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²éѯ½á¹û£º¹²²éµ½1856¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . vernolic acid C18H32O3 ÏàËÆ¶È:88.2% Natural Product Research and Development 2000 12(2) 1-3 A NEW ALKALOID FROM THE SEEDS OF ALLIUM TUBEROSUM Sang Shengmin; Mao Shilong; Lao Aina; Chen Zhongliang Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . methyl (9Z,12R)-12-methoxy-9-octadecenoate ÏàËÆ¶È:77.7% Russian Journal of Organic Chemistry 2001 37 608-611 Catalytic Cyclopropanation of Ricinolic Acid Derivatives with Diazomethane A. M. Davletbakova, I. O. Maidanova, N. Z. Baibulatova, V. A. Dokichev and Yu. V. Tomilov, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3(¦Î)-hydroxy-hexadeca- 4(E),6(Z)-dienoic acid C16H28O3 ÏàËÆ¶È:76.4% Phytochemistry 2008 69 2495-2500 Antineoplastic unsaturated fatty acids from Fijian macroalgae Ren-Wang Jiang, Mark E. Hay, Craig R. Fairchild, Jacques Prudhomme, Karine Le Roch,William Aalbersberg, Julia Kubanek Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . topsentolide B2 C20H32O4 ÏàËÆ¶È:75% Journal of Natural Products 2006 69(4) 567-571 Cytotoxic Oxylipins from a Marine Sponge Topsentia sp. Xuan Luo, Famei Li, Jongki Hong, Chong-O. Lee, Chung Ja Sim, Kwang Sik Im, and Jee H. Jung Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (E)-11-oxo-octadeca-12-enoic acid C19H34O3 ÏàËÆ¶È:72.2% Zeitschrift f¨¹r Naturforschung B 2009 64b 1199-1207 Three New Unsaturated Fatty Acids from the Marine Green Alga Ulva fasciata Delile Ghada S. E. Abou-ElWafa, Mohamed Shaaban, Khaled A. Shaaban,Mohamed E. E. El-Naggar, and Hartmut Laatsch Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Octanoate C18H32O3 ÏàËÆ¶È:72.2% Journal of Agricultural and Food Chemistry 2002 50 3522-3526 Antimicrobial and Bactericidal Activities of Esters of 2-endo-Hydroxy-1,8-cineole as New Aroma Chemicals Mitsuo Miyazawa and Yuya Hashimoto Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Gloeosporone C18H30O5 ÏàËÆ¶È:72.2% Helvetica Chimica Acta 1987 70 281-291 Revised Structure of the Fungal Germination Self-Inhibitor Gloeosporone Walter L. Meyer, W. Bernd Schweizer, Albert K. Beck, Werner Scheifele, Dieter Seebach, Stuart L. Schreiber and Sarah E. Kelly Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 9,10-Dihydroxystearic acid ÏàËÆ¶È:70.5% 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 9 . (S)-13-hydroxy-9Z,11E-octadecadienoic acid C18H32O3 ÏàËÆ¶È:70.5% China Journal of Chinese Materia Medica 2004 29 1108-1109 Èý·Öµ¤»¯Ñ§³É·ÖµÄÑо¿ »ÆÑ§Ê¯, Û¬ áÔ, ·¶Àö»ª, â×ʯɽ , ÁºÏþÌì Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 29 C16H30O4 ÏàËÆ¶È:70.5% Heterocycles 2008 76 1313-1328 2, 6-Dimethyl-4-nitrobenzoic Anhydride (DMNBA): An Effective Coupling Reagent for the Synthesis of Carboxylic Esters and Lactones Isamu Shiina and Ryo Miyao Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (8S,11S,E)-11-hydroxyoctadec-9-en-8-yl acetate C20H38O3 ÏàËÆ¶È:70.5% The Journal of Organic Chemistry 2010 75 4230-4243 Asymmetric Synthesis of the Cytotoxic Marine Natural Product (t)-Awajanomycin and Its C-11 Epimer Rui Fu, Jian-Liang Ye, Xi-Jie Dai, Yuan-Ping Ruan, and Pei-Qiang Huang Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 9(S),12(R),13(S)-trihydroxystearic acid C18H32O4 ÏàËÆ¶È:70.5% Tetrahedron 1980 36 993-996 Malyngic acid, a new fatty acid from Lyngbya majuscula Original Research Article John H. Cardellina II, Richard E. Moore Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Hexanoate C16H28O3 ÏàËÆ¶È:70.5% Journal of Agricultural and Food Chemistry 2002 50 3522-3526 Antimicrobial and Bactericidal Activities of Esters of 2-endo-Hydroxy-1,8-cineole as New Aroma Chemicals Mitsuo Miyazawa and Yuya Hashimoto Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Heptanoate C17H30O3 ÏàËÆ¶È:70.5% Journal of Agricultural and Food Chemistry 2002 50 3522-3526 Antimicrobial and Bactericidal Activities of Esters of 2-endo-Hydroxy-1,8-cineole as New Aroma Chemicals Mitsuo Miyazawa and Yuya Hashimoto Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . methyl ester of (9Z,12R)-12-(methoxycarbonylmethoxy)octadec-9-enoic