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Holophyllin A,a rearranged abietane-type diterpenoid from the trunk of Abies holophylla
Authors:Chung Sub Kim  Bora Shin  Oh Wook Kwon  Sun Yeou Kim  Sang Un Choi  Dong-Chan Oh  Ki Hyun Kim  Kang Ro Lee
Institution:1. Natural Products Laboratory, School of Pharmacy, Sungkyunkwan University, 300 Chonchon-dong, Jangan-ku, Suwon 440-746, Republic of Korea;2. Natural Products Research Institute, College of Pharmacy, Seoul National University, Seoul 151-742, Republic of Korea;3. Graduate School of East-West Medical Science, Kyung Hee University, Yongin 446-701, Republic of Korea;4. Gachon Institute of Pharmaceutical Science, Gachon University, Incheon 406-799, Republic of Korea;5. College of Pharmacy, Gachon University, Incheon 406-799, Republic of Korea;6. Korea Research Institute of Chemical Technology, Daejeon 305-343, Republic of Korea
Abstract:Holophyllin A (1), a novel rearranged abietane-type diterpenoid was isolated, together with a new diterpene glycoside, holophyllin B (2), from the trunk of Abies holophylla. The structures of 1 and 2 were established by extensive spectroscopic analyses and their absolute configurations were determined by ECD calculation. All the isolates were tested for their inhibitory effects on NO production in LPS-activated murine microglial cells.
Keywords:Abies holophylla  Pinaceae  Abietane diterpene  Spiro compound
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