Luteolin 6-C-β-ristobioside from Poa annua - ScienceDirect
ExportJavaScript is disabled on your browser. Please enable JavaScript to use all the features on this page., 1987, Pages 859-860Author links open overlay panelShow moreAbstractA new glycoflavone, luteolin 6-C-(2″-O-α-D-mannosyl-β-D-glucoside), was characterized from whole plants of Poa annua.KeywordsPoa annuaGramineaeflavone C-glycosidesalditolluteolin 6-C-β-ristobioside2″-O-α-D-mannopyranosylisoorientinorientinisoorientintrieinmannitol.Choose an option to locate/access this article:Check if you have access through your login credentials or your institution.ororRecommended articlesCiting articles (0)中草药高纯度化合物生产
中草药高纯度化合物生产
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按汉语拼音分类:
&Ferullic acid
Epicatechin (EC)
表儿茶素没食子酸酯
Epicatechin-3-gallate (ECG)
表没食子儿茶素
Epigallocatechin (EGC)
表没食子儿茶素没食子酸酯
Epigallocatechin-3-gallate (EGCG)
补骨脂二氢黄酮甲醚
Bavachinin
穿心莲内酯
Andrographolide
Chrysophanol
对羟基苯甲醛&
p-Hydroxybenzaldehyde
Tetrandrine
Xanthotoxin
芦荟大黄素
Aloe-emodin
Gallic acid
没食子酸丙酯
Propyl gallate
没食子儿茶素没食子酸酯
Gallocatechin-3-gallate (GCG)
Imperatorin
Oleanolic acid
山奈酚（药典山奈素）
Kaempferol
Kaempferide
脱水穿心莲内酯琥珀酸半酯&&&&&&&&&
Dehydroandrographolide succinate
脱水淫羊藿素（淫羊藿甙元）
Anhydroicaritin
五味子甲素
Deoxyschizandin
Ursolic acid
延胡索乙素
Tetrahydropalmatine
盐酸小檗碱
Berberine hydrochloride
Folic acid
异补骨脂素
Isopsoralen
异欧前胡素
Isoimperatorin
Isofraxidin
Protocatechuic aldehyde
Protocatechuic acid
Geniposide
紫草素(右旋）
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(小有名气)
在线: 47.5小时
虫号: 628910
注册: 专业: 天然药物化学
求助化合物微谱检索（相似度大于80%）
要开题了，好长时间都没解出来，急
平时上网不多，金币没几个，见谅！
化合物1（DMSO）
193.0, 164.1, 156.4, 151.9, 148.7, 147.1, 131.5, 130.2, 123.0, 120.3, 117.4, 109.3, 104.7, 104.3, 103.7, 102.1, 92.2, 41.6, 29.5
化合物2（CDCl3）
137.6, 125.3, 125.2, 120.3, 120.2, 120.0, 112.7, 42.2, 20.8
化合物3（CDCl3）
200.1, 161.7, 150.9, 150.3, 140.5, 135.1, 134.4, 131.1, 128.9, 123.0, 117.8, 117.3, 115.8, 115.5, 113.5, 38.2, 37.1, 30.7
化合物4（DMSO）
167.0, 160.5, 151.5, 150.6, 149.2, 147.8, 146.1, 146.0, 141.1, 135.2, 133.8, 130.8, 130.0, 129.5, 127.2, 125.1, 122.3, 119.6, 116.0, 114.5, 111.7, 103.8, 102.5, 101.1, 79.6, 61.7, 56.1, 55.7, 52.1, 48.5, 44.9
化合物5（CDCl3）
190.7, 159.4, 150.7, 149.6, 147.1, 147.0, 146.6, 134.6, 127.6, 120.5, 118.7, 114.5, 113.5, 112.3, 109.8, 108.1, 102.7, 102.1, 39.7, 29.0
[ Last edited by ssfcydp on
at 09:11 ]
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(正式写手)
药理学博士
在线: 196.9小时
虫号: 970186
注册: 性别: GG专业: 药物毒理
【答案】应助回帖
★ ★ ★ ★ ★ ★ ★ ★ ★ ★ 感谢参与，应助指数 +1ssfcydp: 金币+10, ★★★很有帮助, 谢谢！能否帮忙查下其他几个？麻烦了！
化合物1的50%以上的匹配信息如下
查询结果：共查到27个化合物(查询结果仅供参考)
& & 1 .& &&&5,7,4'-trihydroxy-6,3',5'-trimethoxyflavone
& && &&&相似度:57.8%
& & Phytochemistry& && && & 1980& && && & 19& && && & 669-672
& & Isolation and synthesis of two new flavones from Conoclinium coelestinum
& & Werner Herz, Seringolam V. Govindan, Ingrid Riess-Maurer, B. Kreil, Hildebert Wagner, Lorand Farkas, Janos Strelisky
& & Structure& && &13C NMR& &碳谱模拟图
& & 2 .& &&&5-羟基-3',4',6,7-四甲氧基黄酮
& & C19H18O7& &&&相似度:57.8%
& & Chinese Pharmaceutical Journal& && && & 2008& && && & 43& && && & 417-419
& & Study on Flavanoids in the Leaves of Premna szemaoensis Pei
& & LI Qin LI Ping SHEN Yue-mao
& & Structure& && &13C NMR& &碳谱模拟图
& & 3 .& &&&5,6-dihydroxy-7,3',4'-trimethoxyflavone
& && &&&相似度:57.8%
& & Biological and Pharmaceutical Bulletin& && && & 2002& && && & 25& && && & 875-879
& & Antiproliferative Constituents in Plants 10. Flavones from the Leaves of Lantana montevidensis BRIQ. and Consideration of Structure–Activity Relationship
& & Tsuneatsu Nagao, Fumiko Abe, Junei Kinjo, Hikaru Okabe
& & Structure& && &13C NMR& &碳谱模拟图
& & 4 .& &&&7-(thiophen-2-yl)-7,13-dihydro-5-oxa-13-aza-indeno[2,1-b]phenanthrene-6,8-dione
& & C23H13NSO3& &&&相似度:57.8%
& & Heterocycles& && && & 2012& && && & 85& && && &
& & An Efficient One-Pot Three-Component Synthesis of Highly Functionalized Coumarin Fused Indenodihydropyridine and Chromeno[4,3-b]quinoline Derivatives
& & Naseem Ahmed,* B. Venkata Babu, Sandeep Singh, and Petar M. Mitrasinovic
& & Structure& && &13C NMR& &碳谱模拟图
& & 5 .& &&&pongapinnol-A
& & C19H14O6& &&&相似度:52.6%
& & Phytochemistry& && && & 2004& && && & 65& && && & 439-443
& & Furanoflavonoids from Pongamia pinnata fruits
& & Prem P. Yadav, Ghufran Ahmad, Rakesh Maurya
& & Structure& && &13C NMR& &碳谱模拟图
& & 6 .& &&&5,5'-dihydroxy-2' ,4' ,8-trimethoxyflavone
& & C18H16O7& &&&相似度:52.6%
& & Planta Medica& && && & 1996& && && & 62& && && & 160-162
& & Two Flavones from Artemisia giraldil and their Antimicrobial Activity
& & W. F. Zheng, R. X. Tan1, L. Yang, and Z. L. Liu
& & Structure& && &13C NMR& &碳谱模拟图
& & 7 .& &&&6-C-methylluteolin 7-methyl ether
& & C17H14O6& &&&相似度:52.6%
& & Planta Medica& && && & 2003& && && & 69& && && & 623-627
& & Antimicrobial Constituents from Goldenseal (the Rhizomes of Hydrastis canadensis) against Selected Oral Pathogens
& & Bang Yeon Hwang,Sara K.Roberts,Lucas R.Chadwick,Christine D.Wu,A.Douglas Kinghorn
& & Structure& && &13C NMR& &碳谱模拟图
& & 8 .& &&&5-羟基-6, 7, 3', 4'-四甲氧基黄酮
& & C19H18O7& &&&相似度:52.6%
& & Acta Botanica Yunnanica& && && & 2004& && && & 26(5)& && && & 563-568
& & Chemical Constituents from Clerodendranthus spicatus
& & ZHAO Ai-Hua, ZHAO Qin-Shi, LI Rong-Tao, SUN Han-Dong
& & Structure& && &13C NMR& &碳谱模拟图
& & 9 .& &&&5-hydroxy-3',4',6,7-tetramethoxyflavone
& && &&&相似度:52.6%
& & China Journal of Chinese Materia Medica& && && & 2002& && && & 27& && && & 749-751
& & A Study on Chemical Constituents in the Herb of Mentha spicata
& & ZHENG Jian, ZHAO Dongsheng, WU Bin, WU Lijun
& & Structure& && &13C NMR& &碳谱模拟图
& & 10 .& &&&5,8-dihydroxyl-7,3',4'-trimethoxyflavone
& && &&&相似度:52.6%
& & China Journal of Chinese Materia Medica& && && & 1998& && && & 23& && && & 293-295
& & Studies on Chemical constituents of Conyza blinii Lévl.
