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²éѯ½á¹û£º¹²²éµ½1415¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 2 C20H36O3 ÏàËÆ¶È:80% Journal of Natural Products 2002 65 1712-1714 Aldehyde Dehydrogenase Inhibitors from the Mushroom Clitocybe clavipes Hirokazu Kawagishi, Toshiyuki Miyazawa,Hiroko Kume,Yasushi Arimoto, and Takahiro Inakuma Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 9,10-Dihydroxystearic acid ethyl ester C20H40O4 ÏàËÆ¶È:75% 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 5 18H32O3 ÏàËÆ¶È:73.6% Journal of Natural Products 2002 65 1712-1714 Aldehyde Dehydrogenase Inhibitors from the Mushroom Clitocybe clavipes Hirokazu Kawagishi, Toshiyuki Miyazawa,Hiroko Kume,Yasushi Arimoto, and Takahiro Inakuma Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 6,7,10-trihydroxy-8-octadecenoic acid ÏàËÆ¶È:73.6% 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 5 . tianshic acid ÏàËÆ¶È:73.6% 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 6 . camptosoric acid C18H34O5 ÏàËÆ¶È:73.6% 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 7 . 6,7,10-trihydroxy-8-octadecenoic acid ÏàËÆ¶È:73.6% 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 8 . sanleng acid ÏàËÆ¶È:73.6% Chinese Traditional and Herbal Drugs 1995 26 125-126 ÖÐÒ©ÈýÀâÖеÄл¯ºÏÎïÈýÀâËá ÕÅÎÀ¶«,Ф¿,Ñî¸ùÈ«,³Âº£Éú Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . methyl (9R,10R,12S,13S)-9,12-epoxy-10,13-dihydroxy-octadecanoante ÏàËÆ¶È:73.6% 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 10 . methyl (9R,10R,12S,13S)-10,13-epoxy-9,12-dihydroxy-octadecanonate ÏàËÆ¶È:73.6% 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 11 . 12,13,15-trihydroxy-9-octadecenoic acid ÏàËÆ¶È:73.6% 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 12 . [2',3'-dihydroxy-tetracosanolyamino]-1,3-dihydroxy-octadecane C40H81NO5 ÏàËÆ¶È:73.6% Acta Scientiarum Naturalium Universitatis Sunyatseni 2003 42(6) 122-123 The Novel Ceramides from a Mangrove Endophytic Fungus No12524 LI Hou-jin, YAO Jun- hua, CHEN Yi-guang, LIN Yong-cheng, L.L.P. Vrijmoed Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . [2',3'-dihydroxy-docosanoylamino]-1,3-dihydroxy-octadecane C42H85NO5 ÏàËÆ¶È:73.6% Acta Scientiarum Naturalium Universitatis Sunyatseni 2003 42(6) 122-123 The Novel Ceramides from a Mangrove Endophytic Fungus No12524 LI Hou-jin, YAO Jun- hua, CHEN Yi-guang, LIN Yong-cheng, L.L.P. Vrijmoed Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 9,10,13-ÈýôÇ»ù-·´-11-Ê®°ËÏ©Ëá ÏàËÆ¶È:73.6% Journal of Chinese Medicinal Materials 2011 34 546-548 Studies on the Chemical Constituents of Codonopsis pilosula QI Huan-yang, WANG Rui, LIU Yong, SHI Yan-ping Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 11,12,15-trehydroxy-13-en-octadecenoic acid ÏàËÆ¶È:73.6% Journal of Shenyang Pharmaceutical University 2013 30 674-682 Constituents from starfish Asterina pectinifer LI Zhan-qiang, CHEN Gang, WANG Hai-feng, LU Xuan, FENG Bao-min, PEI Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . Soyasphingosine A C43H87NO5 ÏàËÆ¶È:70% Journal of China Pharmaceutical University 2003 34 506-508 Two New Soyasphingosines in the Stem of Glycine max Merr DU Cheng-Lin; DING Xing-Bao Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (e)-8-oxo-9-oactadecenoic acid C18H32O3 ÏàËÆ¶È:68.4% Journal of Natural Products 2002 65 1712-1714 Aldehyde Dehydrogenase Inhibitors from the Mushroom Clitocybe clavipes Hirokazu Kawagishi, Toshiyuki Miyazawa,Hiroko Kume,Yasushi Arimoto, and Takahiro Inakuma Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . compound 3 C18H30O3 ÏàËÆ¶È:68.4% Journal of Natural Products 2002 65 1712-1714 Aldehyde Dehydrogenase Inhibitors from the Mushroom Clitocybe clavipes Hirokazu Kawagishi, Toshiyuki Miyazawa,Hiroko Kume,Yasushi Arimoto, and Takahiro Inakuma Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . (9R,10E,12S,13S)-9,12,13-Trihydroxyoctadec-10-enoic Acid ÏàËÆ¶È:68.4% 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 20 . lactariolide I C18H30O2 ÏàËÆ¶È:68.4% 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 21 . 