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13C NMR ÈܼÁCDCL3 17.6,20.9,27.7,33.4,65.6,70.3,82.5,100.9,106.6,107.9,118.0,140.1,157.2,159.5,170.6,178.0,187.8 |
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²éѯ½á¹û£º¹²²éµ½420¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . dicerandrol A C34H34O14 ÏàËÆ¶È:100% Journal of Natural Products 2001 64 1006-1009 Dicerandrols, New Antibiotic and Cytotoxic Dimers Produced by the Fungus Phomopsis longicolla Isolated from an Endangered Mint Melissa M. Wagenaar and Jon Clardy Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . dicerandrol C C38H38O16 ÏàËÆ¶È:84.2% Journal of Natural Products 2001 64 1006-1009 Dicerandrols, New Antibiotic and Cytotoxic Dimers Produced by the Fungus Phomopsis longicolla Isolated from an Endangered Mint Melissa M. Wagenaar and Jon Clardy Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Penexanthone B C19H20O8 ÏàËÆ¶È:77.7% Journal of Natural Products 2012 75 793-797 Inhibition of Tumor Cells Interacting with Stromal Cells by Xanthones Isolated from a Costa Rican Penicillium sp. Shugeng Cao, Douglas W. McMillin, Giselle Tamayo, Jake Delmore, Constantine S. Mitsiades, and Jon Clardy Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . rugulotrosin A C32H30O14 ÏàËÆ¶È:76.4% Journal of Natural Products 2004 67 728-730 Rugulotrosins A and B: Two New Antibacterial Metabolites from an Australian Isolate of a Penicillium sp. Michael Stewart, Robert J. Capon, Jonathan M. White, Ernest Lacey, Shaun Tennant, Jennifer H. Gill, and Martin P. Shaddock Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . secalonic acid D ÏàËÆ¶È:70.5% Natural Product Research and Development 2013 25 1-6 Secondary Metabolites of Marine-derived Fungus Penicillium oxalicum SCSGAF 0023 and Their Antifouling and Enzyme-inhibitory Activities SUN Yu-lin, CHEN Yin, XU Xin-ya, ZHANG Xiao-yong, ZHENG Zhi-hui, NONG Xu-hua, BAO Jie, QI Shu-hua Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . phomoxanthone A C38H38O16 ÏàËÆ¶È:68.4% Journal of Natural Products 2001 64 1015-1018 Phomoxanthones A and B, Novel Xanthone Dimers from the Endophytic Fungus Phomopsis Species Masahiko Isaka, Amonlaya Jaturapat, Kamolchanok Rukseree, Kannawat Danwisetkanjana,Morakot Tanticharoen, and Yodhathai Thebtaranonth Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . photinide E C16H16O7 ÏàËÆ¶È:64.7% Journal of Natural Products 2009 72 942-945 Photinides A-F, Cytotoxic Benzofuranone-Derived ¦Ã-Lactones from the Plant Endophytic Fungus Pestalotiopsis photiniae Gang Ding, Zhihui Zheng, Shuchun Liu, Hua Zhang, Liangdong Guo, and Yongsheng Che Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 6-(Butyloxymethyl)-3-hexylfuro[2,3-d]pyrimidin-2(3H)-one C17H26N2O3 ÏàËÆ¶È:64.7% Canadian Journal of Chemistry 2006 84 561-568 Synthesis of 6-(alkoxymethyl)- and 6-(alkylsulfanylmethyl)furo[2,3-d]pyrimidin-2(3H)-one analogues1,2 Zlatko Janeba, Noha Maklad, and Morris J. Robins Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . SAD(secalonic acid D) C32H30O14 ÏàËÆ¶È:64.7% Chinese Journal of Marine Drugs 2011 30(4) 18-24 Bioactive secondary metabolites produced by an Antarctic marine-derived fungus Penicil l ium chrysogenum PR4-1-3 MA Hong-yan,LI De-hai,GU Qian-qun,ZHU T