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57-60-1
DMSO   13C NMR
7.5,16.1,18.3,21.3,28.8,31.1,43.3,55.2,59.3,61.8,108.8,111.0,118.2,118.9,120.7,124.5,127.9,136.0,166.3,167.3
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zchangll: ½ð±Ò+8, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-04-24 16:01:58
1 .     cyclo[Trp-Val]
    ÏàËÆ¶È:80%
Chinese Journal of Marine Drugs          2009          28(2)          6-10
Studies on the chemical constituents of the fermentation liquid from marine bacteria Roseobacter sp.
MENG Xu-peng, TIAN Li, LIN Wen-han, LI Qing-shan
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     »·-(É«°±Ëá-çÓ°±Ëá)-¶þëÄ
C16H19N3O2     ÏàËÆ¶È:80%
Chinese Journal of Medicinal Chemistry          2012          22          38-43
Chemical constituents from the endophyte Bacillus pumilus derived from Breynia fruticosa
HUO Pei-yuan; CHEN Hua-hong; JIANG Yi; HAN Li; XU Li-hua; HUANG Xue-shi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     cyclo(L-Leu-L-Trp)
C17H21N3O2     ÏàËÆ¶È:70%
Bioorganic & Medicinal Chemistry          2012          20          2002-2009
Cyclic dipeptides exhibit potency for scavenging radicals
Tadashi Furukawa, Takashi Akutagawa, Hitomi Funatani, Toshikazu Uchida, Yoshihiro Hotta, Masatake Niwa, Yoshiaki Takaya
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     cyclo-(L-Trp-D-Val)
C16H19N3O2     ÏàËÆ¶È:70%
Chinese Journal of Marine Drugs          2013          32          37-45
ä°Ì¦¹²ÉúÕæ¾úHT-2´ÎÉú´úл²úÎïµÄÑо¿
ËïÀ¤À´, Íõ, ¸¶Åô, ÁõÅàÅà, ÖìΰÃ÷
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     N'-Prenyl-cyclo-L-tryptophan-L-proline
C21H26N3O2     ÏàËÆ¶È:66.6%
Bioorganic & Medicinal Chemistry          2000          8          2407-2415
Synthesis and evaluation of microtubule assembly inhibition and cytotoxicity of prenylated derivatives of cyclo-l-Trp-l-Pro
Juan F Sanz-Cervera, Emily M Stocking, Takeo Usui, Hiroyuki Osada, Robert M Williams
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     cyclo[Trp-lle]
    ÏàËÆ¶È:65%
Chinese Journal of Marine Drugs          2009          28(2)          6-10
Studies on the chemical constituents of the fermentation liquid from marine bacteria Roseobacter sp.
MENG Xu-peng, TIAN Li, LIN Wen-han, LI Qing-shan
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     cyclo[Trp-Phe]
    ÏàËÆ¶È:65%
Chinese Journal of Marine Drugs          2009          28(2)          6-10
Studies on the chemical constituents of the fermentation liquid from marine bacteria Roseobacter sp.
