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刘敏8998

金虫 (小有名气)

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氘代丙酮作谱:197.3, 162.7, 155.8, 138.2, 134.3, 128.4, 127.2, 124.8, 123.1, 75.3, 72.3, 68.9, 63.6, 55.0, 53.4, 49.3, 45.5, 36.6, 36.0, 35.5, 33.9, 33.7, 25.2,22.6, 16.4,15.4
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有所不为

至尊木虫 (著名写手)

【答案】应助回帖

感谢参与,应助指数 +1
按从小到大顺序输入,数字间用英文半角逗号(,)分隔例如:
如:21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2
与君初相识,犹如故人归。
2楼2013-12-12 21:19:35
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刘敏8998

金虫 (小有名气)

引用回帖:
2楼: Originally posted by 有所不为 at 2013-12-12 21:19:35
按从小到大顺序输入,数字间用英文半角逗号(,)分隔例如:
如:21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2

15.4,16.4,22.6, 25.2, 33.7,33.9, 35.5,36.0,36.6,45.5,49.3,53.4, 55.0, 63.6, 68.9,72.3,75.3,123.1,124.8,127.2, 128.4, 134.3, 138.2, 155.8,162.7, 197.3,
3楼2013-12-12 21:50:39
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有所不为

至尊木虫 (著名写手)

引用回帖:
3楼: Originally posted by 刘敏8998 at 2013-12-12 21:50:39
15.4,16.4,22.6, 25.2, 33.7,33.9, 35.5,36.0,36.6,45.5,49.3,53.4, 55.0, 63.6, 68.9,72.3,75.3,123.1,124.8,127.2, 128.4, 134.3, 138.2, 155.8,162.7, 197.3,...

亲 是半角逗号 半角。。。半角。。。半角。。。
与君初相识,犹如故人归。
4楼2013-12-12 21:57:29
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刘敏8998

金虫 (小有名气)

引用回帖:
4楼: Originally posted by 有所不为 at 2013-12-12 21:57:29
亲 是半角逗号 半角。。。半角。。。半角。。。...

15.4,16.4, 22.6, 25.2, 33.7, 33.9, 35.5, 36.0, 36.6, 45.5, 49.3, 53.4, 55.0, 63.6, 68.9, 72.3, 75.3, 123.1, 124.8, 127.2, 128.4, 134.3, 138.2, 155.8, 162.7,  197.3
5楼2013-12-13 09:52:17
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有所不为

至尊木虫 (著名写手)

