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39.491  39.629  39.770  39.907  40.048  40.185  40.327  56.042  56.168  60.341  94.716  103.676  104.545  109.638  111.888  120.284  123.278  131.719  149.349  152.458  152.805  153.152  157.672  163.676  182.561
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14.091  22.670  25.016  25.920  28.635  29.143  29.223  29.238  29.257  29.341  29.459  29.513   29.562  29.589  29.639  29.681  31.904  34.407  64.388  76.773  76.987  77.196  109.993  110.004  
»¯ºÏÎï4 ë®´úÂÈ·Â
11.837  11.963   12.024   12.237  18.764  18.966  19.019  19.387  19.805  21.049  21.060  21.079  21.205  23.040  24.283   24.344  25.389  26.042  28.231  28.906  19.120  31.603  31.870  33.915  36.127  36.485  37.233  39.655  39.751  40.487  42.184  42.249  42.295  45.800  50.103  50.126  51.217  55.920  56.030  56.740  56.839  71.753  76.800  77.013  77.223  110.000  110.016  121.672  129.240  138.295  140.721  
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11.837  11.963  12.024  12.233  18.764  18.966  19.019  19.374  19.801  21.052  21.071  21.205  23.043  24.283  24.344  25.386  26.053  28.227  28.902  29.127  31.607  31.859  31.874  31.889  33.918  36.127  36.478  36.485  37.237  39.659  39.754  40.479  42.188  42.257  42.295  45.804  50.107  50.133  51.217  55.927  56.038  56.740  56.834  71.750  76.796  77.006  77.219  121.669  121.676  129.244  138.295  140.725
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1 .     2-bromo-1-tridecen-3-ol
C13H25BrO     ÏàËÆ¶È:75%
European Journal of Organic Chemistry          2011                   2278-2285
An Efficient Approach to 2-Bromoalken-3-ols by Regioselective Bromohydroxylation Reaction of Simple Allenes with NBS
Wangqing Kong, Binjie Guo, Chunling Fu and Shengming Ma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     undecanoic acid
C11H22O2     ÏàËÆ¶È:66.6%
Acta Botanica Yunnanica          1999          21(2)          265-268
A Acetylenic Acid from Diploclisia glaucescens
YANG Ye-Kun, GAO Cheng-Wei ,QIU Ming-Hua, NIE Rui-Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     fatty acid ester part of III
    ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1988          36          1180-1184
Chemical Studies on the COnstituents of Hyphear Tanakae HOSOKAWA from Different Host Trees
TAKEHIKO FUKUNAGA,KOICHI NISHIYA,IKUKO KAJIKAWA,YOSHIKUNI WATANABE,NOBUO SUZUKI,KOICHI TAKEYA and HIDEJI ITOKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     Palmitic acid
    ÏàËÆ¶È:66.6%
Chemistry of Natural Compounds          2004          40          457-459
A NEW HYDROQUINONE DIGLUCOSIDE FROM Lysimachia fordiana
Xin-an Huang and Ren-Zhou Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     1-Nonanethiol
    ÏàËÆ¶È:66.6%
Molecules          2009          14          4634-4643
3-(2-Aminophenyl)-4-methyl-1, 3-thiazole-2(3H)-thione as an Ecofriendly Sulphur Transfer Agent to Prepare Alkanethiols in High Yield and High Purity
Mohammed Amine Mehdid, Ayada Djafri, Christian Roussel and Federico Andreoli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     1-Decanethiol
    ÏàËÆ¶È:66.6%
Molecules          2009          14          4634-4643
3-(2-Aminophenyl)-4-methyl-1, 3-thiazole-2(3H)-thione as an Ecofriendly Sulphur Transfer Agent to Prepare Alkanethiols in High Yield and High Purity
Mohammed Amine Mehdid, Ayada Djafri, Christian Roussel and Federico Andreoli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     1-Dodecanethiol
    ÏàËÆ¶È:66.6%
Molecules          2009          14          4634-4643
3-(2-Aminophenyl)-4-methyl-1, 3-thiazole-2(3H)-thione as an Ecofriendly Sulphur Transfer Agent to Prepare Alkanethiols in High Yield and High Purity
Mohammed Amine Mehdid, Ayada Djafri, Christian Roussel and Federico Andreoli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     1-Octadecanethiol
    ÏàËÆ¶È:66.6%
Molecules          2009          14          4634-4643
3-(2-Aminophenyl)-4-methyl-1, 3-thiazole-2(3H)-thione as an Ecofriendly Sulphur Transfer Agent to Prepare Alkanethiols in High Yield and High Purity
