• Archives of Plastic Surgery
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• v.42 no.6
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• pp.791-793
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• 2015

• Archives of Plastic Surgery
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• v.44 no.4
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• pp.352-353
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• 2017

• Archives of Pharmacal Research
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• v.21 no.1
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• pp.62-66
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• 1998

The resistance inhibitory activities of 54 odorant mixtures (essential oil) from 41 Korean aromatic herbs were tested against multi-drug resistant Staphylococcus aureus SA2, which has resistances to 10 usual antibiotics including chloramphenicol. As results, combinations of 28 kinds of samples from 21 herbs and chloramphenicol have resistance inhibitory activities in dose dependent manner.

• Archives of Pharmacal Research
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• v.13 no.4
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• pp.374-378
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• 1990

From the stem of Prunus davidiana, naringenin and its glucoside, kaempferol and its glucoside, dihydrokaempferol, kaempferide glucoside, hesperetin glucoside, quercetin glucoside, d-catechin and $\beta$-sitosterol glucoside were isolated.

• Archives of Pharmacal Research
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• v.13 no.2
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• pp.204-206
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• 1990

Certain pyrazolin-5-one and pyrazole derivatives bearing uracil-6-yl or tetrazol-5-yl moiety in position 1 have been synthesized. The anti-inflammatory activity of six representative compounds have been tested and the results are reported.

• Archives of Pharmacal Research
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• v.18 no.5
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• pp.364-365
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• 1995

• Archives of Pharmacal Research
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• v.22 no.5
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• pp.496-501
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• 1999

The reaction of epi-androsterone with cyanoacetyl hydrazine (2) gave the hydrazone derivative 3. The reactivity of 3 towards chemical reagents was studied to give pyridine, thiazole and thiophene derivatives.

• Archives of Pharmacal Research
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• v.10 no.4
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• pp.258-259
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• 1987

An alkaloid was isolated form water-soluble fraction of Panax ginseng roots. It was characterized by spectroscopic data and dynthesis as 4, 5, 6, 7-tetrahydroimidazo (4, 5-c) pyridine-6-carboxylic acid or spinacine, which was first isolated from the plant kingdom.

• Archives of Pharmacal Research
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• v.18 no.1
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• pp.44-47
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• 1995

The synthesis of osme quinoxaline derivatives containing indoline-2, 3-dione or thiazolidlinone residue is described. The synthesized derivatives were sureened in vitro for their growth inhibitory activity against six species of bacteria, viz. Staphylococcus aureus, Streptococcus faecalis, Escherichia coli, Pseudomonas aeruginosa, Serratia marcescens and Mycobacterium semegmatils. Most of the compounds exhibited antimicrobial activity especially those having indoline-2, 3-dione moiety.