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Chemical constituents of Abies delavayi.
Yang, Xian-Wen; Li, Su-Mei; Li, Yong-Li; Feng, Lin; Shen, Yun-Heng; Lin, Shen; Tian, Jun-Mian; Zeng, Hua-Wu; Wang, Ning; Steinmetz, Andre; Liu, Yonghong; Zhang, Wei-Dong.
Affiliation
  • Yang XW; Department of Natural Product Chemistry, School of Pharmacy, Second Military Medical University, China; Key Laboratory of Marine Bio-Resources Sustainable Utilization, Guangdong Key Laboratory of Marine Materia Medica, South China Sea Institute of Oceanology, Chinese Academy of Sciences, China; Luxe
  • Li SM; Key Laboratory of Marine Bio-Resources Sustainable Utilization, Guangdong Key Laboratory of Marine Materia Medica, South China Sea Institute of Oceanology, Chinese Academy of Sciences, China.
  • Li YL; Department of Natural Product Chemistry, School of Pharmacy, Second Military Medical University, China.
  • Feng L; Department of Natural Product Chemistry, School of Pharmacy, Second Military Medical University, China.
  • Shen YH; Department of Natural Product Chemistry, School of Pharmacy, Second Military Medical University, China.
  • Lin S; Department of Natural Product Chemistry, School of Pharmacy, Second Military Medical University, China.
  • Tian JM; Department of Natural Product Chemistry, School of Pharmacy, Second Military Medical University, China.
  • Zeng HW; Department of Natural Product Chemistry, School of Pharmacy, Second Military Medical University, China.
  • Wang N; Luxembourg Public Research Centre for Health (CRP-SANTE), 84 Val Fleuri, L-1526 Luxembourg, Luxembourg.
  • Steinmetz A; Luxembourg Public Research Centre for Health (CRP-SANTE), 84 Val Fleuri, L-1526 Luxembourg, Luxembourg.
  • Liu Y; Key Laboratory of Marine Bio-Resources Sustainable Utilization, Guangdong Key Laboratory of Marine Materia Medica, South China Sea Institute of Oceanology, Chinese Academy of Sciences, China.
  • Zhang WD; Department of Natural Product Chemistry, School of Pharmacy, Second Military Medical University, China. Electronic address: wdzhangy@hotmail.com.
Phytochemistry ; 105: 164-70, 2014 Sep.
Article in En | MEDLINE | ID: mdl-24916321
ABSTRACT
Systematic phytochemical investigations on Abies delavayi afforded 110 compounds, including 49 terpenoids, 13 lignans, 20 flavonoids, three coumarins, and 25 other chemical constituents. By detailed analysis of one- and two-dimensional NMR spectroscopic and high-resolution mass spectrometric data, 10 previously unreported compounds were identified they comprised three sesquiterpenoids, two diterpenoids, one triterpenoid, one monoterpenoid, one flavonoid, and two phenols. These 10 compounds and some previously known ones were subjected to two cytotoxic bioassays against three human tumor cell lines and NO production inhibition on RAW264.7 macrophages, respectively. (25R)-24,25-Dihydroabieslactone had the strongest cytotoxic activity against Colo-205 cells with an IC50 value of 19.0±3.7µg/mL. (+)-T-cadinol, 8,11,13-abietatrien-15-ol-18-yl acetate, 18-acetoxy-13-epi-manool, imperatorin, bergapten, and 5,7-O-dimethyl poriol exhibited weak inhibitory activity against LPS-induced NO production in RAW264.7 macrophages with IC50 values of approximately 50µg/mL.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Flavonoids / Drugs, Chinese Herbal / Abies / Diterpenes / Anti-Inflammatory Agents Limits: Animals / Humans Language: En Journal: Phytochemistry Year: 2014 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Flavonoids / Drugs, Chinese Herbal / Abies / Diterpenes / Anti-Inflammatory Agents Limits: Animals / Humans Language: En Journal: Phytochemistry Year: 2014 Document type: Article