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ninahan

铜虫 (著名写手)

[求助] 微谱求助

碳谱数据:
14.7,22.3,23.2,24.5,25.2,27.0,28.8,32.8,35.2,36.2,37.0,37.1,41.9,48.6,50.3,53.1,55.0,65.4,68.4,75.0,127.4,128.2,129.9,132.1,135.4,136.2,170.4,207.8,211.2
溶剂是氘代氯仿
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lifeliuyan

至尊木虫 (职业作家)

【答案】应助回帖

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感谢参与,应助指数 +1
ninahan: 金币+10, ★★★★★最佳答案, 谢谢! 2013-11-13 16:03:38
查询结果:共查到1255个化合物(查询结果仅供参考)  
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1 .     2-[1'-(p-Methoxyphenyl)-3'-phenyl-propyl-3'-one]-5a-cholestan-3-one
C43H60O3     相似度:67.7%
Steroids          2013          78          387-395
Microwave-promoted and Lewis acid catalysed synthesis of steroidal A- and D-ring fused 4,6-diarylpyridinesOriginal Research Article
Mandakini Dutta, Pallabi Saikia, Sanjib Gogoi, Romesh C. Boruah
Structure      13C NMR   碳谱模拟图

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2 .     grandol A
C27H44O3     相似度:65.5%
Steroids          2013          78          210-219
Steroids from Dysoxylum grande (Meliaceae) leaves
Low Kok Wah, Faridah Abas, Geoffrey A. Cordell, Hideyuki Ito, Intan Safinar Ismail
Structure      13C NMR   碳谱模拟图

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3 .     2-[3'-(p-Chlorophenyl)-1'-(p-flurophenyl)-propyl-3'-one]-5α-cholestan-3-one
C42H56ClFO2     相似度:62.5%
Steroids          2013          78          387-395
Microwave-promoted and Lewis acid catalysed synthesis of steroidal A- and D-ring fused 4,6-diarylpyridinesOriginal Research Article
Mandakini Dutta, Pallabi Saikia, Sanjib Gogoi, Romesh C. Boruah
Structure      13C NMR   碳谱模拟图

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4 .     (14S,17S,18R)-[(5S,8R,9S,10S,13S,14S,17S)-10,13-dimethyl-3-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl] 18-amino-17-hydroxy-14-isobutyl-13,16-dioxo-19-phenyl-3,6,9-trioxa-12,15-diazanonadecan-1-oate
C43H67N3O9     相似度:62.0%
Bioorganic & Medicinal Chemistry          2011          19          6768-6778
Design, synthesis and biological evaluation of nuclear receptor-degradation inducers
Yukihiro Itoh, Risa Kitaguchi, Minoru Ishikawa, Mikihiko Naito, Yuichi Hashimoto
Structure      13C NMR   碳谱模拟图

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5 .     (S*,R*)-N-[1-(cyclohexyhnethyl)-3-ethoxy-2-hydroxy-3-oxopropyl]-N2-[N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanyl]-L-leucinamide
C32H51N3O7     相似度:62.0%
Journal of Medicinal Chemistry          1993          36          2431-2447
Activated ketone based inhibitors of human renin
Dinesh V. Patel, Katherine Rielly-Gauvin, Denis E. Ryono, Charles A. Free, Sandra A. Smith, Edward W. Petrillo Jr.
Structure      13C NMR   碳谱模拟图

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6 .     (R,R)-N-[1-(cyclohexylinethyl)-3-ethoxy-2-hydroxy-3-oxopropyl]-N2-[N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanyl]-L-leucinamide
C32H51N3O7     相似度:62.0%
Journal of Medicinal Chemistry          1993          36          2431-2447
Activated ketone based inhibitors of human renin
Dinesh V. Patel, Katherine Rielly-Gauvin, Denis E. Ryono, Charles A. Free, Sandra A. Smith, Edward W. Petrillo Jr.
Structure      13C NMR   碳谱模拟图

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7 .     (1S,2S)-N-[1-(cyclohexylmethyl)-2-(dimethoxyphosphinyl)-2-hydroxyethyl]-N2-[N-(4-morpholinylcarbonyl)-L-phenylalanyl]-L-leucinamide
C31H51N4O8P     相似度:62.0%
Journal of Medicinal Chemistry          1995          38          4557-4569
alpha.-Hydroxy Phosphinyl-Based Inhibitors of Human Renin
Dinesh V. Patel, Katherine Rielly-Gauvin, Denis E. Ryono, Charles A. Free, W. Lynn Rogers, Sandra A. Smith, Jack M. DeForrest, Robert S. Oehl, Edward W. Petrillo Jr.
Structure      13C NMR   碳谱模拟图

