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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
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