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xzhfood: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2014-01-11 23:08:40
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1 . methyl 17-hydroxydocosanoate C23H46O3 ÏàËÆ¶È:72.7% Journal of Natural Products 2002 65 108-114 Emmyguyacins A and B: Unusual Glycolipids from a Sterile Fungus Species That Inhibit the Low-pH Conformational Change of Hemagglutinin A during Replication of Influenza Virus Christie Boros, Barry Katz, Scott Mitchell, Cedric Pearce, Karra Swinbank, and Debra Taylor Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 9,10-dihydroxystearic acid ethyl ester C23H44O4 ÏàËÆ¶È:68.1% Steroids 2008 73 1098-1109 Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1] Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Compound 2 C33H63NO5 ÏàËÆ¶È:68.1% Bioorganic & Medicinal Chemistry Letters 2007 17 3426-3430 Annonaceous acetogenin mimics bearing a terminal lactam and their cytotoxicity against cancer cells Hai-Xia Liu, Guo-Rui Huang, Huan-Ming Zhang, Jia-Rui Wu, Zhu-Jun Yao Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 2-(13-methyl)-tridecanecaproate ÏàËÆ¶È:68.1% Chinese Traditional and Herbal Drugs 2010 41 1421-1423 Chemical constituents of Toosendan Fructus(¢ñ) ZHOU Ying; WANG Hui-juan; GUO Dong-gui; WANG Zheng-lin; ZHU Xun; HU Fang; LI Zhou-yang Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ethyl 10,16-dihydroxyhexadecanoate ÏàËÆ¶È:68.1% molecules 2011 16 4923-4936 Derivatives of 10,16-Dihydroxyhexadecanoic Acid Isolated from Tomato (Solanum lycopersicum) as Potential Material for Aliphatic Polyesters Daniel Arrieta-Baez, Miguel Cruz-Carrillo, Mayra Beatriz G¨®mez-Patiño and L. Gerardo Zepeda-Vallejo Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Compound 4 C35H67NO5 ÏàËÆ¶È:65.2% Bioorganic & Medicinal Chemistry Letters 2007 17 3426-3430 Annonaceous acetogenin mimics bearing a terminal lactam and their cytotoxicity against cancer cells Hai-Xia Liu, Guo-Rui Huang, Huan-Ming Zhang, Jia-Rui Wu, Zhu-Jun Yao Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (¡À)-1-(Tetrahydrofuran-2-yl)-tridecanol C17H34O2 ÏàËÆ¶È:64% Archiv der Pharmazie 2003 336 381-384 Syntheses of 2,5-Dialkylfuran and Tetrahydrofuran Carbinols and Their Cytotoxic Activity J¨¹rgen Krauss, Doris Unterreitmeier and Dorothee Antlsperger Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . nerifol [methyl (8,16)-dihydroxyhexadecanoate] C17H34O4 ÏàËÆ¶È:63.6% Planta Medica 1987 53 47-49 Isolation and Structure of Neriumol and Nerifol from the Leaves of Nerium odorum Salimuzzaman Siddiqui, Sabira Begum, Farrukh Hafeez and Bina S. Siddiqui Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Methyl 10-ketolactobacillate (Methyl (Z)-10-(2-hexylcyclopropane-1-yl)-10-oxodecanoate) C20H36O3 ÏàËÆ¶È:63.6% Organic Letters 2006 Vol. 8, No. 1 79-81 Configurational Analysis of Cyclopropyl Fatty Acids Isolated from Escherichia coli Laura J. Stuart, James P. Buck, Amy E. Tremblay, and Peter H. Buist Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Methyl 13-ketolactobacillate (Methyl (Z)-10-(2-(1-oxo)-hexylcyclopropane-1-yl)-decanoate) C20H36O3 ÏàËÆ¶È:63.6% Organic Letters 2006 Vol. 8, No. 1 79-81 Configurational Analysis of Cyclopropyl Fatty Acids Isolated from Escherichia coli Laura J. Stuart, James P. Buck, Amy E. Tremblay, and Peter H. Buist Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 10,13-Dimethyl-9-tetradecen-1-ol C16H32O ÏàËÆ¶È:63.6% |

