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bacel1213ͳæ (³õÈëÎÄ̳)
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ÇóÁ½¸ö»¯ºÏÎï΢Æ× ÒÑÓÐ1È˲ÎÓë
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»¯ºÏ1 K18-22 CDCl3 CÆ×£º14.2, 40.8, 44.1, 45.3, 56.3, 60.8, 71.4, 72.8, 101.4, 106.3, 108.5, 109.8, 131.2, 133.3, 135.5, 147.7, 147.8, 152.6, 174.5 »¯ºÏ2 E52-G1 d6-DMSO CÆ×£º19.3, 26.0, 53.8, 60.3, 60.8, 65.0, 71.8, 106.0, 106.3, 110.7, 113.1, 116.3, 123.9, 126.9, 128.5, 129.0, 134.0, 134.7, 134.8, 150.1, 151.8, 152.1, 154.9, 155.7, 174.9, 175.6 |
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1 . ¹í¾Ê¶¾ËØ ÏàËÆ¶È:94.7% Chinese Traditional and Herbal Drugs 2010 41 1619-1622 ÌÒ¶ùÆß»¯Ñ§³É·ÖºÍϸ°û¶¾ÐÔÑо¿ ³ÂÓиù;ÕÅÀö·¼;ÁõÓý³½;Íõ±ÌËÉ;½ðöÎ;¸µÐÀÍ®;Öܽ¨Æ½;¹ùºé×£ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . (-)-podophyllotoxin ÏàËÆ¶È:94.7% Chinese Pharmaceutical Journal 2014 49 1306-1309 Lignans Constituents from Callus Culture of Dysosma versipellis DUAN Rui-gang, LI Jun-wei, ZOU Jian-hua*, LI Qiu-hong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . podophyllotoxin ÏàËÆ¶È:89.4% Natural Product Research and Development 2005 17 588-591 Chemical Constituents of Sabina vulgaris Antoine WANG Wu-bao; BA Hang; HAJIA Aisa; LIAO Li-xin; DUO Li-kun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . Podophyllotoxin ÏàËÆ¶È:89.4% Molecules 2012 17 9506-9519 Cytotoxic Podophyllotoxin Type-Lignans from the Steam Bark of Bursera fagaroides var. fagaroides Andr¨¦s M. Rojas-Sep¨²lveda, Mario Mendieta-Serrano, Mayra Y. Ant¨²nez Mojica, Enrique Salas-Vidal, Silvia Marquina, Mar¨ªa Luisa Villarreal, Ana Mar¨ªa Puebla, Jorge I. Delgado and Laura Alvarez Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . Podophyllotoxin C22H22O8 ÏàËÆ¶È:89.4% Helvetica Chimica Acta 1994 77 771-777 A Novel Rearrangement Product of Podophyllotoxone ¨C Ester Derivatives and in vitro cytotoxicity studies Peter H. Höfert and Rudolf Matusch Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . podophyllotoxin ÏàËÆ¶È:85.7% Phytochemistry 1980 19 1527-1530 13C NMR analysis of podophyllotoxin and some of its derivatives Sebasti¨¢o F. Fonseca, Edmundo A. R¨²veda, James D. McChesney Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . Desoxypodophyllotoxin ÏàËÆ¶È:85% Molecules 2012 17 9506-9519 Cytotoxic Podophyllotoxin Type-Lignans from the Steam Bark of Bursera fagaroides var. fagaroides Andr¨¦s M. Rojas-Sep¨²lveda, Mario Mendieta-Serrano, Mayra Y. Ant¨²nez Mojica, Enrique Salas-Vidal, Silvia Marquina, Mar¨ªa Luisa Villarreal, Ana Mar¨ªa Puebla, Jorge I. Delgado and Laura Alvarez Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . ¹í¾Ê¶¾ËØ ÏàËÆ¶È:84.2% Journal of Anhui Agricultural Sciences 2011 39 19781-19782 Chemical Components of CHINESE UMBRELLALEAF RHIZOME AND ROOT in Taibai Mountains MA Yang-min et al Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . Podophyllotoxin C22H22O8 ÏàËÆ¶È:84.2% Journal of Separation Science 2013 36 1022-1028 Novel linear and step-gradient counter-current chromatography for bio-guided isolation and purification of cytotoxic podophyllotoxins from Dysosma versipellis (Hance) (pages 1022¨C1028) Zhi Yang, Xiaoman Liu, Kuiwu Wang, Xiaoji Cao and Shihua Wu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . compound