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°´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½447¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (+)-1-acetoxypinoresinol C22H24O8 ÏàËÆ¶È:68.1% Chemical & Pharmaceutical Bulletin 1984 32 2730-2735 Lignans from Bark of the Olea Plants. I HIROKI TSUKAMOTO,SUEO HISADA and SANSEI NISHIBE Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (+)-acetoxy-pinoresinol C22H24O8 ÏàËÆ¶È:68.1% Chinese Journal of Natural Medicines 2003 1 79-81 Studies on the Chemical Constituents of Fraxinus chinensis Roxb. ZHANG Dong Mei; HU Li Hong; YE Wen Cai; ZHAO Shou Xun Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (+)-1-acetoxypinoresinol ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 1985 33 1232-1241 Lignans from Bark of the Olea Plants. II HIROKI TSUKAMOTO,SUEO HISADA and SANSEI NISHIBE Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . lariciresinol ÏàËÆ¶È:66.6% China Journal of Chinese Materia Medica 2008 33 1453-1464 Studies on Chemical Constituents of Daphne holosericea (Diels) Hamaya CHEN Yuqi, SU Juan, SHEN Yunheng, ZHANG Wei, HU Xiaojia, XU Wenzheng, ZHANG Weidong, KONG Lingyi Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . lariciresinol ÏàËÆ¶È:66.6% China Journal of Chinese Materia Medica 2007 32 688-691 Studies on chemical constituents in root of Isatis indigotica ZUO Li, LI Jianbei, XU Jing, YANG Jingzhi, ZHANG Dongming, TONG Yongling Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Olivil C20H24O7 ÏàËÆ¶È:66.6% Fitoterapia 2001 72 80-82 Lignans from Strophanthus gratus S. Cowan, M. Stewart, D.K. Abbiw, Z. Latif ,S.D. Sarker,U, R.J. Nash Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . lariciresinol ÏàËÆ¶È:66.6% Chinese Pharmaceutical Journal 2008 43 1453-1456 Studies on Chemical Constituents of Daphne holosericea (Diels) Hamaya CHEN Yu-qi, SU Juan, SHEN Yun-heng, ZHANG Wei, HU Xiao-jia, XU Wen-zheng, ZHANG Wei-dong, KONG Ling-yi Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . diosniponol A C19H22O4 ÏàËÆ¶È:66.6% Bioorganic & Medicinal Chemistry Letters 2013 23 3806-3809 Anti-neuroinflammatory diarylheptanoids from the rhizomes of Dioscorea nipponica Kyeong Wan Woo, Eunjung Moon, Oh Wook Kwon, Sung Ok Lee, Sun Yeou Kim, Sang Zin Choi, Mi Won Son, Kang Ro Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . metasequirin E C19H22O7 ÏàËÆ¶È:66.6% Journal of Natural Products 2011 74 234-239 Terpenoids and Norlignans from Metasequoia glyptostroboides Liao-Bin Dong, Juan He, Yuan-Yuan Wang, Xing-De Wu, Xu Deng, Zheng-Hong Pan, Gang Xu, Li-Yan Peng, Yu Zhao, Yan Li, Xun Gong, and Qin-Shi Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (-)-berchemol C26H30O10 ÏàËÆ¶È:61.9% Chemical & Pharmaceutical Bulletin 1989 37 3311-3315 A New Lignan, (-)-Berchemol, from Berchemia racemosa Nobuko SAKURAI,Shin-ichi NAGASHIMA,Ken-ichi KAWAI and Takao INOUE Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (-)-olivil C20H24O7 ÏàËÆ¶È:61.9% Chemical & Pharmaceutical Bulletin 1988 36 795-799 Lignans Related to Olivil from Genus Cerbera : Cerbera. VI FUMIKO ABE,TATSUO YAMAUCHI and ALFRED S.C. WAN Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (+)-1-hydroxy-2-epipinoresinol C20H22O7 ÏàËÆ¶È:61.9% Chemical & Pharmaceutical Bulletin 1985 33 1232-1241 Lignans from Bark of the Olea Plants. II HIROKI TSUKAMOTO,SUEO HISADA and SANSEI NISHIBE Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (+)-1-acetoxy-2-epipinoresinol C22H24O8 ÏàËÆ¶È:61.9% Chemical & Pharmaceutical Bulletin 1985 33 1232-1241 Lignans from Bark of the Olea Plants. II HIROKI TSUKAMOTO,SUEO HISADA and SANSEI NISHIBE Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Cyclocurcumin ÏàËÆ¶È:61.9% Biochemical Systematics and Ecology 2008 36 476-780 Diaryl derivatives from the root tuber of Curcuma longa Li-Yao Wang, Mian Zhang, Chao-Feng Zhang, Zheng-Tao Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 4,4',8,8',9-pentahydroxy-3,3'-dimethoxy-7,9'-monoepoxylignan ÏàËÆ¶È:61.9% Acta Pharmaceutica Sinica 2004 Vol 39 190-193 Isolation and structure identification of the chemical constituents from pine needles of Pinus massoniana Lamb FENG Wei-sheng; WANG Yan-zhi; ZHENG Xiao-ke; BI Yue-feng Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (+)-1-hydroxypinoresinol C20H22O7 ÏàËÆ¶È:61.9% Acta Pharmaceutica Sinica 2004 Vol 39 534-537 Identification of the structure of two new nitro group phenolic glycosides from Schisandra propinqua (Wall.) Baill var. intermidia A.C.Smith WU Tong; KONG De-yun; LI Hui-ting Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (-)-Tanegool-7'-methyl ether C21H26O7 ÏàËÆ¶È:61.9% Planta Medica 2012 78 480-484 Four New Cytotoxic Tetrahydrofuranoid Lignans from Sinopodophyllum emodi Yan-Jun Sun,Zhan-Lin Li,Hong Chen,Xiao-Qiu Liu,Wei Zhou,Hui-Ming Hua Structure 13C NMR ̼Æ×Ä£Äâͼ |

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