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²éѯ½á¹û£º¹²²éµ½22¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 18-oxotryprostatin A C22H25N3O4 ÏàËÆ¶È:55.5% Journal of Natural Products 2008 71(6) 985-989 Cytotoxic Alkaloids and Antibiotic Nordammarane Triterpenoids from the Marine-Derived Fungus Aspergillus sydowi Min Zhang, Wen-Liang Wang, Yu-Chun Fang, Tian-Jiao Zhu, Qian-Qun Gu, and Wei-Ming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . tert-Butyloxycarbonyl-leucyl-tryptophanyl-prolyl-glycine methyl ester C30H43N5O7 ÏàËÆ¶È:55.5% Archives of Pharmacal Research 2007 30 1380-1386 Synthetic and Biological Studies on Natural Cyclic Heptapeptide: Segetalin E Rajiv Dahiya and Komalpreet Kaur Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . compound 6 C27H33N3O6 ÏàËÆ¶È:55.5% Tetrahedron 2008 64 7986-7991 Seven new prenylated indole diketopiperazine alkaloids from holothurian-derived fungus Aspergillus fumigatus Fazuo Wang, Yuchun Fang, Tianjiao Zhu, Min Zhang, Aiqun Lin, Qianqun Gu, Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 12,13-dihydroxyfumitremorgin C C22H25N3O5 ÏàËÆ¶È:51.8% Chemistry of Natural Compounds 2004 40 615-617 FUMITREMORGINS FROM THE MARINE ISOLATE OF THE FUNGUS Aspergillus fumigatus Sh. Sh. Afiyatullov, A. I. Kalinovskii, M. V. Pivkin,P. S. Dmitrenok, and T. A. Kuznetsova Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . Diethyl [(17¦Â-hydroxy-3-methoxy-estra-1,3,5(10)-trien-16¦Â-ylamino)methylene]malonate C27H37NO6 ÏàËÆ¶È:51.8% Steroids 2002 67 835-849 Synthesis, structure and catechol-oxidase activity of copper(II) complexes of 17-hydroxy-16-(N-3-oxo-prop-1-enyl)amino steroids Rainer Wegner, Manuela Dubs, Helmar Görls, Christian Robl, Bruno Schönecker, Ernst-G. Jäger Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 16¦Á-Toluene-p-sulfonyloxymethyl-3-methoxy-13¦Á-estra-1,3,5(10)-trien-17¦Â-ol C27H34O5S ÏàËÆ¶È:51.8% Steroids 2003 68 451-458 Stereoselective halogenation of the 16-hydroxymethyl-3-methoxy-13¦Á-estra-1,3,5(10)-trien-17-ols and their solvolytic investigation J¨¢nos Wölfling, Erzs¨¦bet Merny¨¢k, P¨¦ter Forg¨®, Gyula Schneider Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 16¦Á-toluenep-sulfonyloxymethyl-3-methoxy-13 -estra-1,3,5(10)-trien-17 -acetate 3i ÏàËÆ¶È:51.8% Steroids 2003 68 451-458 Stereoselective halogenation of the 16-hydroxymethyl-3-methoxy-13¦Á-estra-1,3,5(10)-trien-17-ols and their solvolytic investigation J¨¢nos Wölfling, Erzs¨¦bet Merny¨¢k, P¨¦ter Forg¨®, Gyula Schneider Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . acetyl-hobartidiol ÏàËÆ¶È:51.8% Journal of Natural Products 1990 Vol 53 713 Alcaloïdes Indoliques Isoles d'Aristotelia australasica J. C. Quirion, C. Kan, H. P. Husson, I. R. C. Bick Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 10,11-dihydroxy-fumitremorgin C C23H21N5O4 ÏàËÆ¶È:51.8% Phytochemistry 1990 29 1025-1026 12,13-Dihydroxy-fumitremorgin C from Aspergillus fumigatus Wolf-Rainer Abraham,Hans-Adolf Arfmann Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . tricarbonyl[(¦Ç4-6,7,8,9)-(2E,4Z,6E,8E)-7-(3-indolyl)methyl-3-methyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonate-traenenitrile]iron C31H32FeN2O3 ÏàËÆ¶È:51.8% Journal of Heterocyclic Chemistry 2001 38 259-264 Synthesis of 11Z-9-demethyl-9-((3-indolyl)methyl)retinal Akimori Wada, Naoko Fujioka and Masayoshi Ito Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . compound 11 ÏàËÆ¶È:51.8% Steroids 1994 59 305-309 Synthesis of new 16-spirosteroids Lutz F. Tietze, J¨¢nos Wölfling, Gyula Schneider, Mathias Noltemeyer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . Xylogranatin F C26H27NO6 ÏàËÆ¶È:51.8% Chemistry-A European Journal 2008 14 1129-1144 Xylogranatins F¨CR: Antifeedants from the Chinese Mangrove, Xylocarpus granatum, A New Biogenetic Pathway to Tetranortriterpenoids Jun Wu, Si Zhang, Torsten Bruhn, Qiang Xiao, Haixin Ding and Gerhard Bringmann Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . N¦Á-(tert-butyloxycarbonyl)-(R)-tryptophan di-n-pentylamide ÏàËÆ¶È:51.8% Journal of Medicinal Chemistry 1991 34 3350-3359 Cholecystokinin (CCK) antagonists: (R)-tryptophan-based hybrid antagonists of high affinity and selectivity for CCK-A receptors James F. Kerwin Jr., Frank Wagenaar, Hana Kopecka, Chun Wel Lin, Thomas Miller, David Witte, Michael Stashko, Alex M. Nadzan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . [4-(tetradecyloxy)phenyl]methylacetyl(2-pyridinylmethyl)carbamate C30H44N2O4 ÏàËÆ¶È:51.8% Journal of Medicinal Chemistry 1993 36 580-590 Analogs of platelet activating factor. 