【答案】应助回帖

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刘敏8998: 金币+10, ★★★★★最佳答案 2013-12-17 11:10:17
查询结果:共查到136个化合物(查询结果仅供参考)
1 .     12β,15α,25,28-tetrahydroxyergosta-4,6,8(14),22-tetraen-3-one
C28H40O5     相似度:92.8%
Helvetica Chimica Acta          2012          95          308-313
Highly Conjugated Ergostane-Type Steroids and Aranotin-Type Diketopiperazines from the Fungus Aspergillus terreus BCC 4651
Rachada Haritakun, Pranee Rachtawee, Somjit Komwijit, Sutichai Nithithanasilp,and Masahiko Isaka
Structure      13C NMR   碳谱模拟图
2 .     12β,15α,25,26-tetrahydroxyergosta-4,6,8(14),22-tetraen-3-one
C28H40O5     相似度:71.4%
Helvetica Chimica Acta          2012          95          308-313
Highly Conjugated Ergostane-Type Steroids and Aranotin-Type Diketopiperazines from the Fungus Aspergillus terreus BCC 4651
Rachada Haritakun, Pranee Rachtawee, Somjit Komwijit, Sutichai Nithithanasilp,and Masahiko Isaka
Structure      13C NMR   碳谱模拟图
3 .     17β-[3-(N-Phenyl)-2-oxazolidon-5-yl]androst-4-en-3-one
    相似度:57.6%
Steroids          2008          73          1375-1384
Neighboring group participation: Part 17 Stereoselective synthesis of some steroidal 2-oxazolidones, as novel potential inhibitors of 17α-hydroxylase-C17,20-lyase
Dóra Ondré, János Wölfling, Zoltán Iványi, Gyula Schneider, István Tóth, Mihály Szécsi, János Julesz
Structure      13C NMR   碳谱模拟图
4 .     17β-(1-p-Chlorophenyl-3-pyrazolyl)androst-4-en-3-one
C28H33ClN2O     相似度:57.6%
Steroids          2010          75          450-456
Synthesis of regioisomeric 17β-N-phenylpyrazolyl steroid derivatives and their inhibitory effect on 17α-hydroxylase/C17,20-lyase
Zoltán Iványi, János Wölfling, Tamás Görbe, Mihály Szécsi, Tibor Wittmann, Gyula Schneider
Structure      13C NMR   碳谱模拟图
5 .     17β-(1-p-Chlorophenyl-5-pyrazolyl)androst-4-en-3-one
C28H33ClN2O     相似度:57.6%
Steroids          2010          75          450-456
Synthesis of regioisomeric 17β-N-phenylpyrazolyl steroid derivatives and their inhibitory effect on 17α-hydroxylase/C17,20-lyase
Zoltán Iványi, János Wölfling, Tamás Görbe, Mihály Szécsi, Tibor Wittmann, Gyula Schneider
Structure      13C NMR   碳谱模拟图
6 .     compound 16b
C32H50O4     相似度:57.6%
Journal of the Chemical Society, Perkin Transactions 1          1989                   165-174
Synthetic photochemistry. Part 44. Total synthesis of ceroplastol II and albolic acid, 5-8-5-membered tricyclic sesterterpenoid insect wax constituents, via stereocontrolled silyloxy-Cope rearrangement with a normally disfavoured transition state
Nobuo Kato, Hitoshi Takeshita, Hideo Kataoka, Shoji Ohbuchi and Shinya Tanaka
Structure      13C NMR   碳谱模拟图
7 .     agelasidine E
C23H41N3O3S     相似度:57.6%
European Journal of Organic Chemistry          2012                   5131-5135
Antifungal Diterpene Alkaloids from the Caribbean Sponge Agelas citrina: Unified Configurational Assignments of Agelasidines and Agelasines
E. Paige Stout, Lily C. Yu and Tadeusz F. Molinski
Structure      13C NMR   碳谱模拟图
8 .     16-O-phenylthiomethylliphagal
C29H34O4S     相似度:55.5%
Organic Letters          2010          Vol.12,No.20          4450-4453
Enantioselective Total Synthesis of the Selective PI3 Kinase Inhibitor Liphagal
Enrique Alvarez-Manzaneda, Rachid Chahboun, Esteban Alvarez, Ma José Cano, Ali Haidour, and Ramón Alvarez-Manzaneda
Structure      13C NMR   碳谱模拟图
9 .     (6β,8aβ)-N,N-Dimethyl-1,2,3,5,6,7,8,8a-octahydro-2-(3-phenyl-2- propen-1-yl)-5,5,8a-trimethyl-6-isoquinolineamine
C23H34N2· 2C7H8O3S     相似度:53.8%
Chemical & Pharmaceutical Bulletin          2002          50(3)          316-329
Structure Activity Relationships of New Inhibitors of Mammalian 2,3-Oxidosqualene Cyclase Designed from Isoquinoline Derivatives
Jean BINET, Didier THOMAS, Abdellah BENMBAREK, Daniel de FORNEL, and Patrice RENAUT
Structure      13C NMR   碳谱模拟图
10 .     13-epi-yosgadensonol
    相似度:53.8%
Journal of Natural Products          1996          59          113-116
Norditerpenes and Norsesterterpenes from Salvia yosgadensis
Gülacüti Topç, and Ayhan Ulubelen
Structure      13C NMR   碳谱模拟图
11 .     17α,21-Dihydroxy-pregna-4,6-diene-3,11,20-trione21-acetate
C23H28O6     相似度:53.8%
Steroids          2005          70          763-769