ian-jiao Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . secalonic acid A C32H30O14 ÏàËÆ¶È:64.7% Phytochemistry 1987 26 1599-1602 Secalonic acid a,a vivotoxin in pink root-infected onion John C. Steffens,David J. Robeson Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ranhuadujuanine D ÏàËÆ¶È:64.7% China Journal of Chinese Materia Medica 2010 35 2568-2571 Five monoterpenes from leaves of Rhododendron anthopogon QIN Changhong; MEI Ying; ZHOU Xianli; A Ping; HUANG Shuai Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Secalonic acid D C16H15O7 ÏàËÆ¶È:64.7% Archives of Pharmacal Research 2006 29 59-63 Secalonic acid D; A cytotoxic constituent from marine lichen-derived fungusGliocladium sp. T31 Hong Ren, Li Tian, Qianqun Gu and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Blennolide A C16H16O7 ÏàËÆ¶È:64.7% Chemistry-A European Journal 2008 14 4913-4923 New Mono- and Dimeric Members of the Secalonic Acid Family: Blennolides A¨CG Isolated from the Fungus Blennoria sp. Wen Zhang, Karsten Krohn, Zia-Ullah, Ulrich Flörke, Gennaro Pescitelli, Lorenzo Di Bari, S¨¢ndor Antus, Tibor Kurt¨¢n, Joachim Rheinheimer, Siegfried Draeger and Barbara Schulz Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . epi-blennolide C ÏàËÆ¶È:64.7% Tetrahedron 2012 68 6218-6223 New dimeric and monomeric chromanones, gonytolides D¨CG, isolated from the fungus Gonytrichum sp. Haruhisa Kikuchi, Masato Isobe, Shoichiro Kurata, Yasuhiro Katou, Yoshiteru Oshima Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . secalonic acid D C32H30O14 ÏàËÆ¶È:64.7% Pharmaceutical Biology 2011 49(3) 796-799 Secalonic acid D as a novel DNA topoisomerase I inhibitor from marine lichen-derived fungus Gliocladium sp. T31 Ren Hong Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (-)-14-O-Acetyl-7-trifluoroacetylindolactam-V C21H24F3N3O4 ÏàËÆ¶È:61.9% Bioorganic & Medicinal Chemistry 2008 16 650-657 Design and physicochemical properties of new fluorescent ligands of protein kinase C isozymes focused on CH/¦Ð interaction Takuya Sugimoto, Koji Itagaki, Kazuhiro Irie Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 6-(Butyloxymethyl)-3-octylfuro[2,3-d]pyrimidin-2(3H)-one C19H30N2O3 ÏàËÆ¶È:61.1% Canadian Journal of Chemistry 2006 84 561-568 Synthesis of 6-(alkoxymethyl)- and 6-(alkylsulfanylmethyl)furo[2,3-d]pyrimidin-2(3H)-one analogues1,2 Zlatko Janeba, Noha Maklad, and Morris J. Robins Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . Penicitrinol F C19H26O7 ÏàËÆ¶È:61.1% Marine Drugs 2013 11 1718-1727 Polyketides from a Marine-Derived Fungus Xylariaceae sp. Xu-Hua Nong, Zhi-Hui Zheng, Xiao-Yong Zhang, Xin-Hua Lu and Shu-Hua Qi Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . cylindrocyclophane B C38H58O7 ÏàËÆ¶È:60% Tetrahedron 1992 48 3001-3006 Structures of cylindrocyphanes a-f Bradley S. Moore, Jian-Lu Chen, Gregory M.L. Patterson, Richard E. Moore Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . photinide F C16H16O7 ÏàËÆ¶È:58.8% Journal of Natural Products 2009 72 942-945 Photinides A-F, Cytotoxic Benzofuranone-Derived ¦Ã-Lactones from the Plant Endophytic Fungus Pestalotiopsis photiniae Gang Ding, Zhihui Zheng, Shuchun Liu, Hua Zhang, Liangdong Guo, and Yongsheng Che Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . lachnone