• 대한화학회지
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• 제54권1호
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• pp.9-12
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• 2010

• Bulletin of the Korean Chemical Society
• /
• 제27권7호
• /
• pp.1075-1078
• /
• 2006

• 대한화학회지
• /
• 제52권3호
• /
• pp.328-337
• /
• 2008

• Bulletin of the Korean Chemical Society
• /
• 제34권6호
• /
• pp.1899-1902
• /
• 2013

• 약학회지
• /
• 제32권3호
• /
• pp.157-163
• /
• 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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• 제32권6호
• /
• pp.2139-2142
• /
• 2011

• 대한의용생체공학회:의공학회지
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• 제7권2호
• /
• 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)

• 대한의용생체공학회:학술대회논문집
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• 대한의용생체공학회 1990년도 추계학술대회
• /
• pp.57-60
• /
• 1990

• Archives of Pharmacal Research
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• 제27권11호
• /
• 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.

• 대한약학회:학술대회논문집
• /
• 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.1
• /
• 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)