ÏàËÆ¶È:81.8% Phytochemistry 1998 49 491-496 Production of Podophyllotoxin in Juniperus Chinensis Callus Cultures Treated with Oligosaccharides and a Biogenetic Precursor in Honour of Professor G. H. Neil Towers 75th Birthday Toshio Muranak¦Á, Masaru Miyat¦Á, Kazutaka Ito, Sanro Tachibana Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . podophyllotoxin C22H22O8 ÏàËÆ¶È:81.8% Journal of Wood Science 1998 44 397-400 Extractives of Juniperus chinensis L. I: Isolation of podophyllotoxin and yatein from the leaves of J.chinensis Masaru Miyata, Kazutaka Itoh, Santo Tachibana Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 4'-demethylpodophyllotoxin ÏàËÆ¶È:80% Journal of the Indian Chemical Society 1997 74 692-694 Carbon-13NMR Chemical Shifts of some Podophyllum Lignans and Analogues JAYATI MITERA and ALOK KUMAR MITRA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . podophyllotoxin C22H20O8 ÏàËÆ¶È:78.9% Journal of Yunnan University 2006 28 521-525 Study on lignans of Dysosma versipellis ZHU Pei-fang, WANG Yun-song, ZHAO Jing-feng, ZHANG Hong-bin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . podophyllotoxin ÏàËÆ¶È:76.1% Journal of the Indian Chemical Society 1997 74 692-694 Carbon-13NMR Chemical Shifts of some Podophyllum Lignans and Analogues JAYATI MITERA and ALOK KUMAR MITRA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . Acetyl podophyllotoxin ÏàËÆ¶È:76.1% Molecules 2012 17 9506-9519 Cytotoxic Podophyllotoxin Type-Lignans from the Steam Bark of Bursera fagaroides var. fagaroides Andr¨¦s M. Rojas-Sep¨²lveda, Mario Mendieta-Serrano, Mayra Y. Ant¨²nez Mojica, Enrique Salas-Vidal, Silvia Marquina, Mar¨ªa Luisa Villarreal, Ana Mar¨ªa Puebla, Jorge I. Delgado and Laura Alvarez Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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2222222222222222 1 . (E)-(3,4,5-Trimethoxy)-{2'-(p-toluenesulfonyloxy)-3'-[(tertbutyldiphenylsilyl)oxy]}stilbene C41H45O8SSi ÏàËÆ¶È:57.6% Journal of Natural Products 2010 73 1093-1101 Regio- and Stereospecific Synthesis of Mono-¦Â-d-Glucuronic Acid Derivatives of Combretastatin A-1 Regio- and Stereospecific Synthesis of Mono-¦Â-d-Glucuronic Acid Derivatives of Combretastatin A-1 Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . (Z)-(3,4,5-Trimethoxy)-{2'-(p-toluenesulfonyloxy)-3'-[(tertbutyldiphenylsilyl)oxy]}stilbene C41H44O8SSi ÏàËÆ¶È:53.8% Journal of Natural Products 2010 73 1093-1101 Regio- and Stereospecific Synthesis of Mono-¦Â-d-Glucuronic Acid Derivatives of Combretastatin A-1 Regio- and Stereospecific Synthesis of Mono-¦Â-d-Glucuronic Acid Derivatives of Combretastatin A-1 Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . compound 10 ÏàËÆ¶È:53.8% Tetrahedron Letters 2003 44 5289-5292 A concise and general methodology for the complete asymmetric synthesis of the orthogonally protected 2-amino-1,3,4-butanetriols (ABTs) Om V Singh, Hyunsoo Han Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 5-Fluoro-2-[5-(isopropylthio)-4-phenyl-4H-1,2,4-triazol-3-yl]-1-methyl-3-[(3-methylpiperidin-1-yl)methyl]-1H-indole C27H32FN5S ÏàËÆ¶È:53.8% European Journal of Medicinal Chemistry 2013 69 125-138 Identification and characterization of novel indole based small molecules as anticancer agents