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| 13C NMR (126 MHz, MeOD) ¦Ä 35.31, 38.83, 42.48, 47.71, 55.26, 56.28, 56.32, 56.40, 72.55, 72.96, 87.47, 110.94, 113.21, 113.84, 116.08, 116.15, 120.05, 122.20, 123.01, 130.76, 131.46, 133.72, 146.08, 147.23, 148.96, 149.00, 149.10, 181.76. |
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´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£º¹²²éµ½361¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . lappaol A ÏàËÆ¶È:80% China Journal of Chinese Materia Medica 2010 35 2852-2861 Constituents of Gymnadenia conopsea YUE Zhenggang; ZI Jiachen; ZHU Chenggen; LIN Sheng; YANG Yongchun; SHI Jiangong Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . deltoignan B C29H30O9 ÏàËÆ¶È:72.4% Fitoterapia 2012 83 1125-1130 Cytotoxic sesquiterpenes and lignans from Saussurea deltoidea Jun-Ju Xu, Huo-Qiang Huang, Guang-Zhi Zeng, Ning-Hua Tan Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . isolappaol C C30H34O10 ÏàËÆ¶È:70% Chemical & Pharmaceutical Bulletin 2007 55(1) 150-152 Lignans from Arctium lappa and Their Inhibition of LPS-Induced Nitric Oxide Production So Young PARK,Seong Su HONG,Xiang Hua HAN,Ji Sang HWANG,Dongho LEE,Jai Seup RO,and Bang Yeon HWANG Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . isocimicifugamide ÏàËÆ¶È:64.2% Acta Pharmaceutica Sinica 1994 29 195-199 STUDIES ON PHENOLIC GLYCOSIDES ISOLATED FRoM CIMICIFUGA DAHURICA CJ LI; DH CHen PG Xiao Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 1 C27H34O11 ÏàËÆ¶È:64.2% Indian Journal of Chemistry Section B 2011 50B 624-626 Saussurea heteromalla (D. Don) Hand.-Mazz.: A new source of arctiin, arctigenin and chlorojanerin Saklani, Arvind; Sahoo, Manas Ranjan; Mishra, Prabhu Dutt; Vishwakarma, Ram Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . dumosaol C30H32O10 ÏàËÆ¶È:63.3% Acta Botanica Yunnanica 2005 27(2) 217-222 A New Sesquilignan from Tsuga dumosa ZHAO You-Xing, LI Cheng-Sen, LUO Xiao-Dong,LIU Yu-Qing,ZHOU Jun Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Spathulatol ÏàËÆ¶È:63.3% Acta Botanica Yunnanica 2010 32 281-284 One New Sesqui-lignan from Illicium spathulatum (Ill iciaceae) LAI Guo-Fang, DONG Xu-Jun, YANG Jian-Kun , LUO Huai-Rong, WANG Yi-Fen Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . clinopodic acid H C29H26O12 ÏàËÆ¶È:62.0% Journal of Natural Products 2009 72 1379-1384 Matrix Metalloproteinase-2 Inhibitors from Clinopodium chinense var. parWiflorum Toshihiro Murata,Kenroh Sasaki,Kumiko Sato, Fumihiko Yoshizaki, Haruna Yamada, Hiromichi Mutoh, Kaoru Umehara,Toshio Miyase,Tsutomu Warashina,Hiroaki Aoshima, Homare Tabata, and Kouichi Matsubara Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3-Formyl-2-(3'',4''-dimethoxy-2''-mesyloxyphenyl)-1-(3',4'-dimethoxyphenyl)-8,9-dimethoxy-5,6-dihydropyrrolo[2,1-a]isoquinoline C32H33NO10S ÏàËÆ¶È:62.0% Tetrahedron Letters 2001 42 1205-1208 An efficient synthesis of lamellarin alkaloids: synthesis of lamellarin G trimethyl ether Somsak Ruchirawat, Thumnoon Mutarapat Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . ningalin B permethyl ether C31H31NO8 ÏàËÆ¶È:62.0% Australian Journal of Chemistry 2009 62 683-691 A Total Synthesis of the Marine Alkaloid Ningalin B from (S)-Proline Katrin Hasse, Anthony C. Willis and Martin G. Banwell Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . styraxlignolide C C26H32O11 ÏàËÆ¶È:60.7% Journal of Natural Products 2004 67 1980-1984 New Furofuran and Butyrolactone Lignans with Antioxidant Activity from the Stem Bark of Styrax japonica Byung-Sun Min, Min-Kyun Na, Sei-Ryang Oh, Kyung-Seop Ahn, Gil-Saeng Jeong, Gao Li, Sang-Ku Lee, Hyouk Joung, and Hyeong-Kyu Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . trachelosiaside C28H36O11 ÏàËÆ¶È:60.7% Chemical & Pharmaceutical Bulletin 1986 34 4340-4345 Lignans from Trachelospermum asiaticum (Tracheolospermum. II) FUMIKO ABE and TATSUO YAMAUCHI Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . isocimicifugamide C25H31NO10 ÏàËÆ¶È:60.7% Chinese Chemical Letters 1993 4 891-892 CIMICIFUGAMIDE AND ISOCIMICIFUGAMIDE,TWO NEW CINNAMAMIDE DERIVATIVES ISOLATED FROM CIMICIFUGA DAHURICA CONG JUN LI ,DI HUA CHEN,PEI GEN XIAO Structure 13C NMR ̼Æ×Ä£Äâͼ |

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