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²éѯ½á¹û£º¹²²éµ½22¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Acetonide of 9,1'-dihydroxy-methyl-12-acetylricinoleic acid C24H44O6 ÏàËÆ¶È:56.5% Bioorganic & Medicinal Chemistry 2011 19 384-392 Antioxidant, anti-inflammatory and anti-hyperglycaemic activities of heterocyclic homoprostanoid derivatives S. A. Manohara Reddy, Jayesh Mudgal, Punit Bansal, S. G. Vasanthraju, K. K. Srinivasan,C. Mallikarjuna Rao, N. Gopalan Kutty Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 1,2-di-(11'-hydroxyundecanoyl)-sn-glycero-3-dithiophosphocholine C30H60NO8PS2 ÏàËÆ¶È:55.5% The Journal of Organic Chemistry 2003 68 7298-7307 Design, Synthesis, and Evaluation of Water-Soluble Phospholipid Analogues as Inhibitors of Phospholipase C from Bacillus cereus Christopher L. Franklin, Hui Li, and Stephen F. Martin Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 6,6-Dichloro-3-[2-cyclohexyl-2-(3-cyclohexyl-ureido)-acetyl]-3-aza-bicyclo[3.1.0]hexane-2-carboxylic acid(2-car-bamoyl-1-cyclobutylmethyl-2-oxo-ethyl)-amide C29H43N5O5Cl2 ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry 2008 16 1874-1883 Potent and selective small molecule NS3 serine protease inhibitors of Hepatitis C virus with dichlorocyclopropylproline as P2 residue Kevin X. Chen, Bancha Vibulbhan, Weiying Yang, Kuo-Chi Cheng, Rong Liu, John Pichardo, Nancy Butkiewicz, F. George Njoroge Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . sinularone I C21H36O5 ÏàËÆ¶È:54.5% Marine Drugs 2012 10 1331-1344 Sinularones A¨CI, New Cyclopentenone and Butenolide Derivatives from a Marine Soft Coral Sinularia sp. and Their Antifouling Activity Haiyan Shi, Shanjiang Yu, Dong Liu, Leen van Ofwegen, Peter Proksch and Wenhan Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Comound 1g ÏàËÆ¶È:54.1% Magnetic Resonance in Chemistry 2007 45 93-98 1H and 13C NMR spectral assignment of alkyl and polyamine-linked bis(2-thioxo-[1, 3, 5]-thiadiazinan-3-yl) carboxylic acids (pages 93¨C98) Dolores Molero, Julieta Coro, Rolando P¨¦rez, Margarita Su¨¢rez, Roberto Mart¨ªnez-¨¢lvarez, Antonio Herrera and Nazario Mart¨ªn Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (2R)-SQDG ÏàËÆ¶È:52.1% Tetrahedron Letters 2000 41 4403-4407 Structural determination of sulfoquinovosyldiacylglycerol by chiral syntheses Shinya Hanashima, Yoshiyuki Mizushina, Takayuki Yamazaki, Keisuke Ohta, Shunya Takahashi, Hiroyuki Koshino, Hiroeki Sahara, Kengo Sakaguchi, Fumio Sugawara Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 1,3-Dihydroxy-5-(12-hydroxyheptadecyl)benzene C23H40O3 ÏàËÆ¶È:52.1% The Journal of Antibiotics 2008 61 192-194 New Sulfoalkylresorcinol from Marine-derived Fungus, Zygosporium sp. KNC52 Kaneo Kanoh, Kyoko Adachi, Satoru Matsuda, Yoshikazu Shizuri, Ko Yasumoto, Takenori Kusumi, Kayo Okumura and Teruo Kirikae Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 3-(2-tert-Butoxycarbonylamino-2-cyclohexyl-acetyl)-6,6-dichloro-3-aza-bicyclo[3.1.0]hexane-2-carboxylic acid C19H28N2O5Cl2 ÏàËÆ¶È:52% Bioorganic & Medicinal Chemistry 2008 16 1874-1883 Potent and selective small molecule NS3 serine protease inhibitors of Hepatitis C virus with dichlorocyclopropylproline as P2 residue Kevin X. Chen, Bancha Vibulbhan, Weiying Yang, Kuo-Chi Cheng, Rong Liu, John Pichardo, Nancy Butkiewicz, F. George Njoroge Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (-)-Pinellic Acid ÏàËÆ¶È:50% Helvetica Chimica Acta 2009 92 2052-2057 Synthesis of (-)-Pinellic Acid and Its (9R,12S,13S)-Diastereoisomer Gowravaram Sabitha, Martha Bhikshapathi, Erigala Venkata Reddy, Jhillu S. Yadav Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 1 C25H52N10O3 ÏàËÆ¶È:50% Journal of Natural Products 1995 Vol 58 843-847 Isolation and Structure of Two Novel Muscarinic Receptor Antagonists Vinod R. Hegde, Jack E. Silver, Mahesh G. Patel, Vincent P. Gullo, Pradip R. Das, Mohindar S. Puar Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Bis{2-[(10-Hydroxydecyl)oxy]ethyl} ester of 9-[2-(phosphonomethoxy)ethyl]adenine C32H59N5O8P ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2011 19 3527-3539 New prodrugs of Adefovir and Cidofovir Tom¨¢š Tichy, Graciela Andrei, Martin Drač¨ªnsky, Anton¨ªn Holy, Jan