Mohammed Amine Mehdid, Ayada Djafri, Christian Roussel and Federico Andreoli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     heneicosanol
C21H44O     ÏàËÆ¶È:66.6%
Acta Pharmaceutica Sinica          1997          32          282-285
STUDIES ON LIPOSOLUBLE CONSTITUENTS FROM THE AERIAL PARTS OF SIEGESBECKIA ORIENTALIS L.
DA Guo; ZG Zhang; GQ Ye and ZC Lou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     palmitic acid
    ÏàËÆ¶È:66.6%
China Journal of Chinese Materia Medica          2007          32          500-503
Studies on chemical constituets of Cynanchum forrestii
LIU Yue, LIU Jing, YU Shishan, HUANG Xiangzhong, HU Youcai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     palmitic acid
    ÏàËÆ¶È:66.6%
China Journal of Chinese Materia Medica          2001          26          692-694
Chemical Constituents of loxocalyx urticifolius Hemsl
ZHANG Xiaorong, WANG Ming'an, ZHANG Yong, WANG Mingkui, IDNG Lisheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     arachidic acid
C20H40O2     ÏàËÆ¶È:66.6%
China Journal of Chinese Materia Medica          1992          17          485-487
Studies on the Chemical Constituents of Pedicularis muscola Maxim
Yang Lianchun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     octacasanoic acid
C28H56O2     ÏàËÆ¶È:66.6%
China Journal of Chinese Materia Medica          1990          15          38-39
Studies on the Chemcial Constituents of Adenophora stricta Miq.
Jiang Peifen and Gao Zehngping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     tetracosanoic acid
C24H48O2     ÏàËÆ¶È:66.6%
Acta Pharmaceutica Sinica          2006          Vol 41          426-430
A new sesquiterpene lactone from the roots of Lasianthus acuminatissimus
LI Bin; ZHANG Dong-ming; LUO Yong-ming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     (S)-5-Ethyl-8, 8-dimethyl nonanal
C13H26O     ÏàËÆ¶È:66.6%
Records of Natural Products          2009          3          204-208
Secondary Metabolites of Curvularia oryzae MTCC 2605
Siddhardha Busi, Prabhakar Peddikotla, Suryanarayana M. Upadyayula, Venkateswarlu Yenamandra
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     n-hexacosanyl-n-decaniate
C26H72O2     ÏàËÆ¶È:66.6%
Indian Journal of Chemistry          2009          48B          1164-1169
A new aliphatic acid from Achyranthes aspera Linn. Roots
Sharma,Surendra Kr; Vasudeva,Neeru; Ali,M
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     pentyl undecanoate
C16H32O2     ÏàËÆ¶È:66.6%
Indian Journal of Chemistry          2006          45B          314-317
Synthesis and antimicrobial screening of 5H,7H-N-(coumarin-6-yl)-2,8-diphenyl-5,7-dioxo-4,5,6,7-tetrahydrobenzimidazo[5,6-c]­furan and 5H,7H-N-(coumarin-6-yl)-2,8-diphenyl-5,7-dioxo-6-(7-methoxy-4-methylcoumarin-6-yl)-4,5,6,7-tetrahydro benzimidazo[5,6-c]
Choudhari,B P; Mulwad,V V
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     6-nonadecanone
C19H38O     ÏàËÆ¶È:66.6%
Indian Journal of Chemistry          2005          44B          1742-1744
Two new lipid constituents of Nigella sativa (Seeds)
Singh,Neelima; Verma,Manjul; Mehta,Darshana; Mehta,B K
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     phthalocyanine
C24H35NO2S2Se     ÏàËÆ¶È:66.6%
Heterocycles          2009          79          1081-1086
Preparation and Electrochemical and Optical Properties of Tetrakis(dithiaselenolo)phthalocyanine
Takeshi Kimura, Toshiharu Namauo, Akio Yamakawa, and Yutaka Takaguchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     Dotriacont-1-ene
C32H64     ÏàËÆ¶È:66.6%
Chemistry & Biodiversity          2010          7          717-721
A New Long-Chain Alkene and Antituberculosis Constituents from the Leaves of Pourthiaea lucida
Jih-Jung Chen, Wen-Jiou Lin, Po-Chuen Shieh, Ih-Sheng Chen, Chien-Fang Peng and Ping-Jyun Sung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-02-27 15:49:49
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1 .     6-Chloro-2-methoxy-N-(3,4,5-trimethoxyphenyl)acridin-9-amine
C23H22ClN2O4     ÏàËÆ¶È:59.2%
Bioorganic & Medicinal Chemistry          2011          19          3312-3319
Exploration of acridine scaffold as a potentially interesting scaffold for discovering novel multi-target VEGFR-2 and Src kinase inhibitors