& & Xu Liping, Liu Jiansheng, Min De, Wang Sanwu, Zhang Zhizhen, Guo Dean and Zheng Junhua
& & Structure& && &13C NMR& &碳谱模拟图
& & 11 .& &&&santoflovone
& && &&&相似度:52.6%
& & Phytochemistry& && && & 1997& && && & 46& && && &
& & A guaianolide and a germacranolide from Achillea santolina
& & Basma A. A. A. Balboul, Ahmed A. Ahmed, Hideaki Otsuka, Masahiko Bando, Masaru Kido, Yoshio Takeda
& & Structure& && &13C NMR& &碳谱模拟图
& & 12 .& &&&1-(4-Hydroxy-5-methoxy-1H-indol-2-yl)-2-pyridin-3-yl-ethanone
& && &&&相似度:52.6%
& & Bioorganic & Medicinal Chemistry& && && & 2011& && && & 19& && && &
& & Indol-2-yl ethanones as novel indoleamine 2,3-dioxygenase (IDO) inhibitors
& & Eduard Dolušić, Pierre Larrieu, Sébastien Blanc, Frédéric Sapunaric, Bernadette Norberg,Laurence Moineaux, Delphine Colette, Vincent Stroobant, Luc Pilotte, Didier Colau, Thierry Ferain,Graeme Fraser, Moreno Galeni, Jean-Marie Frère, Bernard Masereel, Ben
& & Structure& && &13C NMR& &碳谱模拟图
& & 13 .& &&&5-hydroxy-6,7,3',4'-tetramethoxyflavone
& && &&&相似度:52.6%
& & Phytochemistry& && && & 1987& && && & 26& && && &
& & Phenolic and acetylenic metabolites from Artemisia assoana
& & Vicente Martínez,Oscar Barberá,J. Sánchez-Parareda,J. Alberto Marco
& & Structure& && &13C NMR& &碳谱模拟图
& & 14 .& &&&7-O-tosylapigenin
& & C22H16O7S& &&&相似度:52.6%
& & Heterocycles& && && & 2008& && && & 76& && && &
& & Synthesis of Oriented Anti-Virus 7-O-Substituted Apigenins
& & Kin-ichi Oyama, Tadao Kondo, and Kumi Yoshida
& & Structure& && &13C NMR& &碳谱模拟图
& & 15 .& &&&4-(Pyridin-4-ylmethylamino)-N-(3-(trifluoromethyl)phenyl)isothiazole-3-carboxamide
& & C17H13F3N4OS& &&&相似度:52.6%
& & Bioorganic & Medicinal Chemistry Letters& && && & 2009& && && & 19& && && &
& & 3,4-Disubstituted isothiazoles: Novel potent inhibitors of VEGF receptors 1 and 2
& & Alexander S. Kiselyov, Marina Semenova, Victor V. Semenov
& & Structure& && &13C NMR& &碳谱模拟图
& & 16 .& &&&5-羟基-6,7,3',4'-四甲氧基黄酮
& && &&&相似度:52.6%
& & Chinese Traditional and Herbal Drugs& && && & 2006& && && & 37& && && & 512-514
& & 薄荷中黄酮类成分的研究
& & 张援虎;刘颖;胡峻;石任兵;郭亚健
& & Structure& && &13C NMR& &碳谱模拟图
& & 17 .& &&&eupatilin
& && &&&相似度:52.6%
& & Chinese Traditional and Herbal Drugs& && && & 2004& && && & 35& && && & 622-624
& & 沙漠绢蒿化学成分研究
& & 邓雁如,何荔,李维琪,汪汉卿
& & Structure& && &13C NMR& &碳谱模拟图
& & 18 .& &&&Eupatilin
& && &&&相似度:52.6%
& & Natural Product Sciences& && && & 2010& && && & 16& && && & 143-147
& & Inhibitors of Nitric Oxide Production from Artemisia princeps
& & Li, D Han, Xiang H Hong, Seong-Su; Lee, C Lee, Moon-S Lee, Dong-Ho; Lee, Mi-K Hwang, Bang-Yeon
& & Structure& && &13C NMR& &碳谱模拟图
& & 19 .& &&&eupatilin
& && &&&相似度:52.6%
& & Journal of Shenyang Pharmaceutical University& && && & 2010& && && & 27& && && & 440-442
& & Isolation and identification of chemical constituents from testa of Castanea mollissima Blume
& & LU Chuan, WU Di, GAO Hui-yuan, SUN Bo-hang, HUANG Jian, WU Li-jun
& & Structure& && &13C NMR& &碳谱模拟图
& & 20 .& &&&eupatilin
& && &&&相似度:52.6%
& & Natural Product Research and Development& && && & 2006& && && & 18& && && & 71-73
& & Chemical Constituents from Chrysanthemum morifolium Ramat
& & ZHANG J QIAN Da- LI You- YIN Zhi-qi
& & Structure& && &13C NMR& &碳谱模拟图
& & 21 .& &&&N-Methylisocystodamine
& & C19H12N4O& &&&相似度:52.6%
& & Tetrahedron& && && & 2011& && && & 67& && && &
& & Cell differentiation inducers from a marine sponge Biemna sp.
& & Reiko Ueoka, Yuji Ise, Shigeru Okada, Shigeki Matsunaga
& & Structure& && &13C NMR& &碳谱模拟图
& & 22 .& &&&eupatilin
& && &&&相似度:52.6%
& & Phytotherapy Research& && && & 2010& && && & 24& && && &
& & Bioactivity-guided isolation of antiproliferative compounds from Centaurea arenaria
& & Bence Csapi, Zsuzsanna Hajdú, István Zupkó, Ágnes Berényi, Peter Forgo, Pál Szabó and Judit Hohmann
& & Structure& && &13C NMR& &碳谱模拟图
& & 23 .& &&&nitidine
& && &&&相似度:52.3%
& & Chemistry of Natural Compounds& && && & 2007& && && & 43& && && & 100-102
& & ISOQUINOLINE ALKALOIDS FROM Broussonetia papyrifera FRUITS
& & Su-Qiu Pang, Guo-Quan Wang, Bao-Kang Huang,Qiao-Yan Zhang, and Lu-Ping Qin
& & Structure& && &13C NMR& &碳谱模拟图
& & 24 .& &&&compound 8a/6
& & C21H17Cl2N3O2& &&&相似度:50%
& & Journal of Heterocyclic Chemistry& && && & 2001& && && & 38& && && & 199-204
& & Synthesis of novel type pyrazolyl and tetrazolyl isoquinolinium zwitterions
& & Ibolya Prauda and Jozsef Reiter
& & Structure& && &13C NMR& &碳谱模拟图
& & 25 .& &&&(E)-1-(5-bromo-2-hydroxy-4-methoxyphenyl)-3-(2-chloro-6-ethoxyquinolin-3-yl)prop-2-en-1-one
& & C21H17ClBrNO4& &&&相似度:50%
& & Indian Journal of Chemistry& && && & 2009& && && & 48B& && && &
& & Experimental and computational evaluation of new quinolinyl chalcones as potent antiplasmodial agents
& & Dave,Shikha S; Ghatolea,Ajay M; Rahatgaonkar,Anjali M; Chorghade,Mukund S; Chauhan,P M S; Srivastava,Kumkum
& & Structure& && &13C NMR& &碳谱模拟图
& & 26 .& &&&7-(2-nitrophenyl)-7,13-dihydro-5-oxa-13-aza-indeno[2,1-b]phenanthrene-6,8-dione
& & C25H14N2O5& &&&相似度:50%
& & Heterocycles& && && & 2012& && && & 85& && && &
& & An Efficient One-Pot Three-Component Synthesis of Highly Functionalized Coumarin Fused Indenodihydropyridine and Chromeno[4,3-b]quinoline Derivatives
& & Naseem Ahmed,* B. Venkata Babu, Sandeep Singh, and Petar M. Mitrasinovic
& & Structure& && &13C NMR& &碳谱模拟图
& & 27 .& &&&2-(3,4-Dihydroxyphenyl)-7-(4-fluorobenzyloxy)-3,5-dihydroxy-4H-chromen-4-one
& & C22H15FO7& &&&相似度:50%
& & Archives of Pharmacal Research& && && & 2012& && && & 35& && && & 77-85
& & Synthesis and antiviral evaluation of 7-O-arylmethylquercetin derivatives against SARS-associated coronavirus (SCV) and hepatitis C virus (HCV)
& & Hye Ri Park, Hyunjun Yoon, Mi Kyoung Kim, Sung Dae Lee and Youhoon Chong
& & Structure& && &13C NMR& &碳谱模拟图
充满希望的路途胜过终点的到达！
(正式写手)
药理学博士
在线: 196.9小时
虫号: 970186
注册: 性别: GG专业: 药物毒理
【答案】应助回帖
化合物2的匹配度在50%以上的信息
查询结果：共查到44个化合物(查询结果仅供参考)
& & 1 .& &&&1,2,3,4-tetrahydro-1-oxo-β-carboline
& && &&&相似度:81.8%
& & Acta Pharmaceutica Sinica& && && & 1996& && && & 31& && && & 151-155
& & STUDIES ON THE CHEMICAL CONSTITUENTS OF EVODIA RUTAECARPA[JUSS] BENTH
& & YQ T XZ Feng and L Huang
& & Structure& && &13C NMR& &碳谱模拟图
& & 2 .& &&&compound 3
& & C11H10N2O& &&&相似度:81.8%
& & Heterocycles& && && & 2008& && && & 76& && && & 861-865
& & Structure& && &13C NMR& &碳谱模拟图
& & 3 .& &&&1,1,1-tris(3-indolyl)methane
& & C25H19N3& &&&相似度:66.6%
& & Journal of Natural Products& && && & 2003& && && & 66& && && &
& & New Indole Alkaloids from the North Sea Bacterium Vibrio parahaemolyticus Bio2491
& & Ravikanth Veluri,Imelda Oka, Irene Wagner-Döbler, and Hartmut Laatsch
& & Structure& && &13C NMR& &碳谱模拟图
& & 4 .& &&&compound 1f
& & C10H8N2O2& &&&相似度:66.6%
& & Journal of Heterocyclic Chemistry& && && & 2000& && && & 37& && && & 15-24
& & Synthesis and nuclear magnetic resonance spectroscopic studies of 1-arylpyrroles
& & Chang Kiu Lee, Jung Ho Jun and Ji Sook Yu
& & Structure& && &13C NMR& &碳谱模拟图
& & 5 .& &&&harmalan
& & C12H12N2& &&&相似度:58.3%
& & Heterocycles& && && & 2005& && && & 65& && && &
& & A Simple Method for the Synthesis of 1-Substituted β-Carboline Derivatives from Tryptamine and Carboxylic Acids in Polyphosphoric Acid
& & Iliyan Ivanov,* Stoyanka Nikolova, and Stela Statkova-Abeghe
& & Structure& && &13C NMR& &碳谱模拟图
& & 6 .& &&&4,5,6,7-Tetrachloro-2,2-diphenyl-1,3-benzodioxole
& & C19H10Cl4O2& &&&相似度:55.5%
& & Molecules& && && & 2002& && && & 7& && && & 840-847
& & First Example of Direct Transformation of Alkylbenzenes to 1, 3-Benzodioxoles by Oxidation with o-Chloranil
& & Sheikh M. Rahman and Tomoshige Kobayashi
& & Structure& && &13C NMR& &碳谱模拟图
& & 7 .& &&&2,3,6-Tribromo-1-methylindole
& & C9H6NBr3& &&&相似度:55.5%
& & Journal of Natural Products& && && & 2006& && && & 69& && && &
& & Synthesis of Bromoindole Alkaloids from Laurencia brongniartii
& & Oscar R. Surez-Castillo, Lidia Beiza-Granados, Myriam Melndez-Rodrguez,Alejandro lvarez-Hernndez, Martha S. Morales-Ros, and Pedro Joseph-Nathan
& & Structure& && &13C NMR& &碳谱模拟图
& & 8 .& &&&1-amino-2-methylindole
& & C9H10N2& &&&相似度:55.5%
& & Journal of Heterocyclic Chemistry& && && & 2001& && && & 38& && && & 885-893
& & Synthesis and characterization of new heterocyclic derivatives by oxidation of 1-amino-2-methylindoline
& & L. Peyrot, M. Elkhatib, J. R. Vignalou, R. Metz, F. Elomar and H. Delalu
& & Structure& && &13C NMR& &碳谱模拟图
& & 9 .& &&&1H-indole-5-carbonitrile
& & C9H5N& &&&相似度:55.5%
& & Heterocycles& && && & 2007& && && & 72& && && & 293-326
& & Synthesis of 2, 4, 5-Trisubstituted Thiazoles with a 5-(N, N-Dimethylaminomethyl) Substituent
& & Bernhard Stump, Philipp C. Kohler, W. Bernd Schweizer, and François Diederich
& & Structure& && &13C NMR& &碳谱模拟图
& & 10 .& &&&3-(Butylamino)-5-bromopyridine
& & C9H13N2Br& &&&相似度:55.5%
& & Heterocycles& && && & 2011& && && & 83& && && &
