지원사업
학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
커뮤니티
연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
초록· 키워드
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A practical synthesis of natural hydroxycinnamide derived from Hippophae rhamnoides L. has been accomplished. One-pot protection/deprotection and amidation of 4-hydroxycinnamic acid afforded the purposed cinnamide in good yield. The spectral data of synthesized cinnamide were in excellent agreement with the reported data. This synthetic procedure would facilitate synthesis of the natural hydroxycinnamides, and their biological studies.
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참고문헌 (13)
참고문헌 신청
Chen, C / 2016 / Sinapic acid and its derivatives as medicine in oxidative stress-induced diseases and aging / Oxid. Med. Cell Longev :3571614
Alam, M. A / 2016 / Hydroxycinnamic acid derivatives: a potential class of natural compounds for the management of lipid metabolism and obesity / Nutr. Metab 13:27
Yamaguchi, M / 2015 / The flavonoid p-hydroxycinnamic acid exhibits anticancer effects in human pancreatic cancer MIA PaCa-2 cells in vitro: Comparison with gemcitabine / Oncol. Rep 34:3304
Liu, L. Y / 2013 / NHydroxycinnamide derivatives of osthole presenting genotoxicity and cytotoxicity against human colon adenocarcinoma cells in vitro and in vivo / Chem. Res. Toxicol 26:1683
Huang, W. J / 2010 / Synthesis of Nhydroxycinnamides capped with a naturally occurring moiety as inhibitors of histone deacetylase / ChemMedChem 5:598
Alam, M. A / 2016 / Hydroxycinnamic acid derivatives: a potential class of natural compounds for the management of lipid metabolism and obesity / Nutr. Metab 13:27
Yamaguchi, M / 2015 / The flavonoid p-hydroxycinnamic acid exhibits anticancer effects in human pancreatic cancer MIA PaCa-2 cells in vitro: Comparison with gemcitabine / Oncol. Rep 34:3304
Liu, L. Y / 2013 / NHydroxycinnamide derivatives of osthole presenting genotoxicity and cytotoxicity against human colon adenocarcinoma cells in vitro and in vivo / Chem. Res. Toxicol 26:1683
Huang, W. J / 2010 / Synthesis of Nhydroxycinnamides capped with a naturally occurring moiety as inhibitors of histone deacetylase / ChemMedChem 5:598
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