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kaopuma: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2012-11-06 09:20:36
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kaopuma: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2012-11-06 09:20:36
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1 . aquisiflavoside C28H32O15 ÏàËÆ¶È:66.6% Journal of Asian Natural Products Research 2012 14 867-872 Aquisiflavoside, a new nitric oxide production inhibitor from the leaves of Aquilaria sinensis Xin-Bao Yang, Jie Feng, Xiu-Wei Yang, Bo Zhao & Jian-Xun Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 7,3',4'-ÈýôÇ»ù-5-¼×Ñõ»ÆÍª´¼ ÏàËÆ¶È:62.5% Chinese Journal of Marine Drugs 2010 29(1) 41-44 Study on chemical constituents from Ipomoea Pescaprae ( L. ) Sweet- WANG Qing-ji, WANG You-shao*, HE Lei, LOU Zhi-ping, ZHANG Si Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3',5'-dimethoxy-[2'',3'' : 8,7]-furano flavone C19H14O5 ÏàËÆ¶È:62.5% Zeitschrift f¨¹r Naturforschung B 2005 60b 356-358 Prenylated Flavonoids from Pongamia pinnata Hao Yin, Si Zhang, and Jun Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . chrysoeriol ÏàËÆ¶È:62.5% Chinese Traditional and Herbal Drugs 2004 35 622-624 ɳĮ¾îÝﻯѧ³É·ÖÑо¿ µËÑãÈç,ºÎÀó,Àîάç÷,ÍôººÇä Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Geraldone C16H12O5 ÏàËÆ¶È:62.5% Archives of Pharmacal Research 2004 27 593-599 Isolation of flavonoids and a cerebroside from the stem bark of Albizzia julibrissin Mee Jung Jung, Sam Sik Kang, Hyun Ah Jung, Goon Ja Kim and Jae Sue Choi Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . chrysoeriol ÏàËÆ¶È:62.5% Chinese Pharmaceutical Journal 2009 44 1475-1477 Studies on Flavonoids from Galium aparine CAI Xiao-mei, YANG Juan, RAO Qiong-juan Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . boeravinone J C16H10O6 ÏàËÆ¶È:62.5% Journal of Medicinal Chemistry 2007 50 1933-1938 Nonprenylated Rotenoids, a New Class of Potent Breast Cancer Resistance Protein Inhibitors Abdelhakim Ahmed-Belkacem, Sira Macalou, Francesca Borrelli, Raffaele Capasso, Ernesto Fattorusso, Orazio Taglialatela-Scafati, and Attilio Di Pietro Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . apigenin 5-O-monomethyl ether ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 1984 32 5023-5026 Studies on the Constituents of Thalictrum thunbergii DC. I EMIKO SHIMIZU,TOSHIAKI TOMIMATSU and TOSHIHIRO NOHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . cinaroside C21H20O11 ÏàËÆ¶È:60% Chemistry of Natural Compounds 2002 38 358-406 PHENOLIC COMPOUNDS OF PLANTS OF THE Scutellaria L. GENUS. DISTRIBUTION, STRUCTURE, AND PROPERTIES V. M. Malikov and M. P. Yuldashev Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 3,6,7-Trihydroxy-1-methoxyxanthone C14H10O6 ÏàËÆ¶È:60% Journal of Asian Natural Products Research 2007 9 393-397 Xanthones from the roots of Cudrania fruticosa Wight B. LIANG, H.-R. LI, L.-Z. XU and S.-L. YANG Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 3,6,7-tri-hydroxy-1-methoxy-xanthone C14H10O6 ÏàËÆ¶È:60% Natural Product Research 2006 20 1237-1240 Two new xanthones from Hypericum japonicum P. Fu; W. -D. Zhang; R. H. Liu; T. -Z. Li; Y. -H. Shen; H. -L. Li; W. Zhang; H. -S. Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . luteolin-7-O-neohesperidoside ÏàËÆ¶È:60% China Journal of Chinese Materia Medica 2009 34 1377-1380 ¼ÙŠL°üÒ¶¿¹¾ú»îÐԳɷֵÄÑо¿(2) ÌïÒ±, ÌÀº£·å, ÍõÏþ¾ê, Çñ·å , Ѧ¸Ä½ø, Àî¾ü Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 8 ÏàËÆ¶È:60% Phytochemistry 1981 20 1977-1979 An acylated allose-containing 8-hydroxyflavone glycoside from Veronica filiformis V.Mohan Chari, Rence J. Grayer-Barkmeijer, Jeffrey B. Harborne, Bengt-Göran Österdahl Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . luteolin-7-O-¦Â-D-glucosides C21H20O11 ÏàËÆ¶È:60% Chinese Traditional and Herbal Drugs 2006 37 25-27 Isolation and structural elucidation of flavonoid from Pyrethrum tatsienense YANG Ai-mei; LIU Xia; LU Run-hua; SHI Yan-ping Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 5,7-dihydroxy-4-oxo-4H-chromen-3-yl 4-methoxybenzoate C17H12O7 ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry 2010 18 2864-2871 Synthesis of a novel series of diphenolic chromone derivatives as inhibitors of NO production in LPS-activated RAW264.7 macrophages Guo-Biao Liu, Jian-Liang Xu, Mei Geng, Rui Xu, Rong-Rong Hui, Jian-Wei Zhao, Qiang Xu, Hong-Xi Xu, Jian-Xin Li Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 4'-hydroxy-5,7-dimethoxyflavone ÏàËÆ¶È:60% Journal of the Chinese Chemical Society 2004 51 199-204 Flavone Glycosides from Strobilanthes formosanus Kuo-Ching Kao, Yu-Ling Ho, I-Hsin Lin,Li-Kang Ho and Yuan-Shiun Chang* Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 1-methoxy-3,7,8-trihydroxyxanthone C14H10O6 ÏàËÆ¶È:60% Magnetic Resonance in Chemistry 2012 50 642-645 Xanthones from the stems of Cratoxylum cochinchinense Yinghui Duan, Yi Dai, Liuyuan Chen, Mingli Liu, Yaolan Li and Xinsheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . Ethyl 6-(4-methoxyphenyl)-2-oxo-4-trifluoromethyl-1,2-dihydropyrimidine-5-carboxylate C15H13F3N2O4 ÏàËÆ¶È:60% Tetrahedron 2012 68 8408-8415 Heterocyclization of N-(1-chloro-2,2,2-trifluoroethylidene)carbamates with ¦Â-enaminoesters¡ªa novel synthetic strategy to functionalized trifluoromethylated pyrimidines Volodymyr A. Sukach, Viktor M. Tkachuk, Eduard B. Rusanov, Gerd-Volker Röschenthaler, Mykhaylo V. Vovk Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . velutin ÏàËÆ¶È:58.8% Journal of Natural Products 1996 59 701-703 DNA Topoisomerase I Inhibitors: Cytotoxic Flavones from Lethedon tannaensis Abdellatif Zahir, Akino Jossang, and Bernard Bodo Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 5,7-dihydroxy-3',4'-dimethoxyflavone ÏàËÆ¶È:58.8% China Journal of Chinese Materia Medica 2005 30 126-128 Studies on the flavonoid constituents in herb of Eremosparton songoricum DING Lan, LIU Guoan, HE Li, WANG Hanqing Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . luteolin-5,3'-dimethyl ether C17H14O6 ÏàËÆ¶È:58.8% Acta Pharmaceutica Sinica 2007 Vol 42 174-178 Isolation and identification of phenolic constituents from Juncus effusus LI Hong-xia; DENG Tie-zhong; CHEN Yu; FENG Hui-jin; YANG Guang-zhong Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . Gerontoisoflavone A C17H14O6 ÏàËÆ¶È:58.8% Phytochemistry 1995 40 945-947 Flavonoids and a prenylated xanthone from Cudrania cochinchinensis var. gerontogea Cheng-Hsiung Chang, Chun-Ching Lin, Shigetosfi Kadota, Masao Hattori, Tsuneo Namba Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . Quercetin 5,4'-dimethyl ether ÏàËÆ¶È:58.8% Phytochemistry 1995 39 463-464 Quercetin 5, 4'-dimethyl ether from Rhododendron ellipticum Li-Kang Ho, Wen-Neng Lin Structure 13C NMR ̼Æ×Ä£Äâͼ |

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