& & Iwao Okamoto,* Masayuki Terashima, Rempei Yoshioka, Tomonori Muramatsu, Satomi Kojima, Haruka Inoue, Mio Takahashi, Nobuyoshi Morita, and Osamu Tamura
& & Youlai Zhang, Hiroki Tanimoto, Yasuhiro Nishiyama, Tsumoru Morimoto, and Kiyomi Kakiuchi
& & Structure& && &13C NMR& &碳谱模拟图
& & 11 .& &&&Carbazol-1-yldiisopropylfluorlsilan
& && &&&相似度:55.5%
& & Zeitschrift für Naturforschung B& && && & 2004& && && & 59& && && &
& & Carbazolylsilanes: Synthesis and Crystal Structures (In German)
& & V. Liebau, M. Noltemeyer, J. Magull, and U. Klingebie
& & Structure& && &13C NMR& &碳谱模拟图
& & 12 .& &&&4-p-Tolylisoxazole
& && &&&相似度:55.5%
& & Tetrahedron& && && & 2012& && && & 68& && && & 807-812
& & Regioselective conversion of alkynes to 4-substituted and 3,4-disubstituted isoxazoles using titanium-catalyzed multicomponent coupling reactions
& & Amila A. Dissanayake, Aaron L. Odom
& & Structure& && &13C NMR& &碳谱模拟图
& & 13 .& &&&compound 12
& && &&&相似度:55.5%
& & Organic Magnetic Resonance& && && & 1982& && && & 19& && && & 98-101
& & A carbon-13 nuclear magnetic resonance spectral investigation of substituted triphenyl phosphates
& & G. W. Buchanan, R. H. Wightman and M. Malaiyandi
& & Structure& && &13C NMR& &碳谱模拟图
& & 14 .& &&&1-(4-methylpyridin-2yl)-3-phenylthiourea
& && &&&相似度:54.5%
& & Molecules& && && & 2006& && && & 11& && && & 597-602
& & One-Pot Synthesis of 5-Arylidene-2-Imino-4-Thiazolidinones under Microwave Irradiation
& & Souad Kasmi-Mir, Ayada Djafri, Ludovic Paquin, Jack Hamelin and Mustapha Rahmouni
& & Structure& && &13C NMR& &碳谱模拟图
& & 15 .& &&&compound 2d
& && &&&相似度:54.5%
& & Journal of Heterocyclic Chemistry& && && & 2002& && && & 39& && && & 69-75
& & Synthesis and characterization of the novel l-(substituted phenoxy/phenyl)-2-phospholene and phospholane 1-oxide derivatives
& & Vallum Krishna Reddy, Jun-Ichi Onogawa, Lakonda Nagaprasada Rao, Tatsuo Oshikawa, Masaki Takahashi and Mitsuji Yamashita
& & Structure& && &13C NMR& &碳谱模拟图
& & 16 .& &&&1-methyl-4-methoxy-β-carboline
& && &&&相似度:54.5%
& & Chinese Traditional and Herbal Drugs& && && & 2007& && && & 38& && && & 807-810
& & Alkaloids from twigs and leaves of Picrasma quassioides
& & CHEN M FAN Hua- DAI Sheng- LIU Ke
& & Structure& && &13C NMR& &碳谱模拟图
& & 17 .& &&&(±)-Spiro(indoline-2,2'-tetrahydrothiophene)-3-one
& & C11H11NOS& &&&相似度:54.5%
& & Organic & Biomolecular Chemistry& && && & 2006& && && & 4& && && & 691-701
& & Unprecedented chemical structure and biomimetic synthesis of erucalexin, a phytoalexin from the wild crucifer Erucastrum gallicum
& & M. Soledade C. Pedras, Mojmir Suchy and Pearson W. K. Ahiahonu
& & Structure& && &13C NMR& &碳谱模拟图
& & 18 .& &&&4-acetylindole
& && &&&相似度:50%
& & Journal of Natural Products& && && & 2003& && && & 66& && && & 885-887
& & Concise Large-Scale Synthesis of Psilocin and Psilocybin, Principal Hallucinogenic Constituents of “Magic Mushroom”
& & Osamu Shirota,Wataru Hakamata, and Yukihiro Goda
& & Structure& && &13C NMR& &碳谱模拟图
& & 19 .& &&&harman
& && &&&相似度:50%
& & Chemical & Pharmaceutical Bulletin& && && & 1993& && && & 41& && && &
& & The 1H- and 13C-Nuclear Magnetic Resonance Spectra of Harman. Reinvestigation of the Assignments by One- and Two-Dimensional Methods
& & Hiroko SEKI,Akihiro HASHIMOTO and Tohru HINO
& & Structure& && &13C NMR& &碳谱模拟图
& & 20 .& &&&1,6-bromoindolyl-3-acetamide
& & C10H9BrN2O& &&&相似度:50%
& & Journal of Natural Products& && && & 1993& && && & Vol 56& && && &
& & Structure and Synthesis of Bromoindoles from the Marine Sponge Pseudosuberites hyalinus
& & Thomas Rasmussen, Jan Jensen, Uffe Anthoni, Carsten Christophersen, Per H. Nielsen
& & Structure& && &13C NMR& &碳谱模拟图
& & 21 .& &&&vibrindole A
& & C18H16N2& &&&相似度:50%
& & Journal of Natural Products& && && & 1994& && && & Vol 57& && && & 1587
& & Vibrindole A, a Metabolite of the Marine Bacterium, Vibrio parahaemolyticus, Isolated from the Toxic Mucus of the Boxfish Ostracion cubicus
& & Ronit Bell, Shmuel Carmeli, Nehemia Sar
& & Structure& && &13C NMR& &碳谱模拟图
& & 22 .& &&&tryptamine
& && &&&相似度:50%
& & Phytochemistry& && && & 1995& && && & 40& && && & 975-977
& & Alkaloids from leaves of Alangium bussyanum
& & A. O. Diallo, H. Mehri, L. Iouzalen, M. Plat
& & Structure& && &13C NMR& &碳谱模拟图
& & 23 .& &&&(±)-2-methyl-6-nitro-1,2,3,4-tetrahydroquinoline
& & C10H12N2O2& &&&相似度:50%
& & Journal of Heterocyclic Chemistry& && && & 2008& && && & 45& && && &
& & 6-Nitro-1,2,3,4-tetrahydroquinolines by a tandem reductive amination-SNAr reaction
& & Richard A. Bunce and Takahiro Nago
& & Structure& && &13C NMR& &碳谱模拟图
& & 24 .& &&&compound 4
& && &&&相似度:50%
& & Journal of Heterocyclic Chemistry& && && & 2005& && && & 42& && && & 867-875
& & A study of substituent effect on 1H and 13C NMR spectra of mono,di and poly substituted carbazoles
& & Sergio M. Bonesi,Maria A. Ponce and Rosa Erra-Balsells
& & Structure& && &13C NMR& &碳谱模拟图
& & 25 .& &&&compound 3b
& && &&&相似度:50%
& & Journal of Heterocyclic Chemistry& && && & 2004& && && & 41& && && & 161-171
& & A study of substituent effect on 1H and 13C nmr spectra of N-and C-substituted carbazoles
& & Sergio M. Bonesi,Maria A. Ponce and Rosa Erra-Balsells
& & Structure& && &13C NMR& &碳谱模拟图
& & 26 .& &&&2,3,8,9-tetramethyl-5a,10b-dihydrobenzofuro[2,3-b]benzofuran
& && &&&相似度:50%
& & Journal of Heterocyclic Chemistry& && && & 2010& && && & 47& && && &
& & 5a,10b-Dihydrobenzofuro[2,3-b]benzofuran type compounds and related products from P-substituted phenols and glyoxal
& & Ali Rahmatpour
& & Structure& && &13C NMR& &碳谱模拟图
& & 27 .& &&&3-[1-(1H-indol-3-yl)ethyl]-1H-indole
& & C18H16N2& &&&相似度:50%
& & Indian Journal of Chemistry& && && & 2007& && && & 46B& && && & 669-673
& & Efficient synthesis of bis(indolyl) methanes in aqueous medium catalyzed by molybdenyl acetylacetonate
& & Banerjee,B; Mandal,S K; Roy,S C
& & Structure& && &13C NMR& &碳谱模拟图
& & 28 .& &&&3-[1-(1H-indol-3yl)methyl]-1-methylethyl]-1H-indole
& & C19H18N2& &&&相似度:50%
& & Indian Journal of Chemistry& && && & 2007& && && & 46B& && && & 669-673
& & Efficient synthesis of bis(indolyl) methanes in aqueous medium catalyzed by molybdenyl acetylacetonate
& & Banerjee,B; Mandal,S K; Roy,S C
& & Structure& && &13C NMR& &碳谱模拟图
& & 29 .& &&&N-p-tolylbenzo[d]thiazol-2-amine
& && &&&相似度:50%
& & Heterocycles& && && & 2010& && && & 81& && && &
& & Iron-Catalyzed One-Pot Synthesis of 2-Aminobenzothiazoles from 2-Aminobenzenethiols and Isothiocyanates under Ligand-Free Conditions in Water
& & Wenying Wang, Wenying Zhong, Runxia Zhou, Jinsheng Yu, Juan Dai, Qiuping Ding, and Yiyuan Peng
& & Structure& && &13C NMR& &碳谱模拟图
& & 30 .& &&&N-(3-thienyl)carbazole
& & C16H11NS& &&&相似度:50%
& & Heterocycles& && && & 2009& && && & 78& && && &
& & Substituent Effects on Photophysical Properties of N-Thienylcarbazoles
& & Hideyuki Shimizu, Atsushi Kobayashi, Shingo Itoi, Toshitada Yoshihara, Seiji Tobita, Yosuke Nakamura, and Jun Nishimura
& & Structure& && &13C NMR& &碳谱模拟图
& & 31 .& &&&diethyl 2-hydroxy-2-(3'-indolyl)malonate
& & C15H17NO5& &&&相似度:50%
& & Heterocycles& && && & 2005& && && & 65& && && & 37-48
& & First Isolation of Both Indolylcarbinols and Diindolylalkanes from Microwave-assisted Acid (Clay)-catalysed Reaction of Indoles with Diethyl Ketomalonate
& & Manas Chakrabarty,* Sulakshana Karmakar, and Yoshihiro Harigaya
& & Structure& && &13C NMR& &碳谱模拟图
& & 32 .& &&&1-Propyl-3,4-dihydro-9H-β-carboline
& & C14H16N2& &&&相似度:50%
& & Heterocycles& && && & 2005& && && & 65& && && &
& & A Simple Method for the Synthesis of 1-Substituted β-Carboline Derivatives from Tryptamine and Carboxylic Acids in Polyphosphoric Acid
& & Iliyan Ivanov,* Stoyanka Nikolova, and Stela Statkova-Abeghe
& & Structure& && &13C NMR& &碳谱模拟图
& & 33 .& &&&2,3-di(2-methoxyanilino)-8-(2-methoxyphenyl)-7H-isoindolo[5,6-g]quinoxaline-5,7,9,11(8H)-tetraone
& & C35H25N5O7& &&&相似度:50%
& & Heterocycles& && && & 2004& && && & 63& && && & 819-826
& & Synthesis of 2,3,8-Trisubstituted 7H-Isoindolo[5,6-g]quinoxaline-5,7,9,11(8H)-tetraones
& & Heesoon Lee,* Sungmoon Cho, Byeonggil Choi, Kwon Namgoong, and Jae-Kyung Jung
& & Structure& && &13C NMR& &碳谱模拟图
& & 34 .& &&&5-(bromo-1H-indol-3-yl)acetonitrile
& & C10H7N2Br& &&&相似度:50%
& & Heterocycles& && && & 2003& && && & 60& && && & 865-877
& & Synthesis of New Melatonin Analogues from Dimers of Azaindole and Indole by Use of Suzuki Homocoupling
& & Jérôme Guillard, Carlos Larraya, and Marie-Claude Viaud-Massuard*
& & Structure& && &13C NMR& &碳谱模拟图
& & 35 .& &&&compound 5a
& && &&&相似度:50%
& & Tetrahedron Letters& && && & 2002& && && & 43& && && &
& & Fluorinated ketene dithioacetals. Part IX. Synthesis and some chemical properties of new fluorinated 3H-1,2-dithiole-3-thiones
& & Vadim M Timoshenko, Jean-Philippe Bouillon, Yuriy G Shermolovich, Charles Portella
& & Structure& && &13C NMR& &碳谱模拟图
& & 36 .& &&&compound 21
& & C14H13NO& &&&相似度:50%
& & Tetrahedron Letters& && && & 2003& && && & 44& && && &
