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²éѯ½á¹û£º¹²²éµ½4157¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . vermistatin ÏàËÆ¶È:94.7% Heterocycles 2005 65 2771-2776 New Vermistatin Derivatives Isolated from Penicillium simplicissimum Shin-ichirou Komai, Tomoo Hosoe, Takeshi Itabashi, Koohei Nozawa, Takashi Yaguchi, Kazutaka Fukushima, and Ken-ichi Kawai* Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . fijiensin C18H16O6 ÏàËÆ¶È:94.7% Experientia 1990 46 982-984 Fijiensin, the first phytotoxin fromMycosphaerella fijiensis, the causative agent of Black Sigatoka disease R. K. Upadhyay, G. A. Strobel, S. J. Coval and J. Clardy Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . vermistatin C18H16O6 ÏàËÆ¶È:94.7% The Journal of Antibiotics 1986 39 1598-1601 3-N-METHYLPAROMOMYCIN I PRODUCED BY A STREPTOMYCES S. RENGARAJU, S. NARAYANAN, P. L. GANJU, M. A. AMIN, M. R. S. IYENGAR, SHUICHI GOMI, JIRO ITCH, SHINJI MIYADOH, TAKASHI SHOMURA, MASAJI SEZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . dihydrovermistatin C18H18O6 ÏàËÆ¶È:78.9% Heterocycles 2005 65 2771-2776 New Vermistatin Derivatives Isolated from Penicillium simplicissimum Shin-ichirou Komai, Tomoo Hosoe, Takeshi Itabashi, Koohei Nozawa, Takashi Yaguchi, Kazutaka Fukushima, and Ken-ichi Kawai* Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . acetoxydihydrovermistatin C20H20O8 ÏàËÆ¶È:75% Heterocycles 2005 65 2771-2776 New Vermistatin Derivatives Isolated from Penicillium simplicissimum Shin-ichirou Komai, Tomoo Hosoe, Takeshi Itabashi, Koohei Nozawa, Takashi Yaguchi, Kazutaka Fukushima, and Ken-ichi Kawai* Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Methoxyvermistatin C19H18O7 ÏàËÆ¶È:73.6% Helvetica Chimica Acta 2007 Vol. 90 1925 Structural and Biological Properties of Vermistatin and Two New Vermistatin Derivatives Isolated from the Marine-Mangrove Endophytic Fungus Guignardia sp. No. 4382 Xue-Kui Xia, Hua-Rong Huang, Zhi-Gang She, Ji-Wen Cai, Liu Lan, Jian-Ye Zhang, Li-Wu Fu, L. L. P. Vrijmoed, and Yong-Cheng Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . penisimplicissin C16H14O6 ÏàËÆ¶È:73.6% Heterocycles 2005 65 2771-2776 New Vermistatin Derivatives Isolated from Penicillium simplicissimum Shin-ichirou Komai, Tomoo Hosoe, Takeshi Itabashi, Koohei Nozawa, Takashi Yaguchi, Kazutaka Fukushima, and Ken-ichi Kawai* Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 7-(2-Methylallyloxy)-3-(3-(bis(2-chloroethyl)amino)-4-methoxyphenyl)-4H-chromen-4-one ÏàËÆ¶È:70% European Journal of Medicinal Chemistry 2012 54 175-187 Synthesis and antitumor activity of formononetin nitrogen mustard derivatives Jie Ren, Hua-Jin Xu, Hong Cheng, Wen-Qun Xin, Xin Chen, Kun Hu Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 5,7-Dihydroxy-6-(2''-hydroxy-3''-methylbut-3''-enyl)-4'-methoxylisoflavone C21H20O6 ÏàËÆ¶È:68.4% Journal of Natural Products 2009 72 164-167 Prenylated and Benzylated Flavonoids from the Fruits of Cudrania tricuspidata Xiang Hua Han, Seong Su Hong, Qinghao Jin, Dayu Li, Hyun-Kyu Kim, Jeongrai Lee, Suk Hyung Kwon,Dongho Lee,Chong-Kil Lee, Myung Koo Lee,and Bang Yeon Hwang Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 