Xudong Luan,Chunmei Gao, Nannan Zhang , Yuzong Chen, Qinsheng Sun ,Chunyan Tan , Hongxia Liu , Yibao Jin, Yuyang Jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     5-hydroxy-6,7,8,3',4'-pentamethoxyflavone
    ÏàËÆ¶È:56%
Phytochemistry          1991          30          1169-1173
Flavonoid constituents of Stachys aegyptiaca
M.A. El-Ansari, M.F. Abdalla, N.A.M. Saleh, D. Barron, J.L. Le Qu¨¦r¨¦
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     5,8-dihydroxy-6,7,3',4'-tetramethoxy flavone 8-O-¦Â-glucopyranoside
C25H28O13     ÏàËÆ¶È:56%
Biochemical Systematics and Ecology          2012          43          10-13
Glycosides of flavone methyl ethers from Murraya paniculata
Yun Zhang, Jun Li, Shepo Shi, Ke Zan, Pengfei Tu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     lethedoside A
    ÏàËÆ¶È:52%
Chinese Journal of Natural Medicines          2012          10          0287-0291
Flavanoids from the stems of Aquilaria sinensis
Dong CHEN, Dan BI, Yue-Lin SONG, Peng-Fei TU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     5-Demethylnobiletin
    ÏàËÆ¶È:52%
Lishizhen Medicine and Materia Medica Research          2010          21          2469-2470
ZHANG Qing-hua1; 2; JIANG Yi-hao3; GONG Qian-feng1 ; WANG Zhi-ping2
HAN Jin-dan; WANG Kui-wu; SHEN Lian-qing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     lycopodone
C27H24O11     ÏàËÆ¶È:50%
Heterocycles          2005          65          661-666
A New Flavone from Lycopodium japonicum
Jian Yan, Lirong Sun, Xianming Zhang, and Minghua Qiu*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     Methoxyhydnocarpin
    ÏàËÆ¶È:50%
Phytochemistry          1979          18          506-508
13C NMR of flavonolignans from Hydnocarpus wightiana
M. R. Parthasarathy, K. R. Ranganathan, D. K. Sharma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     crysoeriol+diosmetin
    ÏàËÆ¶È:50%
Tetrahedron letters          1980          21          3607-3610
Extractives of Thailand cannabis: Synthesis of canniprene and isolation of new geranylated and prenylated chrysoeriols
Leslie Crombie, W.Mary L. Crombie, Sally V. Jamieson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     (-)-(7''R,8''S)-4'',5,7-Trihydroxy-3',3'',5'-trimethoxy-4',8''-oxyflavonolignan-7'',9''-diol
    ÏàËÆ¶È:50%
Journal of Natural Products          2011          74          1188-1200
Lignans and Neolignans from Sinocalamus affinis and Their Absolute Configurations
Liang Xiong, Chenggeng Zhu, Yanru Li, Ye Tian, Sheng Lin, Shaopeng Yuan, Jinfeng Hu, Qi Hou, Naihong Chen, Yongchun Yang, and Jiangong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3Â¥2013-02-27 15:52:11
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1 .     n-Octacos-9-enyl propionate
C31H60O2     ÏàËÆ¶È:79.1%
Chinese Journal of Chemistry          2007          25          843-848
New Aliphatic Alcohol and Ester Constituents from Rice Hulls of Oryza sativa
ILL-Min Chung, Mohd Ali, Se-Chul Chun, Cheng-Wu Jin, Dong-Ha Cho, Seung-Beom Hong and Ateeque Ahmad
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     10,12-Heptadecadiynoic acid
    ÏàËÆ¶È:79.1%
Journal of the Brazilian Chemical Society          2001          12          64-72
Synthesis of the Diacetylenic Phospholipids 1,2-(10',12'-Heptadecadiynoyl)-sn-Glycero-3-Phophatidylcholine and 1,2-(4',6'-Tricosadiynoyl)-sn-Glycero-3-Phophatidylcholine
Paulo T. Hennies, Maria H. C. Santana and Carlos R. D. Correia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     10,12-Tricosadiynoic acid
    ÏàËÆ¶È:79.1%
Journal of the Brazilian Chemical Society          2001          12          64-72
Synthesis of the Diacetylenic Phospholipids 1,2-(10',12'-Heptadecadiynoyl)-sn-Glycero-3-Phophatidylcholine and 1,2-(4',6'-Tricosadiynoyl)-sn-Glycero-3-Phophatidylcholine
Paulo T. Hennies, Maria H. C. Santana and Carlos R. D. Correia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     1-(2-furyl)pentacosa-16,18-diyne
C29H46O     ÏàËÆ¶È:76%
Planta Medica          2001          67          572-575
2-Substituted Furans from Polyalthia suberosa
