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1 . atractylenolid III C15H20O3 ÏàËÆ¶È:93.3% Planta Medica 1989 55 59-61 Constituents of Atractylis koreana Peter Pachaly , AstridLansing, and Kwan Seog Sin Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . peroxiatractylenolide III C15H21O4 ÏàËÆ¶È:93.3% Chinese Chemical Letters 1998 9 1097-1100 Two New Sesquiterpenes from Atractylodes macrocehpala Qi Feng ZHANG,Shi De LUO,Hui Yin WANG Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 8¦Â-hydroxyasterolide ÏàËÆ¶È:93.3% Biochemical Systematics and Ecology 2002 30 187-188 Triterpenes and a sesquiterpene lactone in the resin of Trattinnickia aspera (Burseraceae) Manuel Aregullin, Matthew E. Gompper, Eloy Rodriguez Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . atractylenolide III ÏàËÆ¶È:93.3% Natural Product Research 2008 22 1418-1427 Anti-inflammatory components isolated from Atractylodes macrocephala Koidz Haiyan Dong; Langchong He; Meng Huang; Yalin Dong Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . atractylenolide ¢ó ÏàËÆ¶È:93.3% China Journal of Chinese Materia Medica 2009 34 1687-1689 Chemical constituents from Xanthium mongolicum ZHANGWenzhi, HAN Wei, LI Ying, ZHANG Shujun, ZHAO Defeng Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . codonolactone C15H20O3 ÏàËÆ¶È:93.3% Acta Pharmaceutica Sinica 2006 Vol 41 426-430 A new sesquiterpene lactone from the roots of Lasianthus acuminatissimus LI Bin; ZHANG Dong-ming; LUO Yong-ming Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . ²ÔÊõÄÚõ¥ III C15H21O3 ÏàËÆ¶È:93.3% Chinese Traditional and Herbal Drugs 2008 39 1149-1151 µØïþµÄ»¯Ñ§³É·ÖÑо¿ ÌÆÂõ;Áα¦Õä;ÁÖËç;µË˼ɺ Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . °×ÊõÄÚõ¥ III ÏàËÆ¶È:93.3% Chinese Traditional and Herbal Drugs 2007 38 499-500 é²ÔÊõ»¯Ñ§³É·ÖµÄÑо¿ ÍôÁùÓ¢;¶Î½ðâÚ;Ǯʿ»Ô;ËÞÊ÷À¼ Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . atractylenolid III C15H20O3 ÏàËÆ¶È:93.3% Chinese Journal of Natural Medicines 2008 6 404-407 A New Sesquiterpenoid from the Roots of Chloranthus fortunei WANG Xia-Chang; WU Wei-Qun; MA Shi-Ping; LIU Jing-Han; HU Li-Hong Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Atractylenolide III ÏàËÆ¶È:93.3% Archives of Pharmacal Research 2008 31 965-969 A new cytotoxic prenylated dihydrobenzofuran derivative and other chemical constituents from the rhizomes of Atractylodes lancea DC Jin-ao Duan, Liuying Wang, Shihui Qian, Shulan Su and Yuping Tang Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . atractylenolide III ÏàËÆ¶È:93.3% Chinese Pharmaceutical Journal 2007 42 1055-1059 Studies on Constituents and Anti-Inflammatory Activity of Rhizoma Atractylodis macrocephalae DONG Hai-yan, DONG Ya-lin, HE Lang-chong, PEI Wei-jing Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . atractylenolid III C15H20O3 ÏàËÆ¶È:93.3% Journal of Shenyang Pharmaceutical University 2002 19 178-179 Studies on the chemical constituents of Atractylodes chinensis(DC.) Koidz. LI Xia, WANG Jin-hui, LI Xian, LIANG Da-lian Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ²ÔÊõÄÚõ¥III ÏàËÆ¶È:93.3% Journal of China Pharmaceutical University 2001 32 94-95 Chemical Study on the Root of Codonopsis pilosula ZHU En Yuan; HE Qing; WANG Zheng Tao; XU Luo Shan; XU Guo Jun Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 1 ÏàËÆ¶È:93.3% Bioscience, Biotechnology, and Biochemistry 2009 73 2803-2805 Biotransformation of a Herb Plant Metabolite by a Cell Disruptant of Chlamydomonas reinhardtii Hyun-Sun PARK and Takeshi