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cliff0223

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[ÇóÖú] ΢Æ×ÇóÖú ÒÑÓÐ2È˲ÎÓë

ÇâÆ×0.753,0.806,0.850,0.855,0.870,0.874,0.895,0.946,0.957,1.047,1.247,1.354,1.546,1.692,1.705,2.063,2.068,4.621,4.637,7.282,
̼Æ×£º14.71,14.73,15.90,16.05,16.35,16.51,17.70,18.20,19.48,21.30,21.48,21.64,22.53,,23.71,25.49,25.63,26.16,27.61,27.95,34.02,34.19,34.40,36.34,36.71,37.04,37.81,38.47,39.24,39.40,41.11,42.35,48.69,48.73,50.37,55.41,76.74,77.00,77.25,80.99,118.89,139.86,170.98,
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cliff0223: ½ð±Ò+5 2015-06-17 14:55:39
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1 .     Calotropterpenylester
C42H82O2     ÏàËÆ¶È:83.3%
Pharmazie          2001          56          175-177
Norditerpenic ester and pentacyclic triterpenoids from root bark of Calotropis procera (Ait) R. Br.
S.H. Ansari - M. Ali
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     16¦Â-hydroxypseudotaraxasterol 3-O-palmitate
C46H80O3     ÏàËÆ¶È:81.3%
Shoyakugaku Zasshi          1990          44          335-338
Studies on the Constituents of Chrysanthemi Flos
YAHARA SHOJI, MORITA YASUSHI,NOHARA TOSHIHIRO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     lupeol 3-hydroxyoctadencanoate
    ÏàËÆ¶È:80.9%
Chemical Journal of Chinese Universities          2003          24          436-441
Chemical Constituents from the Roots of Biondia Hemsleyana
TAN Xing-Gen, ZHANG Xiao-Rong, PENG Shu-Lin, LIAO Xun, DING Li-Sheng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     16¦Â-hydroxypseudotarasterol-3¦Â-O-palmitate
    ÏàËÆ¶È:80.9%
Acta Botanica Sinica          1997          39(1)          85−90
Studies on chemical constituents from Dendranthema morifolium (Ramat.) Tzvel.: structure elucidation of two new triterpenoid esters
Hu Li-hong and Chen Zhong-liang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     faradiol myristic ester
    ÏàËÆ¶È:80.9%
Journal of Ethnopharmacology          1997          57          139-144
Anti-oedematous activities of the main triterpendiol esters of marigold (Calendula officinalis L.)
K Zitterl-Eglseer, S Sosa, J Jurenitsch, M Schubert-Zsilavecz, R Della Loggia, A Tubaro, M Bertoldi, C Franz
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     faradiol palmitic ester
    ÏàËÆ¶È:80.9%
Journal of Ethnopharmacology          1997          57          139-144
Anti-oedematous activities of the main triterpendiol esters of marigold (Calendula officinalis L.)
K Zitterl-Eglseer, S Sosa, J Jurenitsch, M Schubert-Zsilavecz, R Della Loggia, A Tubaro, M Bertoldi, C Franz
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     16¦Â-hydroxypseudo tarsxasterol-3-O-palmitate
    ÏàËÆ¶È:80.9%
Chinese Traditional Patent Medicine          2010          32          636-639
Isolation and structural elucidation of triterpenes from Cremanthodium potaninii C£®Winkl
YANG Ai-mei, ZENG Yan, YANG Lin, YANG Zhong-duo
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     3,5-¶þôÇ»ù¶þÊ®ÍéËáÓðÉȶ¹´¼õ¥
C50H88O4     ÏàËÆ¶È:79.0%
Chemical Journal of Chinese Universities          2003          24          436-441
Chemical Constituents from the Roots of Biondia Hemsleyana
TAN Xing-Gen, ZHANG Xiao-Rong, PENG Shu-Lin, LIAO Xun, DING Li-Sheng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     sambucunlin A
C46H80O2     ÏàËÆ¶È:78.5%
Planta Medica          1988          54          223-224
Antihepatotoxic Principles of Sambucus formosana
Chun-Nan Lin and Whey-Pin Tome
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     ÉßÝÔËØ B
    ÏàËÆ¶È:78.5%
Chinese Traditional and Herbal Drugs          2005          36          830-831
˼éÉßÝԵĻ¯Ñ§³É·ÖÑо¿(¢ñ)
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Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     Lup-3¦Â-O-palmitate
    ÏàËÆ¶È:78.5%
Pharmazie          2006          61          70-73