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8 .     sarain-3
     相似度:62.0%
Bulletin des Sociétés Chimiques Belges          1986          95          783-800
Sarains: A New Class of Alkaloids from the Marine Sponge Reniera Sarai
Guido Cimino, Salvatore De Stefano, Gennaro Scognamiglio, Guido Sodano and Enrico Trivellone
Structure      13C NMR   碳谱模拟图

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9 .     cornusalterin B
C31H52O2     相似度:61.2%
Journal of Natural Products          2011          74          54-59
Tirucallane Triterpenoids from Cornus walteri
Ki Hyun Kim, Sang Un Choi, Young Choong Kim, and Kang Ro Lee
Structure      13C NMR   碳谱模拟图

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10 .     6β-phenylsulfanyl-3α,5α-cyclocholestane
C33H50S     相似度:61.2%
Tetrahedron          2013          69          8904-8913
Electrochemical synthesis of glycoconjugates of 3β-hydroxy-Δ5-steroids by using non-activated sugars and steroidal thioethers
Aneta M. Tomkiel, Krzysztof Brzezinski, Zenon Łotowski, Leszek Siergiejczyk, Piotr Wałejko, Stanisław Witkowski, Jan Kowalski, Jolanta Płoszyńska, Andrzej Sobkowiak, Jacek W. Morzycki
Structure      13C NMR   碳谱模拟图

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11 .     phomopsichalasin
     相似度:60%
Tetrahedron          1995          51          3969-3978
Phomopsichalasin, a novel antimicrobial agent from an endophytic Phomopsis sp.
W.S. Horn, M.S.J. Simmonds, R.E. Schwartz, W.M. Blaney
Structure      13C NMR   碳谱模拟图

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12 .     21-hydroxylanosta-7,9(11),24-trien-3-one
     相似度:60%
Mycosystema          2011          30          459-463
Chemical constituents of Fomitiporia ellipsoidea fruiting bodies
LIU Han-Bin BAO Hai-Ying CUI Bao-Kai
Structure      13C NMR   碳谱模拟图

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13 .     2-[3'-(p-Chlorophenyl)-1'-phenyl-propyl-3'-one]-5α-cholestan-3-one
C42H57ClO2     相似度:60%
Steroids          2013          78          387-395
Microwave-promoted and Lewis acid catalysed synthesis of steroidal A- and D-ring fused 4,6-diarylpyridinesOriginal Research Article
Mandakini Dutta, Pallabi Saikia, Sanjib Gogoi, Romesh C. Boruah
Structure      13C NMR   碳谱模拟图

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14 .     compound (1S,2S)-(-)-cis-10a
C33H39Cl2NO5S     相似度:59.3%
European Journal of Organic Chemistry          2010                   6372-6384
(R)-(+)-[VCD(–)984]-4-Ethyl-4-methyloctane: A Cryptochiral Hydrocarbon with a Quaternary Chiral Center. (1) Synthesis of the Enantiopure Compound and Unambiguous Determination of Absolute Configuration
Takuma Fujita, Kazuhiro Obata, Shunsuke Kuwahara, Atsufumi Nakahashi, Kenji Monde, John Decatur and Nobuyuki Harada
Structure      13C NMR   碳谱模拟图

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15 .     2-[1'-(p-Methylphenyl)-3''-phenyl-propyl-3'-one]-5a-cholestan-3-one
C43H60O2     相似度:59.3%
Steroids          2013          78          387-395
Microwave-promoted and Lewis acid catalysed synthesis of steroidal A- and D-ring fused 4,6-diarylpyridinesOriginal Research Article
Mandakini Dutta, Pallabi Saikia, Sanjib Gogoi, Romesh C. Boruah
Structure      13C NMR   碳谱模拟图

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16 .     orthosiphol I
C31H38O10     相似度:58.6%
Chemical & Pharmaceutical Bulletin          2000          48(11)          1711-1719
Constituents of the Vietnamese Medicinal Plant Orthosiphon stamineus
Yasuhiro TEZUKA,Pavlos STAMPOULIS,Arjun H. BANSKOTA, Suresh AWALE,Kim Qui TRAN,Ikuo SAIKI and Shigetoshi KADOTA
Structure      13C NMR   碳谱模拟图
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