• Journal of the Korean Chemical Society
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• v.54 no.1
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• pp.9-12
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• 2010

• Bulletin of the Korean Chemical Society
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• v.27 no.7
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• pp.1075-1078
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• 2006

• Journal of the Korean Chemical Society
• /
• v.52 no.3
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• pp.328-337
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• 2008

• Bulletin of the Korean Chemical Society
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• v.34 no.6
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• pp.1899-1902
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• 2013

• YAKHAK HOEJI
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• v.32 no.3
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• pp.157-163
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• 1988

4-Aryl-1, 4-dihydropyridines(DHP) derived from Hantsch type condensation of aromatic aldehydes with aminocrotonates and acetoacetic esters are studied as calcium channel blocking drugs. New DHP derivatives containing alkenyl ester show fairly good cardiovascular activity in mice. Preparation of the DHP derivatives and their major biological activity are presented along with their physical data.

• Bulletin of the Korean Chemical Society
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• v.32 no.6
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• pp.2139-2142
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• 2011

• Journal of Biomedical Engineering Research
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• v.7 no.2
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• pp.119-132
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• 1986

Poly (2-Hydroxyethyl methacrylate-co-r-methacryloxypropyl triethyl silane) and Poly (2-HydroHyethyl rnettacrylate-co-r-methacrylonypropylmethyl tistrimethyl siloxysilane)

• Proceedings of the KOSOMBE Conference
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• v.1990 no.11
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• pp.57-60
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• 1990

• Archives of Pharmacal Research
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• v.27 no.11
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• pp.1099-1105
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• 2004

The peroxisome proliferator-activated receptors (PPARs) are a primary regulator of lipid metabolism. Potency for activation of PPAR$\gamma$, one of a subfamily of PPARs, particularly mirrors glucose lowering activity. We prepared thiazolidinediones featuring benzoxazole moiety for subtype selective PPAR$\gamma$ activators. 5-[4-[2-(Benzoxazol-2-yl-alkylamino)ethoxy]benzyl]thiazolidine-2,4-diones have been prepared by Mitsunobu reaction of benzoxazolylalkylaminoethanol 8 and hydroxybenzylthiazolidinedione 6 and their activities were evaluated. Most compounds tested were identified as potent PPAR$\gamma$ agonists.

• Proceedings of the PSK Conference
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• 2003.04a
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• pp.224.2-225
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• 2003

Ginsenoside, major components of ginseng have been reported to show various biological activities including an increase of cholesterol metabolism. stimulation of serum protein synthesis, immunomodulatory effects. To explain these pharmacological actions, it is thought that ginseng saponins should be metabolized by human intestinal bacteria after they are orally administered. (omitted)