OHAMA Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . atractylenolide III C15H20O3 ÏàËÆ¶È:93.3% Biological and Pharmaceutical Bulletin 2012 35 1328-1335 Targeting of the Sonic Hedgehog Pathway by Atractylenolides Promotes Chondrogenic Differentiation of Mesenchymal Stem Cells Xican Li, Gang Wei, Xiaozhen Wang, Dong-Hui Liu, Ru-Dong Deng, Hui Li, Jian-Hong Zhou, Yi-Wei Li, He-Ping Zeng, Dong-Feng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . atractylenolide III ÏàËÆ¶È:93.3% Journal of Guangdong Phamaceutical University 2010 26 331-333 Study on chemical constituents of compound Zhenzhu Tiaozhi XIE Rong-rong, GUO Jiao, ZHANG De-zhi, YAN Chun-yan Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . atractylenolide III ÏàËÆ¶È:93.3% Journal of Asian Natural Products Research 2014 16 123-128 New eudesmane-type sesquiterpenoids from the processed rhizomes of Atractylodes macrocephala Ying Li & Xiu-Wei Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . atractylenolide III ÏàËÆ¶È:93.3% China Journal of Chinese Materia Medica 2011 36 578-581 Chemical constituents from aerial part of Atractylodes macrocephala PENG Wei, HAN Ting, LIU Qingchun, QIN Luping Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . Atractylenolide III C15H20O3 ÏàËÆ¶È:93.3% Chinese Journal of Natural Medicines 2012 10 24-27 A new eudesmane sesquiterpenoid lactone from Chloranthus japonicus Ping-Lei FANG, Hai-Yang LIU, Hui-Min ZHONG Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . atractylenolide III ÏàËÆ¶È:93.3% Shoyakugaku Zasshi 1990 44 1-4 Quantitative Analysis of Atractylenolide III in Atractylodes japonica TAI TAKAAKI, IDAKA KOTARO, KONDO SEIZO, AKAHORI AKIRA Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . ²ÔÊõÄÚõ¥III ÏàËÆ¶È:93.3% Journal of Chinese Medicinal Materials 2011 34 546-548 Studies on the Chemical Constituents of Codonopsis pilosula QI Huan-yang, WANG Rui, LIU Yong, SHI Yan-ping Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . lasianthuslactone A C15H20O3 ÏàËÆ¶È:93.3% Lishizhen Medicine and Materia Medica Research 2014 25 272-273 Study on Chemical Constituents of Chloranthus fortunei MA Xing-xia, LUO Gang, YING Xiao-ying Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . atractylenolide III ÏàËÆ¶È:93.3% Chinese Joumal of Experimental Traditional Medical Fomulae 2013 19 112-114 Study on Chemical Constituents in Water Decoction of Ethyl Acetate Parts of Xiangsha Liujunzi Tang Li Yu-chuan, Jia Bo, Peng Teng, Li Bo-qun, Deng Yun, Yang Jing, Yuan Hai-mei, He Gang-min Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . atracylenolide III ÏàËÆ¶È:92.8% Chinese Archives of Traditional Chinese Medicine 2013 31 993-995 Study on Chemical Constituents Extracted from Atractylodes macrocephala FANG Xuemin, CAO Gang, CAI Yinyan Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . °×ÊõÄÚõ¥III C15H20O3 ÏàËÆ¶È:86.6% Journal of Chinese Medicinal Materials 2009 32 228-229 °×ÊõÜòÜßÌÀµ÷¿ØÆ¢Ðé´óÊóѪ¹Ü»îÐÔ³¦ëÄÓÐЧ²¿Î»µÄ»¯Ñ§³É·ÖÑо¿ ÅíÌÚ, ¼Ö²¨, Åí³É, ÁõÐË¡, ÕÅéª, ºØÐ¡·¼ Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . atractylenolide III ÏàËÆ¶È:85.7% Chinese Joumal of Experimental Traditional Medical Fomulae 2013 19 73-76 Study on Chemical Constituents in Water Decoction of Fengshao Liujunzi HE Gang-min, PENG Teng, LI Bo-qun, DENG Yun, YANG Jing, YUAN Hai-mei, LI Yu-chuan Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . 8-epiatractylenolide III C15H20O3 ÏàËÆ¶È:66.6% Journal of Asian Natural Products Research 2014 16 123-128 New eudesmane-type sesquiterpenoids from the processed rhizomes of Atractylodes macrocephala Ying Li & Xiu-Wei Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . atractylenolidone ÏàËÆ¶È:64.2% Chinese Traditional and Herbal Drugs 2009 40 1192-1195 Chemical constituents of Melastoma dodecandrum(¢ò) LIN Sui; LI Yuan-chao; GUO Yu-yu; GUO Shun-min; QUE Hui-qing; QI Yi-ping Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . 8¦Â-methoxyatractylenolide ÏàËÆ¶È:62.5% Chemistry & Biodiversity 2009 6 1266-1272 New Nitrogen-Containing Sesquiterpenoids from the Taiwanese Soft Coral Cespitularia taeniata May Yuan-Bin Cheng, Ching-Yeu Chen, Yao-Haur Kuo, and Ya-Ching Shen Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . 1¦Â,8¦Â-dihydroxyeudesm-4(15),7(11)-dien-8¦Á,12-olide C15H20O4 ÏàËÆ¶È:60% Phytochemistry 2001 57 1197-1200 Sesquiterpene lactones from Smyrnium olusatrum Ali A. El-Gamal Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . biatractylolide C30H38O4 ÏàËÆ¶È:60% Journal of Natural Products 1997 60 27-28 A Novel Bisesquiterpenoid, Biatractylolide, from the Chinese Herbal Plant Atractylodes macrocephala Yongcheng Lin, Tao Jin, Xiongyu Wu, Zhongqi Huang, and Jingsong Fan Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . Taenialactam B C15H21NO2 ÏàËÆ¶È:60% Chemistry & Biodiversity 2009 6 1266-1272 New Nitrogen-Containing Sesquiterpenoids from the Taiwanese Soft Coral Cespitularia taeniata May Yuan-Bin Cheng, Ching-Yeu Chen, Yao-Haur Kuo, and Ya-Ching Shen Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . atractylenolide III C15H20O3 ÏàËÆ¶È:60% Chinese Chemical Letters 1998 9 1097-1100 Two New Sesquiterpenes from Atractylodes macrocehpala Qi Feng ZHANG,Shi De LUO,Hui Yin WANG Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . lasianthuslactone C15H21O4 ÏàËÆ¶È:60% Acta Pharmaceutica Sinica 2006 Vol 41 426-430 A new sesquiterpene lactone from the roots of Lasianthus acuminatissimus LI Bin; ZHANG Dong-ming; LUO Yong-ming Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . (3R)-3-hydroxyatractylenolide III C15H20O4 ÏàËÆ¶È:60% Chemistry & Biodiversity 2010 7 151-157 Sesquiterpenoids and Diterpenoids from Chloranthus anhuiensis Yong-Jiang Xu, Chun-Ping Tang, Min-Jia Tan, Chang-Qiang Ke, Tao Wu and Yang Ye Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . zedoarolide B ÏàËÆ¶È:60% Chinese Pharmaceutical Journal 2008 43 822-824 Studies on Chemical Constituents in Guiyujin (Report ¢ñ) GE Yue-wei, GAO Hui-min, WANG Wei-hao, WANG Zhi-min Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . compound 2 ÏàËÆ¶È:60% Bioscience, Biotechnology, and Biochemistry 2009 73 2803-2805 Biotransformation of a Herb Plant Metabolite by a Cell Disruptant of Chlamydomonas reinhardtii Hyun-Sun PARK and Takeshi OHAMA Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . biepiasterolid C30H38O4 ÏàËÆ¶È:60% Acta Chimica Sinica 1999 57 1022-1025 Structural Elucidation of Biepiasterolid WANG Bao-De YU Yi-Hua TENG Ning-Ning JIANG Shan-Hao ZHU Da-Yuan Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . Codonolactone C15H20O4 ÏàËÆ¶È:60% Lishizhen Medicine and Materia Medica Research 2014 25 272-273 Study on Chemical Constituents of Chloranthus fortunei MA Xing-xia, LUO Gang, YING Xiao-ying Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . (E)-3-(1',2',2'-Trimethyl-6'-oxo-1'-cyclohexyl)acrylsaure-methyester C13H20O3 ÏàËÆ¶È:57.1% Helvetica Chimica Acta 1980 63 1833-1855 Photochemische Reaktionen 111. Mitteilung [1] Zur Photochemie , -ungesättigter , -Epoxyester I: Singulett- versus Triplettreaktivität Alex Peter Alder, Hans Richard Wolf, Oskar Jeger Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . Taenialactone A C16H22O3 ÏàËÆ¶È:56.2% Chemistry & Biodiversity 2009 6 1266-1272 New Nitrogen-Containing Sesquiterpenoids from the Taiwanese Soft Coral Cespitularia taeniata May Yuan-Bin Cheng, Ching-Yeu Chen, Yao-Haur Kuo, and Ya-Ching Shen Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . 