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Spiroketones and a Biphenyl Analog from Stems and Leaves of Larrea nitida and Their Inhibitory Activity against IL-6 Production.
Ahn, Jongmin; Pei, Yihua; Chae, Hee-Sung; Kim, Seong-Hwan; Kim, Young-Mi; Choi, Young Hee; Lee, Joongku; Chang, Minsun; Song, Yun Seon; Rodriguez, Roberto; Oh, Dong-Chan; Kim, Jinwoong; Choi, Sangho; Joo, Sang Hoon; Chin, Young-Won.
Afiliação
  • Ahn J; College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul 08826, Korea. jm212224@snu.ac.kr.
  • Pei Y; College of Pharmacy and Integrated Research Institute for Drug Development, Dongguk University-Seoul, Gyeonggi-do 10326, Korea. yeahhwa@gmail.com.
  • Chae HS; College of Pharmacy and Integrated Research Institute for Drug Development, Dongguk University-Seoul, Gyeonggi-do 10326, Korea.
  • Kim SH; College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul 08826, Korea. yanberk@hanmail.net.
  • Kim YM; College of Pharmacy and Integrated Research Institute for Drug Development, Dongguk University-Seoul, Gyeonggi-do 10326, Korea. dongchanoh@snu.ac.kr.
  • Choi YH; College of Pharmacy and Integrated Research Institute for Drug Development, Dongguk University-Seoul, Gyeonggi-do 10326, Korea. choiyh@dongguk.edu.
  • Lee J; Department of Environment and Forest Resources, College of Agriculture and Life Sciences, Chungnam National University, Daejeon 34134, Korea. joongku@cnu.ac.kr.
  • Chang M; Department of Biological Sciences, College of Science, Sookmyung Women's University, Seoul 04310, Korea. minsunchang@sookmyung.ac.kr.
  • Song YS; College of Pharmacy, Sookmyung Women's University, Seoul 04310, Korea. yssong@sookmyung.ac.kr.
  • Rodriguez R; Department of Botany, University of Concepcion, Casilla 160C, Concepcion 4080871, Chile. rrodrigu@udec.cl.
  • Oh DC; College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul 08826, Korea. jwkim@snu.ac.kr.
  • Kim J; College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul 08826, Korea.
  • Choi S; International Biological Material Research Center, KRIBB, Daejeon 34141, Korea. decoy0@kribb.re.kr.
  • Joo SH; College of Pharmacy, Daegu Catholic University, Gyeongbuk 38430, Korea. sjoo@cu.ac.kr.
  • Chin YW; College of Pharmacy and Integrated Research Institute for Drug Development, Dongguk University-Seoul, Gyeonggi-do 10326, Korea. f2744@dongguk.edu.
Molecules ; 23(2)2018 Jan 31.
Article em En | MEDLINE | ID: mdl-29385086
ABSTRACT
Bioactivity-guided fractionation for the stems of leaves of Larrea nitida Cav., using interleukin-6 (IL-6) inhibitory assay in human mast cells (HMC-1), led to the isolation of three new compounds with an unprecedented skeleton in nature (1-3) and three known compounds (4-6). Their structures were elucidated through extensive spectroscopic analysis. The three new compounds were elucidated as two new spiroketones, nitidaones A (1), and B (2) and one new biphenyl analog, nitidaol (3). The known compounds were identified as nordihydroguaiaretic acid (4), 7,3',4'-tri-O-methylquercetin (5) and ayanin (6). All the isolates were tested for their inhibitory activity against IL-6 production in HMC-1 cells. Of them, compounds 1, 3-6 showed potent anti-inflammatory activity, with IC50 values of 12.8, 17.5, 14.9, 22.9, and 17.8 µM, respectively.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Espironolactona / Compostos de Bifenilo / Interleucina-6 / Caules de Planta / Folhas de Planta / Larrea / Mastócitos / Anti-Inflamatórios Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Molecules Assunto da revista: BIOLOGIA Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Espironolactona / Compostos de Bifenilo / Interleucina-6 / Caules de Planta / Folhas de Planta / Larrea / Mastócitos / Anti-Inflamatórios Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Molecules Assunto da revista: BIOLOGIA Ano de publicação: 2018 Tipo de documento: Article