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New lignanamides and alkaloids from Chelidonium majus and their anti-inflammation activity.
Huang, Xue-Yan; Shao, Zhao-Xiang; An, Li-Jun; Xue, Jing-Jing; Li, Da-Hong; Li, Zhan-Lin; Hua, Hui-Ming.
Afiliação
  • Huang XY; Key Laboratory of Structure-Based Drug Design & Discovery, Ministry of Education, School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang 110016, People's Republic of China.
  • Shao ZX; Key Laboratory of Structure-Based Drug Design & Discovery, Ministry of Education, School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang 110016, People's Republic of China.
  • An LJ; State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy, Tianjin Key Laboratory of Molecular Drug Research, Nankai University, Tianjin 300350, People's Republic of China.
  • Xue JJ; Key Laboratory of Structure-Based Drug Design & Discovery, Ministry of Education, School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang 110016, People's Republic of China.
  • Li DH; Key Laboratory of Structure-Based Drug Design & Discovery, Ministry of Education, School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang 110016, People's Republic of China.
  • Li ZL; Key Laboratory of Structure-Based Drug Design & Discovery, Ministry of Education, School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang 110016, People's Republic of China.
  • Hua HM; Key Laboratory of Structure-Based Drug Design & Discovery, Ministry of Education, School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang 110016, People's Republic of China. Electronic address: huimhua@163.com.
Fitoterapia ; 139: 104359, 2019 Nov.
Article em En | MEDLINE | ID: mdl-31629049
Two new lignanamides, majusamides A and B (1 and 2), and two new alkaloids, chelidoniumine (3) and tetrahydrocoptisine N-oxide (4), together with six known hydroxycinnamic acid amides (HCCA) were isolated from the 75% ethanol extract of Chelidonium majus through the silica gel, Sephadex LH-20, MCI, ODS column chromatography, and semi-HPLC. Their structures were determined on the basis of spectroscopic data and physico-chemical methods. The absolute configurations of 1-3 were determined by electronic circular dichroism (ECD) calculations. The anti-inflammatory activities of all the isolates on the NO production in lipopolysaccharide (LPS)-induced macrophages were evaluated. Compounds 7 and 9 exhibited moderate inhibitory activity with IC50 values of 25.3 ±â€¯0.5 and 23.5 ±â€¯1.7 µM, respectively.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Lignanas / Chelidonium / Alcaloides / Amidas / Anti-Inflamatórios / Óxido Nítrico País/Região como assunto: Asia Idioma: En Revista: Fitoterapia Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Lignanas / Chelidonium / Alcaloides / Amidas / Anti-Inflamatórios / Óxido Nítrico País/Região como assunto: Asia Idioma: En Revista: Fitoterapia Ano de publicação: 2019 Tipo de documento: Article