8-O-methylzedoarolide B C16H24O5 ÏàËÆ¶È:56.2% Phytochemistry Letters 2013 6 544-551 New derivatives from the aerial parts of Boerhaavia diffusa L. (Nyctaginaceae) Thi My Lien Do, Anh Vu Truong, Thi Nga Vo, Travis G. Pinnock, Lawrence M. Pratt, Dominique Guillaume, Kim Phi Phung Nguyen Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . zedoalactone A ÏàËÆ¶È:53.3% Planta Medica 2005 71 482-484 Anti-Babesial Compounds from Curcuma zedoaria Ken Kasahara,Shinkichi Nomura, Subeki, Hideyuki Matsuura,Masahiro Yamasaki , Osamu Yamato , Yoshimitsu Maede ,Ken Katakura,Mamoru Suzuki ,Trimurningsih, Chairul ,Teruhiko Yoshihara Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . Taenialactam A C15H21NO ÏàËÆ¶È:53.3% Chemistry & Biodiversity 2009 6 1266-1272 New Nitrogen-Containing Sesquiterpenoids from the Taiwanese Soft Coral Cespitularia taeniata May Yuan-Bin Cheng, Ching-Yeu Chen, Yao-Haur Kuo, and Ya-Ching Shen Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . beishulenolide A C15H20O2 ÏàËÆ¶È:53.3% Chinese Chemical Letters 1998 9 1097-1100 Two New Sesquiterpenes from Atractylodes macrocehpala Qi Feng ZHANG,Shi De LUO,Hui Yin WANG Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . atractylenolide I ÏàËÆ¶È:53.3% Natural Product Research 2008 22 1418-1427 Anti-inflammatory components isolated from Atractylodes macrocephala Koidz Haiyan Dong; Langchong He; Meng Huang; Yalin Dong Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . alismoxide ÏàËÆ¶È:53.3% China Journal of Chinese Materia Medica 2009 34 994-998 Chemical constituents of A lisma orientalis and their immunosuppressive function ZHANG Chaofeng, ZHOU Aichun, ZHANG mian Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . hydroxylinderstrenolide ÏàËÆ¶È:53.3% China Journal of Chinese Materia Medica 2001 26 765-767 Studies on Constituetns of the Leaves of Lindera aggregata (Sims) Kosterm. ZHANG Chaofeng, SUN Qishi, WANG Zhentao, CHOU Guixin Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . (+)-7-epi-Junenol ÏàËÆ¶È:53.3% Phytochemistry 1999 52 1519-1524 (-)-7-epi-Isojunenol and (+)-7-epi-junenol, constituents of the liverwort Tritomaria uinquedentata Ute Warmers, Wilfried A. König Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . hydroxylindestenolide ÏàËÆ¶È:53.3% Phytochemistry 1997 46 1283-1284 Bisequiterpenoid from the root of Lindera strychnifolia Isao Kouno, Asuka Hirai, Zhi-Hong Jiang, Takashi Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 51 . neolitamone A ÏàËÆ¶È:53.3% Acta Pharmaceutica Sinica 2007 Vol 42 1062-1065 A new eudesmane sesquiterpene lactone from Curcuma wenyujin WANG Shi-sheng; ZHANG Jin-mei; GUO Xiu-han; SONG Qi-ling; ZHAO Wei-jie Structure 13C NMR ̼Æ×Ä£Äâͼ 52 . Alismoxide C15H26O2 ÏàËÆ¶È:53.3% Phytochemistry 1994 36 119-127 Terpenoids of Alisma orientale rhizome and the crude drug alismatis rhizoma Yoshijiro Nakajima, Yohko Satoh, Masumi Katsumata (nee Ohtsuka), Kazuko Tsujiyama (nee Mikoshiba), Yoshiteru Ida, Junzo Shoji Structure 13C NMR ̼Æ×Ä£Äâͼ 53 . (-)-Hydroxylindestrenolide C15H18O3 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 2011 59(8) 1048-1050 (-)-Hydroxylindestrenolide, a New Sesquiterpenoid from a Gorgonian Coral