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dssjsl: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-12-18 11:06:59
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dssjsl: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-12-18 11:06:59
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Ñ¡ÈܼÁ²éѯÏàËÆ¶È54% £¬ ÏÂÃæÊÇûѡÈܼÁ²éµÄ ²éѯ½á¹û£º¹²²éµ½20¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 6' -hydroxy-3' -methoxy-mitorubrin C22H20O8 ÏàËÆ¶È:63.6% Chemical & Pharmaceutical Bulletin 2010 58 829-832 6¡ä-Hydroxy-3¡ä-methoxy-mitorubrin, a New Potentiator of Antifungal Miconazole Activity, Produced by Penicillium radicum FKI-3765-2 Hiroyuki Yamazaki, Satoshi ¨mura and Hiroshi Tomoda Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 4'-hydroxy-3'-methoxy-(+)-S-mitorubrin C22H20O8 ÏàËÆ¶È:54.5% Natural Product Research 2005 19 739-747 New fungal metabolite geranylgeranyltransferase inhibitors with antifungal activity Sheo B. Singh; Rosemarie Kelly; Ziqiang Guan; Jon D. Polishook; Anne W. Dombrowski; Javier Collado; Antonio Gonz¨¢lez; Fernando Pelaez; Elizabeth Register; Theresa M. Kelly; Cynthia Bonfiglio; Joanne M. Williamson Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . monomethyl-(+)-mitorubrin C22H20O7 ÏàËÆ¶È:54.5% Phytochemistry 1995 39 719-721 An azaphilone from Talaromyces tardifaciens Koohei Nozawa, Ritsuko Saito, Shun-Ichi Udagawa, Shoichi Nakajima, Ken-Ichi Kawai Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . CT2108B C21H22O6 ÏàËÆ¶È:52.3% Journal of Natural Products 2003 66 1041-1046 CT2108A and B: New Fatty Acid Synthase Inhibitors as Antifungal Agents Jodi A. Laakso, Robert Raulli,Gail E. McElhaney-Feser,Paul Actor, Ted L. Underiner,Brian J. Hotovec, Ursula Mocek,Ronald L. Cihlar,and Sheldon E. Broedel, Jr Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 8-Hydroxy-1,10-dimethyl-12H-naphtho[2',3':4,5]furo[3,2-c]chromene-6,11,12-trione C21H12O6 ÏàËÆ¶È:52.3% Organic & Biomolecular Chemistry 2011 9 3484-3493 Synthesis of the reported structure of crassiflorone, a naturally occurring quinone isolated from the African ebony Diospyros crassiflora, and regioisomeric pentacyclic furocoumarin naphthoquinones Jalindar Padwal, William Lewis and Christopher J. Moody Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 5-methoxy-3-(3-methoxybenzyl)-7-methyl-2H-chromen-2-one C19H18O4 ÏàËÆ¶È:52.3% Bioorganic & Medicinal Chemistry 2009 17 2842-2851 Synthesis and pharmacological evaluation of coumarin derivatives as cannabinoid receptor antagonists and inverse agonists Andrea Behrenswerth, Nicole Volz, Jakob Toräng, Sonja Hinz, Stefan Bräse, Christa E. M¨¹ller Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 5-amino-4-phenyl-2-phenylsulfanyl-6,7,8,9-tetrahydrobenzo-[1,8]-naphthyridine-3-carbonitrile C25H20N4S ÏàËÆ¶È:52.3% Journal of Heterocyclic Chemistry 2011 48 397-402 Microwave-assisted expeditious synthesis of novel benzo[1,8]-naphthyridine-3-carbonitriles Satish Kumar Singh and Krishna Nand Singh Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . cyperotundone A ÏàËÆ¶È:52.3% Chinese Traditional and Herbal Drugs 2013 44 1226-1230 Chemical constituents from rhizomes of Cyperus rotundus ZHOU Zhong-liu, YIN Wen-qing, ZHANG Hua-lin, YANG Hong-yan, LIN San-qing, XIA Jing-min Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . bangangxanthone A C23H22O6 ÏàËÆ¶È:52.1% Phytochemistry 2005 66 2351-2355 Bangangxanthone A and B, two xanthones from the stem bark of Garcinia polyantha Oliv. A. Meli