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ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
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²éѯ½á¹û£º¹²²éµ½730¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . L-Tryptophan C11H12N2O2 ÏàËÆ¶È:75% Journal of Chinese Pharmaceutical Sciences 2004 13 18 Chemical Constituents from Starfish Asterias rollestoni LI Guoqiang, DENG Zhi-wei, LI Jun, FU Hon-zheng, and LIN wen-han Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . tryptophan C11H12N2O2 ÏàËÆ¶È:75% Natural Product Research 2006 20 79-83 A new adenosyl-alkaloid from Ostrea rivularis Ming-An Ouyang Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . tryptophan ÏàËÆ¶È:75% Natural Product Sciences 2001 7 107-109 Anti-diabetic Constituent from the Node of Lotus Rhizome (Nelumbo nucifera Gaertn) Lee, Min-Won; Kim, Jun-Sik; Cho, Su-Min; Kim, Ji-Hun; Lee, Jae-Seung Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . tryptophan ÏàËÆ¶È:75% Journal of Shenyang Pharmaceutical University 2010 27 69-74 Isolation and identification of metabolites from amarine bacterial strain Bacillus sp. GAO Hao, CHEN Guo-dong, TANG Jin-shan, ZHANG Shu-dan, WANG Nai-li, YAO Xin-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . tryptophan ÏàËÆ¶È:75% Korean Journal of Pharmacognosy 2011 42 302-308 Inhibitors of Adipogenesis in 3T3-L1 Cells Isolated from Wheat Bran Jeong, Won-Sik; Hong, Seong-Su; Lee, Jung-A; Ahn, Eun-Kyung; Oh, Joa-Sub Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . tryptophan ÏàËÆ¶È:75% Academic Journal of Second Military Medical University 2008 29 1479-1482 Study on chemical constituents of Starfish Asterias amurensis CHENG Ping, TANG Hua, PIAO Shu-juan, LU Yi, WANG Zeng-lei, LIN Hou-wen Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . tryptophan ÏàËÆ¶È:75% China Journal of Chinese Materia Medica 2011 36 458-461 Chemical constituents in herb of Polygonum orientale ¢ò LI Yongjun, LI Cuibing, HE Xun, LIAO Shanggao, LAN Yanyu, WANG Aimin, WANG Yonglin Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . L-Tryptophan C11H12N2O2 ÏàËÆ¶È:75% Journal of Peking University (Health Sciences) 2004 36 12-17 Chemical constituents from chinese marine sponge Cinachyrella australiensis LI Li ya; DENG Zhi wei; LI Jun; FU Hong zheng; LIN Wen han Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . É«°±Ëá ÏàËÆ¶È:75% Chinese Traditional and Herbal Drugs 2011 42 2186-2188 Chemical constituents in water fraction of Abelmoschus esculentus JIA, Lu, ZHONG, Li-jun, LI, Huan-fen, JING, Lin-lin Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Schischkiniin C26H24N6O2 ÏàËÆ¶È:69.2% Tetrahedron 2005 61 9001-9006 Isolation, structure elucidation and bioactivity of schischkiniin, a unique indole alkaloid from the seeds of Centaurea schischkinii Mohammad Shoeb, Sezgin Celik, Marcel Jaspars, Yashodharan Kumarasamy, Stephen M. MacManus, Lutfun Nahar, Paul K. Thoo-Lin, Satyajit D. Sarker Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 4b ÏàËÆ¶È:66.6% Chemistry of Natural Compounds 2004 40 585-590 DIASTEREOTOPIC SYNTHESIS OF 1- AND 1,1-SUBSTITUTED 4-PHENYL-2,3,4,9-TETRAHYDRO-1H-b-CARBOLINES B. B. Semenov, K. A. Novikov, A. N. Spitsin,V. N. Azev, and V. V. Kachala Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . N,N,N-trimethyl-tropaphone inner salt(hypaphorine) ÏàËÆ¶È:66.6% China Journal of Chinese Materia Medica 2004 29 432-434 Studies on chemical constituents from root of Hedysarum polybotrys HAI Liqian, ZHANG Qiangying, ZHAO