acid ÏàËÆ¶È:70% Chemistry of Natural Compounds 2001 37 93-94 Catalytic Synthesis of the Methyl Ester of (9Z,12R)-12-(Methoxycarbonylmethoxy)-octadec-9-enoic Acid A. M. Davletbakova, N. Z. Baibulatova, V. A. Dokichev, M. S. Yunusov Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . cinnabaramide C C19H29NO3 ÏàËÆ¶È:68.4% Journal of Natural Products 2007 70 246-252 Cinnabaramides A-G: Analogues of Lactacystin and Salinosporamide from a Terrestrial Streptomycete Marc Stadler,Jens Bitzer, Anke Mayer-Bartschmid,Hartwig M¨¹ller,Jordi Benet-Buchholz, Florian Gantner,Hans-Volker Tichy,Peter Reinemer,and Kevin B. Bacon Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . methyl (9R,10R,12S,13S)-9,12-epoxy-10,13-dihydroxy-octadecanoante ÏàËÆ¶È:68.4% Tetrahedron 1998 54 2227-2242 Marine nematocides: Tetrahydrofurans from a southern Australian brown alga, Notheia anomala Robert J. Capon, Russell A Barrow, Simone Rochfort, Michael Jobling, Colin Skene, Ernest Lacey, Jennifer H Gill, Thomas Friedel, David Wadsworth Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . methyl (9R,10R,12S,13S)-10,13-epoxy-9,12-dihydroxy-octadecanonate ÏàËÆ¶È:68.4% Tetrahedron 1998 54 2227-2242 Marine nematocides: Tetrahydrofurans from a southern Australian brown alga, Notheia anomala Robert J. Capon, Russell A Barrow, Simone Rochfort, Michael Jobling, Colin Skene, Ernest Lacey, Jennifer H Gill, Thomas Friedel, David Wadsworth Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . (6S,7S,9Z)-nonadeca-9,18-diene-6,7-diol C19H36O2 ÏàËÆ¶È:68.4% Australian Journal of Chemistry 1990 43 895-911 Epoxy Lipids From the Australian Epiphytic Brown Alga Notheia anomala RA Barrow and RJ Capon Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . Nonanoate C19H34O3 ÏàËÆ¶È:68.4% Journal of Agricultural and Food Chemistry 2002 50 3522-3526 Antimicrobial and Bactericidal Activities of Esters of 2-endo-Hydroxy-1,8-cineole as New Aroma Chemicals Mitsuo Miyazawa and Yuya Hashimoto Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . topsentolide C2 C21H34O4 ÏàËÆ¶È:66.6% Journal of Natural Products 2006 69(4) 567-571 Cytotoxic Oxylipins from a Marine Sponge Topsentia sp. Xuan Luo, Famei Li, Jongki Hong, Chong-O. Lee, Chung Ja Sim, Kwang Sik Im, and Jee H. Jung Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . lactariolide I C18H30O2 ÏàËÆ¶È:66.6% Chinese Chemical Letters 1997 8 135-136 LACTARIOLIDE,A NEW 14-MEMBERED-RING COMPOUND FROM LACTARIUS SUBVELLEREUS JING ZHANG,XIAO ZHANG FENG Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 6,7,10-trihydroxy-8-octadecenoic acid ÏàËÆ¶È:66.6% Acta Pharmaceutica Sinica 2008 Vol 43 63-66 Chemical constituents of Sparganium stoleniferum DONG Xue; WANG Guo-rong; YAO Qing-qiang Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 5,12-dihydroxyoctadec-6(Z)-enoic acid C18H34O4 ÏàËÆ¶È:66.6% Indian Journal of Chemistry Section B 2005 44B 1915-1921 Biologically active inositol,sterols and lipid derivatives from Sesbania bispinosa Misra,Laxminarain; Siddiqi,Shahzad A Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . Compound 4 C18H33N ÏàËÆ¶È:66.6% Bioorganic & Medicinal Chemistry Letters 2000 10 1799-1801 The total synthesis of piclavines A1¨C4 and their biological evaluation Hiroki Takahata, Naoki Okamoto Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . tianshic acid ÏàËÆ¶È:66.6% 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 27 . camptosoric acid C18H34O5 ÏàËÆ¶È:66.6% Chinese Traditional and Herbal Drugs 2007 38 970-972 Chemical constituents of organic acid part from Camptosorus sibiricus LI Ning; LI Xian; FENG Zhi-guo; LI Xue-zheng; ZHANG Peng Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . 6,7,10-trihydroxy-8-octadecenoic acid ÏàËÆ¶È:66.6% Chinese Traditional and Herbal Drugs 2005 36 1607-1610 Chemical constituents of Sparganium stoloniferum (¢ñ) YUAN Tao; HUA Hui-ming; PEI Yue-hu Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . sanleng acid ÏàËÆ¶È:66.6% Chinese Traditional and Herbal Drugs 1995 26 125-126 ÖÐÒ©ÈýÀâÖеÄл¯ºÏÎïÈýÀâËá ÕÅÎÀ¶«,Ф¿,Ñî¸ùÈ«,³Âº£Éú Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . (E)-Octadec-9-en-11-olide C18H32O2 ÏàËÆ¶È:66.6% Organic & Biomolecular Chemistry 2007 5 3434-3441 Macrolides from the scent glands of the tropical butterflies Heliconius cydno and Heliconius pachinus Stefan Schulz, Selma Yildizhan, Katja Stritzke, Catalina Estrada and Lawrence E. Gilbert Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . (9Z,11E)-13-hydroxy-9,11-octadecadienoic acid C18H32O3 ÏàËÆ¶È:66.6% Bioscience, Biotechnology, and Biochemistry 2000 64 882-886 (10E,12Z,15Z)-9-Hydroxy-10,12,15-octadecatrienoic Acid Methyl Ester as an Anti-inflammatory Compound from Ehretia dicksonii Mei DONG, Yukiko ODA, Mitsuru HIROTA Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . 9,10,13-trihydroxy-(E)-11-octadecenoic acid C18H32O5 ÏàËÆ¶È:66.6% Natural Product Research and Development 1996 8(4) 28-32 SYNTHESIS OF NATURAL INSECTICIDE p-PHELLANDRENE Lu Kui; Liu Yanqi; Zhao Yingjie; Lu Chunming; Zhang Xiaolin; Jiang Yongjia Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . (S)-3-(cyclopentanecarbonyl)-4-[(R,E)-1-hydroxynon-2-enyl]oxazolidin-2-one C18H29NO4 ÏàËÆ¶È:66.6% Bioorganic & Medicinal Chemistry 2011 19 6174-6181 3,4-Disubstituted oxazolidin-2-ones as constrained ceramide analogs with anticancer activities Alok Singh, Hyun-Joon Ha, Jungchan Park, Jun Hee Kim, Won Koo Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . acido 5-hidroxi-octadeca-6(E)-8(Z)-dienoico C18H32O3 ÏàËÆ¶È:66.6% Qu¨ªmica Nova 2013 36 519-523 PREGNANOS E OUTROS CONSTITUINTES DAS RA¨ªZES DE Macrosiphonia petraea (A. St.-Hil.) Kuntze (Apocynaceae) Luiz Roberto de Assis Junior, Fernanda Rodrigues Garcez e Walmir Silva Garcez, Zaira da Rosa Guterres Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . 7-propioxyheptadecane ÏàËÆ¶È:66.6% Journal of Chemical Ecology 2013 39 28-36 Propionates and Acetates of Chiral Secondary Alcohols: Novel Sex Pheromone Components Produced by a Lichen Moth Barsine expressa (Arctiidae: Lithosiinae) Toru Fujii, Rei Yamakawa, Yoshie Terashima, Shinya Imura, Keiichi Ishigaki, Masakatsu Kinjo, Tetsu Ando Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . (3aR,4R,9S,11aS,E)-4-heptyl-9-hydroxy-2,2-dimethyl-7,8,9,11a-tetrahydro-3aH-[1,3]dioxolo[4,5-c]oxecin-6(4H)-one C19H32O5 ÏàËÆ¶È:66.6% Tetrahedron 2014 70 2634-2642 Asymmetric synthesis of naturally occurring nonenolide xyolide through cross metathesis and macrolactonization reaction Original Research Article Rohan Kalyan Rej, Anuvab Jana, Samik Nanda Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . 12,13,15-trihydroxy-9-octadecenoic acid ÏàËÆ¶È:66.6% 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 38 . (-)-Gloeosporon ÏàËÆ¶È:66.6% Journal of the American Chemical Society 1988 110 6210-6218 Structural and synthetic studies of the spore germination autoinhibitor, gloeosporone Stuart L. Schreiber, Sarah E. Kelly, John A. Porco, Tarek. Sammakia, Edward M. Suh Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . 2-(6-Carboxyhexyl)cyclopentylidenecaproic Acid Hydrazide C18H32O3N2 ÏàËÆ¶È:66.6% Journal of Medicinal Chemistry 1983 26 1056-1060 2-(6-Carboxyhexyl)cyclopentanone hexylhydrazone. A potent and time-dependent inhibitor of platelet aggregation N. I. Ghali, D. L. Venton, S. C. Hung, G. C. Le Breton Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . (¡À)-coriolic acid ÏàËÆ¶È:66.6% Shoyakugaku Zasshi 1987 41 174-179 Studies on the Crude Drug Containing the Angiotensin I Converting Enzyme Inhibitors (II) : On the Active Principles of Fritillaria verticillata WILLDENOW var. thumber gii BAKER NIITSU KAZUAKI,Tsumura Laboratory, IKEYA YUKINOBU,Tsumura Laboratory, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . (¡À)-¦Â-diimorphecolic acid ÏàËÆ¶È:66.6% Shoyakugaku Zasshi 1987 41 174-179 Studies on the Crude Drug Containing the Angiotensin I Converting Enzyme Inhibitors (II) : On the Active Principles of Fritillaria verticillata WILLDENOW var. thumber gii BAKER NIITSU KAZUAKI,Tsumura Laboratory, IKEYA YUKINOBU,Tsumura Laboratory, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ |

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