Lannang, J. Komguem, F. Ngounou Ngninzeko,J. Gustave Tangmouo, D. Lontsi, Asma Ajaz, M. Iqbal Choudhary,Rosa Ranjit, Krishna P. Devkota, B. Luc Sondengam Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . mangostenone D C23H24O6 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2006 54(3) 301-305 Cytotoxic Prenylated Xanthones from the Young Fruit of Garcinia mangostana Sunit SUKSAMRARN,Orapin KOMUTIBAN,Piniti RATANANUKUL,Nitirat CHIMNOI, Nattapat LARTPORNMATULEE,and Apichart SUKSAMRARN Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . fuscaxanthone D C25H28O7 ÏàËÆ¶È:50% Journal of Natural Products 2003 66 200-205 Chemical Constituents of Garcinia fusca: Structure Elucidation of Eight New Xanthones and Their Cancer Chemopreventive Activity Chihiro Ito, Masataka Itoigawa, Tomoko Takakura, Nijisiri Ruangrungsi,Fumio Enjo, Harukuni Tokuda, Hoyoku Nishino, and Hiroshi Furukawa Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . cudraxanthone C ÏàËÆ¶È:50% Planta Medica 1991 57 172-175 Structures of Four New Isoprenylated Xanthones,Cudraxanthones L, M, N, and O from Cudrania tricuspidata Yoshio Hano, Yutaka Matsumoto, Kazuko Shinohara, Jin-Yun Sun, and Taro Nomura Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . cudraxanthone C ÏàËÆ¶È:50% Planta Medica 1990 56 399-402 Structures of Three New Isoprenylated Xanthones,Cudraxanthones E, F, and G Yoshio Hano, Yutaka Matsumoto, Jin-Yun Sun, and Taro Nomura Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . falconensin H C22H18Cl2O7 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1993 41 2040-2041 A New Azaphilone, Falconensin H, from Emericella falconensis Takeshi ITABASHI,Koohei NOZAWA,Shoichi NAKAJIMA and Ken-ichi KAWAI Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . Cochinchinone E C24H26O6 ÏàËÆ¶È:50% Phytochemistry Letters 2008 1 211-214 Antibacterial and cytotoxic xanthones from Cratoxylum cochinchinense Wilawan Mahabusarakam, Suthida Rattanaburi, Souwalak Phongpaichit, Akkharawit Kanjana-Opas Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . falconensin H ÏàËÆ¶È:50% Phytochemistry 1995 39 719-721 An azaphilone from Talaromyces tardifaciens Koohei Nozawa, Ritsuko Saito, Shun-Ichi Udagawa, Shoichi Nakajima, Ken-Ichi Kawai Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . gartanin C23H24O6 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2010 18 6258-6264 Xanthones with neuraminidase inhibitory activity from the seedcases of Garcinia mangostana Hyung Won Ryu, Marcus J. Curtis-Long, Sunin Jung, Young Min Jin, Jung Keun Cho, Young Bae Ryu, Woo Song Lee, Ki Hun Park Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . YT231b C24H18O8 ÏàËÆ¶È:50% Journal of the American Chemical Society 2005 127 12254-12262 Engineered Biosynthesis of Aklanonic Acid Analogues Taek Soon Lee, Chaitan Khosla, and Yi Tang Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . cudraxanthone C C24H26O6 ÏàËÆ¶È:50% Heterocycles 1983 21 213-218 Three New Isoprenylated Xanthones, Cudraxanthone A, B, and C, from the Root Barks of Cudrania tricuspidata (Carr.) Bur Taro Nomura, Yoshio Hano, and Tomoko Fujimoto Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 4',5'-dihydroxy-5,7-dimethoxy-6-(3-methylbut-2-enyl) coumaronochromone C22H20O7 ÏàËÆ¶È:50% Fitoterapia 2014 95 220-228 New flavonoids from Campylotropis hirtella with immunosuppressive activity Original Research Article Xiaoping Li, Bixia Xuan, Qingyao Shou, Zhengwu Shen Structure 13C NMR ̼Æ×Ä£Äâͼ |

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