A concise method for the preparation of deuterium-labeled cortisone: Synthesis of [6,7-2H]cortisone
Agnieszka Sulima, Thomas E. Prisinzano, Thomas Spande, Jeffrey R. Deschamps, Noel Whittaker, Zeev Hochberg, Arthur E. Jacobson, Kenner C. Rice
Structure      13C NMR   碳谱模拟图
12 .     17β-[3-(N-4-Chlorophenyl)-2-oxazolidon-5-yl]androst-4-en-3-one
    相似度:53.8%
Steroids          2008          73          1375-1384
Neighboring group participation: Part 17 Stereoselective synthesis of some steroidal 2-oxazolidones, as novel potential inhibitors of 17α-hydroxylase-C17,20-lyase
Dóra Ondré, János Wölfling, Zoltán Iványi, Gyula Schneider, István Tóth, Mihály Szécsi, János Julesz
Structure      13C NMR   碳谱模拟图
13 .     (5'R)-17β-[2-(4-nitrophenyl)-4,5-dihydrooxazol-5-yl]androst-5-en-3-one
C28H34N2O2     相似度:53.8%
Steroids          2009          74          1025-1032
Steroselective synthesis of some steroidal oxazolines, as novel potential inhibitors of 17α-hydroxylase-C17,20-lyase
Dóra Ondré, János Wölfling, István Tóth, Mihály Szécsi, János Julesz, Gyula Schneider
Structure      13C NMR   碳谱模拟图
14 .     17β-(1-Phenyl-3-pyrazolyl)androst-4-en-3-one
C28H34N2O     相似度:53.8%
Steroids          2010          75          450-456
Synthesis of regioisomeric 17β-N-phenylpyrazolyl steroid derivatives and their inhibitory effect on 17α-hydroxylase/C17,20-lyase
Zoltán Iványi, János Wölfling, Tamás Görbe, Mihály Szécsi, Tibor Wittmann, Gyula Schneider
Structure      13C NMR   碳谱模拟图
15 .     17β-(1-p-Cyanophenyl-3-pyrazolyl)androst-4-en-3-one
C29H33N3O     相似度:53.8%
Steroids          2010          75          450-456
Synthesis of regioisomeric 17β-N-phenylpyrazolyl steroid derivatives and their inhibitory effect on 17α-hydroxylase/C17,20-lyase
Zoltán Iványi, János Wölfling, Tamás Görbe, Mihály Szécsi, Tibor Wittmann, Gyula Schneider
Structure      13C NMR   碳谱模拟图
16 .     longipin-2-ene-7β,9α-diol-1-one diangelate
    相似度:53.8%
Phytochemistry          1989          28          265-268
Isolation and preparation of two longipinene derivatives from Stevia subpubescens
Luisa U. Román,Juan D. Hernández,Raúl Castañeda,Carlos M. Cerda,Pedro Joseph-Nathan
Structure      13C NMR   碳谱模拟图
17 .     2α,15,16-trihydroxy-ent-pimar-7-en
C20H34O3     相似度:53.8%
Phytochemistry          1990          29          573-577
Ent-pimarene derivatives from Palafoxia arida
C. Zdero,F. Bohlmann,R.M. King
Structure      13C NMR   碳谱模拟图
18 .     (3S,4R)-3-((3E,7E)-8-Iodo-3,7-dimethylocta-3,7-dienyl)-2-(4-methoxybenzyloxymethyl)-3,4-dimethylcyclohex-1-enecarbaldehyde
C28H39IO3     相似度:53.8%
Organic & Biomolecular Chemistry          2004          2          466-473
Total synthesis of (±)-phomactin G, a platelet activating factor antagonist from the marine fungus Phoma sp.
William P. D. Goldring and Gerald Pattenden
Structure      13C NMR   碳谱模拟图
19 .     (3E,7E)-(1R,2R,11S,12R,16S)-16-(4-Methoxybenzyloxymethyl)-4,8,11,12-tetramethyl-15-oxatricyclo[9.3.2.01,16]hexadeca-3,7-dien-2-ol
C28H40O4     相似度:53.8%
Organic & Biomolecular Chemistry          2004          2          466-473
Total synthesis of (±)-phomactin G, a platelet activating factor antagonist from the marine fungus Phoma sp.
William P. D. Goldring and Gerald Pattenden
Structure      13C NMR   碳谱模拟图
20 .     compound 15
C27H42O3     相似度:53.8%
Journal of the Chemical Society, Perkin Transactions 1          1989                   165-174
Synthetic photochemistry. Part 44. Total synthesis of ceroplastol II and albolic acid, 5-8-5-membered tricyclic sesterterpenoid insect wax constituents, via stereocontrolled silyloxy-Cope rearrangement with a normally disfavoured transition state
Nobuo Kato, Hitoshi Takeshita, Hideo Kataoka, Shoji Ohbuchi and Shinya Tanaka
Structure      13C NMR   碳谱模拟图
21 .     gephyronic acid hemiketal(β)
C26H46O7     相似度:53.8%
Angewandte Chemie International Edition          2011          50          938-941
Gephyronic Acid, a Missing Link between Polyketide Inhibitors of Eukaryotic Protein Synthesis (Part I): Structural Revision and Stereochemical Assignment of Gephyronic Acid
Lionel Nicolas, Timo Anderl, Florenz Sasse, Heinrich Steinmetz, Rolf Jansen, Gerhard H fle, Sabine Laschat, and Richard E. Taylor
Structure      13C NMR   碳谱模拟图
与君初相识,犹如故人归。
6楼2013-12-13 16:23:34
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