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DTH12-10-9-2-2  M=274
13C NMR ( MeOD) ¦Ä 166.47, 163.75, 159.91, 157.43, 145.45, 142.24, 113.67, 113.42, 113.29, 105.88, 103.69, 24.37, 21.65.
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21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2
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2Â¥2013-11-25 22:35:23
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2Â¥: Originally posted by wangkaibo123 at 2013-11-25 22:35:23
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21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2

DTH12-10-9-2-2  M=274
13C NMR ( MeOD) 21.6,24.3,103.6,105.8,113.2,113.4,113.6,142.2,145.4,157.4,159.9,163.7,166.47
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3Â¥2013-11-26 10:47:54
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PSA: ½ð±Ò+1, 3u 2013-11-26 11:19:46
äìÏæäòäÙ(¶¹¸ç´ú·¢): ½ð±Ò+15, лл 2013-12-02 14:20:17
ÒýÓûØÌû:
3Â¥: Originally posted by äìÏæäòäÙ at 2013-11-26 10:47:54
DTH12-10-9-2-2  M=274
13C NMR ( MeOD) 21.6,24.3,103.6,105.8,113.2,113.4,113.6,142.2,145.4,157.4,159.9,163.7,166.47
(ÁíÒ»¸öÌû×ÓÉÏÒ²ÊÇÀàËÆµÄ»¯ºÏÎлл)...

²éѯ½á¹û£º¹²²éµ½48¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     isohaplopine
C13H11NO4     ÏàËÆ¶È:61.5%
Phytochemistry          1988          27          959-960
Quinoline alkaloids from the leaves of Teclea simplicifolia
Assefa Wondimu,Ermias Dagne,Peter G. Waterman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     lecanorin
    ÏàËÆ¶È:60%
China Journal of Chinese Materia Medica          2001          26          608-610
Studies on Chemical Constituents of Umbilicaria esculenta(Miyoshi)Minks
Qiu Cheng, DING Yi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     3,6,8-Trihydroxy-1-methylxanthone
C14H10O5     ÏàËÆ¶È:57.1%
Journal of Natural Products          2003          66          706-708
Two New Xanthone Derivatives from the Algicolous Marine Fungus Wardomyces anomalus
Ahmed Abdel-Lateff, Christine Klemke, Gabriele M. Knig, and Anthony D. Wright
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     compound 6
C21H22O7     ÏàËÆ¶È:57.1%
Phytochemistry          1985          24          805-813
Coumarins from Musineon divaricatum
Tim M. Swager, John H. CardellinaII
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     methyl 2-hydroxy-4-(3-hydroxy-5-methylphenoxy)-6-methylbenzoate
    ÏàËÆ¶È:56.2%
The Journal of Antibiotics          2011          64          465-467
Diphenyl etheric metabolites from Streptomyces sp. neau50
Dian-Liang Gong, Xiang-Jing Wang, Zhi-Dan Xiang, Ji-Dong Wang, Hui Zhang, Chong-Xi Liu, Ji Zhang and Wen-Sheng Xiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     umbelliferone
    ÏàËÆ¶È:53.8%
Planta Medica          1981          42          89-96
Studies on Coumarins of a Chinese Drug ,,Qian-Hu"
T. Okuyama and S. Shibata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     umbelliferone
    ÏàËÆ¶È:53.8%
China Journal of Chinese Materia Medica          2009          34          1231-1234
Coumarins from Peucedanum harry- smithii var. subglabrum
LIWen, FENG Shilan, HU Fangdi, CHEN Erlin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     Sphondin
    ÏàËÆ¶È:53.8%
Phytochemistry          1983          22          2035-2037
Furocoumarin glucosides of Angelica archangelica subspecies Litoralis
Ole Thastrup, John Lemmich
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     7-hydroxycoumarin
    ÏàËÆ¶È:53.8%
Chinese Pharmaceutical Journal          2011          46          576-579
Study on Chemical Constituents of Hydrangea macrophylla(Thunb.) Seringe
FENG Wei-sheng, ZHANG Yan-li, ZHENG Xiao-ke, WANG Yan-zhi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     Umbelliferone
    ÏàËÆ¶È:53.8%
Journal of the Korean Chemical Society          2010          54          701-706