D C15H16O7 ÏàËÆ¶È:58.8% Journal of Natural Products 2006 69 980-982 Chromone Derivatives from the Filamentous Fungus Lachnum sp. BCC 2424 Vatcharin Rukachaisirikul, Sirinya Chantaruk, Wipapan Pongcharoen, Masahiko Isaka, and Sanisa Lapanun Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . nigrolineaxanthone U C18H18O7 ÏàËÆ¶È:58.8% Journal of Natural Products 2005 68 1218-1221 Benzopyran, Biphenyl, and Tetraoxygenated Xanthone Derivatives from the Twigs of Garcinia nigrolineata Vatcharin Rukachaisirikul, Kwanruthai Tadpetch, Anyarat Watthanaphanit, Neangnoi Saengsanae, and Souwalak Phongpaichit Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 4,4'-dibromorugulotrosin A ÏàËÆ¶È:58.8% Journal of Natural Products 2004 67 728-730 Rugulotrosins A and B: Two New Antibacterial Metabolites from an Australian Isolate of a Penicillium sp. Michael Stewart, Robert J. Capon, Jonathan M. White, Ernest Lacey, Shaun Tennant, Jennifer H. Gill, and Martin P. Shaddock Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 7-acetoxy-8-hydroxy-9-isobutyryloxythymol C16H22O6 ÏàËÆ¶È:58.8% Journal of Natural Products 2001 64 1048-1051 Thymol Derivatives from Eupatorium fortunei Motoo Tori, Yukiko Ohara, Katsuyuki Nakashima, and Masakazu Sono Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 4'-MEM-2'-Prenyl-resacetophenone C17H24O5 ÏàËÆ¶È:58.8% Natural Product Research 1995 7 73-80 Synthesis of 5'-(3,3-Dimethylallyl)-4'-Methoxyethoxymethyl Resacetophenone and Improved Preparation of Broussochalcones A and B Diderot Noungoue-tchamo; Denis Barron; Anne-Marie Mariotte Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . lasiodiplodin ÏàËÆ¶È:58.8% China Journal of Chinese Materia Medica 2009 34 414-418 Chemical constituents in roots of Osbeckia opipara WANG Hongsheng, WANG Yuehu, SHI Yana, LI Xingyu, LONG Chunlin Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . 3-Hexyl-6-(hexyloxymethyl)furo[2,3-d]pyrimidin-2(3H)-one C19H30N2O3 ÏàËÆ¶È:58.8% Canadian Journal of Chemistry 2006 84 561-568 Synthesis of 6-(alkoxymethyl)- and 6-(alkylsulfanylmethyl)furo[2,3-d]pyrimidin-2(3H)-one analogues1,2 Zlatko Janeba, Noha Maklad, and Morris J. Robins Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . 6-(Hexyloxymethyl)-3-octylfuro[2,3-d]pyrimidin-2(3H)-one C21H34N2O3 ÏàËÆ¶È:58.8% Canadian Journal of Chemistry 2006 84 561-568 Synthesis of 6-(alkoxymethyl)- and 6-(alkylsulfanylmethyl)furo[2,3-d]pyrimidin-2(3H)-one analogues1,2 Zlatko Janeba, Noha Maklad, and Morris J. Robins Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . (¡À)cis-9',10'-dihydro-4',9',10'-trihydroxyspiro[cycloheptane-1,8'-8'H-pyrano[2,3-h]quinolin-2'(1'H)-one] C18H21NO5 ÏàËÆ¶È:58.8% Chemical & Pharmaceutical Bulletin 2009 57 446-452 Synthesis of Some New Spiropyranoquinolines and Evaluation of Their Free Radical Scavenging Activity Vassiliki Panteleon, Ioannis K. Kostakis, Panagiotis Marakos, Nicole Pouli and Ioanna Andreadou Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . 8-prenylkaempferol ÏàËÆ¶È:58.8% Chinese Journal of Natural Medicines 2006 4 159-160 Chemical Study on the Rhizome of Acorus tatarinowii TAO Hong; ZHU En-Yuan; WANG Zheng-Tao Structure 13C NMR ̼Æ×Ä£Äâͼ |
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