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aiwen747: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-08-26 20:24:37
²éѯ½á¹û£º¹²²éµ½480¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     indole-3-acetic acid
    ÏàËÆ¶È:90%
Natural Product Research and Development          2009          21          379-381
Compounds from Culture Broth of Paenibacillus polymyxa HY96-2
GONG Chun-yan; ZHANG Dao-jing; WEI Hong-gang; LI Shu-lan; SHEN Guo-min; LI Yuan-guang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     Tryptophol[2-(3-indolyl)-ethanol]
    ÏàËÆ¶È:80%
Biochemical Systematics and Ecology          2006          34          453-456
Indole alkaloids from a sponge Sarcotragus species
Yonghong Liu, Jee H. Jung, Si Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     compound
C25H19N3     ÏàËÆ¶È:80%
Journal of Heterocyclic Chemistry          2009          46          535-539
A new catalytic method for ecofriendly synthesis of bis-and trisindolylmethanes by zirconyldodecylsulfate under mild conditions
Maasoumeh Jafarpour,Abdolreza Rezaeifard and Tayebeh Golshani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     1-¼×»ù-1H-ßÅßá-2-ôÈËá
    ÏàËÆ¶È:80%
Modern Chinese Medicine          2008          10(12)          29-31
Studies on the Metabolites of Salvianolic Acid B
Yuan Zheng, Li Guoyu, , Zeng Yimei, Wang Jinhui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     tris(1H-indol-3-yl)methane
C25H19N3     ÏàËÆ¶È:80%
Bioorganic & Medicinal Chemistry          2010          18          6905-6913
Synthesis and cytotoxic potency of novel tris(1-alkylindol-3-yl)methylium salts: Role of N-alkyl substituents
Sergey N. Lavrenov, Yuriy N. Luzikov, Evgeniy E. Bykov, Marina I. Reznikova, Evgenia V. Stepanova, Valeria A. Glazunova, Yulia L. Volodina, Victor V. Tatarsky Jr., Alexander A. Shtil, Maria N. Preobrazhenskaya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     3-indolelactic acid methyl ester
C12H13NO3     ÏàËÆ¶È:75%
Heterocycles          2007          72          91-94
A New Method for Efficient Coupling of Indole and Epoxide Catalyzed with Yb(OTf)3, and Application to the Total Synthesis of Kurasoin B
Satoshi Tsuchiya, Toshiaki Sunazuka, Tatsuya Shirahata, Tomoyasu Hirose, Eisuke Kaji, and Satoshi Omura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     compound 6
    ÏàËÆ¶È:75%
Heterocycles          2000          53          37-48
Preparation of Lavendamycin Analogues
Christine Barbier, Arnaud Joissains, Alain Commerçon, Jean-François Riou, and François Huet*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (¡À)-indollactic acid methyl ester
C12H13NO3     ÏàËÆ¶È:75%
The Journal of Antibiotics          1996          49          886-889
Kurasoins A and B, New Protein Earnesyltransferase Inhibitors Produced by Paedlomyces sp. FO-3684 II. Structure Elucidation and Total Synthesis
RYUJI UCHIDA, KAZURO SHIOMI, TOSHIAKI SUNAZUKA, JUNJI INOKOSHI, AI NISHIZAWA, TOMOYASU HIROSE, HARUO TANAKA, YUZURU IWAI, SATOSHI OMURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     N,N-dimethyltryptamine-N-oxide
    ÏàËÆ¶È:72.7%
Magnetic Resonance in Chemistry          2007          45          359-361
NMR spectral assignments of a new chlorotryptamine alkaloid and its analogues from Acacia confusa (pages 359¨C361)
Malcolm S. Buchanan, Anthony R. Carroll, David Pass and Ronald J. Quinn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     2,2'-thiobis(1H-indole-3-propanamide)
C22H22N4O2S     ÏàËÆ¶È:72.7%
Journal of Medicinal Chemistry          1994          37          598-609
Tyrosine kinase inhibitors. 2. Synthesis of 2,2'-dithiobis(1H-indole-3-alkanamides) and investigation of their inhibitory activity against epidermal growth factor receptor and pp60v-src protein tyrosine kinases
Andrew M. Thompson, David W. Fry, Alan J. Kraker, William A. Denny
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     2,5-bis(3-indolylmethyl)pyrazine
C22H18N4     ÏàËÆ¶È:70%
Journal of Natural Products          2002          65          1660-1663
Pharacine, a Natural p-Cyclophane and Other Indole Derivatives from Cytophaga sp. Strain AM13.11
Mohamed Shaaban,Rajendra P. Maskey, Irene Wagner-Döbler, and Hartmut Laatsch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     corynantheine
    ÏàËÆ¶È:70%
Journal of Natural Products          1985          Vol 48          571-580
Chemistry of the Annonaceae, Part 18. Benzylated Indoles and Dihydrochalcones in Uvaria angolensis from Tanzania
Ilias Muhammad, Peter G. Waterman
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