Chemical Constituents of the Halophyte Glehnia littoralis
Young Ran Um, Jung Im Lee, Jinhyeok Lee, Haejin Kim, Sung Su Yea, Youngwan Seo*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     7-hydroxycoumarin
C9H6O3     ÏàËÆ¶È:53.8%
Natural Product Research and Development          2010          22          1003-1005
ZHOU Song-lin1; CHEN Shuang-lin2; TAN Guang-hong1; WANG Hua1; HUANG Yong-hao1; CHEN Fan11Hainan
XU Wei;SONG Qi-shi; WANG Pei; LI Shang-zhen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     umbelliferone
    ÏàËÆ¶È:53.8%
Natural Product Research and Development          2010          22          181-184
Chemical Constituents from the Leaves of Morus mongolica
JING Ying;ZHANG Xiao-qi;HAN Wei-li; ZHANG Yun-tian; YE Wen-cai;
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4Â¥2013-11-26 10:58:13
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²éѯ½á¹û£º¹²²éµ½48¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     isohaplopine
C13H11NO4     ÏàËÆ¶È:61.5%
Phytochemistry          1988          27          959-960
Quinoline alkaloids from the leaves of Teclea simplicifolia
Assefa Wondimu,Ermias Dagne,Peter G. Waterman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     lecanorin
    ÏàËÆ¶È:60%
China Journal of Chinese Materia Medica          2001          26          608-610
Studies on Chemical Constituents of Umbilicaria esculenta(Miyoshi)Minks
Qiu Cheng, DING Yi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     3,6,8-Trihydroxy-1-methylxanthone
C14H10O5     ÏàËÆ¶È:57.1%
Journal of Natural Products          2003          66          706-708
Two New Xanthone Derivatives from the Algicolous Marine Fungus Wardomyces anomalus
Ahmed Abdel-Lateff, Christine Klemke, Gabriele M. Knig, and Anthony D. Wright
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     compound 6
C21H22O7     ÏàËÆ¶È:57.1%
Phytochemistry          1985          24          805-813
Coumarins from Musineon divaricatum
Tim M. Swager, John H. CardellinaII
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     methyl 2-hydroxy-4-(3-hydroxy-5-methylphenoxy)-6-methylbenzoate
    ÏàËÆ¶È:56.2%
The Journal of Antibiotics          2011          64          465-467
Diphenyl etheric metabolites from Streptomyces sp. neau50
Dian-Liang Gong, Xiang-Jing Wang, Zhi-Dan Xiang, Ji-Dong Wang, Hui Zhang, Chong-Xi Liu, Ji Zhang and Wen-Sheng Xiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     umbelliferone
    ÏàËÆ¶È:53.8%
Planta Medica          1981          42          89-96
Studies on Coumarins of a Chinese Drug ,,Qian-Hu"
T. Okuyama and S. Shibata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     umbelliferone
    ÏàËÆ¶È:53.8%
China Journal of Chinese Materia Medica          2009          34          1231-1234
Coumarins from Peucedanum harry- smithii var. subglabrum
LIWen, FENG Shilan, HU Fangdi, CHEN Erlin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     Sphondin
    ÏàËÆ¶È:53.8%
Phytochemistry          1983          22          2035-2037
Furocoumarin glucosides of Angelica archangelica subspecies Litoralis
Ole Thastrup, John Lemmich
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     7-hydroxycoumarin
    ÏàËÆ¶È:53.8%
Chinese Pharmaceutical Journal          2011          46          576-579
Study on Chemical Constituents of Hydrangea macrophylla(Thunb.) Seringe
FENG Wei-sheng, ZHANG Yan-li, ZHENG Xiao-ke, WANG Yan-zhi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     Umbelliferone
    ÏàËÆ¶È:53.8%
Journal of the Korean Chemical Society          2010          54          701-706
Chemical Constituents of the Halophyte Glehnia littoralis
Young Ran Um, Jung Im Lee, Jinhyeok Lee, Haejin Kim, Sung Su Yea, Youngwan Seo*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
5Â¥2013-11-26 11:39:01
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