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paopaoxiaozhu: ½ð±Ò+9, ¡ïÓаïÖú 2013-03-23 19:25:44
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. sclerotioramine C21H24ClNO4 ÏàËÆ¶È:95.2% Journal of Natural Products 2010 73 942-948 Chemical Epigenetics Alters the Secondary Metabolite Composition of Guttate Excreted by an Atlantic-Forest-Soil-Derived Penicillium citreonigrum Xiaoru Wang, Jos¨¦ G. Sena Filho, Ashley R. Hoover, Jarrod B. King, Trevor K. Ellis, Douglas R. Powell and Robert H. Cichewicz Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 3-N-methylsclerotiorinamine C22H26NO4Cl ÏàËÆ¶È:86.3% Journal of Natural Products 2000 63 1303-1305 8-O-Methylsclerotiorinamine, Antagonist of the Grb2-SH2 Domain, Isolated from Penicillium multicolor Ji-Youn Nam,Hyae-Kyeong Kim,Ju-Young Kwon,Mi Young Han,Kwang-Hee Son,Un Chul Lee, Jung-Do Choi, and Byoung-Mog Kwon Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . isochromophilone VI C23H28NO5Cl ÏàËÆ¶È:82.6% The Journal of Antibiotics 1995 48 696-702 Isochromophilones III - VI, Inhibitors of Acyl-CoA: Cholesterol Acyltransferase Produced by Penicillium multicolor FO-3216 NORIKO ARAI, KAZURO SHIOMI, HIROSHI TOMODA, NORIKO TABATA, DA JUN YANG, ROKURO MASUMA, TOMOYA KAWAKUBO, SATOSHI OMURA Structure 13C NMR ̼Æ×Ä£Äâͼ |
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1 . sclerotioramine C21H24ClNO4 ÏàËÆ¶È:95.2% Journal of Natural Products 2010 73 942-948 Chemical Epigenetics Alters the Secondary Metabolite Composition of Guttate Excreted by an Atlantic-Forest-Soil-Derived Penicillium citreonigrum Xiaoru Wang, Jos¨¦ G. Sena Filho, Ashley R. Hoover, Jarrod B. King, Trevor K. Ellis, Douglas R. Powell and Robert H. Cichewicz Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 3-N-methylsclerotiorinamine C22H26NO4Cl ÏàËÆ¶È:86.3% Journal of Natural Products 2000 63 1303-1305 8-O-Methylsclerotiorinamine, Antagonist of the Grb2-SH2 Domain, Isolated from Penicillium multicolor Ji-Youn Nam,Hyae-Kyeong Kim,Ju-Young Kwon,Mi Young Han,Kwang-Hee Son,Un Chul Lee, Jung-Do Choi, and Byoung-Mog Kwon Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . isochromophilone VI C23H28NO5Cl ÏàËÆ¶È:82.6% The Journal of Antibiotics 1995 48 696-702 Isochromophilones III - VI, Inhibitors of Acyl-CoA: Cholesterol Acyltransferase Produced by Penicillium multicolor FO-3216 NORIKO ARAI, KAZURO SHIOMI, HIROSHI TOMODA, NORIKO TABATA, DA JUN YANG, ROKURO MASUMA, TOMOYA KAWAKUBO, SATOSHI OMURA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . isochromophilone VI C25H30NO6Cl ÏàËÆ¶È:82.6% Australian Journal of Chemistry 2003 56 13-15 Isochromophilone IX, a Novel GABA-Containing Metabolite Isolated from a Cultured Fungus, Penicillium sp. Adam P. Michael, Emily J. Grace, Mike Kotiw and Russell A. Barrow Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 7-epi-sclerotiorin ÏàËÆ¶È:76.1% Chemical & Pharmaceutical Bulletin 1995 43 1307-1310 Four New Chlorinated Azaphilones, Helicusins A-D, Closely Related to 7-epi-Sclerotiorin, from an Ascomycetous Fungus, Talaromyces helicus Eiji YOSHIDA,Haruhiro FUJIMOTO,Miyuki BABA and Mikio YAMAZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (+)-sclerotiorin ÏàËÆ¶È:76.1% The Journal of Antibiotics 1995 48 913-923 Azaphilones with Endothelin Receptor Binding Activity Produced by Penicillium sclerotiorum: Taxonomy, Fermentation, Isolation, Structure Elucidation and Biological Activity