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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½24¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . asperentin-8-O-methyl ether C17H22O5 ÏàËÆ¶È:88.8% Zeitschrift f¨¹r Naturforschung C 2012 67c 587-593 Plant Growth Activities of Aspyran, Asperentin,and its Analogues Produced by the Fungus Aspergillus sp. Yasuo Kimura, Naomi Shimomura, Fumiaki Tanigawa, Shozo Fujioka, and Atsumi Shimad Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . MT-5 ÏàËÆ¶È:83.3% Chemical & Pharmaceutical Bulletin 1999 47 1426-1432 Immunomodulatory Constituents from an Ascomycete, Microascus tardifaciens Haruhiro FUJIMOTO,Toshiyuki FUJIMAKI,Emi OKUYAMA and Mikio YAMAZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . MT-5 ÏàËÆ¶È:61.1% Chemical & Pharmaceutical Bulletin 1999 47 1426-1432 Immunomodulatory Constituents from an Ascomycete, Microascus tardifaciens Haruhiro FUJIMOTO,Toshiyuki FUJIMAKI,Emi OKUYAMA and Mikio YAMAZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . MT-4 ÏàËÆ¶È:55.5% Chemical & Pharmaceutical Bulletin 1999 47 1426-1432 Immunomodulatory Constituents from an Ascomycete, Microascus tardifaciens Haruhiro FUJIMOTO,Toshiyuki FUJIMAKI,Emi OKUYAMA and Mikio YAMAZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . asperentin-6-O-methyl ether C17H22O5 ÏàËÆ¶È:55.5% Zeitschrift f¨¹r Naturforschung C 2012 67c 587-593 Plant Growth Activities of Aspyran, Asperentin,and its Analogues Produced by the Fungus Aspergillus sp. Yasuo Kimura, Naomi Shimomura, Fumiaki Tanigawa, Shozo Fujioka, and Atsumi Shimad Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Paecilomycin L C19H26O7 ÏàËÆ¶È:52.6% Tetrahedron Letters 2013 54 2648-2650 Paecilomycins J¨CM, four new ¦Â-resorcylic acid lactones from Paecilomyces sp. SC0924 Liang-Xiong Xu, Ping Wu, Huan-Huan Wei, Jing-Hua Xue, Xiao-Peng Hu, Xiao-Yi Wei Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (7'R)-7-hydroxyspirolaxine C23H32O7; ÏàËÆ¶È:52.1% Chemistry & Biodiversity 2007 Vol. 4 2772 Microbial Transformation of Spirolaxine, a Bioactive Undecaketide Fungal Metabolite from the Basidiomycete Sporotrichum laxum Gianluca Nasini, Adriana Bava, Giovanni Fronza, and Giuseppe Giannini Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (¡À)-2-(4-Hydroxy-6-methyl-2-oxo-1,2-dihydropyridin-3-yl)-7-methyl-4-phenyl-3,4-dihydro-2Hpyrano-[3,2-c]pyridin-5(6H)-one C21H20N2O4 ÏàËÆ¶È:50% Molecules 2009 14 4973-4986 Synthesis and Phytotoxic Activity of New Pyridones Derived from 4-Hydroxy-6-Methylpyridin-2(1H)-one Antonio Jacinto Demuner, Vania Maria Moreira Valente, Luiz Cl¨¢udio Almeida Barbosa, Akshat Rathi, Timothy J. Donohoe and Amber L. Thompson Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . MT-4 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1999 47 1426-1432 Immunomodulatory Constituents from an Ascomycete, Microascus tardifaciens Haruhiro FUJIMOTO,Toshiyuki FUJIMAKI,Emi OKUYAMA and Mikio YAMAZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 11¦Â-hydroxy-11¦Â,1-dihydromedicarpin C16H16O5 ÏàËÆ¶È:50% Phytochemistry 1998 48 187-190 Pterocarpans from Ononis viscosa subsp. breviflora Alejandro F. Barrero, Eduardo Cabrera, Ignacio Rodriguez Garcia Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 3,4-dihydro-6,8-dimethoxxy-3-(2-hydroxypentyl)isocoumarin C16H22O5 ÏàËÆ¶È:50% Journal of Natural Products 2010 73 75-78 An Antimycobacterial Cyclodepsipeptide from the Entomopathogenic Fungus Ophiocordyceps communis BCC 16475 Rachada Haritakun, Malipan Sappan, Rapheephat Suvannakad, Kanoksri Tasanathai and Masahiko Isaka Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . capillofuranocarboxylate C18H24O5 ÏàËÆ¶È:50% Journal of Natural Products 2010 73 771-775 Antiviral and Anti-inflammatory Metabolites from the Soft Coral Sinularia capillosa Shi-Yie Cheng, Ki-Jhih Huang, Shang-Kwei Wang, Zhi-Horng Wen, Pei-Wen Chen and Chang-Yih Duh Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . tomentonone ÏàËÆ¶È:50% Phytochemistry 1997 46 1423-1429 Prenylated xanthonoids from Calophyllum apetalum Munekazu Iinuma, Tetsuro Ito, Hideki Tosa, Toshiyuki Tanaka, Ryoko Miyake, Veliah Chelladurai Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . cladosporin ÏàËÆ¶È:50% Journal of Natural Products 