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| 13C NMR (101 MHz, Pyr) ¦Ä: 18.0, 20.1, 22.9, 29.6, 32.2, 34.4, 38.5, 39.1, 41.3, 45.3, 46.7, 63.3, 71.8, 73.7, 76.2, 77.6, 100.0, 130.0, 201.0. |
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²éѯ½á¹û£º¹²²éµ½154¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ent-9¦Á,13-dihydroxy-16¦Â,17-epoxykauran-19-oic acid C20H30O5 ÏàËÆ¶È:60% Journal of Natural Products 2006 69 1450-1455 Transformation of Steviol-16¦Á,17-epoxide by Streptomyces griseus and Cunninghamella bainieri Shwu-Fen Chang, Li-Ming Yang, Feng-Lin Hsu, Ju-Yin Hsu, Jia-Horng Liaw, and Shwu-Jiuan Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . excisanin K C20H30O5 ÏàËÆ¶È:60% Journal of Natural Products 2004 67 373-376 Excisanin H, a Novel Cytotoxic 14,20-Epoxy-ent-Kaurene Diterpenoid,and Three New ent-Kaurene Diterpenoids from Rabdosia excisa Ming-yu Gui, Yutaka Aoyagi, Yong-Ri Jin, Xu-Wen Li, Tomoyo Hasuda, and Koichi Takeya Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Excisanin K ÏàËÆ¶È:60% Zeitschrift f¨¹r Naturforschung B 2005 60b 805-810 Isolation, Characterization and Crystal Structure of Cytotoxic ent-Kaurane Diterpenoids from Isodon weisiensis C.Y. Wu Lan Ding, Zhang-Jing Zhang, Guo-An Liu, Dong-Juan Yang, Guo-Cong Guo, Han Wang, and Kun Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . rabdokunmin D C20H30O5 ÏàËÆ¶È:60% Phytochemistry 1989 28 3405-3409 Diterpenoids from Rabdosia kunmingensis Zhang Hongjie,Sun Handong Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . dihydroponicidin ÏàËÆ¶È:60% Natural Products and Bioprospecting 2011 1 116-120 Isorosthornins A-C, new ent-kaurane diterpenoids from Isodon rosthornii Rui Zhan, Xue Du, Jia Su, Xiao-Nian Li, Wei-Guang Wang, Cheng-Qin Liang, Jian-Hong Yang, Yan Li, Jian-Xin Pu, Han-Dong Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . »Æ»¨Ïã²è²Ë¼×ËØ C20H24O6 ÏàËÆ¶È:60% Chinese Traditional and Herbal Drugs 2012 43 247-250 Studies on diterpenoids from Rabdosia nervosa WEI Zhi-xiong; GAO You-heng; LU Hai-xiao; HOU Yuan-fang; LIU Sha; LI Shu-hua Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . enanderianin N C22H32O6 ÏàËÆ¶È:59.0% Planta Medica 2003 69 1031-1035 Cytotoxic Diterpenoids from Isodon enanderianus Wei Xiang,Zhi Na,Sheng-Hong Li,Ma-Lin Li,Rong-Tao Li,Qin-E Tian,Han-Dong Sun, Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . officinoside B C19H32O8 ÏàËÆ¶È:57.8% Chemical & Pharmaceutical Bulletin 2001 49(8) 974-978 Medicinal Flowers. IV.1) Marigold. (2): Structures of New Ionone and Sesquiterpene Glycosides from Egyptian Calendula officinalis Toshiyuki MARUKAMI, Akinobu KISHI, and Masayuki YOSHIKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . melia-ionoside A C19H36O8 ÏàËÆ¶È:57.8% Chemical & Pharmaceutical Bulletin 1991 39 2529-2533 Phytochemical Studies on Meliaceous Plants. VII. The Structures of Two New Ionone Glucosides from Melia toosendan SIEB. et ZUCC. and a Novel Type of Selective Biooxidation by a Kind of Protease Tsutomu NAKANISHI,Mari KONISHI,Hiroko MURATA,Akira INADA,Atsushi FUJII,Naoki TANAKA and Takaji FUJIWARA Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . melia-ionoside