L. PAIRET, S. K. WRIGLEY, I. CHETLAND, E. E. REYNOLDS, M. A. HAYES, J. HOLLOWAY, A. M. AINSWORTH, W. KATZER, X-M. CHENG, D. J. HUPE, P. CHARLTON, A. M. DOHERTY Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . isochromophilone VIII C21H27O5Cl ÏàËÆ¶È:76.1% The Journal of Antibiotics 1996 49 223-229 New Isochromophilones VII and VIII Produced by Penidllium sp. FO-4164 DA-JUN YANG, HIROSHI TOMODA, NORIKO TABATA, ROKURO MASUMA, SATOSHI OMURA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . compound C21H23O5Cl ÏàËÆ¶È:76.1% Journal of Agricultural and Food Chemistry 2007 55 2879-2883 Sclerotiorin, a Novel Inhibitor of Lipoxygenase from Penicillium frequentans C. Chidananda and A. P. Sattur Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . isochromophilone IX ÏàËÆ¶È:76% Australian Journal of Chemistry 2003 56 13-15 Isochromophilone IX, a Novel GABA-Containing Metabolite Isolated from a Cultured Fungus, Penicillium sp. Adam P. Michael, Emily J. Grace, Mike Kotiw and Russell A. Barrow Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . rotiorinol A C23H26O5 ÏàËÆ¶È:69.5% Journal of Natural Products 2006 69 891-895 Antifungal Azaphilones from the Fungus Chaetomium cupreum CC3003 Somdej Kanokmedhakul, Kwanjai Kanokmedhakul, Pitak Nasomjai, Sysavad Louangsysouphanh,Kasem Soytong, Minoru Isobe, Palangpon Kongsaeree, Samran Prabpai, and Apichart Suksamrarn Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 8-O-methylsclerotiorinamine C22H26NO4Cl ÏàËÆ¶È:68.1% Journal of Natural Products 2000 63 1303-1305 8-O-Methylsclerotiorinamine, Antagonist of the Grb2-SH2 Domain, Isolated from Penicillium multicolor Ji-Youn Nam,Hyae-Kyeong Kim,Ju-Young Kwon,Mi Young Han,Kwang-Hee Son,Un Chul Lee, Jung-Do Choi, and Byoung-Mog Kwon Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . Comazaphilone F C22H26O8 ÏàËÆ¶È:68.1% Journal of Natural Products 2011 74 256-261 Comazaphilones A−F, Azaphilone Derivatives from the Marine Sediment-Derived Fungus Penicillium commune QSD-17 Shu-Shan Gao, Xiao-Ming Li, Yi Zhang, Chun-Shun Li, Chuan-Ming Cui, and Bin-Gui Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . rotiorinol A acetate derivative C25H28O6 ÏàËÆ¶È:68% Journal of Natural Products 2006 69 891-895 Antifungal Azaphilones from the Fungus Chaetomium cupreum CC3003 Somdej Kanokmedhakul, Kwanjai Kanokmedhakul, Pitak Nasomjai, Sysavad Louangsysouphanh,Kasem Soytong, Minoru Isobe, Palangpon Kongsaeree, Samran Prabpai, and Apichart Suksamrarn Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 3,3a-dibutyl-5-phenyl-3,3a-dihydro-5H-imidazo[4,5-c]quino-line-2,4-dione C24H27N3O2 ÏàËÆ¶È:66.6% Journal of Heterocyclic Chemistry 2006 43 1251-1260 Molecular rearrangement of 1-substituted 3-aminoquinoline-2,4-diones in their reaction with urea and nitrourea synthesis and transformations of reaction intermediates Anton¨ªn Kl¨¢sek,Michal Kov¨¢ř,Ign¨¢c Hoza,Anton¨ªn Lyčka and Michal Holčapek Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 2-butyl-7-butyryloxy-5-chloro-3-(3-hydroxypropyl)-7-methyl-2H,7H-isoquinoline-6,8-dione C21H28ClNO5 ÏàËÆ¶È:66.6% Journal of the American Chemical Society 2007 129 9860-9861 Total Synthesis, Stereochemical Reassignment, and Absolute Configuration of Chlorofusin Sang Yeul Lee, Ryan C. Clark, and Dale L. Boger Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . helicusin A methyl ester C26H29ClO7 ÏàËÆ¶È:65.3% Chemical & Pharmaceutical Bulletin 1995 43 1307-1310 Four New Chlorinated Azaphilones, Helicusins A-D, Closely Related