through SIRT1 inhibition Original Research Article Naveen Panathur, Udayakumar Dalimba, Pulla Venkat Koushik, Mallika Alvala, Perumal Yogeeswari, Dharmarajan Sriram, Vijith Kumar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 5-(3,4-Difluorophenyl)-3-cyclopropylimino-2-(2-methoxy-3-pyridyl)amino-3,5-dihydrophenazine C27H21F2N5O ÏàËÆ¶È:53.8% Molecules 2014 19 4380-4394 Synthesis and Biological Evaluation of Novel 2-Methoxypyridylamino-Substituted Riminophenazine Derivatives as Antituberculosis Agents Dongfeng Zhang, Yang Liu, Chunlin Zhang, Hao Zhang, Bin Wang, Jian Xu, Lei Fu, Dali Yin, Christopher B. Cooper, Zhenkun Ma, Yu Lu and Haihong Huang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . cambodianin B C27H28O7 ÏàËÆ¶È:51.8% Planta Medica 2011 77 2053-2056 Cytotoxic and Antibacterial Flavonoids from Dragon's Blood of Dracaena cambodiana Luo, Ying; Wang, Hui; Zhao, You-Xing; Zeng, Yan-Bo; Shen, Hai-Yan; Dai, Hao-Fu; Mei, Wen-Li: Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . N-(2,6-dimethylphenyl)-2-(6-methoxy-7-(3-morpholinopropoxy)quinazolin-4-ylamino)benzo[d]thiazole-6-carboxamide C32H34N6O4S ÏàËÆ¶È:51.8% European Journal of Medicinal Chemistry 2013 63 702-712 Design and synthesis of novel 4-benzothiazole amino quinazolines Dasatinib derivatives as potential anti-tumor agents Jin Cai, Min Sun, Xiaoqing Wu, Junqing Chen, Peng Wang, Xi Zong, Min Ji Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 5-(3,4-Difluorophenyl)-3-(4-tetrahydropyranyl)imino-2-(2-methoxy-3-pyridyl)amino-3,5-dihydrophenazine C29H25F2N5O2 ÏàËÆ¶È:51.8% Molecules 2014 19 4380-4394 Synthesis and Biological Evaluation of Novel 2-Methoxypyridylamino-Substituted Riminophenazine Derivatives as Antituberculosis Agents Dongfeng Zhang, Yang Liu, Chunlin Zhang, Hao Zhang, Bin Wang, Jian Xu, Lei Fu, Dali Yin, Christopher B. Cooper, Zhenkun Ma, Yu Lu and Haihong Huang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . methyl (2R,3S)-2-((4-methoxybenzyloxy)methyl)-3-(2-(2-(allyloxycarbonyl)-3,5,6-trimethoxy-4-methylphenyl)-1-(diethyl(isopropyl)silyloxy) ethyl)aziridine-1-carboxylate ÏàËÆ¶È:51.7% Heterocycles 2006 67 597-619 Improved Syntheses of the FR900482 and Mitomycin Benzazocine Ring Core via Mitsunobu Cyclization Pascal Ducept, Daniel A. Gubler, and Robert M. Williams* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 3-Bromo-4,4',5-trimethoxy-3'-O-tert-butyldiphenylsilyl-Z-stilbene C33H35O4SiBr2 ÏàËÆ¶È:50% Journal of Natural Products 2005 68 1450-1458 Antineoplastic Agents. 509. Synthesis of Fluorcombstatin Phosphate and Related 3-Halostilbenes George R. Pettit, Mathew D. Minardi, Heidi J. Rosenberg, Ernest Hamel, Michael C. Bibby, Sandie W. Martin, M. Katherine Jung, Robin K. Pettit, Timothy J. Cuthbertson, and Jean-Charles Chapuis Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

3Â¥2015-02-27 14:12:22
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4Â¥2015-02-27 15:16:23