Patoomratana Tuchinda,Manat Pohmakotr, Vichai Reutrakul, Wanpen Thanyachareon ,Samaisukh Sophasan, Chalobon Yoosook, Thawatchai Santisuk, John M. Pezzuto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     compound 1
    ÏàËÆ¶È:75%
Phytochemistry          1996          42          997-998
Nematicidal hydrocarbons from Mucuna aterrima
Marisa A. Nogueira, João S. de Oliveira, Silamar Ferraz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     1-(2-furyl)pentacosa-7,9-diyne
C29H46O     ÏàËÆ¶È:70.8%
Journal of Natural Products          2006          69(1)          68-72
2-Substituted Furans from the Roots of Polyalthia evecta
Somdej Kanokmedhakul, Kwanjai Kanokmedhakul, Itsara Kantikeaw, and Nutchanat Phonkerd
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     methyl ester of peroxyacarnoic acids D
C24H44NO5     ÏàËÆ¶È:70.8%
Journal of Natural Products          2001          64          131-133
New Acetogenin Peroxides from the Indian Sponge Acarnus bicladotylota
Angelo Fontana,Giuliana d¡¯Ippolito, Lisette D¡¯Souza, Ernesto Mollo, P. S. Parameswaram, and Guido Cimino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     (3R*,4R*)-4-[N-(tert-Butoxycarbonyl)-11-aminoundecyl]-3-(non-8-enyl)-oxetan-2-one
C28H51NO4     ÏàËÆ¶È:70.8%
Bioorganic & Medicinal Chemistry          2012          20          583-591
Development and characterization of improved b-lactone-based anti-virulence drugs targeting ClpP
Evelyn Zeiler, Vadim S. Korotkov, Katrin Lorenz-Baath, Thomas Böttcher, Stephan A. Sieber
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     cis,cis-diunsaturated a-meromycolic acid
C50H96O2     ÏàËÆ¶È:70.8%
Tetrahedron Letters          2012          53          214-216
Synthesis of cis,cis-diunsaturated ¦Á-meromycolic acid by a palladium-catalysed alkyl¨Calkyl Negishi reaction
Giacomo Berretta, Geoffrey D. Coxon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     6-Bromohexyl 3,4,5-Tris(tetradecyloxy)benzoate
C55H100BrO5     ÏàËÆ¶È:68%
Helvetica Chimica Acta          2009          92          2024-2037
Concise Synthesis of [1,1¡ä-Biisoquinoline]-4,4¡ä-diol via a Protecting Group Strategy and Its Application for Potential Liquid-Crystalline Compounds
Elisabeth Kapatsina, Markus Mateescu, Angelika Baro, Wolfgang Frey, Sabine Laschat
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     6-Bromohexyl 3,4,5-Tris(hexadecyloxy)benzoate
C61H112BrO5     ÏàËÆ¶È:68%
Helvetica Chimica Acta          2009          92          2024-2037
Concise Synthesis of [1,1¡ä-Biisoquinoline]-4,4¡ä-diol via a Protecting Group Strategy and Its Application for Potential Liquid-Crystalline Compounds
Elisabeth Kapatsina, Markus Mateescu, Angelika Baro, Wolfgang Frey, Sabine Laschat
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     5-Bromo-1,4-dimethyl-6-hexadecyl-2,3-dihydro-1Hpyrrolo[2,3-b]pyridine
C25H43N2Br     ÏàËÆ¶È:68%
Bioorganic & Medicinal Chemistry          2012          20          3584-3595
Simplified bicyclic pyridinol analogues protect mitochondrial function Original Research Article
Xiaoqing Cai, Omar M. Khdour, Jennifer Jaruvangsanti, Sidney M. Hecht
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     2-pentacosa-7,9-diynylfuran
C29H46O     ÏàËÆ¶È:67.8%
Journal of Natural Products          2009          72          857-860
Synthesis of Natural Polyacetylenes Bearing Furan Rings
Daniela A. Barancelli, Anderson C. Mantovani, Cristiano Jesse, Cristina W. Nogueira, and Gilson Zeni
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     Dodecyl (Z)-9-hexadecenoate
    ÏàËÆ¶È:67.8%
Journal of Natural Products          2011          74          1364-1369
Lizard Epidermal Gland Secretions. II. Chemical Characterization of the Generation Gland Secretion of the Sungazer, Cordylus giganteus
Stefan Louw, Ben V. Burger, Maritha Le Roux, and Johannes H. Van Wyk
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     majoranolide
C19H34O3     ÏàËÆ¶È:66.6%
Chemistry & Biodiversity          2008          Vol. 5          2690
Antimycobacterial Butanolides from the Root of Lindera akoensis
Su-Yen Chang, Ming-Jen Cheng, Chien-Fang Peng, Hsun-Shuo Chang, and Ih-Sheng Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