9,10-Dihydroxystearic acid ÏàËÆ¶È:68.4% 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 22 . (S)-13-hydroxy-9Z,11E-octadecadienoic acid C18H32O3 ÏàËÆ¶È:68.4% 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 23 . hyeronimone C19H31NO3 ÏàËÆ¶È:68.4% Journal of Natural Products 1991 Vol 54 1309 Constituents of Hyeronima alchorneoides Winston F. Tinto, Gregory Blyden, William F. Reynolds, Stewart McLean Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . (E)-11-oxo-octadeca-12-enoic acid C19H34O3 ÏàËÆ¶È:68.4% 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 25 . 6,7,10-trihydroxy-8-octadecenoic acid ÏàËÆ¶È:68.4% 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 26 . compound 29 C16H30O4 ÏàËÆ¶È:68.4% 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 27 . (2E)-4,5-Dihydroxy-2-hexadecenoic acid ethyl ester C18H36O4 ÏàËÆ¶È:68.4% Tetrahedron Letters 2002 43 891-893 Synthesis of podoscyphic acid Johan Eriksson, Martin Johansson, Olov Sterner Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . 9,10,13-trihydroxy-(E)-11-octadecenoic acid C18H32O5 ÏàËÆ¶È:68.4% 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 29 . (6S,9R,10R)-10-hydroxy-6,9-epoxynonadec-18-en-7-one C19H34O3 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 30 . methyl(10E)-12-octadec-10-enoate ÏàËÆ¶È:68.4% Russian Journal of Organic Chemistry 2001 37 781-783 Isomerization of Methyl (9Z)-12-Oxooctadec-9-enoate A. M. Davletbakova, N. Z. Baibulatova, V. A. Dokichev, S. G. Yunusova and M. S. Yunusov Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . (4S,5S,E)-ethyl 4,5-dihydroxyheptadec-2-enoate C19H36O4 ÏàËÆ¶È:68.4% European Journal of Organic Chemistry 2011 1106-1112 Stereoselective Total Synthesis of (+)-Nephrosteranic Acid and (+)-Roccellaric Acid through Asymmetric Dihydroxylation and Johnson¨CClaisen Rearrangement Rodney A. Fernandes and Asim K. Chowdhury Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . (6S,7S,9R,10R)-6,9-epoxynonadec-18-ene-7,10-diol 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 33 . mixturre of N-(2',3'-dihydroxytetracosyl)-1,3-dihydroxy-2-amino-octadecane and N-(2',3'-dihydroxyhexacosyl)-1,3-dihydroxy-2-amino-octadecane ÏàËÆ¶È:68.4% Chemistry and Industry of Forest Products 2004 24 11-14 SPHINGOSINE DERIVATIVES ISOLATED FROM MONGROVE FUNGI 2526~# AND 1850~# FROM THE SOUTH SEA IN CHINA ZHU Feng, LIN Yong-cheng, ZHOU Shi-ning, VRIJMOED L L P Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . 10,12-dihydroxystearic acid ÏàËÆ¶È:68.4% Applied Microbiology and Biotechnology 2013 97 8987-8995 Production of a novel compound, 10,12-dihydroxystearic acid from ricinoleic acid by an oleate hydratase from Lysinibacillus fusiformis Min-Ho Seo, Kyoung-Rok Kim, Deok-Kun Oh Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . methyl 11,12,15-trihydroxy-13(14)-octadecenoate C19H36O5 ÏàËÆ¶È:68.4% Indian Journal of Chemistry Section B 2003 42B 1782-1785 Terpenoid and lipid constituents from Artemisia annua Amit Tewari & Singh Bhakuni Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . 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 37 . compound 2d ÏàËÆ¶È:68.4% Magnetic Resonance in Chemistry 2012 50 823-828 1H, 13C and 15N NMR assignments for N- and O-acylethanolamines, important family of naturally occurring bioactive lipid mediators Roberta Ottria, Silvana Casati and Pierangela Ciuffreda Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . (¡À)-¦Â-diimorphecolic acid ÏàËÆ¶È:68.4% 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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