A C19H36O8 ÏàËÆ¶È:57.8% Chemical & Pharmaceutical Bulletin 1990 38 830-832 THE STRUCTURES OF TWO NEW IONONE GLUCOSIDES FROM MELIA TOOSENDAN AND A NOVEL TYPE OF SELECTIVE BIO-OXIDATION Tsutomu NAKANISHI,Mari KONISHI,Hiroko MURATA,Akira INADA,Atsushi FUJII,Naoki TANAKA and Takaji FUJIWARA Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . icariside B6 C19H32O7 ÏàËÆ¶È:57.8% Chemical & Pharmaceutical Bulletin 1988 36 2475-2484 Studies on the Glycosides of Epimedium grandiflorum MORR. var. thunbergianum (MIQ.) NAKAI. III TOSHIO MIYASE,AKIRA UENO,NOBUO TAKIZAWA,HIROMI KOBAYASHI and HIROKO OGUCHI Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Gynostemoside C C19H34O8 ÏàËÆ¶È:57.8% Phytochemistry 2010 71 693-700 Gynostemosides A¨CE, megastigmane glycosides from Gynostemma pentaphyllum Zhen Zhang, Wei Zhang, Yan-Ping Ji, Yun Zhao, Chuan-Gui Wang, Jin-Feng Hu Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (-)-6,6-dimethyl-4-methylenebicyclo[3.1.1]heptane-1¦Á,3¦Á-diol-3-O-¦Â-D-glucopyranoside ÏàËÆ¶È:57.8% Records of Natural Products 2013 7 351-354 Two New Monoterpenes from Tithonia diversifolia and Their Anti-Hyperglycemic Activity Xia Li, Guanghui Huang, Guijun Zhao, Wansheng Chen, Junli Li and Lianna Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . dendronobiloside E C21H34O8 ÏàËÆ¶È:57.1% Planta Medica 2002 68 723-729 New Alloaromadendrane,Cadinene and Cyclocopacamphane Type Sesquiterpene Derivatives and Bibenzyls from Dendrobium nobile Qinghua Ye,Weimin Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . isoscoparin H C20H30O5 ÏàËÆ¶È:55% Journal of Natural Products 2009 72 125-129 ent-Kaurane Diterpenoids from Isodon scoparius Yong Zhao,Jian-Xin Pu, Sheng-Xiong Huang, Ying-Li Wu, Li-Bin Yang, Wei-Lie Xiao, Quan-Bin Han,Guo-Qiang Chen, and Han-Dong Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . maoecrystal A ÏàËÆ¶È:55% Helvetica Chimica Acta 2003 Vol. 86 299 Novel ent-Abietane Diterpenoids from Isodon eriocalyx var. laxiflora Xuemei Niu, Shenghong Li, Qinshi Zhao, Shuangxi Mei, Zhongwen Lin, Handong Sun,Yang Lu, Cheng Wang, and Qitai Zheng Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . viteagnusin C C20H36O2 ÏàËÆ¶È:55% Chemical & Pharmaceutical Bulletin 2008 56(11) 1621-1624 Five New Diterpenoids, Viteagnusins A¡ªE, from the Fruit of Vitex agnus-castus Masateru ONO,Toru YAMASAKI,Masatarou KONOSHITA,Tsuyoshi IKEDA,Masafumi OKAWA,Junei KINJO,Hitoshi YOSHIMITSU,and Toshihiro NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . excoagallochaol A C20H34O2 ÏàËÆ¶È:55% Phytochemistry 2007 68 2426-2431 Elucidation of excogallochaols A¨CD, four unusual diterpenoids from the Chinese mangrove Excoecaria agallocha Ji-Dong Wang, Wen Zhang, Zhen-Yu Li, Wen-Sheng Xiang,Yue-Wei Guo, Karsten Krohn Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . ent-9¦Á,13,16¦Â,17-tetrahydroxykauran-19-oic acid C20H32O6 ÏàËÆ¶È:55% Journal of Natural Products 2006 69 1450-1455 Transformation of Steviol-16¦Á,17-epoxide by Streptomyces griseus and Cunninghamella bainieri Shwu-Fen Chang, Li-Ming Yang, Feng-Lin Hsu, Ju-Yin Hsu, Jia-Horng Liaw, and