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Çå·çÓÄÀ¼: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, thank u very much£¡ 2013-03-16 08:42:38
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Çå·çÓÄÀ¼: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, thank u very much£¡ 2013-03-16 08:42:38
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1 . Compound 3 ÏàËÆ¶È:68.7% Magnetic Resonance in Chemistry 2007 45 705-709 Xylocarpins A and B, two new mexicanolides from the seeds of a Chinese mangrove Xylocarpus granatum: NMR investigation in mixture (pages 705¨C709) Minyi Li, Jun Wu, Si Zhang, Qiang Xiao and Qingxin Li Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . methyl 3¦Â-tigloyloxy-2,6-dihydroxy-1-oxo-meliac-8(30)-enate C32H40O10 ÏàËÆ¶È:62.5% Chemical & Pharmaceutical Bulletin 1998 46 523-525 Tetranortriterpenoids from Swietenia macrophylla Keisuke KOJIMA,Kimio ISAKA and Yukio OGIHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 12-O-methylvolkensin C33H42O10 ÏàËÆ¶È:61.7% Phytochemistry 1999 51 787-791 Limonoids from fruit of Melia toosendan and their cytotoxic activity Kiyomi Tada, Michio Takido, Susumu Kitanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Munronoid N C34H46O9 ÏàËÆ¶È:61.7% Journal of Agricultural and Food Chemistry 2012 60 4289-4295 The Limonoids and Their Antitobacco Mosaic Virus (TMV) Activities from Munronia unifoliolata Oliv. Yong-hui Ge, Kai-xing Liu, Jian-xin Zhang, Shu-zhen Mu, and Xiao-jiang Hao Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . methyl 3¦Â-tigloyloxy-2-hydroxy-1-oxo-meliac-8(30)-enate C32H40O9 ÏàËÆ¶È:59.3% Chemical & Pharmaceutical Bulletin 1998 46 523-525 Tetranortriterpenoids from Swietenia macrophylla Keisuke KOJIMA,Kimio ISAKA and Yukio OGIHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . methyl-2-hydroxy-3¦Â-tigloyloxy-1-oxomeliac-8(30)-enate ÏàËÆ¶È:59.3% Phytochemistry 1998 49 1981-1988 Limonoids from Swietenia humilis and Guarea grandiflora (Meliaceae)Taken in part from the PhD and MS theses of C. Villarreal and M. A. Jim¨¦nez, respectively. Adelina Jimenez, Claudina Villarreal, Ruben Alfredo Toscano, Mathew Cook, John T. Arnason, Robert Bye, Rachel Mata Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . methyl-3¦Â-tigloyloxy-2,6-dihydroxy-1-oxo-meliac-8(30)-enate ÏàËÆ¶È:58.0% Natural Product Research 2008 22 763-800 13C NMR spectroscopy of D and B, D-ring seco-limonoids of Meliaceae family T. Narender; T. Khaliq; Shweta Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . anguinomycin C C31H46O4 ÏàËÆ¶È:58.0% The Journal of Antibiotics 1995 48 954-961 Anguinomycins C and D, New Antitumor Antibiotics with Selective Cytotoxicity against Transformed Cells YOICHI HAYAKAWA, KIN-YA SOHDA, KAZUO SHIN-YA, TOMOMI HIDAKA, HARUO SETO Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3¦Â-acetoxy-5-en-benzo[g]androst[17,16-b]quinoline C32H35NO2 ÏàËÆ¶È:58.0% Steroids 2012 77 1438-1445 A microwave promoted solvent-free approach to steroidal quinolines and their in vitro evaluation for antimicrobial activities Shyamalee Gogoi, Kommuri Shekarrao, Aparajita Duarah, Tarun C. Bora, Sanjib Gogoi, Romesh C. Boruah Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . caseobliquin A C33H40O10 ÏàËÆ¶È:57.5% Journal of Natural Products 2009 72 1847-1850 Cytotoxic Clerodane Diterpenoids from Casearia obliqua Gerardo Magela Vieira J¨²nior, Tiago de Oliveira Gonc¸alves, Luis O. Regasini, Paulo M. Pinheiro Ferreira,Cl¨¢udia do ¨® Pessoa, Let¨ªcia V. Costa Lotufo, Roseli Buzanelli Torres, Nivaldo Boralle, Vanderlan da Silva Bolzani, and Alberto Jos¨¦ Cavalheiro Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 1¦Á-tigloyloxy-3¦Á-acetoxyl-7¦Á-hydroxyl-12¦Á-ethoxylnimbolinin C35H48O9 ÏàËÆ¶È:57.1% Chinese Chemical Letters 2010 21 838-841 New limonoids from the fruits of Melia toosendan Qiong Zhang; Jing Yu Liang; Qing Shan Li; Zhi Da Min Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Meliatoosenin O C35H48O9 ÏàËÆ¶È:57.1% Phytochemistry 2012 73 106-113 