Balzarini ,Robert Snoeck , Marcela Krečmerov¨¢ Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (2S)-SQDG ÏàËÆ¶È:50% Tetrahedron Letters 2000 41 4403-4407 Structural determination of sulfoquinovosyldiacylglycerol by chiral syntheses Shinya Hanashima, Yoshiyuki Mizushina, Takayuki Yamazaki, Keisuke Ohta, Shunya Takahashi, Hiroyuki Koshino, Hiroeki Sahara, Kengo Sakaguchi, Fumio Sugawara Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 6,7,10-trihydroxy-8-octadecenoic acid ÏàËÆ¶È:50% China Journal of Chinese Materia Medica 2010 35 865-868 Chemical constituents from Myricaria alopecuroides LI Zhanjun; XUE Peifeng; XIE Hongxia; LI Xiaojuan; XIE Min Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 6,6-Dichloro-3-aza-bicyclo[3,1,0]hexane-2,3-dicar-boxylic acid di-tert-butyl ester C15H23NO4Cl2 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2008 16 1874-1883 Potent and selective small molecule NS3 serine protease inhibitors of Hepatitis C virus with dichlorocyclopropylproline as P2 residue Kevin X. Chen, Bancha Vibulbhan, Weiying Yang, Kuo-Chi Cheng, Rong Liu, John Pichardo, Nancy Butkiewicz, F. George Njoroge Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . SQGD C37H69O12SNa ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry Letters 2010 20 6699-6702 Identification of a sulfonoquinovosyldiacylglyceride from Azadirachta indica and studies on its cytotoxic activity and DNA binding properties Ratna Chatterjee, Omkar Singh, Lalawmpuii Pachuau, Shiba Prasad Malik, Mausumi Paul, Kakali Bhadra, Santanu Paul, Gopinatha Suresh Kumar, Nirup Bikash Mondal, Sukdeb Banerjee Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . tianshic acid ÏàËÆ¶È:50% Chinese Traditional and Herbal Drugs 2009 40 1858-1860 A new flavone glycoside from Salsola collina XIANG Yu; YAO Yuan-zhang; ZHOU Qiu-xiang; LI Ping; LI You-bin Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . Biotinyl-N-¦Å-aminocaproyl-N-cystamine C25H45O5N5S3 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 1995 3 907-915 Bifunctional activity labels for selection of filamentous bacteriophages displaying enzymes Sophie Vanwetswinkel, Roland Touillaux, Jacques Fastrez, Jacqueline Marchand-Brynaert Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . Biofinyl-N-¦Å-anfinocaproyl-N-cystamine-N'-BOC C20H38O3N5S3 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 1995 3 907-915 Bifunctional activity labels for selection of filamentous bacteriophages displaying enzymes Sophie Vanwetswinkel, Roland Touillaux, Jacques Fastrez, Jacqueline Marchand-Brynaert Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 12,13,15-trihydroxy-9-octadecenoic acid ÏàËÆ¶È:50% Chinese Journal of Natural Medicines 2011 9 94-97 A Novel Ceramide from the Roots of Derris elliptica LU Hai-Ying, LIANG Jing-Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . compound 19 C75H130IN3O16 ÏàËÆ¶È:50% European Journal of Organic Chemistry 2012 1130-1137 Dendritic Architectures with Positively Charged Cores and Negatively Charged Shells Torsten Schunk and Andreas Hirsch Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . protolichesterinic acid C19H32O4 ÏàËÆ¶È:50% Journal of Agricultural and Food Chemistry 2011 59 2299-2307 Isolation, Characterization and Antifungal Activity of Major Constituents of the Himalayan Lichen Parmelia reticulata Tayl.† Mayurika Goel, Prem Dureja, Archna Rani, Prem L. Uniyal, and Hartmut Laatsch Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . protolichesterinic acid C19H32O4 ÏàËÆ¶È:50% Journal of Agricultural and Food Chemistry 2011 59 2299-2307 Isolation, Characterization and Antifungal Activity of Major Constituents of the Himalayan Lichen Parmelia reticulata Tayl. Mayurika Goel,Prem Dureja,Archna Rani,Prem L. Uniyal,and Hartmut Laatsch Structure 13C NMR ̼Æ×Ä£Äâͼ |

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