8. Antagonists of PAF containing an aromatic ring linked to a pyridinium ring Michael P. Trova, Allan Wissner, Marion L. Carroll, Suresh S. Kerwar, Walter C. Pickett, Robert E. Schaub, Lawrence W. Torley, Constance A. Kohler Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . N-carboxamido-staurosporine C29H27N5O4 ÏàËÆ¶È:51.7% The Journal of Antibiotics 2006 59 331-337 N-Carboxamido-staurosporine and Selina-4(14),7(11)-diene-8,9-diol, New Metabolites from a Marine Streptomyces sp. FREE Shao Jie Wu, Serge Fotso, Fuchao Li, Song Qin, Gerhard Kelter, Heinz H Fiebig and Hartmut Laatsch Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . Methyl 2-{(3R)-3-[(tert-butoxycarbonyl)amino]piperidin-1-yl}-3-(5-fluoro-2-methylbenzyl)-5-methyl-4-oxo-4,5-dihydro-3H-imidazo[4,5-c]quinoline-7-carboxylate C31H36O5N5F ÏàËÆ¶È:51.7% Bioorganic & Medicinal Chemistry 2012 20 5864-5883 Discovery of 3H-imidazo[4,5-c]quinolin-4(5H)-ones as potent and selective dipeptidyl peptidase IV (DPP-4) inhibitors Yohei Ikuma, Hitoshi Hochigai, Hidenori Kimura, Noriko Nunami, Tomonori Kobayashi, Katsuya Uchiyama, Yudai Furuta, Mutsuko Sakai, Masakuni Horiguchi, Yumi Masui, Kazuhiko Okazaki, Yasuhiro Sato, Hiroyuki Nakahira Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . tricarbonyl[ethyl (¦Ç4-4,5,6,7)-(2E,4E,6E)-5-(3-indolyl)methyl-7-(2,6,6-trimethyl-1-cyclo-hexen-1-yl)-2,4,6-heptatrienoate]iron C30H33FeNO5 ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2001 38 259-264 Synthesis of 11Z-9-demethyl-9-((3-indolyl)methyl)retinal Akimori Wada, Naoko Fujioka and Masayoshi Ito Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . compound 12h ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 1998 6 2029-2039 New 1¦Á,25-dihydroxy vitamin D3 analogues with side chains attached to C-18: synthesis and biological activity Gunnar Grue-Sørensen, Christina Mørk Hansen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . (2S,4S,5S,7S)-5-Azido-N-(3-amino-2,2-dimethylpropyl)-4-hydroxy-2-isopropyl-7-(4-methoxy-3-(3-methoxypropoxy) benzyl)-8-methylnonanamide C30H52N7O5 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2011 19 4238-4249 Synthesis, biological evaluation and docking studies of octane-carboxamide based renin inhibitors with extended segments toward S3' site of renin Yong Wu, Chen Shi, Xiaowei Sun, Xiaoming Wu, Hongbin Sun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . (2S,4S,5S,7S)-5-Azido-N-(2,2-dimethyl-3-(2,2,2-trifluor oacetamido)propyl)-4-hydroxy-2-isopropyl-7-(4-methoxy-3-(3-methoxypropoxy)benzyl)-8-methylnonanamide C32H52N5O6F3 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2011 19 4238-4249 Synthesis, biological evaluation and docking studies of octane-carboxamide based renin inhibitors with extended segments toward S3' site of renin Yong Wu, Chen Shi, Xiaowei Sun, Xiaoming Wu, Hongbin Sun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . Ethyl (3-((2S,4S,5S,7S)-5-Azido-4-hydroxy-2-isopropyl-7-(4-methoxy-3-(3-methoxypropoxy)benzyl)-8-methyl nonanamido)-2,2-dimethylpropyl)carbamate C33H57N5O7 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2011 19 4238-4249 Synthesis, biological evaluation and docking studies of octane-carboxamide based renin inhibitors with extended segments toward S3' site of renin Yong Wu, Chen Shi, Xiaowei Sun, Xiaoming Wu, Hongbin Sun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . (2S,4S,5S,7S)-5-Azido-N-(3-(3,3-dimethylureido)-2,2-dimethylpropyl)-4-hydroxy-2-isopropyl-7-(4-methoxy-3-(3-methoxypropoxy)benzyl)-8-methylnonanamide C33H58N6O6 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2011 19 4238-4249 Synthesis, biological evaluation and docking studies of octane-carboxamide based renin inhibitors with extended segments toward S3' site of renin Yong Wu, Chen Shi, Xiaowei Sun, Xiaoming Wu, Hongbin Sun Structure 13C NMR ̼Æ×Ä£Äâͼ |
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