to 7-epi-Sclerotiorin, from an Ascomycetous Fungus, Talaromyces helicus Eiji YOSHIDA,Haruhiro FUJIMOTO,Miyuki BABA and Mikio YAMAZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . (-)-rotiorin C23H24O5 ÏàËÆ¶È:65.2% Journal of Natural Products 2006 69 891-895 Antifungal Azaphilones from the Fungus Chaetomium cupreum CC3003 Somdej Kanokmedhakul, Kwanjai Kanokmedhakul, Pitak Nasomjai, Sysavad Louangsysouphanh,Kasem Soytong, Minoru Isobe, Palangpon Kongsaeree, Samran Prabpai, and Apichart Suksamrarn Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . Chaetomugilin O C23H25ClO5 ÏàËÆ¶È:65.2% Tetrahedron 2009 65 7580-7586 Chaetomugilins I¨CO, new potent cytotoxic metabolites from a marine-fish-derived Chaetomium species. Stereochemistry and biological activities Yasuhide Muroga, Takeshi Yamada, Atsushi Numata, Reiko Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . chaetomugilin F C23H25ClO5 ÏàËÆ¶È:65.2% The Journal of Antibiotics 2008 61 615-622 Chaetomugilins, New Selectively Cytotoxic Metabolites, Produced by a Marine Fish-derived Chaetomium Species Muroga Yasuhide, Takeshi Yamada, Atsushi Numata and Reiko Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . Chaetoviridin G C23H25ClO5 ÏàËÆ¶È:65.2% Journal of Natural Products 2011 74 1182-1187 Azaphilones from the Endophyte Chaetomium globosum Warley S. Borges, Gabriela Mancilla, Denise O. Guimarães, Rosa Dur¨¢n-Patr¨®n, Isidro G. Collado, and Mnica T. Pupo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . helicusin D C25H27ClO7 ÏàËÆ¶È:64% Chemical & Pharmaceutical Bulletin 1995 43 1307-1310 Four New Chlorinated Azaphilones, Helicusins A-D, Closely Related to 7-epi-Sclerotiorin, from an Ascomycetous Fungus, Talaromyces helicus Eiji YOSHIDA,Haruhiro FUJIMOTO,Miyuki BABA and Mikio YAMAZAKI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . Compound 11 ÏàËÆ¶È:63.6% Magnetic Resonance in Chemistry 2004 42 648-658 You have full text access to this contentStructural assignment of regioisomeric 3-[2-or 5-anilino-2-(alkylamino)phenyl]propanoic acids, 2H-1, 4-benzothiazin-3(4H)-ones and 2, 3-dihydro-1, 5-benzothiazepin-4(5H)-ones by 1D NOE and gHMBC NMR techniques Alan R. Katritzky, Novruz G. Akhmedov, Mingyi Wang, Charles J. Rostek and Peter J. Steel Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . Comazaphilone B C22H26O8 ÏàËÆ¶È:63.6% Journal of Natural Products 2011 74 256-261 Comazaphilones A−F, Azaphilone Derivatives from the Marine Sediment-Derived Fungus Penicillium commune QSD-17 Shu-Shan Gao, Xiao-Ming Li, Yi Zhang, Chun-Shun Li, Chuan-Ming Cui, and Bin-Gui Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . bharangin ÏàËÆ¶È:61.9% Bioorganic & Medicinal Chemistry Letters 2011 21 4581-4584 Cytotoxic diterpenoid quinonemethides from the roots of Pygmacopremna herbacea K. Satish, M. V. P. S. Vishnuvardhan, V. Lakshma Nayak, G. Srihari, M. Subrahamanyam, T. Prabhakar Rao, S. Ramakrishna, K. Ravikumar, B. Sridhar, M. Marthanda Murthy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . ethyl 4-(4-hydroxy-3-methoxyphenyl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate C22H27NO5 ÏàËÆ¶È:61.9% Journal of Heterocyclic Chemistry 2010 47 194-198 Glycine-catalyzed easy and efficient one-pot synthesis of polyhydroquinolines through Hantzsch multicomponent condensation under controlled microwave Satish Kumar Singh and Krishna Nand Singh Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . compound (S)8-FBS C22H25F2N2O2 