& & An efficient total synthesis of 9-methoxycarbazole-3-carbaldehyde based on a novel methodology for the preparation of methoxyindoles
& & N. Selvakumar, Manoj Kumar Khera, B.Yadi Reddy, D. Srinivas, A.Malar Azhagan, Javed Iqbal
& & Structure& && &13C NMR& &碳谱模拟图
& & 37 .& &&&6-Chloro-3-(methylthiomethyl)-1H-indole
& & C10H10ClNS& &&&相似度:50%
& & Tetrahedron& && && & 2012& && && & 68& && && &
& & A novel NH4OAc and CuBr(PPh3)3-induced intermolecular Pummerer-type reaction between free (NH)-indoles and dimethylsulfoxide: facile synthesis of 3-methylthiomethyl substituted indoles
& & Jin Liu, Xianxue Wang, Han Guo, Xiaokang Shi, Xiaoyu Ren, Guosheng Huang
& & Structure& && &13C NMR& &碳谱模拟图
& & 38 .& &&&3-(Hydroxymethyl)indole-2-methylsulfoxide
& & C10H11NO2S& &&&相似度:50%
& & Organic & Biomolecular Chemistry& && && & 2006& && && & 4& && && &
& & Metabolism of crucifer phytoalexins in Sclerotinia sclerotiorum: detoxification of strongly antifungal compounds involves glucosylation
& & M. Soledade C. Pedras and Mohammad Hossain
& & Structure& && &13C NMR& &碳谱模拟图
& & 39 .& &&&rutaecarpene
& & C18H15N3& &&&相似度:50%
& & Bioorganic & Medicinal Chemistry& && && & 2009& && && & 17& && && &
& & Synthesis and vasodilator effects of rutaecarpine analogues which might be involved transient receptor potential vanilloid subfamily, member 1 (TRPV1)
& & Zhuo Chen, Gaoyun Hu, Dai Li, Jun Chen, Yuanjian Li, Huayong Zhou, Ye Xie
& & Structure& && &13C NMR& &碳谱模拟图
& & 40 .& &&&1,3-diphenylbut-1-ene
& && &&&相似度:50%
& & European Journal of Organic Chemistry& && && & 2010& && && && && && &
& & Amberlyst-15 in Ionic Liquid: An Efficient and Recyclable Reagent for Nucleophilic Substitution of Alcohols and Hydroamination of Alkenes
& & Ziyauddin S. Qureshi, Krishna M. Deshmukh, Pawan J. Tambade, Kishor P. Dhake and Bhalchandra M. Bhanage
& & Structure& && &13C NMR& &碳谱模拟图
& & 41 .& &&&isopropyl N-phenylmaleamate
& & C13H15NO3& &&&相似度:50%
& & European Journal of Organic Chemistry& && && & 2010& && && && && && &
& & Esterification of Maleamic Acids without Double Bond Isomerization
& & Albert Sánchez, Enrique Pedroso and Anna Grandas
& & Structure& && &13C NMR& &碳谱模拟图
& & 42 .& &&&N-(n-Butyl)-2,7-dibromocarbazole
& & C16H15Br2N& &&&相似度:50%
& & Tetrahedron& && && & 2012& && && & 68& && && &
& & Efficient synthesis of N-alkyl-2,7-dihalocarbazoles by simultaneous carbazole ring closure and N-alkylation
& & Drahomír Výprachtický, Ivan Kmínek, Veronika Pokorná, Věra Cimrová
& & Structure& && &13C NMR& &碳谱模拟图
& & 43 .& &&&N-(n-Butyl)-2,7-dichlorocarbazole
& & C16H15Cl2N& &&&相似度:50%
& & Tetrahedron& && && & 2012& && && & 68& && && &
& & Efficient synthesis of N-alkyl-2,7-dihalocarbazoles by simultaneous carbazole ring closure and N-alkylation
& & Drahomír Výprachtický, Ivan Kmínek, Veronika Pokorná, Věra Cimrová
& & Structure& && &13C NMR& &碳谱模拟图
& & 44 .& &&&7-Bromo-3-methyl-5-(trimethylsilyl)iso-benzofuran-1(3H)-one
& && &&&相似度:50%
& & Tetrahedron& && && & 2012& && && & 68& && && &
& & Cyclotrimerization of unsymmetrically bromo-substituted diynes: toward the synthesis of potential selective inhibitors of tyrosine kinase 2
& & Silje Melnes, Annette Bayer, Odd Reidar Gautun
& & Structure& && &13C NMR& &碳谱模拟图
充满希望的路途胜过终点的到达！
(正式写手)
药理学博士
在线: 196.9小时
虫号: 970186
注册: 性别: GG专业: 药物毒理
【答案】应助回帖
化合物3的匹配度在80%以上的信息
1 .& &&&wuchuyuamide III
C18H17N3O3& &&&相似度:88.8%
Journal of Asian Natural Products Research& && && & 2007& && && & 9& && && & 685-688
A novel alkaloid from the fruits of Evodia officinalis
HUI-ZI JIN, JING-LING DU, WEI-DONG ZHANG, HAI-SHENG CHEN,JEONG-HYUNG LEE and JUNG-JOON LEE
Structure& && &13C NMR& &碳谱模拟图
充满希望的路途胜过终点的到达！
(正式写手)
药理学博士
在线: 196.9小时
虫号: 970186
注册: 性别: GG专业: 药物毒理
【答案】应助回帖
化合物4的匹配度在50%的信息
查询结果：共查到39个化合物(查询结果仅供参考)
& & 1 .& &&&(E)-3(5)-[β-(4-hydroxy-3-methoxyphenyl)-ethenyl]-5(3)-phenyl-1H-pyrazole
& & C18H16N2O2& &&&相似度:61.2%
& & Bioorganic & Medicinal Chemistry& && && & 2009& && && & 17& && && &
& & Synthesis and biological evaluation of curcuminoid pyrazoles as new therapeutic agents in inflammatory bowel disease: Effect on matrix metalloproteinases
& & R.M. Claramunt, L. Bouissane, M.P. Cabildo, M.P. Cornago, J. Elguero, A. Radziwon, C. Medina
& & Structure& && &13C NMR& &碳谱模拟图
& & 2 .& &&&9-O-[3-(ferulic acid)propyl] berberine bromide
& & C32H28NO8Br& &&&相似度:59.3%
& & Bioorganic & Medicinal Chemistry& && && & 2011& && && & 19& && && &
& & Benzenediol-berberine hybrids: Multifunctional agents for Alzheimer’s disease
& & Huailei Jiang, Xu Wang, Ling Huang, Zonghua Luo, Tao Su, Ke Ding, Xingshu Li
& & Structure& && &13C NMR& &碳谱模拟图
& & 3 .& &&&Okaramine E
& & C32H32N4O4& &&&相似度:56.2%
& & Bioscience, Biotechnology, and Biochemistry& && && & 1995& && && & 59& && && & 246-250
& & New Okaramine Congeners, Okaramines D, E, and F, from Penicillium simplicissimum ATCC 90288
& & Hideo Hayashi, Yoshihide Asabu, Sawao Murao, Motoo Arai
& & Structure& && &13C NMR& &碳谱模拟图
& & 4 .& &&&N-(1,2-Bis(4-isopropoxy-3-methoxyphenyl)-2-oxoethyl)-1-benzyl-5-(benzyloxy)-6-methoxy-1H-indole-2-carboxamide
& & C46H48N2O8& &&&相似度:55.8%
& & Bioorganic & Medicinal Chemistry& && && & 2011& && && & 19& && && &
& & Synthesis and topoisomerase I inhibitory activity of a novel diazaindeno[2, 1-b]phenanthrene analogue of Lamellarin D
& & Salvatore Cananzi, Lucio Merlini, Roberto Artali, Giovanni Luca Beretta, Nadia Zaffaroni, Sabrina Dallavalle
& & Structure& && &13C NMR& &碳谱模拟图
& & 5 .& &&&lamellarin C 20-sulfate
& & C30H26NO12S& &&&相似度:54.8%
& & Journal of Natural Products& && && & 1999& && && & 62& && && & 419-424
& & New Lamellarin Alkaloids from the Australian Ascidian, Didemnum chartaceum
& & Rohan A. Davis, Anthony R. Carroll, Gregory K. Pierens, and Ronald J. Quinn
& & Structure& && &13C NMR& &碳谱模拟图
& & 6 .& &&&ferulic acid
& && &&&相似度:54.8%
& & Phytochemistry& && && & 2009& && && & 70& && && & 147-155
& & On the role of the monolignol γ-carbon functionality in lignin biopolymerization
& & Anders Holmgren, Magnus Norgren , Liming Zhang , Gunnar Henriksson
& & Structure& && &13C NMR& &碳谱模拟图
& & 7 .& &&&O-2-(3-Hydroxy-4-methoxyphenyl)ethyl-O-α-Lrhamnopyranosyl-(1 3)-(4-O-cis-feruloyl)-β-Dglucopyranoside
& & C31H40O15& &&&相似度:54.8%
& & Chemistry of Natural Compounds& && && & 2002& && && & 38& && && & 473-519
& & PHENOLIC COMPOUNDS OF PLANTS OF THE Scutellaria GENUS. DISTRIBUTION, STRUCTURE, AND PROPERTIES
& & V. M. Malikov and M. P. Yuldashev
& & Structure& && &13C NMR& &碳谱模拟图
& & 8 .& &&&2,3,5,4'-tetrahydroxystilbene-2-O- (2''-O-feruloyl)-β-D-glucopyranoside
& & C30H30O12& &&&相似度:54.8%
& & Chinese Chemical Letters& && && & 2001& && && & 12& && && & 503-506
& & Two New Glucosides from Radix Polygoni multiflori Preparata
& & Wan Sheng CHEN, Wei Dong ZHANG, Gen Jing YANG, Hai Sheng CHEN,Chuan Zhuo QIAO
& & Structure& && &13C NMR& &碳谱模拟图
& & 9 .& &&&cistanoside D
& && &&&相似度:54.8%
& & Chinese Traditional and Herbal Drugs& && && & 1999& && && & 30(7)& && && & 487-490
& & Phenylpropanold Glycosides of Ningpo Figwort (Scrophularia ningpoensis)
& & Li Y Jiang S Gao Wenyun
& & Structure& && &13C NMR& &碳谱模拟图
& & 10 .& &&&1-[4-(4-{4-[5-(2,4-dichloro-phenyl)-3-oxo-penta-1,4-dienyl]-2-methoxy-phenoxymethyl}-[1,2,3] triazol-1-yl)-5-hydroxymethyl-tetrahydro-furan-2-yl]-5-methyl-1H-pyri-midine-2,4-dione
& & C31H29Cl2N5O7& &&&相似度:54.8%
& & Bioorganic & Medicinal Chemistry& && && & 2010& && && & 18& && && &
& & Design, synthesis and in vitro antimalarial evaluation of triazole-linked chalcone and dienone hybrid compounds
& & Eric M. Guantai, Kanyile Ncokazi, Timothy J. Egan, Jiri Gut, Philip J. Rosenthal, Peter J. Smith, Kelly Chibale
& & Structure& && &13C NMR& &碳谱模拟图
& & 11 .& &&&Zanthocapensine
& & C30H27NO6& &&&相似度:54.8%
& & Planta Medica& && && & 2012& && && & 78& && && & 148-153
& & Antibacterial Benzofuran Neolignans and Benzophenanthridine Alkaloids from the Roots of Zanthoxylum capense
& & Luo, X Pedro, L Milic, V Mulhovo, S Duarte, A Duarte, Noé Ferreira, Maria-José U.:
& & Structure& && &13C NMR& &碳谱模拟图
& & 12 .& &&&scroside E
& & C30H38O16& &&&相似度:51.6%
& & Helvetica Chimica Acta& && && & 2004& && && & Vol. 87& && && & 598
& & Phenyl and Phenylethyl Glycosides from Picrorhiza scrophulariiflora
& & Sheng-Xiong Huang, Xun Liao, Quan-Jiang Nie, Li-Sheng Ding, and Shu-Lin Peng
& & Structure& && &13C NMR& &碳谱模拟图
& & 13 .& &&&lamellarin B 20-sulfate
& & C30H24NO12S& &&&相似度:51.6%
& & Journal of Natural Products& && && & 1999& && && & 62& && && & 419-424
& & New Lamellarin Alkaloids from the Australian Ascidian, Didemnum chartaceum
& & Rohan A. Davis, Anthony R. Carroll, Gregory K. Pierens, and Ronald J. Quinn
& & Structure& && &13C NMR& &碳谱模拟图
& & 14 .& &&&compound 4a
& & C31H26O11& &&&相似度:51.6%
& & Chemical & Pharmaceutical Bulletin& && && & 1991& && && & 39& && && &
& & Studies on Nepalese Crude Drugs. XIV. New Flavonoids from the Root of Scutellaria prostrata JACQ. ex BENTH.