Shwu-Jiuan Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . ent-9¦Á,13,16¦Á,17-tetrahydroxykauran-19-oic acid C20H32O6 ÏàËÆ¶È:55% Journal of Natural Products 2006 69 1450-1455 Transformation of Steviol-16¦Á,17-epoxide by Streptomyces griseus and Cunninghamella bainieri Shwu-Fen Chang, Li-Ming Yang, Feng-Lin Hsu, Ju-Yin Hsu, Jia-Horng Liaw, and Shwu-Jiuan Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . alboatisin B C20H28O5 ÏàËÆ¶È:55% Journal of Natural Products 2007 70 1053-1055 Alboatisins A-C, ent-Atisene Diterpenoids from Isodon albopilosus Sheng-Xiong Huang,Yan Zhou,Li-Bin Yang, Yong Zhao, Sheng-Hong Li, Li-Guang Lou, Quan-Bin Han,Li-Sheng Ding, and Han-Dong Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . ent-12¦Á,15¦Á-dihydroxy-16-ketobeyeran-19-oic acid C20H29O5 ÏàËÆ¶È:55% Journal of Natural Products 2002 65 273-277 Microbial Transformations of Isosteviol Feng-Lin Hsu, Chia-Chung Hou, Li-Ming Yang, Juei-Tang Cheng, Tzong-Cherng Chi, Pang-Chun Liu, and Shwu-Jiuan Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . minheryin G C20H30O5 ÏàËÆ¶È:55% Planta Medica 2009 75 65-69 Cytotoxic ent-Kaurane Diterpenoids from Isodon henryi Yong Zhao, Sheng-Xiong Huang, Li-Bin Yang, Jian-Xin Pu,Wei-Lie Xiao, Li-Mei Li, Chun Lei, Zhi-Ying Weng, Quan-Bin Han, Han-Dong Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . excoecarin B C20H32O3 ÏàËÆ¶È:55% Chemical & Pharmaceutical Bulletin 1996 44 2100-2102 Chemical Structures of Excoecarins A, B and C : Three New Labdane-Type Diterpenes from Wood, Excoecaria agallocha Tenji KONISHI,Shiu KIYOSAWA,Takao KONOSHIMA and Yasuhiro FUJIWARA Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . adenostemmoic acid G C20H30O5 ÏàËÆ¶È:55% Chemical & Pharmaceutical Bulletin 1990 38 1308-1312 Kaurane-Type Diterpenes from Adenostemma lavenia O. KUNTZE Shigeru SHIMIZU,Toshio MIYASE,Kaoru UMEHARA and Akira UENO Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . compound 15 C20H34O3 ÏàËÆ¶È:55% Chemical & Pharmaceutical Bulletin 1983 31 4409-4416 Chemische und Chemotaxonomische Untersuchungen der Pterophyten. XLIV. Chemische Untersuchungen der Inhaltsstoffe von Microlepia marginata (PANZER) C. CHR. (2) TADAYUKI KURAISHI,TAKAO TANIGUCHI,KAZUYUKI HORI,TAKAO MURAKAMI,NOBUTOSHI TANAKA,YASUHISA SAIKI and CHIUMING CHEN Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . enmenol C20H30O6 ÏàËÆ¶È:55% Acta Botanica Sinica 1994 36 813-816 Chemical Structure of Macrocalyxin H Wang Xian-rong and Wang Hong-ping Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . Sculponcatin D C20H28O8 ÏàËÆ¶È:55% Chinese Chemical Letters 1991 2 293-296 DITERPENOIDS FROM RABDOSIA SCULPONEATA RONG PIN ZHANG,HONG JIE ZHANG,YU LIN ZHEN AND HAN DONG SUN Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . kirtenol ÏàËÆ¶È:55% Chinese Chemical Letters 2001 12 51-54 New diterpenoid glucosides from Siegesbeckia pubescens Jiang XIONG, Qi Duan JIN, Yun Long XU Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . ponicidin C20H26O6 ÏàËÆ¶È:55% China Journal of Chinese Materia Medica 1994 19 295-296 Studies on Chemical Constituetns of Rabdosia nervosa (Hemsl) C.Y.Wu et H.W.Li Gao Youheng, Wan Zhenxian, Lai Xuewen and Zhu Ying Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . 8¦Â-hydroxystemodin C20H34O3 ÏàËÆ¶È:55% Journal of Natural Products 1991 Vol 54 1543 Preparation, Characterization, and Antiviral Activity of Microbial Metabolites of Stemodin Charles D. Hufford, Farid A. Badria, Mohamed Abou-Karam, W. Thomas Shier, Robin D. Rogers Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . 7¦Â,8¦Â-dihydroxystemodin C20H34O4 ÏàËÆ¶È:55% Journal of Natural Products 1991 Vol 54 1543 Preparation, Characterization, and Antiviral Activity of Microbial Metabolites of Stemodin Charles D. Hufford, Farid A. Badria, Mohamed Abou-Karam, W. Thomas Shier, Robin D. Rogers Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . stemodin ÏàËÆ¶È:55% Journal of Natural Products 1992 Vol 55 48 New Stemodane Diterpenes from Stemodia maritima Charles D. Hufford, Babajide O. Oguntimein, Ilias Muhammad Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . kirenol C20H34O4 ÏàËÆ¶È:55% Natural Product Sciences 1997 3 14-18 The Constituents of Siegesbeckia orientalis Xiong, Jiang; Ma, Yunbao; Xu, Yunlong Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . Enmenol C20H30O6 ÏàËÆ¶È:55% Phytochemistry 1995 38 921-926 Structures of macrocalyxin B, F, G and H, and maoyerabdosin from Isodon macrocalyx Wang Xian-Rong, Wang Hong-Ping, Hu Hui-Ping, Sun Han-Dong, Wang Su-Qing, Shinichi Ueda, Yoshihiro Kuroda, Tetsuro Fujita Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . kirenol C20H34O4 ÏàËÆ¶È:55% Phytochemistry 1992 31 917-921 Diterpenoids from Siegesbeckia pubescens Jiang Xiong, Yunbao Ma, Yunlong Xu Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . kirenol ÏàËÆ¶È:55% Chinese Traditional and Herbal Drugs 2002 33 495-496 Studies on chemical constituents of Siegesbeckia pubescens (¢ñ) GAO Hui; LI Ping ya; LI De kun; DU Xiao ping Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . Excisanin D ÏàËÆ¶È:55% Pharmazie 2005 60 458-460 Cytotoxic ent-kaurane diterpenoids from Isodon weisiensis C. Y. Wu Lan Ding, Guo-Ah Liu, Dong-Juan Yang, Han Wang, Lai Wang and Kun Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . kochianic acid A C20H32O6 ÏàËÆ¶È:55% Fitoterapia 2012 83 1-5 Two new abietane diterpenoids from the caulis and leaves of Callicarpa kochiana Chao-Zhan Lin, Chen-Chen Zhu, Zhong-Xiang Zhao, Xiao-Hui Li, Tian-Qin Xiong, Yu-Ying Xia, Yu Ning Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . ponicidin ÏàËÆ¶È:55% Chinese Journal of Natural Medicines 2012 10 464-470 Three new ent-kaurane diterpenoids from Isodon rubescens and their cytotoxicities Xu LIU, Yong-Bo XUE, Ke DONG, Xiao-Nian LI, Yan LI, Jian-Xin PU, Ji-Zhou WU, Han-Dong SUN Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . kirenol ÏàËÆ¶È:55% Journal of Chinese Pharmaceutical Sciences 2013 22 197-200 A new entpimarane diterpenoid from Siegesbeckia pubescens Kehui Xie, Jianbin Wang, Rong Yang, Qiong Wu, Xiaoxue Pi, Hongzheng Fu Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . compound 6 C20H32O5 ÏàËÆ¶È:55% Phytochemistry 2013 95 268-276 Biotransformation of dihydroisosteviol and the effects of