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方小平

金虫 (小有名气)

[求助] 微谱求助-331c 已有1人参与

13C NMR (126 MHz, Acetone) δ 16.48,18.18,19.45,20.09,20.43,21.40,21.79,27.62,31.34,31,96,33.95,34.84,36.00,39.92,40.85,43.84,44.24,47.25,51.33,84.96,123.68,126.00,133.05,136.81,159.12,168.80,188.12,199.18.
溶剂:氘代丙酮
相似度要求:>50%
谢谢!
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sydong

铁杆木虫 (著名写手)

【答案】应助回帖

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感谢参与,应助指数 +1
方小平: 金币+10, ★★★很有帮助 2014-06-07 09:36:25
查询结果:共查到15个化合物(查询结果仅供参考)
1 .     Cholest-4α-methyl-8-en-7α-acetoxy-3-one
C30H48O3     相似度:56.6%
Steroids          2006          71          476-483
Synthesis and antitumor activity of cholest-4α-methyl-7-en-3β-ol derivatives
Lan He, Yumei Liu, Jiangong Shi, Qiang Pei
Structure      13C NMR   碳谱模拟图
2 .     Penicisteroid A
C30H50O6     相似度:56.6%
Bioorganic & Medicinal Chemistry Letters          2011          21          2894-2897
Penicisteroids A and B, antifungal and cytotoxic polyoxygenated steroids from the marine algα-derived endophytic fungus Penicillium chrysogenum QEN-24S
Shu-Shan Gao, Xiao-Ming Li, Chun-Shun Li, Peter Proksch, Bin-Gui Wang
Structure      13C NMR   碳谱模拟图
3 .     3β-hydroxy-12-keto-9(11)-ursen-28,13β-olide
C30H44O4     相似度:53.3%
Molecules          2007          12          2599-2604
Two New Triterpenoids from Photinia serrulata
Yaling Song, Yuehu Wang, Qing Lu, Jinming Gao, Minggang Bi and Yongxian Cheng
Structure      13C NMR   碳谱模拟图
4 .     Cholest-4α-methyl-8-en-7α-ecetoxy-3β-ol
C28H46O     相似度:53.3%
Steroids          2006          71          476-483
Synthesis and antitumor activity of cholest-4α-methyl-7-en-3β-ol derivatives
Lan He, Yumei Liu, Jiangong Shi, Qiang Pei
Structure      13C NMR   碳谱模拟图
5 .     cholest-4-ene-3,6-dione
    相似度:51.7%
China Journal of Chinese Materia Medica          2009          34          60-63
Bioactivity sterols from red alga Acanthophora spicifera boergesen
HAN Lijun, SHI Dayong, XU Feng, YUAN Zhaohui, SUN Jie, SHI Jiangong
Structure      13C NMR   碳谱模拟图
6 .     5α,8α-环二氧麦角甾-6,22-二烯-3β-醇
C28H44O3     相似度:51.7%
Chinese Traditional and Herbal Drugs          2006          37          823-824
软骨凹顶藻中的甾醇化合物
徐石海;杨晓燕;郭书好;廖小建
Structure      13C NMR   碳谱模拟图
7 .     3β-acetoxy-17-ylideneamino(N-2'-pyrimidylbenzenesulfonamide)-5α-androstane
C31H40N4O4S     相似度:51.7%
Bioorganic & Medicinal Chemistry          2011          19          6860-6872
Cytotoxicity and gene expression profiles of novel synthesized steroid derivatives as chemotherapeutic anti-breast cancer agents
Gamal A. Elmegeed, Wagdy K.B. Khalil, Rafat M. Mohareb, Hanaa H. Ahmed, Mervat M. Abd-Elhalim, Ghada H. Elsayed
Structure      13C NMR   碳谱模拟图
8 .     stigmast-4-en-3-one
    相似度:51.7%
Chinese Journal of Oceanology and Limnology          2008          26          190-192
The chemical constituents from red alga Gymnogongrus flabelliformis Harv.
YUAN Zhaohui, HAN Lijun, SU Hua, SHI Dayong, SUN Jie, LI Shuai, SHI Jiangong
Structure      13C NMR   碳谱模拟图
9 .     cholest-4-ene-3,6-dione
C27H42O2     相似度:51.7%
Chinese Journal of Oceanology and Limnology          2011          29          674-678
A new ketosteroid from red alga Acanthophora spicifera*
SHI Dayong, GUO Shuju, FAN Xiao
Structure      13C NMR   碳谱模拟图
10 .     ergosta-4,6,8(14),22-tetraen-3-one
    相似度:51.7%
China Journal of Chinese Materia Medica          2014          39          442-447
Chemical constituents from Pleione bulbocodioides
WANG Chao, HAN Shao-wei, CUI Bao-song, WANG Xiao-juan, LI Shuai
Structure      13C NMR   碳谱模拟图
11 .     (24R)-24-豆甾-4,22-二烯-3-酮
    相似度:51.7%
China Journal of Chinese Materia Medica          2012          37          2092-2099
Non-anthraquinones constituents from the roots of Knoxia valerianoides
ZHAO Feng; WANG Sujuan; WU Xiuli; YU Yang; YUE Zhenggang; LIU Bo; LIN Sheng; ZHU Chenggen; YANG Yongchun; SHI Jiangong
Structure      13C NMR   碳谱模拟图
12 .     Cholest-4α-methyl-8-en-7α-ethoxy-3β-ol
C30H52O2     相似度:50%
Steroids          2006          71          476-483
Synthesis and antitumor activity of cholest-4α-methyl-7-en-3β-ol derivatives
Lan He, Yumei Liu, Jiangong Shi, Qiang Pei
Structure      13C NMR   碳谱模拟图
13 .     26-hydroxy-1,3-friedelanedione
    相似度:50%
Chemical & Pharmaceutical Bulletin          1999          47          1725-1729
Antidiabetic Principles of Natural Medicines. IV. Aldose Reductase and α-Glucosidase Inhibitors from the Roots of Salacia oblonga WALL. (Celastraceae) : Structure of a New Friedelane-Type Triterpene, Kotalagenin 17-Acetate
Hisashi MATSUDA,Toshiyuki MURAKAMI,Kenichi YASHIRO,Johji YAMAHARA and Masayuki YOSHIKAWA
Structure      13C NMR   碳谱模拟图
14 .     compound 2
    相似度:50%
Fitoterapia          2012          83          1238-1241
A convenient and efficient one-pot conversion of peimisine into cyclopamine
Shu-Yan Zheng, Hong-Sheng Tan, Jian-Sheng Tao, Zheng-Wu Shen
Structure      13C NMR   碳谱模拟图
15 .     integracide A
    相似度:50%
Bioorganic & Medicinal Chemistry          2003          11          1577-1582
Integracides: tetracyclic triterpenoid inhibitors of HIV-1 integrase produced by Fusarium sp.
Sheo B Singh, Deborah L Zink, Anne W Dombrowski, Jon D Polishook, John G Ondeyka, Jorden Hirshfield, Peter Felock, Daria J Hazuda
Structure      13C NMR   碳谱模拟图
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