& & Yuichi KIKUCHI,Yukinori MIYAICHI and Tsuyoshi TOMIMORI
& & Structure& && &13C NMR& &碳谱模拟图
& & 15 .& &&&1,2-dihydro-6,8- dimethoxy-7-1-(3,5-dimethoxy-4-hydroxyphenyl)-N1,N2-bis-[2-(4- hydroxyphenyl)ethyl]-2,3-naphthalene dicarboxamide
& && &&&相似度:51.6%
& & Biochemical Systematics and Ecology& && && & 2007& && && & 35& && && & 621-623
& & Chemical Constituents of Commelina communis Linn.
& & Qin Yang, Guan Ye, Wei-Min Zhao
& & Structure& && &13C NMR& &碳谱模拟图
& & 16 .& &&&quassidine B
& & C27H24N4O3& &&&相似度:51.6%
& & Journal of Natural Products& && && & 2010& && && & 73& && && & 167-171
& & Quassidines A−D, Bis-β-carboline Alkaloids from the Stems of Picrasma quassioides
& & Wei-Hua Jiao, Hao Gao, Chen-Yang Li, Feng Zhao, Ren-Wang Jiang, Ying Wang, Guang-Xiong Zhou and Xin-Sheng Yao
& & Structure& && &13C NMR& &碳谱模拟图
& & 17 .& &&&cistanoside D
& && &&&相似度:51.6%
& & Phytochemistry& && && & 1992& && && & 31& && && & 263-266
& & Phenylpropanoid and iridoid glycosides from Pedicularis lasiophrys
& & Jia Zhongjian, Liu Zimin, Wang Changzeng
& & Structure& && &13C NMR& &碳谱模拟图
& & 18 .& &&&picrasmalignan A
& & C30H30O9& &&&相似度:51.6%
& & Chemistry & Biodiversity& && && & 2011& && && & Vol.8& && && &
& & A New Neolignan and a New Sesterterpenoid from the Stems of Picrasma quassioides Bennet
& & Wei-Hua Jiao, Hao Gao, Feng Zhao, Fei He, Guang-Xiong Zhou, and Xin-Sheng Yao
& & Structure& && &13C NMR& &碳谱模拟图
& & 19 .& &&&(-)-secoisolariciresinol 4-O-β-D-glucopyranoside
& & C26H36O11& &&&相似度:51.6%
& & Chemical & Pharmaceutical Bulletin& && && & 2002& && && & 50& && && & 73-77
& & Constituents of the Underground Parts of Glehnia littoralis
& & Zhong Yuan, Yasuhiro Tezuka, Wenzhe Fan, Shigetoshi Kadota and Xian Li
& & Structure& && &13C NMR& &碳谱模拟图
& & 20 .& &&&(5α,7α)-4,5-Epoxy-3,6-dimethoxy-17-methyl-6,14-ethenomorphinan-7-carboxylic Acid 2-{[(3-Methoxyphenyl)amino]carbonyl}hydrazide
& & C30H34N4O6& &&&相似度:51.6%
& & Helvetica Chimica Acta& && && & 2010& && && & 93& && && &
& & Synthesis and Characterization of New 7-Substituted 6,14-Ethenomorphinane Derivatives: N-{5-[(5,7)-4,5-Epoxy-3,6-dimethoxy-17-methyl-6,14-ethenomorphinan-7-yl]-1,3,4-oxadiazol-2-yl}arenamines
& & Serkan Yavuz and Yılmaz Yıldırır
& & Structure& && &13C NMR& &碳谱模拟图
& & 21 .& &&&N-{5-[(5α,7α)-4,5-Epoxy-3,6-dimethoxy-17-methyl-6,14-ethenomorphinan-7-yl]-1,3,4-oxadiazol-2-yl}-3-methoxybenzenamine
& & C30H32N4O5& &&&相似度:51.6%
& & Helvetica Chimica Acta& && && & 2010& && && & 93& && && &
& & Synthesis and Characterization of New 7-Substituted 6,14-Ethenomorphinane Derivatives: N-{5-[(5,7)-4,5-Epoxy-3,6-dimethoxy-17-methyl-6,14-ethenomorphinan-7-yl]-1,3,4-oxadiazol-2-yl}arenamines
& & Serkan Yavuz and Yılmaz Yıldırır
& & Structure& && &13C NMR& &碳谱模拟图
& & 22 .& &&&2-[1-(4-Methoxyphenyl)-9H-β-carbolin-3-yl]-4-(3-nitrobenzylidene)-4H-oxazol-5-one
& & C28H18N4O5& &&&相似度:51.6%
& & Molecules& && && & 2012& && && & 17& && && &
& & Synthesis and Evaluation of New β-Carboline-3-(4-benzylidene)-4H-oxazol-5-one Derivatives as Antitumor Agents
& & Franciele Cristina Savariz, Mary Ann Foglio, João Ernesto de Carvalho, Ana Lúcia T. G. Ruiz, Marta C. T. Duarte, Mauricio Ferreira da Rosa, Emerson Meyer and Maria Helena Sarragiotto
& & Structure& && &13C NMR& &碳谱模拟图
& & 23 .& &&&3-[4-{5-benzyl-2-[4-(N'-hydroxycarbamimidoyl)-phenyl]-5-methyl-4,5-dihydrofuran-3-ylsulfonyl}phenylamino]-N'-hydroxybenzimidamide
& & C32H31N5O5S& &&&相似度:51.6%
& & Bioorganic & Medicinal Chemistry& && && & 2010& && && & 18& && && &
& & Synthesis and evaluation of original amidoximes as antileishmanial agents
& & Ahlem Bouhlel, Christophe Curti, Aurélien Dumètre, Michèle Laget, Maxime D. Crozet, Nadine Azas, Patrice Vanelle
& & Structure& && &13C NMR& &碳谱模拟图
& & 24 .& &&&2-[4-{5-benzyl-2-[4-(N'-hydroxycarbamimidoyl)-phenyl]-5-methyl-4,5-dihydrofuran-3-ylsulfonyl}phenyl-amino]-N'-hydroxybenzimidamide
& & C32H31N5O5S& &&&相似度:51.6%
& & Bioorganic & Medicinal Chemistry& && && & 2010& && && & 18& && && &
& & Synthesis and evaluation of original amidoximes as antileishmanial agents
& & Ahlem Bouhlel, Christophe Curti, Aurélien Dumètre, Michèle Laget, Maxime D. Crozet, Nadine Azas, Patrice Vanelle
& & Structure& && &13C NMR& &碳谱模拟图
& & 25 .& &&&2-[4-{5-benzyl-3-[4-(N'-hydroxycarbamimidoyl)phenylsulfonyl]-5-methyl-4,5-dihydrofuran-2-yl}phenylamino]-N'-hydroxybenzimidamide
& & C32H31N5O5S& &&&相似度:51.6%
& & Bioorganic & Medicinal Chemistry& && && & 2010& && && & 18& && && &
& & Synthesis and evaluation of original amidoximes as antileishmanial agents
& & Ahlem Bouhlel, Christophe Curti, Aurélien Dumètre, Michèle Laget, Maxime D. Crozet, Nadine Azas, Patrice Vanelle
& & Structure& && &13C NMR& &碳谱模拟图
& & 26 .& &&&3-hydroxy-2,11,12-trimethoxy-14-[4-methoxy-3-(methoxymethoxy)phenyl]-6H-[1]benzopyrano[4',3':4,5]pyrrolo[2,1-a]isoquinolin-6-one
& & C31H27NO9& &&&相似度:51.6%
& & Bioorganic & Medicinal Chemistry& && && & 2011& && && & 19& && && &
& & Synthesis, structure–activity relationships, and mechanism of action of anti-HIV-1 lamellarin α 20-sulfate analogues
& & Haruka Kamiyama, Yoshinao Kubo, Hironori Sato, Naoki Yamamoto, Tsutomu Fukuda, Fumito Ishibashi, Masatomo Iwao
& & Structure& && &13C NMR& &碳谱模拟图
& & 27 .& &&&5-{3-hydroxy-2,11,12-trimethoxy-6-oxo-6H-[1]benzopyrano[4',3':4,5]pyrrolo[2,1-a]isoquinolin-14-yl}-2-methoxyphenyl 2,2,2-trichloroethyl sulfate
& & C31H24Cl3NO11S& &&&相似度:51.6%
& & Bioorganic & Medicinal Chemistry& && && & 2011& && && & 19& && && &
& & Synthesis, structure–activity relationships, and mechanism of action of anti-HIV-1 lamellarin α 20-sulfate analogues
& & Haruka Kamiyama, Yoshinao Kubo, Hironori Sato, Naoki Yamamoto, Tsutomu Fukuda, Fumito Ishibashi, Masatomo Iwao
& & Structure& && &13C NMR& &碳谱模拟图
& & 28 .& &&&5-amino-1-(benzothiazol-2'-ylthio)-4-imino-3-(p-methoxy-phenyl)-7-phenyl-3,4-dihydrophthalazine-6,6(7H)-dicarbonitrile hydrochloride
& & C30H22ClN7OS2& &&&相似度:51.6%
& & Journal of Heterocyclic Chemistry& && && & 2011& && && & 48& && && & 241-248