ÏàËÆ¶È:61.9% Tetrahedron Letters 2005 46 2623-2626 Self-assembly of chiral mesoionic heterocycles into smectic phases: a new class of polar liquid crystal C.V. Yelamaggad, Manoj Mathews, Uma S. Hiremath, D.S. Shankar Rao, S. Krishna Prasad Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . isochromophilone IV C21H27O5Cl ÏàËÆ¶È:61.9% The Journal of Antibiotics 1995 48 696-702 Isochromophilones III - VI, Inhibitors of Acyl-CoA: Cholesterol Acyltransferase Produced by Penicillium multicolor FO-3216 NORIKO ARAI, KAZURO SHIOMI, HIROSHI TOMODA, NORIKO TABATA, DA JUN YANG, ROKURO MASUMA, TOMOYA KAWAKUBO, SATOSHI OMURA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . carbazoquinocin D C21H25NO2 ÏàËÆ¶È:61.9% The Journal of Antibiotics 1995 48 326-328 Isolation and Structural Elucidation of Antioxidative Substances, Carbazoquinocins A to F MASAHIRO TANAKA, KAZUO SHIN-YA, KAZUO FURIHATA, HARUO SETO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . pre-kinamycin diacetate ÏàËÆ¶È:61.9% The Journal of Antibiotics 1989 42 189-197 NEW PRODUCTS RELATED TO KINAMYCIN FROM STREPTOMYCES MURAYAMAENSIS II. STRUCTURES OF PRE-KINAMYCIN, KETO-ANHYDROKINAMYCIN, AND KINAMYCINS E AND F PAMELA J. SEATON, STEVEN J. GOULD Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . JBIR-120 C18H18N2O3 ÏàËÆ¶È:61.9% The Journal of Antibiotics 2012 65 373-375 JBIR-120: a new growth inhibitor of hormone-refractory prostate cancer cells Teppei Kawahara, Takahiro Hosoya, Masao Tsukamoto, Sachiko Okabe, Hideki Yamamura, Masayuki Hayakawa, Hiroyuki Seimiya, Motoki Takagi and Kazuo Shin-ya Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . 3-Butyl-1,2,3,4-tetrahydro-1-methyl-2,4-dioxoquinolin-3-yl Butylcarbamate C19H26N2O4 ÏàËÆ¶È:61.9% Helvetica Chimica Acta 2011 94 78-91 Reaction of 3-Hydroxyquinoline-2, 4-diones with Isocyanates and Thermally Induced Transformation of the Reaction Products Vladim¨ªr Mrkvička, Anton¨ªn Lyčka, Robert V¨ªcha and Anton¨ªn Kl¨¢sek Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . rotiorinol B C23H26O6 ÏàËÆ¶È:60.8% Journal of Natural Products 2006 69 891-895 Antifungal Azaphilones from the Fungus Chaetomium cupreum CC3003 Somdej Kanokmedhakul, Kwanjai Kanokmedhakul, Pitak Nasomjai, Sysavad Louangsysouphanh,Kasem Soytong, Minoru Isobe, Palangpon Kongsaeree, Samran Prabpai, and Apichart Suksamrarn Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 33 . rotiorinol C C23H26O6 ÏàËÆ¶È:60.8% Journal of Natural Products 2006 69 891-895 Antifungal Azaphilones from the Fungus Chaetomium cupreum CC3003 Somdej Kanokmedhakul, Kwanjai Kanokmedhakul, Pitak Nasomjai, Sysavad Louangsysouphanh,Kasem Soytong, Minoru Isobe, Palangpon Kongsaeree, Samran Prabpai, and Apichart Suksamrarn Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 34 . chaetoviridin B C23H29ClO7 ÏàËÆ¶È:60.8% Chemical & Pharmaceutical Bulletin 1990 38 625-628 Four New Azaphilones from Chaetomium globosum var. flavo-viridae Masanao TAKAHASHI,Kiyotaka KOYAMA and Shinsaku NATORI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 35 . Chaetomugilin D C23H27O6Cl ÏàËÆ¶È:60.8% Bioorganic & Medicinal Chemistry Letters 2009 19 1572-1574 Bioactive metabolites produced by Chaetomium globosum, an endophytic fungus isolated from Ginkgo biloba Jian-Chun Qin, Ya-Mei Zhang, Jin-Ming Gao, Ming-Sheng Bai, Sheng-Xiang Yang, Hartmut Laatsch, An-Ling Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ |
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