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1 . Ethyl 10-cyclopropyl-5-fluoro-2-methyl-7-oxo-3-(phenyldiazenyl)-7,10-dihydropyrido-[2,3-f]quinoxaline-8-carboxylate C24H20FN5O3 ÏàËÆ¶È:59.0% Zeitschrift f¨¹r Naturforschung B 2007 62 1045-1051 Synthesis of Some Ethyl 3-(Aryldiazenyl)-7-oxo-dihydropyrido[2,3-f]quinoxaline-8-carboxylates J. A. Zahra, M. A. Khanfar, M. M. El-Abadelah, B. A. A. Thaher, N. S. El-Abadla, and W. Voelter Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 3-(2-benzofuryl)azuleno[1,2-c]thiophene-9-carbonitrile C21H11NOS ÏàËÆ¶È:59.0% Heterocycles 2002 58 405-419 A New Synthetic Approach to Azuleno[1,2-c]thiophenes Kimiaki Imafuku* and Dao-Lin Wang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . N-(2-(4-Chlorophenylamino)pyridin-3-yl)-2-(3,4,5-trimethoxyphenylamino)nicotinamide C26H24O4N5Cl ÏàËÆ¶È:59.0% Bioorganic & Medicinal Chemistry 2014 22 6755-6767 Synthesis of 2-anilinopyridine dimers as microtubule targeting and apoptosis inducing agents Ahmed Kamal, S.M. Ali Hussaini, V. Lakshma Nayak, M. Shaheer Malik, M. Lakshmi Sucharitha, Thokhir Basha Shaik, Md. Ashraf, Chandrakant Bagul Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . (E)-pent-2-en-4-ynoic acid [4-(3-chloro-4-fluorophe-nylamino)-3-cyano-7-ethoxyquinolin-6-yl]-amide C23H16N4O2FCl ÏàËÆ¶È:56.5% Bioorganic & Medicinal Chemistry 2010 18 6634-6645 Development of a new epidermal growth factor receptor positron emission tomography imaging agent based on the 3-cyanoquinoline core: Synthesis and biological evaluation Federica Pisaneschi, Quang-De Nguyen, Elham Shamsaei, Matthias Glaser, Edward Robins, Maciej Kaliszczak, Graham Smith, Alan C. Spivey, Eric O. Aboagye Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 5-(3,4-Difluorophenyl)-3-cyclopropylimino-2-(2-methoxy-3-pyridyl)amino-3,5-dihydrophenazine C27H21F2N5O ÏàËÆ¶È:56% Molecules 2014 19 4380-4394 Synthesis and Biological Evaluation of Novel 2-Methoxypyridylamino-Substituted Riminophenazine Derivatives as Antituberculosis Agents Dongfeng Zhang, Yang Liu, Chunlin Zhang, Hao Zhang, Bin Wang, Jian Xu, Lei Fu, Dali Yin, Christopher B. Cooper, Zhenkun Ma, Yu Lu and Haihong Huang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 7-hydroxy-4-methoxy-phenanthrene-2-O-¦Â-D-glucoside ÏàËÆ¶È:54.5% China Journal of Chinese Materia Medica 2005 30 1827-1830 Chemical constituents from tuber of Cremastra appendiculata Xia Wenbin, XUE Zhen, LI Shuai, WANG Sujuan, YANG Yongchun, HE Dingxiang, RAN Guanglun, KONG Lingzhong, SHI Jiangong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 1-benzyloxy-8,9-methylenedioxyphenanthridine ÏàËÆ¶È:54.5% Phytochemistry 1996 41 323-326 Alkaloids from Crinum firmifolium var. hygrophilum Judith Razafimbelo, Marta Andriantsiferana, Genevieve Baudouin, François Tillequin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 4d C22H19N5O3 ÏàËÆ¶È:54.5% Journal of Heterocyclic Chemistry 2006 43 1513-1521 Synthesis of ethyl 6-aryl-4-oxo-4,6-dihydro-1(12)(13)h-pyrimido-[2',1':4,5][1,3,5]triazino[1,2-a]benzimidazole-3-carboxylates Anton V. Dolzhenko,Wai-Keung Chui and Anna V. Dolzhenko Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 8r C21H19BrO5 ÏàËÆ¶È:54.5% Archiv der Pharmazie 1997 330 215-224 Synthesis and Antitumour Activity of New Derivatives of Flavone-8-acetic Acid (FAA). Part 2: Ring-Substituted Derivatives R. Alan Aitken, Michael C. Bibby, John A. Double, Andrea L. Laws, Robert B. Ritchie and David W. J. Wilson Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

5Â¥2015-02-27 15:48:57














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