& & Studies with 2-(acetonylthio)benzothiazole: Novel synthesis of pyridazin-6(1H)-one, pyridazin-6(1H)-imine, and phthalazine derivatives of antimicrobial and antifungal activities
& & Fatima A. Al-Omran and Adel A. El-Khair
& & Structure& && &13C NMR& &碳谱模拟图
& & 29 .& &&&lamellarin T
& & C30H27NO9& &&&相似度:51.6%
& & Heterocycles& && && & 2012& && && & 84& && && &
& & Convergent Total Syntheses of the Pentacyclic Lamellarins K, T, U and W via the Addition of Azomethine Ylides to Tethered Tolans
& & Bernard L. Flynn and Martin G. Banwell
& & Structure& && &13C NMR& &碳谱模拟图
& & 30 .& &&&lariciresinol 4'-O-β-D-glucopyranoside
& & C26H34O11& &&&相似度:51.6%
& & Chinese Traditional and Herbal Drugs& && && & 2011& && && & 42& && && & 25-30
& & Lignans and flavonoids from rhizome of Drynaria fortunei
& & LIANG Yong-hong, YE Min, HAN Jian, WANG Bao-rong, GUO De-an
& & Structure& && &13C NMR& &碳谱模拟图
& & 31 .& &&&Janceolaroside A
& & C27H36O12& &&&相似度:51.6%
& & Natural Product Communications& && && & 2011& && && & 6& && && & 749-752
& & Janceolaroside A and Janceoside A, Two New Compounds from the Stems and Roots of Jasminum lanceolarium
& & Lili Lou, Lingfei Han, Dali Meng*, Ning Li and Xian Li
& & Structure& && &13C NMR& &碳谱模拟图
& & 32 .& &&&bastadin 7
& && &&&相似度:50%
& & Journal of Natural Products& && && & 1996& && && & 59& && && &
& & Bastadin 20 and Bastadin O-Sulfate Esters from Ianthella basta: Novel Modulators of the Ry1R FKBP12 Receptor Complex
& & Melanie A. Franklin, Sharron G. Penn, Carlito B. Lebrilla, Tien H. Lam, Isaac N. Pessah, and Tadeusz F. Molinski
& & Structure& && &13C NMR& &碳谱模拟图
& & 33 .& &&&artselaeroside B
& & C37H50O20& &&&相似度:50%
& & Planta Medica& && && & 1998& && && & 64& && && & 720-723
& & Iridoid and Phenyipropanoid Glycosides from Pedicularis artselaeri
& & Bao Ning Su, Lan Ping Ma, and Zhongjian Jia
& & Structure& && &13C NMR& &碳谱模拟图
& & 34 .& &&&(2S)-5,7,2',5'-tetrahydroxy-6-methoxyflavanone 2'-O-β-D-(2-O-feruloyl)glucopyranoside
& & C32H32O15& &&&相似度:50%
& & Chemical & Pharmaceutical Bulletin& && && & 1988& && && & 36& && && &
& & Studies on the Nepalese Crude Drugs. IX. : On the Flavonoid Constituents of the Root of Scutellaria scandens BUCH.-HAM. ex D. DON
& & YUKINORI MIYAICHI,YOSHITAKA IMOTO,TSUYOSHI TOMIMORI and TUSNEO NAMBA
& & Structure& && &13C NMR& &碳谱模拟图
& & 35 .& &&&2(S)-5,7,5'-Trihydroxy-6-methoxy-2'-O-β-D-(2-O-feruloyl)-glucopyranosylflavanone
& & C32H32O15& &&&相似度:50%
& & Chemistry of Natural Compounds& && && & 2002& && && & 38& && && & 473-519
& & PHENOLIC COMPOUNDS OF PLANTS OF THE Scutellaria GENUS. DISTRIBUTION, STRUCTURE, AND PROPERTIES
& & V. M. Malikov and M. P. Yuldashev
& & Structure& && &13C NMR& &碳谱模拟图
& & 36 .& &&&bastadin 25
& & C34H26Br4N4O12S& &&&相似度:50%
& & Journal of Natural Products& && && & 2010& && && & 73& && && &
& & A Bastadin with Potent and Selective δ-Opioid Receptor Binding Affinity from the Australian Sponge Ianthella flabelliformis
& & Anthony R. Carroll, Sonya M. Kaiser, Rohan A. Davis, Roger W. Moni, John N. A. Hooper and Ronald J. Quinn
& & Structure& && &13C NMR& &碳谱模拟图
& & 37 .& &&&15-O-sulfonatobastadin 11
& & C34H26Br4N4O11S& &&&相似度:50%
& & Journal of Natural Products& && && & 2010& && && & 73& && && &
& & A Bastadin with Potent and Selective δ-Opioid Receptor Binding Affinity from the Australian Sponge Ianthella flabelliformis
& & Anthony R. Carroll, Sonya M. Kaiser, Rohan A. Davis, Roger W. Moni, John N. A. Hooper and Ronald J. Quinn
& & Structure& && &13C NMR& &碳谱模拟图
& & 38 .& &&&1-[5-hydroxymethyl-4-(4-{2-methoxy-4-[5-(4-methoxy-phenyl)-3-oxo-penta-1,4-dienyl]-phenoxymethyl}-[1,2,3]triazol-1-yl)-tetrahydro-furan-2-yl]-5-methyl-1H-pyrimidine-2,4-dione
& & C32H33N5O8& &&&相似度:50%
& & Bioorganic & Medicinal Chemistry& && && & 2010& && && & 18& && && &
& & Design, synthesis and in vitro antimalarial evaluation of triazole-linked chalcone and dienone hybrid compounds
& & Eric M. Guantai, Kanyile Ncokazi, Timothy J. Egan, Jiri Gut, Philip J. Rosenthal, Peter J. Smith, Kelly Chibale
& & Structure& && &13C NMR& &碳谱模拟图
& & 39 .& &&&balajaponin E
& & C32H44O16& &&&相似度:50%
& & Planta Medica& && && & 2011& && && & 77& && && & 477-481
& & New Phenylpropanoids and In Vitro α-Glucosidase Inhibitors from Balanophora japonica
& & Tong Zhou, Xiao-hui Zhang, Shu-wei Zhang, Shan-shan Liu, Li-jiang Xuan
& & Structure& && &13C NMR& &碳谱模拟图
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化合物5的匹配度在50%的信息
查询结果：共查到132个化合物(查询结果仅供参考)
& & 1 .& &&&8-oxoepiberberine
& && &&&相似度:70%
& & Chinese Journal of Natural Medicines& && && & 2007& && && & 5& && && & 348-350
& & Isoquinoline Alkaloids from the Rhizoma of Coptis chinensis
& & WANG W ZHANG Qing-W YE Wen-C WANG Yi-Tao
& & Structure& && &13C NMR& &碳谱模拟图
& & 2 .& &&&3-hydroxy-2-methoxy-9,10-methylenedioxy-8-oxoprotoberberine
& & C19H15NO5& &&&相似度:65%
& & Phytotherapy Research& && && & 2010& && && & 24& && && &
& & A new and weakly antispasmodic protoberberine alkaloid from Rhizoma Coptidis
& & Ming Zhao, Yan-Fang Xian, Siu-Po Ip, Harry HS Fong and Chun-Tao Che
& & Structure& && &13C NMR& &碳谱模拟图
& & 3 .& &&&2,3,9,10-dimethylenedioxy-8-oxoprotoberberine
& & C19H13NO5& &&&相似度:60%
& & Planta Medica& && && & 2001& && && & 67& && && & 189-190
& & Isoquinoline Alkaloids from Thalictrum delavayi
& & Mai Li, Xin Chen, Qin-Mei Tang, Jin-Sheng Zhang
& & Structure& && &13C NMR& &碳谱模拟图
& & 4 .& &&&8-Oxo-epiberberine
& & C20H17NO5& &&&相似度:60%
& & Archives of Pharmacal Research& && && & 2006& && && & 29& && && & 757-761
& & Protoberberine alkaloids and their reversal activity of P-gp expressed multidrug resistance (MDR) from the rhizome ofCoptis japonica Makino
& & Yong Deuk Min, Min Cheol Yang, Kyu Ha Lee, Kyung Ran Kim and Sang Un Choi, et al.
& & Structure& && &13C NMR& &碳谱模拟图
& & 5 .& &&&8-Oxocoptisine
& && &&&相似度:60%
& & Archives of Pharmacal Research& && && & 2006& && && & 29& && && & 757-761
& & Protoberberine alkaloids and their reversal activity of P-gp expressed multidrug resistance (MDR) from the rhizome ofCoptis japonica Makino
& & Yong Deuk Min, Min Cheol Yang, Kyu Ha Lee, Kyung Ran Kim and Sang Un Choi, et al.