16 .     plakorsin A
C23H40O3     ÏàËÆ¶È:66.6%
Journal of Natural Products          2001          64          324-327
Three New Furan Derivatives and a New Fatty Acid from a Taiwanese Marine Sponge Plakortis simplex
Ya-Ching Shen, Chaturvedula V. S. Prakash, and Yao-Haur Kuo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




17 .     plakorsin b
C22H38O3     ÏàËÆ¶È:66.6%
Journal of Natural Products          2001          64          324-327
Three New Furan Derivatives and a New Fatty Acid from a Taiwanese Marine Sponge Plakortis simplex
Ya-Ching Shen, Chaturvedula V. S. Prakash, and Yao-Haur Kuo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




18 .     9,10-dihydroxystearic acid
C21H40O4     ÏàËÆ¶È:66.6%
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

--------------------------------------------------------------------------------




19 .     Ethyl Heptadecanoate
    ÏàËÆ¶È:66.6%
Journal of Natural Products          1989          Vol 52          180
Long Chain Esters of Aesculus indica
Bikram Singh, Pawan K. Agrawal, Raghunath S. Thakur
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




20 .     3-hydroxy-9-oxo-4-tetradecyl-5-oxa-1-azabicyclo[4.3.0]nonane-2- methanol
C22H41NO4     ÏàËÆ¶È:66.6%
Phytochemistry          1992          31          3757-3759
Two sphingoid derivatives from stromata of Epichloe typhin A on Phleum pratense
Hiroyuki Koshino, Teruhiko Yoshihara, Akitami Ichihara, Akitoshi Tajimi, Tadayuki Shimanuki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4Â¥2013-02-27 15:54:11
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¡¾´ð°¸¡¿Ó¦Öú»ØÌû

µÚÎå¸ö
1 .     N-(Cholest-5-en-3¦Â-yl)-3¦Â-hydroxyandrost-5-ene-17¦Â-carboxamide
C47H75NO2     ÏàËÆ¶È:70.5%
Steroids          2009          74          88-94
Steroids linked with amide bond¡ªExtended cholesterol
Ivan Černý, Miloš Bud¨§š¨ªnský, Vladim¨ªr Pouzar, Pavel Drašar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




2 .     (20R)-26-methylcholest-5-en-3¦Â-ol and (20R)-26-methylcholestan-3¦Â-ol
C31H56OSi     ÏàËÆ¶È:69.6%
Bioorganic & Medicinal Chemistry          2012          20          4064-4081
Substrate analog studies of the ¦Ø-regiospecificity of Mycobacterium tuberculosis cholesterol metabolizing cytochrome P450 enzymes CYP124A1, CYP125A1 and CYP142A1
Jonathan B. Johnston, Arti A. Singh, Anaelle A. Clary, Chiung-Kuan Chen, Patricia Y. Hayes, Sharon Chow, James J. De Voss, Paul R. Ortiz de Montellano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




3 .     (3¦Â,22E)-stigmasta-5,22-dien-3-yl-(3¦Á,5¦Â,7¦Á,12¦Á)-7,12-bis(formyloxy)-3-hydroxycholan-24-oate
C55H86O7     ÏàËÆ¶È:67.2%
Bioorganic & Medicinal Chemistry          2010          18          8194-8203
Steroid conjugates: Synthesis and preliminary biological testing of pro-juvenoids
Hana Svobodov¨¢, Hana Ryšav¨¢, Milan Pavl¨ªk, David Šaman, Pavel Drašar, Zden¨§k Wimmer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




4 .     3¦Á-Hydroxy-5¦Â-cholan-24-oic acid (cholan-24-oicacid methyl ester)-3-yl ester
C49H81O5     ÏàËÆ¶È:66.6%
Steroids          2003          68          1157-1161
Synthesis of ester-linked lithocholic acid dimers
Lutfun Nahar, Alan B. Turner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




5 .     daucosterol-6'-linoleate
    ÏàËÆ¶È:66.0%
Journal of Shenyang Pharmaceutical University          2008          25          883-885
Chemical constituents from the seeds of Castanea mollissima Blume(III)
LONG Zhi-min, WU Li-jun, JIANG Bing-ya, SUN Bo-hang, HUANG Jian, GAO Hui-yuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

6 .     lanoscopariol
C46H80O3     ÏàËÆ¶È:64.7%
Journal of Natural Products          1996          59          181-184
New 9¦Â-Lanostane-Type Triterpenic and 13, 14-seco-Steroidal Esters from the Roots of Artemisia scoparia
Surendra Kumar Sharma and Mohammad Ali
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




7 .     balanoinvolin
C53H90O7     ÏàËÆ¶È:64.7%
Chemistry of Natural Compounds          2009          45          371-373
BALANOINVOLIN, A NEW STEROID DERIVATIVEFROM Balanophora involucrate
Bing Luo, Kun Zou, Zhiyong Guo, Feijun Dan, Juizhi Wang, and Hui Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




8 .     3-Oxo-5¦Â-cholan-24-oic acid (cholan-24-oic acidmethyl ester)-3-yl ester
C49H79O5     ÏàËÆ¶È:64.7%
Steroids          2003          68          1157-1161
Synthesis of ester-linked lithocholic acid dimers
Lutfun Nahar, Alan B. Turner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