Yuying, LIANG Hong, DU Niansheng Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . N,N-Diethyltryptamine C14H20N2 ÏàËÆ¶È:66.6% Bioorganic & Medicinal Chemistry 2011 19 3120-3127 Tryptamine derivatives as novel non-nucleosidic inhibitors against hepatitis B virus Shi-Jin Qu , Gui-Feng Wang ,Wen-Hu Duan,Shan-Yan Yao, Jian-Ping Zuo , Chang-Heng Tan ,Da-Yuan Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Compound 6 C12H12N2O3 ÏàËÆ¶È:66.6% Tetrahedron Letters 2011 52 7042-7045 Histone deacetylase inhibitor induced the production of three novel prenylated tryptophan analogs in the entomopathogenic fungus,Torrubiella luteorostrata Teigo Asai, Takashi Yamamoto, Yoshiteru Oshima Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . compound 6 C15H10N2 ÏàËÆ¶È:66.6% Tetrahedron Letters 2002 43 3327-3328 A photochemical route to synthesize cryptosanguinolentine R.Nandha Kumar, T. Suresh, P.S. Mohan Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 6-Chloro-L-tryptophan C11H11ClN2O ÏàËÆ¶È:66.6% Tetrahedron Letters 2004 45 8569-8573 Synthesis of optically active ring-A substituted tryptophans as IDO inhibitors Xiaoyan Li, Wenyuan Yin, P.V.V. Srirama Sarma, Hao Zhou, Jun Ma, James M. Cook Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 6 ÏàËÆ¶È:66.6% Heterocycles 2000 53 37-48 Preparation of Lavendamycin Analogues Christine Barbier, Arnaud Joissains, Alain Commerçon, Jean-François Riou, and François Huet* Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (1H-indol-3-yl)-(trimethylsiloxy)acetonitrile ÏàËÆ¶È:66.6% Tetrahedron 2002 58 2813-2819 Synthesis of the marine alkaloids rhopaladins A, B, C and D Tomasz Janosik, Ann-Louise Johnson, Jan Bergman Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . Sch 725418 C24H24N4O2 ÏàËÆ¶È:66.6% The Journal of Antibiotics 2004 57 345-347 Structure Elucidation of a New Diketopiperazine Sch 725418 from Micromonospora sp. SHU-WEI YANG,TZE-MING CHAN,JOSEPH TERRACCIANO,DAVID LOEBENBERG,GUODONG CHEN,MAHESH PATEL,VINCENT GULLO,BIRENDRA PRAMANIK and MIN CHU Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 3-indolethanol C10H11NO ÏàËÆ¶È:66.6% Academic Journal of Second Military Medical University 2008 29 1234-1238 Isolation,identification and biological characterization of secondary metabolites produced by a marine Bacillus subtilis HAN Wen-ju, LU Xiao-ling, XU Qiang-zhi, LIU Xiao-yu, JIAO Bing-hua Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 2,6-Dibromo-3-bromomethyl-1-carbomethoxyindole C11H8NO2Br3 ÏàËÆ¶È:66.6% Natural Product Communications 2011 6 451-456 C-6 Regioselective Bromination of Methyl Indolyl-3-acetate Oscar R. Su¨¢rez-Castillo, Myriam Mel¨¦ndez-Rodr¨ªguez, Lidia Beiza-Granados, Indira C. Cano-Escudero, Martha S. Morales-R¨ªos and Pedro Joseph-Nathan Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 2,2'-(1,1'-methylenebis(1H-indole-3,1-diyl))diethanol C16H21O6N ÏàËÆ¶È:66.6% Journal of Asian Natural Products Research 2011 13 1042-1046 Two new compounds from the endophytic fungus Colletotrichum sp. L10 of Cephalotaxus hainanensis Gang Chen, Hao-Fu Dai, Yi Sha and Yue-Hu Pei Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . tryptophan C11H12N2O2 ÏàËÆ¶È:66.6% Chinese Journal of Natural Medicines 2012 10 68-71 A new perylenequinone from a halotolerant fungus, Alternaria sp. M6 Song-Ya ZHANG, Zhan-Lin LI, Jiao BAI, Yu WANG, Li-Min ZHANG, Xin WU, Hui-Ming HUA Structure 13C NMR ̼Æ×Ä£Äâͼ |
4Â¥2013-12-11 10:11:14









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