Triterpenoids from Pyrethrum tatsienense
Yang Ai-Mei, Liu Xia, Lu Run-Hua and Shi Yan-Ping
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     lupeol palmitate
    ÏàËÆ¶È:78.5%
Chinese Pharmaceutical Journal          2011          46          11-13
Constituents of Viscum ovalifolium DC(¢ò)
YANG Yan-jun, SHA Cong-wei, CHEN Mei-guo
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     compound 24
    ÏàËÆ¶È:78.5%
Qu¨ªmica Nova          2008          31          20-24
Chemical constituents from Tabernaemontana catharinensis root bark: a brief NMR review of indole alkaloids and in vitro cytotoxicity
Pereira, Paulo S¨¦rgio; França, Suzelei de Castro; Oliveira, Paulo Vinicius Anderson de; Breves, Camila Moniz de Souza; Pereira, Sarazete Izidia Vaz; Sampaio, Suely Vilela; Nomizo, Auro; Dias, Diones Aparecida
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     pseudotaraxasterol-3¦Â-O-palmitate
C46H80O2     ÏàËÆ¶È:78.5%
Chinese Joumal of Experimental Traditional Medical Fomulae          2011          17          121-124
Chemical Constituents from Gentiana algida
YANG Ai-mei, HAN Han, SUN Jing, MIAO Zhong-huan, SHI Xiao-long
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     balanophorin B
C46H80O2     ÏàËÆ¶È:78.5%
Acta Botanica Yunnanica          1998          20          369-373
Triterpene constituents from Balanophora indica
Liu Xi-Kui, Li Zhong-Rong, Qiu Ming-Hua, Nie Rui-Lin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     (3b,20R)-20- hydroxylanost-25-en-3-yl palmitate
C46H82O3     ÏàËÆ¶È:76.1%
Helvetica Chimica Acta          2006          Vol. 89          558
Terpenoids from Eupatorium fortunei TURCZ
Hai-Xia Jiang, Ya Li, Jing Pan, and Kun Gao
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     Taraxast-20(30)-ene-3¦Â-O-palmitate
    ÏàËÆ¶È:76.1%
Chemistry of Natural Compounds          2008          44          399-401
TRITERPENOIDS AND STEROIDS FROM Ixeridium gracile
Xue-Mei Ma, Duo-Long Di, and Yan-Ping Shi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     N-[3¦Â-acetoxy-20(29)-lupen-28-oyl]-9-amino acid Methyl Ester
    ÏàËÆ¶È:76.1%
Chemistry of Natural Compounds          2002          38          331-339
SYNTHESIS OF BETULONIC ACID DERIVATIVES CONTAINING AMINO-ACID FRAGMENTS
N. I. Petrenko, N. V. Elantseva, V. Z. Petukhova,M. M. Shakirov, E. E. Shul'ts, and G. A. Tolstikov
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     3¦Â-acetoxy-11¦Á[2',3'-epoxyferulyloxy]-olean-13(18)-ene
C42H60O7     ÏàËÆ¶È:76.1%
Natural Product Research          2001          15          339-344
A New Oleanane Triterpenoid from Gordonia ceylanica
H. M. T. B. Herath; P. S. Athukoralage; Joanne F. Jamie
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     Taraxast-20(30)-ene-3¦Â,16¦Â-diol-3-O-palmitate
    ÏàËÆ¶È:76.1%
Pharmazie          2006          61          70-73
Triterpenoids from Pyrethrum tatsienense
Yang Ai-Mei, Liu Xia, Lu Run-Hua and Shi Yan-Ping
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
21 .     lupeol stearate
    ÏàËÆ¶È:76.1%
Chinese Pharmaceutical Journal          2011          46          11-13
Constituents of Viscum ovalifolium DC(¢ò)
YANG Yan-jun, SHA Cong-wei, CHEN Mei-guo
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
22 .     compound 7
C37H60O7     ÏàËÆ¶È:76.1%
Tetrahedron          2005          61          10569-10582
Triterpenoids from Cedrela sinensis
Kumiko Mitsui, Masato Maejima, Hiroaki Saito, Haruhiko Fukaya, Yukio Hitotsuyanagi, Koichi Takeya
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
23 .     taraxasteryl palmitate
C46H80O2     ÏàËÆ¶È:76.1%
Journal of Northwest A&F University (Natural Science)          2005          33          90-94
Anti-fungi active compounds from Inula britannica
DING Hai-xin, Li Guang-ze, FENG Jun-tao, ZHANG Xing
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
24 .     compound 1b
C37H58O8     ÏàËÆ¶È:76.1%