9 .     (3¦Â,22E)-stigmasta-5,22-dien-3-yl-(3¦Á,5¦Â,7¦Á,12¦Á)-3,7,12-tris(formyloxy)cholan-24-oate
C56H86O8     ÏàËÆ¶È:64.2%
Bioorganic & Medicinal Chemistry          2010          18          8194-8203
Steroid conjugates: Synthesis and preliminary biological testing of pro-juvenoids
Hana Svobodov¨¢, Hana Ryšav¨¢, Milan Pavl¨ªk, David Šaman, Pavel Drašar, Zden¨§k Wimmer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

10 .     daucosterol linoleate
    ÏàËÆ¶È:64.1%
Chinese Pharmaceutical Journal          2007          42          661-663
Studies on Chemical Constituents of Paeonia veitchii L.
WANG Rui, CHOU Gui-xin, ZHU En-yuan, WANG Zheng-tao, BI Kai-shun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ


11 .     5¦Á,14¦Á-cevanin-6-O-20¦Â-hydroxy-3¦Â-yl-3¦Á,7¦Á-dihydroxy-5¦Â-cholan-24-oate
C51H81NO6     ÏàËÆ¶È:62.7%
Steroids          2009          74          424-434
Structural analysis and antitussive evaluation of five novel esters of verticinone and bile acids
Jiu-liang Zhang, Hui Wang, Hui-fang Pi, Han-li Ruan, Peng Zhang, Ji-zhou Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




12 .     5¦Á,14¦Á-cevanin-6-O-20¦Â-hydroxy-3¦Â-yl-3¦Á,7¦Â-dihydroxy-5¦Â-cholan-24-oate
C51H81NO6     ÏàËÆ¶È:62.7%
Steroids          2009          74          424-434
Structural analysis and antitussive evaluation of five novel esters of verticinone and bile acids
Jiu-liang Zhang, Hui Wang, Hui-fang Pi, Han-li Ruan, Peng Zhang, Ji-zhou Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




13 .     5¦Á,14¦Á-cevanin-6-O-20¦Â-hydroxy-3¦Â-yl-3¦Á,6¦Á-dihydroxy-5¦Â-cholan-24-oate
C51H81NO6     ÏàËÆ¶È:62.7%
Steroids          2009          74          424-434
Structural analysis and antitussive evaluation of five novel esters of verticinone and bile acids
Jiu-liang Zhang, Hui Wang, Hui-fang Pi, Han-li Ruan, Peng Zhang, Ji-zhou Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




14 .     Sitosterol-3-O-12',13'-epoxy-9'-oxo-(10'E)-octadecenoate
C47H78O4     ÏàËÆ¶È:62.7%
Journal of Asian Natural Products Research          2003          5          215-221
THE CHEMICAL CONSTITUENTS OF MUNRONIA HENRYI
SHU-HUA QI, DA-GANG WU, YUN-BAO MA and XIAO-DONG LUO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




15 .     ¦Â-sitosterol linoleate
    ÏàËÆ¶È:62.7%
Chinese Pharmaceutical Journal          2007          42          661-663
Studies on Chemical Constituents of Paeonia veitchii L.
WANG Rui, CHOU Gui-xin, ZHU En-yuan, WANG Zheng-tao, BI Kai-shun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

16 .     (cis)-2-(4-{2-[(ethoxycarbonyl)amino]ethoxy}benzyl)cyclohexyl (3¦Â,22E)-stigmasta-5,22-dien-3-yl butanedioate
    ÏàËÆ¶È:62.7%
Bioorganic & Medicinal Chemistry          2010          18          8194-8203
Steroid conjugates: Synthesis and preliminary biological testing of pro-juvenoids
Hana Svobodov¨¢, Hana Ryšav¨¢, Milan Pavl¨ªk, David Šaman, Pavel Drašar, Zden¨§k Wimmer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




17 .     xestosterol ester of 18-bromooctadeca-(9E,17E)-diene-7,15-diynoic acid
C48H71O2Br     ÏàËÆ¶È:60.7%
Journal of Natural Products          1999          62          1439-1442
Isolation of Xestosterol Esters of Brominated Acetylenic Fatty Acids from the Marine Sponge Xestospongia testudinaria
Ngoc B. Pham, Mark S. Butler, John N. A. Hooper, Roger W. Moni, and Ronald J. Quinn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




18 .     xestosterol ester of 18-bromooctadeca-(9E,17E)-diene-5,7,15-triynoic acid
C48H67O2Br     ÏàËÆ¶È:60.7%
Journal of Natural Products          1999          62          1439-1442
Isolation of Xestosterol Esters of Brominated Acetylenic Fatty Acids from the Marine Sponge Xestospongia testudinaria
Ngoc B. Pham, Mark S. Butler, John N. A. Hooper, Roger W. Moni, and Ronald J. Quinn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