Menella sp. (Plexauridae) Shih-Yao KAO, Yu-Chia CHANG, Jui-Hsin SU, Mei-Chin LU, Yung-Husan CHEN,Jyh-Horng SHEU, Zhi-Hong WEN, Wei-Hsien WANG, Yueh-Hsiung KUO,Tsong-Long HWANG, and Ping-Jyun SUNG Structure 13C NMR ̼Æ×Ä£Äâͼ 54 . Ë«°×ÊõÄÚõ¥ ÏàËÆ¶È:53.3% Chinese Traditional and Herbal Drugs 2007 38 1460-1462 Chemical constituents in rhizome of Atractylodes macrocephala LI Wei; WEN Hong-mei; CUI Xiao-bing; ZHANG Fa-cheng; DONG Jie Structure 13C NMR ̼Æ×Ä£Äâͼ 55 . atractylenolide I ÏàËÆ¶È:53.3% Chinese Pharmaceutical Journal 2007 42 1055-1059 Studies on Constituents and Anti-Inflammatory Activity of Rhizoma Atractylodis macrocephalae DONG Hai-yan, DONG Ya-lin, HE Lang-chong, PEI Wei-jing Structure 13C NMR ̼Æ×Ä£Äâͼ 56 . zedoalactone A ÏàËÆ¶È:53.3% Chinese Pharmaceutical Journal 2008 43 822-824 Studies on Chemical Constituents in Guiyujin (Report ¢ñ) GE Yue-wei, GAO Hui-min, WANG Wei-hao, WANG Zhi-min Structure 13C NMR ̼Æ×Ä£Äâͼ 57 . zedoalactone A ÏàËÆ¶È:53.3% Journal of Shenyang Pharmaceutical University 2008 25 188-190 Guaiane sesquiterpenes of Curcuma wenyujin HU Dan, MA Ning, LOU Yan, QU Ge-xia, QIU Feng Structure 13C NMR ̼Æ×Ä£Äâͼ 58 . (4aS,8aR,9aS)-3,8a-dimethyl-5-methylidene-4a,5,6,7,8,8a,9,9a-octahydronaphtho[2,3-b]furan-2(4H)-one ÏàËÆ¶È:53.3% Russian Journal of Organic Chemistry 2010 46 1719-1734 Synthetic transformations of methylenelactones of eudesmanic type. Behavior of isoalantolactone under the conitions of heck reaction A. V. Belovodskii, E. E. Shults, M. M. Shakirov, I. Yu. Bagryanskaya and Yu. V. Gatilov, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 59 . atractylenolide I ÏàËÆ¶È:53.3% Journal of Ethnopharmacology 2007 114 212-217 Screening for the anti-inflammatory activity of fractions and compounds from Atractylodes macrocephala koidz Cui-Qin Li, Lang-Chong He, Hai-Yan Dong, Ju-Qing Jin Structure 13C NMR ̼Æ×Ä£Äâͼ 60 . phaeocaulisin G C15H20O4 ÏàËÆ¶È:53.3% Journal of Natural Products 2013 76 1150-1156 Guaiane-Type Sesquiterpenes from Curcuma phaeocaulis and Their Inhibitory Effects on Nitric Oxide Production Yue Liu, JiangHao Ma, Qian Zhao, ChunRu Liao, LiQin Ding, LiXia Chen, Feng Zhao, and Feng Qiu Structure 13C NMR ̼Æ×Ä£Äâͼ 61 . phaeocaulisin H C15H20O5 ÏàËÆ¶È:53.3% Journal of Natural Products 2013 76 1150-1156 Guaiane-Type Sesquiterpenes from Curcuma phaeocaulis and Their Inhibitory Effects on Nitric Oxide Production Yue Liu, JiangHao Ma, Qian Zhao, ChunRu Liao, LiQin Ding, LiXia Chen, Feng Zhao, and Feng Qiu Structure 13C NMR ̼Æ×Ä£Äâͼ 62 . atractylenolide I ÏàËÆ¶È:53.3% China Journal of Chinese Materia Medica 2011 36 578-581 Chemical constituents from aerial part of Atractylodes macrocephala PENG Wei, HAN Ting, LIU Qingchun, QIN Luping Structure 13C NMR ̼Æ×Ä£Äâͼ 63 . asterolid ÏàËÆ¶È:53.3% Acta Chimica Sinica 1999 57 1022-1025 Structural Elucidation of Biepiasterolid WANG Bao-De YU Yi-Hua TENG Ning-Ning JIANG Shan-Hao ZHU Da-Yuan Structure 13C NMR ̼Æ×Ä£Äâͼ 64 . biatractylolide C30H38O4 ÏàËÆ¶È:53.3% Acta Scientiarum Naturalium Universitatis Sunyatseni 1996 35(2) 75-76 A Unique Bisesquiterpenoid from the Chinese Herb Medicine Atractylodes marocephala Koidz Lin Yongcheng, Jin Tao, Yuan Zhimei, Wu Xiongyu, Fan Jinsong, Huang Zhongqi Structure 13C NMR ̼Æ×Ä£Äâͼ 65 . Chlojaponilactone A C15H20O3 ÏàËÆ¶È:53.3% Chinese Journal of Natural Medicines 2012 10 24-27 A new eudesmane sesquiterpenoid lactone from Chloranthus japonicus Ping-Lei FANG, Hai-Yang LIU, Hui-Min ZHONG Structure 13C NMR ̼Æ×Ä£Äâ |

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