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flyawu

至尊木虫 (职业作家)

[求助] 微谱求助,谢谢! 已有1人参与

溶剂:  DMSO
C谱: 15.4, 18.7, 18.8, 20.9, 25.2, 26.5, 27.3, 29.3, 31.3, 34.9, 35.8, 36.0, 37.4, 37.7, 43.4, 46.0, 48.2, 48.5, 70.7, 71.1, 75.4, 116.9, 119.6, 127.9, 139.3, 143.7, 171.4, 177.7

样品名:2146-1
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yangyinhe

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2楼2015-01-13 13:09:01
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yangyinhe

至尊木虫 (著名写手)

【答案】应助回帖

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感谢参与,应助指数 +1
flyawu: 金币+10, ★★★★★最佳答案, 非常感谢!下回会注意空格! 2015-01-13 14:08:32
1 .     borrelidin
C28H43NO6     相似度:78.5%
Journal of Agricultural and Food Chemistry          2012          60          1251-1257
Antifungal Activity of Borrelidin Produced by a Streptomyces Strain Isolated from Soybean
Chong-Xi Liu, Ji Zhang, Xiang-Jing Wang, Ping-Ting Qian, Ji-Dong Wang, Ya-Mei Gao, Yi-Jun Yan, Shu-Zhen Zhang, Peng-Fei Xu, Wen-Bin Li, and Wen-Sheng Xiang
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

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2 .     Schiglausin D
C30H46O5     相似度:66.6%
Planta Medica          2012          78          472-479
Lanostane Triterpenoids from the Stems of Schisandra glaucescens
Juan Zou,Li-Bin Yang,Jing Jiang,Yan-Yan Diao,Xiao-Nian Li,Jin Huang,Jian-Hong Yang,Hong-Lin Li,Wei-Lie Xiao,Xue Du,Shan-Zhai Shang,Jian-Xin Pu,Han-Dong Sun
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

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3 .     7α,12α-Diacetoxy-5β-cholestan-3α-ol
C31H52O5     相似度:65.5%
Steroids          2013          78          927-937
An efficient synthesis of 7α,12α-dihydroxy-4-cholesten-3-one and its biological precursor 7α-hydroxy-4-cholesten-3-one: Key intermediates in bile acid biosynthesis
Shoujiro Ogawa, Biao Zhou, Yusuke Kimoto, Kaoru Omura, Akiko Kobayashi, Tatsuya Higashi, Kuniko Mitamura, Shigeo Ikegawa, Lee R. Hagey, Alan F. Hofmann, Takashi Iida
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

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4 .     Gummiferolic acid Methyl ester
C26H38O4     相似度:64.2%
Phytochemistry          1978          17          1636-1637
Gummiferolic acid, a new ent-atis-16-ene diterpenoid from Margotia gummifera
Mariano Pinar, Benjamin Rodriguez and Antonio Alemany
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

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5 .     (24S)-24-ethyl-5α-cholestan-3β,4β-diol
C29H50O2     相似度:64.2%
Marine Drugs          2012          10          2448-2466
Preliminary Structure-Activity Relationship on Theonellasterol, a New Chemotype of FXR Antagonist, from the Marine Sponge Theonella swinhoei
Valentina Sepe, Raffaella Ummarino, Maria Valeria D'Auria, Orazio Taglialatela-Scafati, Simona De Marino, Claudio D'Amore, Barbara Renga, Maria Giovanna Chini, Giuseppe Bifulco, Yoichi Nakao, Nobuhiro Fusetani, Stefano Fiorucci and Angela Zampella
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

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6 .     (24E)-3,4-secocucurbita- 4,24-diene-3,26-dioic acid
C30H47O4     相似度:63.3%
Helvetica Chimica Acta          2000          Vol. 83          3191
New Terpenoids from Basidiomycetes Russula lepida
Tan Jian-Wen, Dong Ze-Jun, and Liu Ji-Kai
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

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7 .     kuguacin A
C30H46O4     相似度:63.3%
Phytochemistry          2008          69          1043-1048
Trinorcucurbitane and cucurbitane triterpenoids from the roots of Momordica charantia
Jianchao Chen, Renrong Tian, Minghua Qiu, Lu Lu,Yongtang Zheng, Zhongquan Zhang
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

--------------------------------------------------------------------------------

8 .     Ganodermanontriol
C30H48O4     相似度:63.3%
Molecules          2007          12          2038-2046
Two Novel Lanostane Triterpenoids from Ganoderma Sinense
Yin Qiao, Xian-min Zhang and Ming-hua Qiu
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

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9 .     brumollisol A
C30H48O5     相似度:63.3%
Chemistry & Biodiversity          2013          10          695-702
Tirucallane Triterpenoids from the Stems of Brucea mollis
Hui Chen, Shuang-Gang Ma, Zhen-Feng Fang, Jian Bai, Shi-Shan Yu, Xiao-Guang Chen, Qi Hou, Shao-Peng Yuan and Xia Chen
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

--------------------------------------------------------------------------------

10 .     spinogenin C6
C29H46O5     相似度:62.0%
Phytochemistry          1997          46          1255-1259
3α-hydroxy-oleanene type triterpene glycosyl esters from leaves of Acanthopanax spinosus
Masazumi Miyakoshi, Susumu Isoda, Hirotoshi Sato, Yasuaki Hirai, Junzo Shoji, Yoshiteru Ida
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图
3楼2015-01-13 13:11:14
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