19 .     Stigmast-5-en-3¦Â-ol linoleate
C17H18O6     ÏàËÆ¶È:60.7%
Acta Botanica Yunnanica          2001          23(3)          368-372
Chemical Constituents from Dysoxylum hainanense
LUO Xiao-Dong,WU Shao-Hua,MA Yun-Bao,WU Da-Gang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




20 .     5,6¦Â-Epoxysitosteryl-9,10-di-tertbutyldimethylsilyloxystearate
C59H112O5Si2     ÏàËÆ¶È:60.7%
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
5Â¥2013-02-27 16:01:20
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¡¾´ð°¸¡¿Ó¦Öú»ØÌû

µÚËĸö
1 .     N-(Cholest-5-en-3¦Â-yl)-3¦Â-hydroxyandrost-5-ene-17¦Â-carboxamide
C47H75NO2     ÏàËÆ¶È:64.7%
Steroids          2009          74          88-94
Steroids linked with amide bond¡ªExtended cholesterol
Ivan Černý, Miloš Bud¨§š¨ªnský, Vladim¨ªr Pouzar, Pavel Drašar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




2 .     (20R)-26-methylcholest-5-en-3¦Â-ol and (20R)-26-methylcholestan-3¦Â-ol
C31H56OSi     ÏàËÆ¶È:64.2%
Bioorganic & Medicinal Chemistry          2012          20          4064-4081
Substrate analog studies of the ¦Ø-regiospecificity of Mycobacterium tuberculosis cholesterol metabolizing cytochrome P450 enzymes CYP124A1, CYP125A1 and CYP142A1
Jonathan B. Johnston, Arti A. Singh, Anaelle A. Clary, Chiung-Kuan Chen, Patricia Y. Hayes, Sharon Chow, James J. De Voss, Paul R. Ortiz de Montellano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




3 .     (3¦Â,22E)-stigmasta-5,22-dien-3-yl-(3¦Á,5¦Â,7¦Á,12¦Á)-7,12-bis(formyloxy)-3-hydroxycholan-24-oate
C55H86O7     ÏàËÆ¶È:63.6%
Bioorganic & Medicinal Chemistry          2010          18          8194-8203
Steroid conjugates: Synthesis and preliminary biological testing of pro-juvenoids
Hana Svobodov¨¢, Hana Ryšav¨¢, Milan Pavl¨ªk, David Šaman, Pavel Drašar, Zden¨§k Wimmer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




4 .     daucosterol-6'-linoleate
    ÏàËÆ¶È:62.2%
Journal of Shenyang Pharmaceutical University          2008          25          883-885
Chemical constituents from the seeds of Castanea mollissima Blume(III)
LONG Zhi-min, WU Li-jun, JIANG Bing-ya, SUN Bo-hang, HUANG Jian, GAO Hui-yuan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




5 .     balanoinvolin
C53H90O7     ÏàËÆ¶È:60.7%
Chemistry of Natural Compounds          2009          45          371-373
BALANOINVOLIN, A NEW STEROID DERIVATIVEFROM Balanophora involucrate
Bing Luo, Kun Zou, Zhiyong Guo, Feijun Dan, Juizhi Wang, and Hui Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




6 .     3¦Á-Hydroxy-5¦Â-cholan-24-oic acid (cholan-24-oicacid methyl ester)-3-yl ester
C49H81O5     ÏàËÆ¶È:60.7%
Steroids          2003          68          1157-1161
Synthesis of ester-linked lithocholic acid dimers
Lutfun Nahar, Alan B. Turner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




7 .     5¦Á,14¦Á-cevanin-6-O-20¦Â-hydroxy-3¦Â-yl-3¦Á,7¦Á-dihydroxy-5¦Â-cholan-24-oate
C51H81NO6     ÏàËÆ¶È:60.7%
Steroids          2009          74          424-434
Structural analysis and antitussive evaluation of five novel esters of verticinone and bile acids
Jiu-liang Zhang, Hui Wang, Hui-fang Pi, Han-li Ruan, Peng Zhang, Ji-zhou Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




8 .     (cis)-2-(4-{2-[(ethoxycarbonyl)amino]ethoxy}benzyl)cyclohexyl (3¦Â,22E)-stigmasta-5,22-dien-3-yl butanedioate
    ÏàËÆ¶È:60.7%
Bioorganic & Medicinal Chemistry          2010          18          8194-8203
Steroid conjugates: Synthesis and preliminary biological testing of pro-juvenoids
Hana Svobodov¨¢, Hana Ryšav¨¢, Milan Pavl¨ªk, David Šaman, Pavel Drašar, Zden¨§k Wimmer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

9 .     pseudolaridimer B
C50H78O5     ÏàËÆ¶È:60.7%
Organic Letters          2012          14          5432-5435
Pseudolaridimers A and B, Hetero-Cycloartane¨CLabdane Diels¨CAlder Adducts from the Cone of Pseudolarix amabilis
Bo Li, De-Yun Kong, Yun-Heng Shen, Hu Yuan, Rong-Cai Yue, Yi-Ren He, Lu Lu, Lei Shan, Hui-Liang Li, Ji Ye, Xian-Wen Yang, Juan Su, Run-Hui Liu, and Wei-Dong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




