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xiling0505

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[求助] 求助微谱数据 已有1人参与

12.8,13.8,17.0,24.7,33.0,33.9,36.5,41.1,41.6,42.3,43.3,44.1,45.9,52.1,58.0,58.6,61.3,62.8,69.0,70.7,73.9,79.0,84.5,112.6,125.7,140.1
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cjpballack

铁杆木虫 (正式写手)

【答案】应助回帖

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感谢参与,应助指数 +1
xiling0505: 金币+8, ★★★★★最佳答案 2014-11-19 22:39:26
查询结果:共查到369个化合物(查询结果仅供参考)  
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1 .     cepagenin
    相似度:66.6%
Chemistry of Natural Compounds          1987          23          700-706
STEROIDS OF THE SPIROSTAN AND FUROSTAN SERIES OF PLANTS OF THE Allium GENUS. XXIII. STRUCTURE OF CEPAGENIN AND OF ALLIOSPIROSIDES C AND D FROM Allium cepa
S. D. Kravets, Yu. S. Vollerner, A. S. Shashkov, M. B. Gorovits, and N. K. Abubakir
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图
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2 .     (25S*)-Cholest-5-ene-l(R*),3(R*),16(S*),22(S*),26-pentaol
    相似度:66.6%
Phytochemistry          1996          41          907-917
Cholestane- and pregnane-type glycosides from the roots of Tribulus cistoides
Hans Achenbach, Harald Hübner, Melchior Reiter
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图
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3 .     cepagenin
    相似度:66.6%
Magnetic Resonance in Chemistry          1995          33          923-953
NMR spectroscopy of steroidal sapogenins and steroidal saponins: An update
Pawan K. Agrawal, Dharam C. Jain and Ashish K. Pathak
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图
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4 .     Cholest-5-ene-1(R*),3(R*),16(S*),22(S*)-tetraol
    相似度:62.9%
Phytochemistry          1996          41          907-917
Cholestane- and pregnane-type glycosides from the roots of Tribulus cistoides
Hans Achenbach, Harald Hübner, Melchior Reiter
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图
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5 .     (22S)-3β,16β,22,25-tetrahydroxycholest-5-en-1β-yl β-D-glucopyranoside aglycone
C27H46O5     相似度:62.9%
Chemical & Pharmaceutical Bulletin          2012          60(2)          275-279
New Cholestane Glycosides from the Leaves of Cordyline terminalis
Akihito Yokosuka,Takeyuki Suzuki,and Yoshihiro Mimaki
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图
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6 .     14,15-dihydroajugapitin
    相似度:62.9%
Phytochemistry          1990          29          2931-2933
Neo-clerodane diterpenoids from Ajuga chamaepitys
Iva M. Boneva,Bozhana P. Mikhova,Peter Y. Malakov,Georgy Y. Papanov,Helmut Duddeck,Stefan L. Spassov
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图
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7 .     22-methoxyfurostanol saponin
C49H76O20     相似度:60.7%
Molecules          2012          17          14002-14014
Novel Steroidal Components from the Underground Parts of Ruscus aculeatus L.
Simona De Marino, Carmen Festa, Franco Zollo and Maria Iorizzi
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图
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8 .     jasnudifloside F
C27H42O13     相似度:59.2%
Chemical & Pharmaceutical Bulletin          2002          50(3)          384-389
Nine New Secoiridoid Glucosides from Jasminum nudiflorum
Yukiko TAKENAKA,Takao TANAHASHI, Hiromi TAGUCHI,Naotaka NAGAKURA, and Toyoyuki NISHI
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图
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9 .     (20R)-5α-cholestane-3α,4β,21-triol 3,21-disulfate
C27H46O9S2Na2     相似度:59.2%
Journal of Natural Products          2003          66          298-301
Hemolytic Steroid Disulfates from the Far Eastern Starfish Pteraster pulvillus
Natalia V. Ivanchina, Alla A. Kicha, Anatoly I. Kalinovsky, Pavel S. Dmitrenok, and Valentin A. Stonik
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图
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10 .     certonardoside G
C27H46O4     相似度:59.2%
Journal of Natural Products          2003          66          384-391
Bioactive Sterols from the Starfish Certonardoa semiregularis
Weihong Wang, Famei Li, Yujin Park, Jongki Hong, Chong-Ok Lee, Jae Yang Kong, Sook Shin, Kwang Sik Im, and Jee H. Jung
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图
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