& & Structure& && &13C NMR& &碳谱模拟图
& & 6 .& &&&compound
& && &&&相似度:60%
& & Bioorganic & Medicinal Chemistry& && && & 1998& && && & 6& && && &
& & Synthesis and activity of bivalent FKBP12 ligands for the regulated dimerization of proteins
& & Terence Keenan, David R. Yaeger, Nancy L. Courage, Carl T. Rollins, Mary Ellen Pavone, Victor M. Rivera, Wu Yang, Tao Guo, Jane F. Amara, Tim Clackson, Michael Gilman, Dennis A. Holt
& & Structure& && &13C NMR& &碳谱模拟图
& & 7 .& &&&9-(3,4-dimethoxyphenyl)-5,9-dihydro-8H-furo[3',4':6,7]naphtho[2,3-d][1,3]dioxol-6-one
& & C21H18O6& &&&相似度:57.1%
& & Journal of Natural Products& && && & 1996& && && & 59& && && & 493-494
& & Lignans from Bupleurum handiense
& & H. López and A. Valera
& & Structure& && &13C NMR& &碳谱模拟图
& & 8 .& &&&methyl 3-{[2-(4-hydroxy-3-methoxyphenyl)imidazo[1,2-a]-pyrimidin-3-yl]amino}benzoate
& & C21H18N4O4& &&&相似度:57.1%
& & Journal of Heterocyclic Chemistry& && && & 2008& && && & 45& && && &
& & First example of the groebke mcr using hydoxybenzal dehydes and substituted 2-aminopyrimidines
& & Anatoliy I. Polyakov,Vera A. Eryomina,Lidiya A. Medvedeva,Nadezhda I. Tihonova and LeoniD. G. Voskressensky
& & Structure& && &13C NMR& &碳谱模拟图
& & 9 .& &&&methyl 2-{[2-(4-hydroxy-3-methoxyphenyl)imidazo[1,2-a]-pyrimidin-3-yl]amino}benzoate
& & C21H18N4O4& &&&相似度:57.1%
& & Journal of Heterocyclic Chemistry& && && & 2008& && && & 45& && && &
& & First example of the groebke mcr using hydoxybenzal dehydes and substituted 2-aminopyrimidines
& & Anatoliy I. Polyakov,Vera A. Eryomina,Lidiya A. Medvedeva,Nadezhda I. Tihonova and LeoniD. G. Voskressensky
& & Structure& && &13C NMR& &碳谱模拟图
& & 10 .& &&&compound 12b
& && &&&相似度:57.1%
& & Bioorganic & Medicinal Chemistry Letters& && && & 2011& && && & 21& && && &
& & Synthesis of substituted triazolyl curcumin mimics that inhibit RANKL-induced osteoclastogenesis
& & Sang-Kyu Park, Sangtae Oh, Hye Kyoung Shin, Seong Hwan Kim, Jungyeob Ham, Jae-Seok Song, Seokjoon Lee
& & Structure& && &13C NMR& &碳谱模拟图
& & 11 .& &&&compound 12j
& && &&&相似度:57.1%
& & Bioorganic & Medicinal Chemistry Letters& && && & 2011& && && & 21& && && &
& & Synthesis of substituted triazolyl curcumin mimics that inhibit RANKL-induced osteoclastogenesis
& & Sang-Kyu Park, Sangtae Oh, Hye Kyoung Shin, Seong Hwan Kim, Jungyeob Ham, Jae-Seok Song, Seokjoon Lee
& & Structure& && &13C NMR& &碳谱模拟图
& & 12 .& &&&compound 12k
& && &&&相似度:56.5%
& & Bioorganic & Medicinal Chemistry Letters& && && & 2011& && && & 21& && && &
& & Synthesis of substituted triazolyl curcumin mimics that inhibit RANKL-induced osteoclastogenesis
& & Sang-Kyu Park, Sangtae Oh, Hye Kyoung Shin, Seong Hwan Kim, Jungyeob Ham, Jae-Seok Song, Seokjoon Lee
& & Structure& && &13C NMR& &碳谱模拟图
& & 13 .& &&&(-)-8-oxo-10-hydroxy-2,3,9-trimethoxyberberine
& & C20H21NO5& &&&相似度:55%
& & Journal of Natural Products& && && & 2009& && && & 72& && && &
& & Constituents of Polyalthia longifolia var. pendula
& & Tzong-Huei Lee, Mei-Jhen Wang, Pi-Yu Chen, Tung-Ying Wu, Wu-Che Wen, Fu-Yu Tsai, and Ching-Kuo Lee
& & Structure& && &13C NMR& &碳谱模拟图
& & 14 .& &&&vitexdoin E
& & C19H16O6& &&&相似度:55%
& & Journal of Natural Products& && && & 2009& && && & 72& && && &
& & Nitric Oxide Scavenging Lignans from Vitex negundo Seeds
& & Cheng-Jian Zheng, Bao-Kang Huang, Ting Han, Qiao-Yan Zhang,Hong Zhang, Khalid Rahman, and Lu-Ping Qin
& & Structure& && &13C NMR& &碳谱模拟图
& & 15 .& &&&denthyrsin
& & C21H18O7& &&&相似度:55%
& & Phytochemistry& && && & 2005& && && & 66& && && &
& & Bi-bicyclic and bi-tricyclic compounds from Dendrobium thyrsiflorum
& & Guang-Nong Zhang, Ling-Yan Zhong, S.W. Annie Bligh, Ying-Li Guo,Chao-Feng Zhang, Mian Zhang, Zheng-Tao Wang, Luo-Shan Xu
& & Structure& && &13C NMR& &碳谱模拟图
& & 16 .& &&&palmarumycin CP17
& & C20H14O5& &&&相似度:55%
& & Journal of Natural Products& && && & 2008& && && & 71(12)& && && &
& & Antileishmanial Constituents of the Panamanian Endophytic Fungus Edenia sp.
& & Sergio Martínez-Luis, Gina Della-Togna, Phyllis D. Coley,Thomas A. Kursar, William H. Gerwick, and Luis Cubilla-Rios
& & Structure& && &13C NMR& &碳谱模拟图
& & 17 .& &&&synthetic 8-oxyberberubine
& && &&&相似度:55%
& & Molecules& && && & 2009& && && & 14& && && & 726-737
& & Total Syntheses of (±)-Gusanlung A, (±)-Gusanlung D and 8-Oxyberberrubine and the Uncertainty Concerning the Structures of (-)-Gusanlung A, (-)-Gusanlung D and 8-Oxyberberrubine
& & Surachai Nimgirawath, Phansuang Udomputtimekakul, Thitima Apornpisarn, Asawin Wanbanjob and Thongchai Taechowisan
& & Structure& && &13C NMR& &碳谱模拟图
& & 18 .& &&&compound 12
& & C21H20O5& &&&相似度:55%
& & Journal of Asian Natural Products Research& && && & 2009& && && & 11& && && & 202-209
& & Isolation and synthesis of a new chromenochalcone and a new chromene from Orthosiphon glabratus
& & Biswanath Das, Ponnaboina Thirupathi, Rathod Aravind Kumar, Akella Venkata Subramanya Sarma and Shaik Jilani Basha
& & Structure& && &13C NMR& &碳谱模拟图
& & 19 .& &&&Olivil
& & C20H24O7& &&&相似度:55%
& & Fitoterapia& && && & 2001& && && & 72& && && & 80-82
& & Lignans from Strophanthus gratus
& & S. Cowan, M. Stewart, D.K. Abbiw, Z. Latif ,S.D. Sarker,U, R.J. Nash
& & Structure& && &13C NMR& &碳谱模拟图
& & 20 .& &&&methylchasnarolid
& & C21H20O7& &&&相似度:55%
& & Journal of Natural Products& && && & 1993& && && & Vol 56& && && & 1177
& & New Lignan Butenolides from Bupleurum salicifolium
& & R. Estévez-Reyes, A. Estévez-Braun, A. G. González
& & Structure& && &13C NMR& &碳谱模拟图
& & 21 .& &&&8-Oxyberberrubine
& & C19H15NO5& &&&相似度:55%
& & Phytochemistry& && && & 1995& && && & 39& && && & 439-442
& & Isoquinoline alkaloids from Acangelisia gusanlung
& & Jin-Sheng Zhang, Louisette Le Men-Olivier, Georges Massiot
& & Structure& && &13C NMR& &碳谱模拟图
& & 22 .& &&&(±)-8-oxohypecorinine
& & C20HI5NO7& &&&相似度:55%
& & Phytochemistry& && && & 1995& && && & 38& && && &
& & (±)-8-oxohypecorinine from Hypecoum procumbens var. glaucescens
& & Hassan-Elrady A. Saad
& & Structure& && &13C NMR& &碳谱模拟图
& & 23 .& &&&Compound 4b
& & C22H20N4O2& &&&相似度:55%
& & Bioorganic & Medicinal Chemistry Letters& && && & 1999& && && & 9& && && &
& & Synthesis and anticonvulsant activity of 3-aryl-5H-2,3-benzodiazepine ampa antagonists
& & Benjamin A. Anderson, Nancy K. Harn, Marvin M. Hansen, Allen R. Harkness, David Lodge, J. David Leander
& & Structure& && &13C NMR& &碳谱模拟图
& & 24 .& &&&fumaramine
& & C21H22N2O6& &&&相似度:55%
& & Phytochemistry& && && & 1980& && && & 19& && && &
& & Fumschleicherine, an alkaloid of Fumaria schleicheri
& & H.G. Kiryakov, Z.H. Mardirossian, Donald W. Hughes, David B. MacLean
& & Structure& && &13C NMR& &碳谱模拟图
& & 25 .& &&&cavidilinine
& & C19H13NO4& &&&相似度:55%
& & Chinese Journal of Natural Medicines& && && & 2009& && && & 7& && && & 414-416
& & A New Alkaloid from the Herb of Corydalis saxicola
& & WANG Qi-Z LIANG Jing-Yu; FENG Xu
& & Structure& && &13C NMR& &碳谱模拟图
& & 26 .& &&&chamaecypanone B
& & C20H16O6& &&&相似度:55%
& & Tetrahedron Letters& && && & 2001& && && & 42& && && &
& & Three novel and one new lignan, chamaecypanones A, B, obtulignolide and isootobanone from the heartwood of Chamaecyparis obtusa var. formosana
& & Yueh-Hsiung Kuo, Chia-Hsien Chen, Yi-Ming Chiang
& & Structure& && &13C NMR& &碳谱模拟图
& & 27 .& &&&compound
& & C18H18O4Cl3& &&&相似度:55%
& & Marine Drugs& && && & 2012& && && & 10& && && &
& & Geographic Variability and Anti-Staphylococcal Activity of the Chrysophaentins and Their Synthetic Fragments
& & Jessica L. Keffer, Jared T. Hammill, John R. Lloyd, Alberto Plaza, Peter Wipf and Carole A. Bewley
& & Structure& && &13C NMR& &碳谱模拟图
& & 28 .& &&&5,6-dihydro-2,3,10,11-tetramethoxyisoquino[1,2-b]quinazolin-8-one
& & C20H20N2O5& &&&相似度:55%
& & Heterocycles& && && & 2002& && && & 57& && && &
& & Controlled Synthesis of Electron Deficient Nitro-1H-benzotriazoles
& & Callum J. McHugh, Daniel R. Tackley, and Duncan Graham*
& & Structure& && &13C NMR& &碳谱模拟图
& & 29 .& &&&1-(2-bromo-4,5-methylenedioxybenzyl)-6,7-dimethoxy1,2,3,4-tetrahydroisoquinoline
& && &&&相似度:55%
& & Journal of the Chinese Chemical Society& && && & 2006& && && & 53& && && & 443-447
& & Synthesis of Thalicthuberine
& & Surachai Nimgirawath* and Suppisak Chaturonrugsamee
& & Structure& && &13C NMR& &碳谱模拟图
& & 30 .& &&&13-oxoprotopine
& & C20H17NO6& &&&相似度:55%
& & Natural Product Communications& && && & 2012& && && & 7& && && & 575-580
& & Phytochemical and Biological Activity Studies of the Bhutanese Medicinal Plant Corydalis crispa
& & Phurpa Wangchuk, Paul A. Keller, Stephen G. Pyne, Thanapat Sastraruji, Malai Taweechotipatr, Roonglawan Rattanajak, Aunchalee Tonsomboon and Sumalee Kamchonwongpaisan
& & Structure& && &13C NMR& &碳谱模拟图
& & 31 .& &&&3-(1,3-benzodioxol-5-yl)-1-(4-methoxyphenyl)-5(-furan-2-yl)-1H-pyrazole
& & C22H18N2O4& &&&相似度:55%
& & European Journal of Organic Chemistry& && && & 2011& && && && && && &