10 .     (3¦Â,22E)-stigmasta-5,22-dien-3-yl-(3¦Á,5¦Â,7¦Á,12¦Á)-3,7,12-tris(formyloxy)cholan-24-oate
C56H86O8     ÏàËÆ¶È:60.7%
Bioorganic & Medicinal Chemistry          2010          18          8194-8203
Steroid conjugates: Synthesis and preliminary biological testing of pro-juvenoids
Hana Svobodov¨¢, Hana Ryšav¨¢, Milan Pavl¨ªk, David Šaman, Pavel Drašar, Zden¨§k Wimmer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




11 .     daucosterol linoleate
    ÏàËÆ¶È:60.3%
Chinese Pharmaceutical Journal          2007          42          661-663
Studies on Chemical Constituents of Paeonia veitchii L.
WANG Rui, CHOU Gui-xin, ZHU En-yuan, WANG Zheng-tao, BI Kai-shun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




12 .     xestosterol ester of 18-bromooctadeca-(9E,17E)-diene-7,15-diynoic acid
C48H71O2Br     ÏàËÆ¶È:58.8%
Journal of Natural Products          1999          62          1439-1442
Isolation of Xestosterol Esters of Brominated Acetylenic Fatty Acids from the Marine Sponge Xestospongia testudinaria
Ngoc B. Pham, Mark S. Butler, John N. A. Hooper, Roger W. Moni, and Ronald J. Quinn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




13 .     xestosterol ester of 18-bromooctadeca-(9E,17E)-diene-5,7,15-triynoic acid
C48H67O2Br     ÏàËÆ¶È:58.8%
Journal of Natural Products          1999          62          1439-1442
Isolation of Xestosterol Esters of Brominated Acetylenic Fatty Acids from the Marine Sponge Xestospongia testudinaria
Ngoc B. Pham, Mark S. Butler, John N. A. Hooper, Roger W. Moni, and Ronald J. Quinn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




14 .     lanoscopariol
C46H80O3     ÏàËÆ¶È:58.8%
Journal of Natural Products          1996          59          181-184
New 9¦Â-Lanostane-Type Triterpenic and 13, 14-seco-Steroidal Esters from the Roots of Artemisia scoparia
Surendra Kumar Sharma and Mohammad Ali
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




15 .     3-Oxo-5¦Â-cholan-24-oic acid (cholan-24-oic acidmethyl ester)-3-yl ester
C49H79O5     ÏàËÆ¶È:58.8%
Steroids          2003          68          1157-1161
Synthesis of ester-linked lithocholic acid dimers
Lutfun Nahar, Alan B. Turner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




16 .     5,6¦Â-Epoxysitosteryl-9,10-di-tertbutyldimethylsilyloxystearate
C59H112O5Si2     ÏàËÆ¶È:58.8%
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


17 .     5¦Á,14¦Á-cevanin-6-O-20¦Â-hydroxy-3¦Â-yl-3¦Á,7¦Â-dihydroxy-5¦Â-cholan-24-oate
C51H81NO6     ÏàËÆ¶È:58.8%
Steroids          2009          74          424-434
Structural analysis and antitussive evaluation of five novel esters of verticinone and bile acids
Jiu-liang Zhang, Hui Wang, Hui-fang Pi, Han-li Ruan, Peng Zhang, Ji-zhou Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




18 .     Sitosterol-3-O-12',13'-epoxy-9'-oxo-(10'E)-octadecenoate
C47H78O4     ÏàËÆ¶È:58.8%
Journal of Asian Natural Products Research          2003          5          215-221
THE CHEMICAL CONSTITUENTS OF MUNRONIA HENRYI
SHU-HUA QI, DA-GANG WU, YUN-BAO MA and XIAO-DONG LUO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




19 .     ¦Â-sitosteryl-3¦Â-glucopyranoside-6'-O-palmitate
    ÏàËÆ¶È:58.8%
Fitoterapia          2004          75          500-504
Cytotoxic constituents from Plumbago zeylanica
A.T. Nguyen , H. Malonne , P. Duez , R. Vanhaelen-a,b, b a anhaelen-Fastrea,M. Vanhaelen, J. Fontaine
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




20 .     compound 16a+17a
    ÏàËÆ¶È:58.4%
Steroids          2012          77          780-790
A new approach to the side chain formation of 24-alkyl-22-hydroxy steroids: Application to the preparation of early brassinolide biosynthetic precursorsOriginal Research Article
Alaksiej L. Hurski, Vladimir N. Zhabinskii, Vladimir A. Khripach
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6Â¥2013-02-27 16:05:41
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