Limonoids from the fruits of Melia toosendan Yi Zhang, Chun-Ping Tang, Chang-Qiang Ke, Xi-Qiang Li, Hua Xie, Yang Ye Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . barbatin A C34H38O8 ÏàËÆ¶È:56.2% Phytochemistry 2006 67 1326-1330 neo-Clerodane diterpenoids from Scutellaria barbata with cytotoxic activities Sheng-Jun Dai, Jia-Yi Tao, Ke Liu, Yong-Tao Jiang, Li Shen Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . chaetoglobosin S C32H38N2O3 ÏàËÆ¶È:56.2% Journal of Natural Products 2004 67 1722-1725 Chaetoglobosins Q, R, and T, Three Further New Metabolites from Chaetomium globosum Wenxu Jiao, Yunjiang Feng, John W. Blunt, Anthony L. J. Cole, and Murray H. G. Munro Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . swietenin F C34H38O9 ÏàËÆ¶È:56.2% Chemical & Pharmaceutical Bulletin 1990 38 639-651 Constituents of the Seeds of Swietenia mahagoni JACQ. I. : Isolation, Structures, and 1H- and 13C-Nuclear Magnetic Resonance Signal Assignments of New Tetranortriterpenoids Related to Swietenine and Swietenolide Shigetoshi KADOTA,Lamek MARPAUNG,Tohru KIKUCHI and Hisao EKIMOTO Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . Amphidinolide D C32H50O8 ÏàËÆ¶È:56.2% Journal of Natural Products 1989 Vol 52 1036 Cytotoxic Macrolides from a Cultured Marine Dinoflagellate of the Genus Amphidinium Jun'ichi Kobayashi, Masami Ishibashi, Hideshi Nakamura, Yasushi Ohizumi, Terufumi Yamasu, Yoshimasa Hirata, Takuma Sasaki, Tomihisa Ohta, Shigeo Nozoe Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . xylogodavarin D C32H38O8 ÏàËÆ¶È:56.2% Chemistry-A European Journal 2012 18 14342-14351 Andhraxylocarpins A¨CE: Structurally Intriguing Limonoids from the True Mangroves Xylocarpus granatum and Xylocarpus moluccensis Jun Li, Dr. Min-Yi Li, Dr. Torsten Bruhn, Dr. Daniel C. G. Götz, Prof. Dr. Qiang Xiao, Tirumani Satyanandamurty, Prof. Dr. Jun Wu and Prof. Dr. Gerhard Bringmann Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . chisomicine A C32H38O8 ÏàËÆ¶È:56.2% Journal of Natural Products 2011 74 1313-1317 Chisomicines A−C, Limonoids from Chisocheton ceramicus Ibrahim A. Najmuldeen, A. Hamid A. Hadi, Khalijah Awang, Khalit Mohamad, Kamal Aziz Ketuly, Mat Ropi Mukhtar, Soon-Lim Chong, Gomathi Chan, Mohd Azlan Nafiah, Ng Seik Weng, Osamu Shirota, Takahiro Hosoya, Alfarius E. Nugroho, and Hiroshi Morita Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . humilinolide E C34H42O11 ÏàËÆ¶È:55.8% Phytochemistry 1998 49 1981-1988 Limonoids from Swietenia humilis and Guarea grandiflora (Meliaceae)Taken in part from the PhD and MS theses of C. Villarreal and M. A. Jim¨¦nez, respectively. Adelina Jimenez, Claudina Villarreal, Ruben Alfredo Toscano, Mathew Cook, John T. Arnason, Robert Bye, Rachel Mata Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 6-O-acetyl-2-hydroxyswietenin C34H42O11 ÏàËÆ¶È:55.8% Heterocycles 2004 63 389-399 Three New Mexicanolides from the Stem Bark of Swietenia mahogani Jacq. Mona M. G. Saad, Tetsuo Iwagawa, Hiroaki Okamura, Matsumi Doe, and Munehiro Nakatani* Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 17-benzoyloxy-3-O-(2,3-dimethylbutanoyl)-20-deoxyingenol C33H42O7 ÏàËÆ¶È:54.8% Phytochemistry 2008 69 812-819 Ingenane diterpenoids from Euphorbia esula Zhi-Qiang Lu, Min Yang, Jin-Qiang Zhang, Guang-Tong Chen, Hui-Lian Huang,Shu-Hong Guan, Chao Ma, Xuan Liu, De-An Guo Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 7,9,13-trideacetylbaccatin VI C31H40O11Na ÏàËÆ¶È:54.8% Phytochemistry 2000 54 221-230 Taxoids from the needles of the Canadian yew Junzeng Zhang, Francoise Sauriol, Orval Mamer, Lolita O. Zamir Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . (13E,17E)-12-phenylsulfonylbicyclogeranylfarnesol ÏàËÆ¶È:54.8% Chemistry of Natural Compounds 2007 43 268-273 SUPERACID CYCLIZATION OF(2E,6E,10E,14E)-8- PHENYLSULFONYLGERANYLFARNESOL TETRAHYDROPYRANYL ETHER V. Kulcitki, M. Grin'ko, A. Barba,N. Ungur, and P. F. Vlad Structure 13C NMR ̼Æ×Ä£Äâͼ |

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