& & Facile Access to 3,5-Dihalogenated Pyrazoles by Sydnone Cycloaddition and their Versatile Functionalization by Pd-Catalyzed Cross-Coupling Processes
& & Thierry Delaunay, Mazen Es-Sayed, Jean-Pierre Vors, Nuno Monteiro and Geneviève Balme
& & Structure& && &13C NMR& &碳谱模拟图
& & 32 .& &&&(Z)-2-[(2-Furyl)methylidene]-5,6-di(2-furyl)-6H-pyran-3-one
& && &&&相似度:55%
& & Journal of Agricultural and Food Chemistry& && && & 2001& && && & 49& && && &
& & Structure Determination of a Novel 3(6H)-Pyranone Chromophore and Clarification of Its Formation from Carbohydrates and Primary Amino Acids
& & O. Frank, S. Heuberger, and T. Hofmann
& & Structure& && &13C NMR& &碳谱模拟图
& & 33 .& &&&dehydrocorydaline
& && &&&相似度:54.5%
& & Journal of Asian Natural Products Research& && && & 2008& && && & 10& && && &
& & Two new protoberberine quaternary alkaloids from Corydalis yanhusuo
& & Xing-Ye Cheng, Yue Shi, Shun-Liang Zheng, Wen Jin and Hong Sun
& & Structure& && &13C NMR& &碳谱模拟图
& & 34 .& &&&compound 13k
& && &&&相似度:54.5%
& & Bioorganic & Medicinal Chemistry Letters& && && & 2011& && && & 21& && && &
& & Synthesis of substituted triazolyl curcumin mimics that inhibit RANKL-induced osteoclastogenesis
& & Sang-Kyu Park, Sangtae Oh, Hye Kyoung Shin, Seong Hwan Kim, Jungyeob Ham, Jae-Seok Song, Seokjoon Lee
& & Structure& && &13C NMR& &碳谱模拟图
& & 35 .& &&&compound 12i
& && &&&相似度:54.1%
& & Bioorganic & Medicinal Chemistry Letters& && && & 2011& && && & 21& && && &
& & Synthesis of substituted triazolyl curcumin mimics that inhibit RANKL-induced osteoclastogenesis
& & Sang-Kyu Park, Sangtae Oh, Hye Kyoung Shin, Seong Hwan Kim, Jungyeob Ham, Jae-Seok Song, Seokjoon Lee
& & Structure& && &13C NMR& &碳谱模拟图
& & 36 .& &&&3-(3,4-dimethoxyphenyl)-1-(5-hydroxy-2,2-dimethyl-2H-chromen-6-yl)-propanone
& & C22H24O5& &&&相似度:52.3%
& & Phytochemistry& && && & 2002& && && & 60& && && & 931-936
& & Isolation and synthesis of chalcones with different degrees of saturation
& & Karsten Krohn, Klaus Steingröver, M. Srinivasa Rao
& & Structure& && &13C NMR& &碳谱模拟图
& & 37 .& &&&(2S)-3',4'-Methylenedioxy-6'',6''-dimethylchromeno-[2'',3'':7,8]-flavanone
& && &&&相似度:52.3%
& & Phytochemistry& && && & 1996& && && & 42& && && &
& & Twenty-three flavonoids from Lonchocarpus subglaucescens
& & Aderbal F. Magalhães, Ana Maria G. Azevedo Tozzi, Beatriz Helena L. Noronha Sales, Eva G. Magalhães
& & Structure& && &13C NMR& &碳谱模拟图
& & 38 .& &&&Paprafumine
& & C22H23NO8& &&&相似度:52.3%
& & Phytochemistry& && && & 1995& && && & 40& && && & 593-596
& & Alkaloidal constituents of Fumaria indica
& & Atta-ur-Rahman, Shakil Ahmad, M. Khalid Bhatti, M. Iqbal Choudhary
& & Structure& && &13C NMR& &碳谱模拟图
& & 39 .& &&&Pyranojacureubin
& && &&&相似度:52.3%
& & Phytochemistry& && && & 1993& && && & 33& && && & 727-728
& & Xanthones from Garcinia forbesii
& & Leslie J. Harrison, Lup-San Leong, Guat-Lee Sia, Keng-Yeow Sim, Hugh T.-W. Tan
& & Structure& && &13C NMR& &碳谱模拟图
& & 40 .& &&&6,8-bis[5-(tert-butyl)-2-furyl]-8H-[1,3]dioxolo[4,5-g][3,1]-benzothiazine
& & C25H27NO4S& &&&相似度:52.3%
& & Journal of Heterocyclic Chemistry& && && & 2008& && && & 45& && && & 475-481
& & Synthesis of 2,4-difuryl-4H-3,1-benzothiazines via a furan ring migration reaction
& & Vladimir T. Abaev,Fatima A. Tsiunchik,Alexander V. Butin and Andrey V. Gutnov
& & Structure& && &13C NMR& &碳谱模拟图
& & 41 .& &&&Compound 2
& && &&&相似度:52.3%
& & Magnetic Resonance in Chemistry& && && & 2009& && && & 47& && && & 523-526
& & Complete assignments of 1H and 13C NMR spectral data for 7, 7′-dihydroarylnaphthalene lignan lactones (pages 523–526)
& & Rosangela da Silva, João Henrique Carvalho Batista, Carine da Silva Maringolo and Paulo Marcos Donate
& & Structure& && &13C NMR& &碳谱模拟图
& & 42 .& &&&taiwanin C
& && &&&相似度:52.3%
& & Magnetic Resonance in Chemistry& && && & 2006& && && & 44& && && & 727-730
& & Complete assignments of 1H and 13C NMR data for seven arylnaphthalide lignans from Justicia procumbens (pages 727–730)
& & Meihua Yang, Jun Wu, Fan Cheng and Yuan Zhou
& & Structure& && &13C NMR& &碳谱模拟图
& & 43 .& &&&Dehydrocorydaline
& && &&&相似度:52.3%
& & Journal of China Pharmaceutical University& && && & 2002& && && & 33& && && & 483-486
& & Alkaloids from Rhizoma corydalis
& & XU Xiang-H WANG Zheng-T YU Guo-D RUAN Bi-F LI Jun
& & Structure& && &13C NMR& &碳谱模拟图
& & 44 .& &&&3-(benzo[d][1,3]dioxol-5-yl)-7-hydroxy-6-(3-methylbut-2-enyl)-4H-chromen-4-one
& & C21H17NO5& &&&相似度:52.3%
& & Bioorganic & Medicinal Chemistry& && && & 2010& && && & 18& && && & 249-266
& & The synthesis and evaluation of flavone and isoflavone chimeras of novobiocin and derrubone
& & Jared R. Mays, Stephanie A. Hill, Justin T. Moyers, Brian S.J. Blagg
& & Structure& && &13C NMR& &碳谱模拟图
& & 45 .& &&&compound 26a
& & C21H16O6& &&&相似度:52.3%
& & European Journal of Organic Chemistry& && && & 2011& && && && && && &
& & Synthesis of Biologically Active Nonnatural Palmarumycin Derivatives
& & Abdulselam Aslan, Sultan Altun, Ishtiaq Ahmed, Ulrich Flörke, Barbara Schulz and Karsten Krohn
& & Structure& && &13C NMR& &碳谱模拟图
& & 46 .& &&&ethyl 3-(3,5-bis(4-hydroxy-3-methoxystyryl)isoxazol-4-yl)propanoate
& & C26H27NO7& &&&相似度:52.1%
& & Bioorganic & Medicinal Chemistry& && && & 2009& && && & 17& && && & 360-367
& & Synthesis and evaluation of electron-rich curcumin analogues
& & Michael W. Amolins, Laura B. Peterson, Brian S.J. Blagg
& & Structure& && &13C NMR& &碳谱模拟图
& & 47 .& &&&compound 26c
& & C24H20O6& &&&相似度:52.1%
& & European Journal of Organic Chemistry& && && & 2011& && && && && && &
& & Synthesis of Biologically Active Nonnatural Palmarumycin Derivatives
& & Abdulselam Aslan, Sultan Altun, Ishtiaq Ahmed, Ulrich Flörke, Barbara Schulz and Karsten Krohn
& & Structure& && &13C NMR& &碳谱模拟图
& & 48 .& &&&phyllanthusmin A
& & C21H16O7& &&&相似度:50%
& & Chemical & Pharmaceutical Bulletin& && && & 2006& && && & 54(8)& && && &
& & Cytotoxic Arylnaphthalene Lignans from Phyllanthus oligospermus
& & Shwu-Jen WU,and Tian-Shung WU
& & Structure& && &13C NMR& &碳谱模拟图
& & 49 .& &&&artekeiskeanol B
& & C20H24O5& &&&相似度:50%
& & Journal of Natural Products& && && & 2001& && && & 64& && && &
& & Four New Coumarin Derivatives from Artemisia keiskeana
& & Jong Hwan Kwak, Kyung Bok Lee,and Francis J. Schmitz
& & Structure& && &13C NMR& &碳谱模拟图
& & 50 .& &&&3-(4-hydroxy-3-methoxyphenyl)-2-hydroxymethyl-8-methoxy-2,3-dihydrobenzo[1,4]dioxine-6-carbaldehyde
& & C18H16O7& &&&相似度:50%
& & Journal of Natural Products& && && & 2000& && && & 63& && && &
& & Synthesis and Structures of Regioisomeric Hydnocarpin-Type Flavonolignans
& & Nathan R. Guz and Frank R. Stermitz
& & Structure& && &13C NMR& &碳谱模拟图
& & 51 .& &&&justicidin A
& && &&&相似度:50%
& & Journal of Natural Products& && && & 1999& && && & 62& && && &
& & Cytotoxic Lignans of Justicia ciliata
& & Shiow-Hwa Day, Nien-Yung Chiu, Shen-Jeu Won, and Chun-Nan Lin
& & Structure& && &13C NMR& &碳谱模拟图
& & 52 .& &&&fissilandione
& & C19H15NO5& &&&相似度:50%
& & Journal of Natural Products& && && & 1998& && && & 61& && && &
& & Two p-Quinonoid Aporphine Alkaloids from Fissistigma balansae
& & Yi-Chen Chia, Fang-Rong Chang, and Yang-Chang Wu
& & Structure& && &13C NMR& &碳谱模拟图
& & 53 .& &&&garcibiphenyl D
& & C18H20O4& &&&相似度:50%
& & Planta Medica& && && & 2006& && && & 72& && && & 473-477
& & Benzopyrans, Biphenyls and Xanthones from the Root of Garcinia linii and their Activity against Mycobacterium tuberculosis
& & Chen, Jih-J Peng, Chien-F Huang, Hung-Yi; Chen, Ih-Sheng
& & Structure& && &13C NMR& &碳谱模拟图
& & 54 .& &&&9-methyldecumbenine C
& & C20H13NO6& &&&相似度:50%
& & Planta Medica& && && & 2009& && && & 75& && && & 547-549
& & A New Alkaloid from Corydalis hendersonii
& & Yu Fu, Yan Zhou, Xun Liao, Bingru Bai, Shulin Peng, Lisheng Ding
& & Structure& && &13C NMR& &碳谱模拟图
& & 55 .& &&&hortiolone
& && &&&相似度:50%
& & Planta Medica& && && & 1982& && && && && && & 250-251
& & Carbon-13 Spectral Data of Prenylated Coumarins
& & Marcello Nicoletti, Franco Delle Monache and Giovanni Battista MariniBettoI
& & Structure& && &13C NMR& &碳谱模拟图
& & 56 .& &&&kaerophyllin
& & C21H20O6& &&&相似度:50%
& & Planta Medica& && && & 1981& && && & 43& && && & 378-380
& & Kaerophyllin, A New Lignan from Chaerophyllum maculatum
& & G. A. Mikaya, O. G. Turabelidze, E. P. Kemertelidze and N. S. Wulfson
& & Structure& && &13C NMR& &碳谱模拟图
& & 57 .& &&&4-methyl-2,9-dioxo-8,9-dihydro-2H-furo[2,3-h]chromen-8-ylcarboxyloate
& & C19H12O6& &&&相似度:50%
& & Chinese Chemical Letters& && && & 2008& && && & 19& && && & 791-794
& & Studies on the esterifications of 9-(hydroxyimino)-4-methyl-8,9-dihydrofuro[2,3-h]chromen-2-one with acid chlorides under different cond tions
& & Ru Shu Sun, Yang Wang, Peng Xia
& & Structure& && &13C NMR& &碳谱模拟图
& & 58 .& &&&2-[(5,6-Dimethoxybenzofuran-2-carbonyl)-amino]benzoic acid methyl ester
& & C19H17NO6& &&&相似度:50%
& & Molecules& && && & 2002& && && & 7& && && & 353-362
& & Synthesis}