7-¦Ã,¦Ã-Dimethylallyloxy-5-hydroxy-4'-methoxyisoflavone C21H20O5 ÏàËÆ¶È:68.4% Phytochemistry Letters 2008 1 23-26 O-Prenylated flavonoids from Dalbergia sissoo Ramireddy V. Narahari Reddy, Nimmanapalli P. Reddy, Shaik I. Khalivulla, Mopuru V. Bhaskar Reddy, Duvvuru Gunasekar, Alain Blond, Bernard Bodo Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . kaempferol-7,4'-dimethyl ether ÏàËÆ¶È:68.4% Journal of Asian Natural Products Research 2006 8 401-409 New flavonol glycosides and new xanthone from Polygala japonica T.-Z. LI, W.-D. ZHANG, G.-J. YANG, W.-Y. LIU, R.-H. LIU, C. ZHANG and H.-S. CHEN Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 3,7-dihydroxy-5-4'-dunethoxyflavone ÏàËÆ¶È:68.4% Phytochemistry 1999 50 899-902 Eicosenones and methylated flavonols from Amomum koenigii Hui Dong, Yu-Lin Gou, Shu-Geng Cao, Shao-Xing Chen, Keng-Yeow Sim,Swee-Hock Goh, R. Manjunatha Kini Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . kaempferol-7,4'-dimethylether ÏàËÆ¶È:68.4% Natural Product Sciences 1998 4 215-220 Sulphated Flavonols of the Flowers of Tamarix amplexicaulis Souleman, Ahmed M.A. Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 2-(2,4-dimethoxyphenyl)-5-(E)-propenylbenzofuran ÏàËÆ¶È:68.4% Phytochemistry 1987 26 2041-2043 Ramosissin and other methoxylated nor-neolignans from Krameria ramosissima Hans Achenbach,Johann Grob,Xorge A. Dominguez,Julia Verde Star,Fernando Salgado Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . ratanhiaphenol III ÏàËÆ¶È:68.4% Phytochemistry 1989 28 1959-1962 Neolignans and nor-neolignans from Krameria lanceolata Hans Achenbach,Johann Groß,Peter Bauereiß,Xorge A. Dominguez,Humberto Sanchez Vega,Julia Verde Star,Carlos Romboldt Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . hydroxydihydrovermistatin C18H18O7 ÏàËÆ¶È:68.4% Heterocycles 2005 65 2771-2776 New Vermistatin Derivatives Isolated from Penicillium simplicissimum Shin-ichirou Komai, Tomoo Hosoe, Takeshi Itabashi, Koohei Nozawa, Takashi Yaguchi, Kazutaka Fukushima, and Ken-ichi Kawai* Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . Compound 3 ÏàËÆ¶È:68.4% Magnetic Resonance in Chemistry 2006 44 99-101 Complete assignment of 1H and 13C NMR data of dihydroxyflavone derivatives (pages 99¨C101) Byoung-Ho Moon, Youngshim Lee, Joong-Hoon Ahn and Yoongho Lim Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . Kaempferol 7,4'dimethyl ether ÏàËÆ¶È:68.4% Phytochemistry 1984 23 2347-2349 Flavonoids of the flowers of tamarix nilotica M.A.M. Nawwar, A.M.A. Souleman, J. Buddrus, M. Linscheid Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 7,4'-dimethoxykaemferol ÏàËÆ¶È:68.4% Chinese Traditional and Herbal Drugs 2006 37 1764-1768 Chemical constituents of Tamarix ramosissima ZHANG Yuan; TU Peng-fei Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . compound 9h ÏàËÆ¶È:68.4% Archiv der Pharmazie 1997 330 215-224 Synthesis and Antitumour Activity of New Derivatives of Flavone-8-acetic Acid (FAA). Part 2: Ring-Substituted Derivatives R. Alan Aitken, Michael C. Bibby, John A. Double, Andrea L. Laws, Robert B. Ritchie and David W. J. Wilson Structure 13C NMR ̼Æ×Ä£Äâͼ |
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