1993 Vol 56 1397 Isocladosporin, a Biologically Active Isomer of Cladosporin from Cladosporium cladosporioides John M. Jacyno, John S. Harwood, Horace G. Cutler, Mee-Kyoung Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (10'R)-5-(10-hydroxytridecyl)-1-O-methylresorcinol C20H34O3 ÏàËÆ¶È:50% Phytochemistry 1994 36 189-194 Resorcinol derivatives and other components from Ononis viscosa subsp. breviflora Alejandro.F. Barrero, Eduardo Cabrera, Ignacio Rodr¨ªguez, Eva M. Fern¨¢ndez-Gallego Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (20S)-16-Ene-22-thia-24-nor-26,27-dimethyl-8-ol C18H32O2S ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2008 16 1796-1815 Synthesis and structure¨Cactivity relationships of 16-ene-22-thia-1¦Á,25-dihydroxy-26,27-dimethyl-19-norvitamin D3 analogs having side chains of different sizes Hajime Takaku, Yukiko Miyamoto, Shiori Asami, Mika Shimazaki, Sachiko Yamada, Keiko Yamamoto, Nobuyuki Udagawa, Hector F. DeLuca, Masato Shimizu Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 10¦Â-hydroxymonocillin II C18H22O5 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2009 17 4622-4635 Synthesis and structure¨Cactivity relationships of radicicol derivatives and WNT-5A expression inhibitory activity Hideki Shinonaga, Toshiya Noguchi, Akiko Ikeda, Mari Aoki, Natsuko Fujimoto, Akira Kawashima Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . cladosporin C16H20O5 ÏàËÆ¶È:50% Chemistry of Natural Compounds 2012 48 467-469 Secondary metabolites of the marine fungus Aspergillus ustus KMM 4640 G. K. Oleinikova, V. A. Denisenko, N. N. Slinkina and Sh. Sh. Afiyatullov Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 2-((4S,6S)-6-(2-((R,Z)-3-methoxy-2-methylbut-1-enyl)oxazol-4-yl)-2,2-dimethyl-1,3-dioxan-4-yl)ethanol C17H27NO5 ÏàËÆ¶È:50% Journal of the American Chemical Society 2010 132 10286-10292 Total Synthesis of Enigmazole A from Cinachyrella enigmatica. Bidirectional Bond Constructions with an Ambident 2,4-Disubstituted Oxazole Synthon Colin K. Skepper, Tim Quach and Tadeusz F. Molinski Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 4-((4S,6R)-6-(2-iodoethyl)-2,2-dimethyl-1,3-dioxan-4-yl)-2-((R,Z)-3-methoxy-2-methylbut-1-enyl)oxazole C17H26NO4I ÏàËÆ¶È:50% Journal of the American Chemical Society 2010 132 10286-10292 Total Synthesis of Enigmazole A from Cinachyrella enigmatica. Bidirectional Bond Constructions with an Ambident 2,4-Disubstituted Oxazole Synthon Colin K. Skepper, Tim Quach and Tadeusz F. Molinski Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 3-(2-methoxy-1-methyl-vinyl)-4,6,6-trimethyl-5-methylene-3-vinyl-bicyclo[2.2.2]octan-2-one C18H26O2 ÏàËÆ¶È:50% Canadian Journal of Chemistry 2004 82 227-239 Part 2: Efficient strategies for the construction of variably substituted bicyclo[5.3.1]undecenones (AB-taxane ring systems) and their conversion to tricyclo[9.3.1.03,8]pentadecenones (ABC taxane ring systems) and bicyclo[2.2.2]octanones Nidia P Villalva-Serv¨ªn, Alain Laurent, Alex G Fallis Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . E-1-(Tetrahydro-2-pyranyloxy)-8-dodecen-3,6-diyne ÏàËÆ¶È:50% Journal of the Brazilian Chemical Society 2004 15 372-377 Electroantennographic Responses of Heterotermes tenuis (Isoptera: Rhinotermitidae) to Synthetic (3Z,6Z,8E)-Dodecatrien-1-ol Luciane G. Batista-Pereira, M¨¢rcio G. dos Santos, Arlene G. Corr¨ºa, João B. Fernandes, C¨¦lia R. R. C. Dietrich, Dilmar A. Pereira, Odair C. Bueno and Ana Maria Costa-Leonardo Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 9-methylene-9,11-secopodocarp-11-ene C18H30 ÏàËÆ¶È:50% Australian Journal of Chemistry 1981 34 1959-1973 Structure odour studies with some diterpene derived acetals PK Grant and DD Rowan Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . N-(L-Valyl-L-methionyl)-8-amino-2,6-anhydro-3,8-dideoxy-8-glycero-D-talo-octonic Acid ÏàËÆ¶È:50% Journal of Medicinal Chemistry 1987 30 2309-2313 Design and synthesis of peptide derivatives of a 3-deoxy-D-manno-2-octulosonic acid (KDO) analog as novel antibacterial agents acting upon lipopolysaccharide biosynthesis Alf Claesson, Anita M. Jansson, Brian G. Pring, Stephen M. Hammond, Bertil Ekstroem Structure 13C NMR ̼Æ×Ä£Äâͼ |
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