transformed products on steroidogenic gene expressions Shwu-Fen Chang, Li-Ming Yang, Tsurng-Juhn Huang, Chin-Yang Chen, Shiow-Yunn Sheu, Pan-Chun Liu, Shwu-Jiuan Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . neorabdosin C24H30O7 ÏàËÆ¶È:55% Acta Chimica Sinica 1985 43 481-483 THE STRUCTURE OF NEORABDOSIN SUN HAN-DONG LIN ZHONG-WEN WAN DE-ZU GONG YUN-HUAI ; ZHAO QING-ZHI CHA JIN-HUA WAN HAN-QING Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . gelomulide U C22H30O6 ÏàËÆ¶È:54.5% Phytochemistry 2008 69 276-287 Cytotoxic ent-abietane diterpenes from Gelonium aequoreum Chia-Lin Lee,Fang-Rong Chang,Pei-Wen Hsieh,Michael-Y. Chiang,Chin-Chung Wu,Zih-You Huang,Yu-Hsuan Lan,Mei Chen,Kuo-Hsiung Lee,Hsin-Fu Yen,Wen-Chun Hung,Yang-Chang Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . eriocalyxin C C22H28O7 ÏàËÆ¶È:54.5% Journal of Natural Products 1999 62 782-784 Diterpenoids from Isodon eriocalyx Shao-Nong Chen, Jian-Min Yue, Shao-Yuan Chen, Zhong-Wen Lin, Guo-Wei Qin, Han-Dong Sun, and Yao-Zu Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . eriocalyxin C C22H28O7 ÏàËÆ¶È:54.5% Chinese Chemical Letters 1998 9 1025-1028 Three New Diterpenoids from Isodon Eriocalyx shao Nong CHEN,Shao Yuan CHEN,Jian Min YUE,Zhong Wen LIN,Guo Wei QIN,Han Dong SUN,and Yao Zu CHEN Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . flexicaulin A C22H32O6 ÏàËÆ¶È:54.5% Phytochemistry 1989 28 3534-3536 Diterpenoids from Rabdosia flexicaulis Ziiang Hongjie,Sun Handong Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . 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(2): Structures of New Ionone and Sesquiterpene Glycosides from Egyptian Calendula officinalis Toshiyuki MARUKAMI, Akinobu KISHI, and Masayuki YOSHIKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . umbrosianin C20H30O5 ÏàËÆ¶È:52.6% Chemical & Pharmaceutical Bulletin 1989 37 1213-1215 Diterpenoid Constituents of Rabdosia umbrosa (MAXIM.) : Isolation and Structure Elucidation of Two New Diterpenoids, Umbrosianin and Rabdoumbrosanin Yoshio TAKEDA,Teruyoshi ICHIHARA,Tetsuro FUJITA and Akira UENO Structure 13C NMR ̼Æ×Ä£Äâͼ 51 . compound 5 C10H20O2 ÏàËÆ¶È:52.6% Chemical & Pharmaceutical Bulletin 1981 29 1636-1643 The Constituents of Schizonepeta tenuifolia BRIQ. I. Structures of Two New Monoterpene Glucosides, Schizonepetosides A and B HIROSHI SASAKI,HEIHACHIRO TAGUCHI,TOHRU ENDO,ITIRO YOSIOKA and YOICHI IITAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 52 . icariside B2 C19H30O8 ÏàËÆ¶È:52.6% Chemical & Pharmaceutical Bulletin 1987 35 1109-1117 Studies on the Glycosides of Epimedium grandiflorum MORR. 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Johnson, Harry H. S. Fong, Norman R. Farnsworth, and Geoffrey A. Cordell Structure 13C NMR ̼Æ×Ä£Äâͼ 93 . ent-12¦Â-hydroxy-16- oxobeyeran-19-oic acid C20H30O4 ÏàËÆ¶È:50% Planta Medica 2007 73 1581-1587 Novel ent-Beyeran-19-oic Acids from Biotransformations of Isosteviol Metabolites by Mortierella isabellina Che-Ling Lin1,Shwu-Jiuan Lin,Wei-Jan Huang,Yuan-Ling Ku,Tung-Hu Tsai,Feng-Lin Hsu Structure 13C NMR ̼Æ×Ä£Äâͼ |

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