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sherrywh: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-06-30 09:36:24
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sherrywh: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-06-30 09:36:24
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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£º¹²²éµ½86¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . N-(indol-3-ylethyl)-2-hydroxy-3-methylpentanamide C16H22N2O2 ÏàËÆ¶È:68.7% Journal of Natural Products 1996 59 1157-1158 N-(Indol-3-ylethyl)-2'-hydroxy-3'-methylpentanamide, a Novel Indole Derivative from Xenorhabdus nematophilus Jianxiong Li, Genhui Chen, and John M. Webster Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (2'S,3'S)-N-(Indol-3-ylethyl)-2'-hydroxy-3'-methylpentanamide C16H22N2O2 ÏàËÆ¶È:68.7% Bulletin of the Korean Chemical Society 2003 24 623-626 Isolation and Synthesis of Tryptamine Derivatives from a Symbiotic Bacterium Xenorhabdus nematophilus PC Seunguk Paik, Myung Kwang Park, Seong Hoon Jhun, Heai Ku Park, Chun Soo Lee, Bum Rae Cho, Hong Sik Byun, Seok Burm Choe, Seong Il Suh Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (2'R,3'S)-N-(Indol-3-ylethyl)-2'-hydroxy-3'-methylpentanamide C16H22N2O2 ÏàËÆ¶È:68.7% Bulletin of the Korean Chemical Society 2003 24 623-626 Isolation and Synthesis of Tryptamine Derivatives from a Symbiotic Bacterium Xenorhabdus nematophilus PC Seunguk Paik, Myung Kwang Park, Seong Hoon Jhun, Heai Ku Park, Chun Soo Lee, Bum Rae Cho, Hong Sik Byun, Seok Burm Choe, Seong Il Suh Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Nb-acetyltryptamine C12H14N2O ÏàËÆ¶È:66.6% Archives of Pharmacal Research 2003 26 21-23 Indolyl alkaloid derivatives,Nb-acetyltryptamine and oxaline from a marine-derived fungus Yong Li, Xi Feng Li, Dong Soo Kim, Hong Dae Choi and Byeng Wha Son Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . N-fatty acyl trptamine ÏàËÆ¶È:62.5% Phytochemistry 1993 34 1633-1635 N-fatty acyl tryptamines from Annona reticulata Uki Maeda, Noriyuki Hara, Yoshinori Fujimoto, Anjani Srivastava, Yogesh Kumar Gupra, Mahendra Sahai Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . compound 13a C14H16N2O3 ÏàËÆ¶È:60% Journal of Natural Products 2005 68 1581-1587 Extraction, Hemisynthesis, and Synthesis of Canthin-6-one Analogues. Evaluation of Their Antifungal Activities Flor Soriano-Agatn, Delphine Lagoutte, Erwan Poupon, Franois Roblot,Alain Fournet, Jean-Charles Gantier, and Reynald Hocquemiller Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . N-acetyl-tryptamine C12H14N2O ÏàËÆ¶È:60% Chemistry of Natural Compounds 2006 42 713-717 INDOLIC METABOLITES FROM THE NEW MARINE BACTERIUM Roseivirga echinicomitans KMM 6058T G. K. Oleinikova,O. I. Ivchuk, V. A. Denisenko, E. L. Chaikina,N. I. Menzorova, O. I. Nedashkovskaya, and T. A. Kuznetsova Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 1-(1H-indol-3-yl)-2,3-dihydroxy-5-methyl-hexane C15H21NO2 ÏàËÆ¶È:60% Journal of Asian Natural Products Research 2009 11 1040-1044 Steroids and alkaloids from the South China Sea sponge Axinella sp Shu-Hua Qia, Yi-Fei Wangb and Si Zhanga Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound C19H20N2O3S ÏàËÆ¶È:60% Heterocycles 2003 60 99-112 Regioselective Reduction of N-Alkyl-3-sulfonyl Glutarimide. Formal Synthesis of 1,2,3,4,6,7,12,12b-Octahydroindolo[2,3-a]quinolizine and Homobaclofen Meng-Yang Chang and Shui-Tein Chen* Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 3-(3-Indolyl)butanenitrile C12H12N2O ÏàËÆ¶È:60% Phytochemistry 2010 71 1952-1962 Indolyl-3-acetaldoxime dehydratase from the phytopathogenic fungus Sclerotinia sclerotiorum: Purification, characterization, and substrate specificity M. Soledade C. Pedras, Zoran Minic, Premila D. Thongbam, Vangala Bhaskar, Sabine Montaut Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . sattazolin C15H19NO2 ÏàËÆ¶È:60% The Journal of Antibiotics 1995 48 967-972 Sattabacins and Sattazolins: New Biologically Active Compounds with Antiviral Properties Extracted from a Bacillus sp. GIORGIO LAMPIS, DELIA DEIDDA, CARLO MAULLU, MARIA A. MADEDDU, RAFFAELLO POMPEI, FRANCO DELLE MONACHE, GIUSEPPE SATTA Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . tetrahydro-2H-pyran-2-yl (2-(1H-indol-3-yl)ethyl)carbamodithioate C16H20N2OS2 ÏàËÆ¶È:60% Bulletin of the Korean Chemical Society 2012 33 4047-4051 A New and Facile Protocol for the Synthesis of Dithiocarbamate-linked 3,4-Dihydro-2H-pyran Using N-Halo Catalysts Under Mild Conditions Reaction Ramin Ghorbani-Vaghei*, Mostafa Amiri, Hojat Veisi Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . six-membered ring amide derivative ÏàËÆ¶È:56.2% Chemical & Pharmaceutical Bulletin 1993 41 1173-1176 The 1H- and 13C-Nuclear Magnetic Resonance Spectra of Manzamine C and Related Compounds Hiroko SEKI,Masako NAKAGAWA,Akihiro HASHIMOTO and Tohru HINO Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 3-(1-(2-Bromophenyl)-2-nitroethyl)-1H-indole C16H13BrN2O2 ÏàËÆ¶È:56.2% Molecules 2009 14 3952-3963 An Efficient Method for the N-Bromosuccinimide Catalyzed Synthesis of Indolyl-Nitroalkanes Chun-Wei Kuo, Chun-Chao Wang, Hu-Lin Fang, B. R. Raju, Veerababurao Kavala, Pateliya M. Habib and Ching-Fa Yao Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . Nematophin C16H20N2O2 ÏàËÆ¶È:56.2% Bulletin of the Korean Chemical Society 2003 24 623-626 Isolation and Synthesis of Tryptamine Derivatives from a Symbiotic Bacterium Xenorhabdus nematophilus PC Seunguk Paik, Myung Kwang Park, Seong Hoon Jhun, Heai Ku Park, Chun Soo Lee, Bum Rae Cho, Hong Sik Byun, Seok Burm Choe, Seong Il Suh Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 23 ÏàËÆ¶È:55.5% Journal of Natural Products 2005 68 1581-1587 Extraction, Hemisynthesis, and Synthesis of Canthin-6-one Analogues. Evaluation of Their Antifungal Activities Flor Soriano-Agatn, Delphine Lagoutte, Erwan Poupon, Franois Roblot,Alain Fournet, Jean-Charles Gantier, and Reynald Hocquemiller Structure 13C NMR ̼Æ×Ä£Äâͼ |

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