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2Â¥2015-05-12 10:04:28
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seuseasoar

ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)

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¡ï ¡ï ¡ï ¡ï ¡ï
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cliff0223: ½ð±Ò+5 2015-06-17 14:55:34
1 .     16¦Â-hydroxypseudotarasterol-3¦Â-O-palmitate
    ÏàËÆ¶È:76.1%
Acta Botanica Sinica          1997          39(1)          85−90
Studies on chemical constituents from Dendranthema morifolium (Ramat.) Tzvel.: structure elucidation of two new triterpenoid esters
Hu Li-hong and Chen Zhong-liang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     compound 1a
    ÏàËÆ¶È:74.4%
Phytochemistry          1991          30          1869-1872
Diterpenic adducts from Xylopia species
Wagner Vilegas, Joana D'Arc Felicio, Nidia F. Roque, Hugo E. Gottlieb
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     faradiol palmitic ester
    ÏàËÆ¶È:73.8%
Journal of Ethnopharmacology          1997          57          139-144
Anti-oedematous activities of the main triterpendiol esters of marigold (Calendula officinalis L.)
K Zitterl-Eglseer, S Sosa, J Jurenitsch, M Schubert-Zsilavecz, R Della Loggia, A Tubaro, M Bertoldi, C Franz
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     16¦Â-hydroxypseudotaraxasterol 3-O-palmitate
C46H80O3     ÏàËÆ¶È:72.0%
Shoyakugaku Zasshi          1990          44          335-338
Studies on the Constituents of Chrysanthemi Flos
YAHARA SHOJI, MORITA YASUSHI,NOHARA TOSHIHIRO
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     sambucunlin A
C46H80O2     ÏàËÆ¶È:71.4%
Planta Medica          1988          54          223-224
Antihepatotoxic Principles of Sambucus formosana
Chun-Nan Lin and Whey-Pin Tome
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     lupeol 3-hydroxyoctadencanoate
    ÏàËÆ¶È:71.4%
Chemical Journal of Chinese Universities          2003          24          436-441
Chemical Constituents from the Roots of Biondia Hemsleyana
TAN Xing-Gen, ZHANG Xiao-Rong, PENG Shu-Lin, LIAO Xun, DING Li-Sheng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     ÉßÝÔËØ B
    ÏàËÆ¶È:71.4%
Chinese Traditional and Herbal Drugs          2005          36          830-831
˼éÉßÝԵĻ¯Ñ§³É·ÖÑо¿(¢ñ)
´÷ÖÒ,Íõ¸ÖÁ¦,Íõ·å,ÂíË«³É,ÁÖÈð³¬
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     lupeol stearate
    ÏàËÆ¶È:71.4%
Chinese Pharmaceutical Journal          2011          46          11-13
Constituents of Viscum ovalifolium DC(¢ò)
YANG Yan-jun, SHA Cong-wei, CHEN Mei-guo
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     lupeol palmitate
    ÏàËÆ¶È:71.4%
Chinese Pharmaceutical Journal          2011          46          11-13
Constituents of Viscum ovalifolium DC(¢ò)
YANG Yan-jun, SHA Cong-wei, CHEN Mei-guo
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     faradiol myristic ester
    ÏàËÆ¶È:71.4%
Journal of Ethnopharmacology          1997          57          139-144
Anti-oedematous activities of the main triterpendiol esters of marigold (Calendula officinalis L.)
K Zitterl-Eglseer, S Sosa, J Jurenitsch, M Schubert-Zsilavecz, R Della Loggia, A Tubaro, M Bertoldi, C Franz
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     balanophorin B
C46H80O2     ÏàËÆ¶È:71.4%
Acta Botanica Yunnanica          1998          20          369-373
Triterpene constituents from Balanophora indica
Liu Xi-Kui, Li Zhong-Rong, Qiu Ming-Hua, Nie Rui-Lin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     compound 9
    ÏàËÆ¶È:69.7%
Phytochemistry          1995          40          607-609
Frutoic acid, a dimeric kaurane diterpene from Xylopia frutescens
Jacqueline A. Takahashi, Maria Am¨¦lia D. Boaventura, Joaquim de Carvalho Bayma, Ala¨ªde B. Oliveira
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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