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1 . (+)-matrine ÏàËÆ¶È:80% Chemical & Pharmaceutical Bulletin 1996 44 1951-1953 (-)-14¦Â-Hydroxymatrine, a New Lupine Alkaloid from the Roots of Sophora tonkinensis Ping XIAO,Jiashi LI,Hajime KUBO,Kazuki SAITO,Isamu MURAKOSHI and Shigeru OHMIYA Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . matrine ÏàËÆ¶È:73.3% China Journal of Chinese Materia Medica 2006 31 557-560 Constituents in the alkaloid fraction of Kushen decoction LIU Bin, SHI Rengbing Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . matrine ÏàËÆ¶È:73.3% China Journal of Chinese Materia Medica 1997 22 741-743 Alkaloids in Sophora alopecuroides Seed and Relevant Tests for Activity Zhang Lanzhen and Li, P J Houghton and S Jackson, P R Twentyman Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . compound ÏàËÆ¶È:73.3% Korean Journal of Pharmacognosy 2000 31(4) 421-425 Isolation and Quantitative Determination of Matrine from Sophorae Radix Kim, Ju-Sun; Lee, Kyong-Soon; Chang, Seung-Yeup; Won, Do-Hee; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . matrine ÏàËÆ¶È:73.3% Natural Product Research and Development 2006 18 408-410 Studies on Cytotoxic Constituents from Sophora tonkinensis DENG Yin-hua; SUN Li; ZHANG Wei; XU Kang-ping; LI Fu-shuang; TAN Jian-bing; CAO Jian-guo; TAN Gui-shan; Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . matrine C15H25N3O ÏàËÆ¶È:73.3% Journal of Northwest A&F University (Natural Science) 2012 40 96-102 Synthesis and identification of artificial antigen of matrine LI Ying, MA Zhi-qing, FENG Jun-tao, ZHANG Xing Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . martrine ÏàËÆ¶È:73.3% Natural Medicines 1994 48 180-184 Analysis of Matrine, Matrine N-Oxide and Sophocarpine N-Oxide in Sophora Root "Kushen" YAMAMOTO KEIICHI,ARIMOTO KEIKO,et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . matrine C15H24N2O ÏàËÆ¶È:66.6% Chemistry of Natural Compounds 1996 32 596-675 ALKALOIDS. PLANTS, STRUCTURES, PROPERTIES" Chapter 2, continued R. Shakirov, M. V. Telezhenetskaya, I. A. Bessonova,S. F. Aripova, I. A. Israilov, M. N. Sultankhodzhaev,V. I. Vinogradova, V. I.Akhmedzhanova, T. S. Tulyaganov,B. T. Salimov, and V. A. Tel'nov Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 15-Hydroxy-11¦ÂH-eudesm-4-en-8¦Â,12-olide C15H22O3 ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 2008 46 1084-1088 Structural determination of three new eudesmanolides from Inula helenium (pages 1084¨C1088) Xiao-Chi Ma, Ke-Xin Liu, Bao-Jing Zhang, Xiu-Lan Xin and Jian Huang Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . ( +)-9¦Á-hydroxymatrine C15H24N2O2 ÏàËÆ¶È:66.6% Phytochemistry 1983 22 2069-2072 (+)-9¦Á-Hydroxymatrine from Sophora macrocarpa Rosa Negrete, Bruce K. Cassels, Gert Eckhardt Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . grandisine F C16H24N2O2 ÏàËÆ¶È:62.5% Journal of Natural Products 2006 69 1295-1299 Grandisines C−G, Indolizidine Alkaloids from the Australian Rainforest Tree Elaeocarpus grandis Peter L. Katavic, Debra A. Venables, Paul I. Forster, Gordon Guymer, and Anthony R. Carroll Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . bacciferin A C15H26O2 ÏàËÆ¶È:60% Journal of Natural Products 2008 71(4) 628-632 Terpenoids from the Stems of Cipadessa baccifera Li-Gen Lin, Chun-Ping Tang, Chang-Qiang Ke, Yi Zhang, and Yang Ye Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (1R,4R)-4-hydroxydauca-7-ene-6-one C15H24O2 ÏàËÆ¶È:60% Journal of Natural Products 2005 68 468-471 Daucane Sesquiterpenes from Ferula hermonis Amlie Lhuillier, Nicolas Fabre, Edmond Cheble, Fathi Oueida,Sverine Maurel, Alexis Valentin, Isabelle Fourast, and Claude Moulis Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 25 ÏàËÆ¶È:60% Journal of Natural Products 2003 66 344-349 Chemical Transformations on Botryane Skeleton. Effect on the Cytotoxic Activity Jos L. Reino, Rosa Durn-Patrn, Inmaculada Segura, Rosario Hernndez-Galn, Hans H. Riese, and Isidro G. Collado Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (8R)-8-acetoxypatchoulol C17H28O3 ÏàËÆ¶È:60% Journal of Natural Products 1999 62 437-440 Biotransformation of the Fungistatic Sesquiterpenoid Patchoulol by Botrytis cinerea Josefina Aleu, James R. Hanson, Rosario Hern¨¢ndez Gal¨¢n, and Isidro G. Collado Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 2¦Á-hydroxy pterodontic acid C15H22O3 ÏàËÆ¶È:60% Journal of Asian Natural Products Research 2007 9 233-237 Two eudesmane sesquiterpenes from Laggera pterodonta Y.-B. LIU†, W. JIA, Z. YAO, Q. PAN, Y. TAKAISHIk and H.-Q. DUAN Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (+)-cycloisolongifolol ÏàËÆ¶È:60% Natural Product Research 2007 21 455-460 Biotransformation of (+)-cycloisolongifolol by plant pathogenic fungus Glomerella cingulata Mitsuo Miyazawa; Kazuki Sakata Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (+)-cycloisolongifol-5¦Â-ol C15H24O ÏàËÆ¶È:60% Zeitschrift f¨¹r Naturforschung B 2006 61b 1035-1038 Microbial Metabolism of (+)-Cycloisolongifol-5¦Â-ol |
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