MENG Xu-peng, TIAN Li, LIN Wen-han, LI Qing-shan
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     »·-(É«°±Ëá-ÒìÁÁ°±Ëá)-¶þëÄ
C17H21N3O2     ÏàËÆ¶È:65%
Chinese Journal of Medicinal Chemistry          2012          22          38-43
Chemical constituents from the endophyte Bacillus pumilus derived from Breynia fruticosa
HUO Pei-yuan; CHEN Hua-hong; JIANG Yi; HAN Li; XU Li-hua; HUANG Xue-shi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     3-isorauniticine
    ÏàËÆ¶È:61.9%
Planta Medica          1981          41          406-418
13C NMR Data of 3-Isoajmalicine and 19-Epiajmalicine
Raimo Uusvuori and Mauri Lounasmaa
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     (+)-6,7-dehydrovincadine
    ÏàËÆ¶È:61.9%
Helvetica Chimica Acta          1976          59          2711-2723
13C-NMR. Spectroscopy of Naturally Occuring Substances. XLII. Conformational analysis of quebrachamine-like indole alkaloids and related substances
Ernest Wenkert, Edward W. Hagaman, Nicole Kunesch, Nai-yi Wang and B¨¦la Zsadon
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     (+)-6,7-dehydrovincadine
    ÏàËÆ¶È:61.9%
Helvetica Chimica Acta          1976          59          2711-2723
13C-NMR. Spectroscopy of Naturally Occuring Substances. XLII. Conformational analysis of quebrachamine-like indole alkaloids and related substances
Ernest Wenkert, Edward W. Hagaman, Nicole Kunesch, Nai-yi Wang and B¨¦la Zsadon
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     tetrahydroalstonine
    ÏàËÆ¶È:61.9%
Natural Product Research and Development          2007          19          235-239
Indole Alkaloids from Rauwolfia vomitoria
LI Lin;HE Hong-ping; ZHOU Hua; HAO Xiao-jiang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     compound 1
C21H27N3O2     ÏàËÆ¶È:61.9%
The Journal of Antibiotics          2003          56          102-106
Novel Antifungal Diketopiperazine from Marine Fungus
HEE-GUK BYUN,HUIPING ZHANG,MASAMI MOCHIZUKI,KYOKO ADACHI,YOSHIKAZU SHIZURI,WON-JAE LEE and SE-KWON KIM
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     (2R,13br)-2-ethyl-2-((methoxymethoxy)methyl)-2,3,4,5,7,8,13,13b-octahydro-1H-azepino[1',2':1,2]pyrido[3,4-b]indole
C21H30N2O2     ÏàËÆ¶È:61.9%
Tetrahedron          2013          69          5525-5536
Enantiospecific total synthesis of indole alkaloids (+)-eburnamonine, (−-aspidospermidine and (−-quebrachamine
John Eugene Nidhiry, Kavirayani R. Prasad
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     compound 9c
    ÏàËÆ¶È:61.9%
Journal of the American Chemical Society          1979          101          5370-5376
Total synthesis of the yohimbines
Ernest Wenkert, Timothy D. J. Halls, Gerhard Kunesch, Kazuhiko Orito, Richard L. Stephens, Wayne A. Temple, Jhillu S. Yadav
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     naucleofficine D
C20H22N2O3     ÏàËÆ¶È:60%
Phytochemistry          2008          69          1405-1410
Indole alkoloids from Nauclea officinalis with weak antimalarial activity
Jingyong Sun, Hongxiang Lou, Shengjun Dai, Hui Xu, Feng Zhao, Ke Liu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     3-[(1H-Indol-3-yl)methyl]-6-benzylpiperazine-2,5-dione
C20H19N3O2     ÏàËÆ¶È:60%
Chemistry of Natural Compounds          2009          45          677-680
iso-¦Á-CYCLOPIAZONIC ACID, A NEW NATURAL PRODUCTISOLATED FROM THE MARINE-DERIVEDFUNGUS Aspergillus flavus C-F-3
Ai-Qun Lin, Lin Du, Yu-Chun Fang, Fa-Zuo Wang,Tian-Jiao Zhu, Qian-Qun Gu, and Wei-Ming Zhu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     voafinidine
C20H28N2O2     ÏàËÆ¶È:60%
Natural Product Research          1996          8          49-53
Voafinidine and Voalenine, Novel Indoles of the Aspidosperma-type from Tabernaemontana
Toh-Seok Kam; S. Anuradha; Kah-Yeng Loh
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     borrerine
    ÏàËÆ¶È:60%
Journal of Natural Products          1985          Vol 48          120-123
RMN du Carbone 13 des Alcaloïdes du Type Borr¨¦rine-Borr¨¦v¨¦rine-Isoborr¨¦v¨¦rine
F. Tillequin, M. Koch, A. Rabaron
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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2Â¥2015-02-06 13:08:25
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