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14.09,16.15,19.70,19.73,22.60,22.69,24.46,24.78,25.13,25.74,27.96,29.35,29.43,29.61,29.69,31.91,32.68,32.78,36.66,37.28,37.35,37.42,39.36,39.86,59.37,63.04,123.11,140.19
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21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2
14.1,16.2,19.7,19.7,22.6,22.7,24.5,24.8,25.1,25.7,28.0,29.4,29.4,29.6,29.7,31.9,32.7,32.8,36.7,37.3,37.4,37.4,39.4,39.9,59.4,63.0,123.1,140.2

  
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1 .     trans-phytyl palmitate
C16H31O     ÏàËÆ¶È:83.8%
Journal of Natural Products          1991          Vol 54          1444
Diterpene Fatty Acid Ester from Leucas nutans
Mashooda Hasan, Dadu Khan Burdi, Viqar Uddin Ahmad
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

2 .     phytyl-1-hexanoate
    ÏàËÆ¶È:75%
Natural Product Research          2007          21          828-833
Lipid constituents of Trifolium resupinatum var. microcephalum
Temine Sabudak; Emel Isik; Sevil Oksuz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

3 .     epoxylycopaene
C40H78O     ÏàËÆ¶È:75%
Phytochemistry          1997          44          671-678
Four polymethylsqualene epoxides and one acyclic tetraterpene epoxide from Botryococcus braunii
V. Delahais, P. Metzger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

4 .     balansenate I
C32H62O2     ÏàËÆ¶È:73.3%
Helvetica Chimica Acta          2003          Vol. 86          2452
New Long-Chain Esters and Adenine Analogs from the Leaves of Formosan Bridelia balansae
Yeh-Hsin Tsai, Ih-Sheng Chen, and Ian-Lih Tsai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

5 .     palmitate
C36H70O2     ÏàËÆ¶È:72.4%
Natural Product Communications          2011          6          767-772
Lipophilic Components from the Ecuadorian Plant Schistocarpha eupatorioides
Gianluca Gilardoni, Solveig Tosi, Giorgio Mellerio, Maria Elena Maldonado, Ximena Chiriboga and Giovanni Vidari
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

6 .     trianthenol
C40H78O     ÏàËÆ¶È:71.4%
Phytochemistry          2001          56          99-102
Trianthenol: an antifungal tetraterpenoid from Trianthema portulacastrum (Aizoaceae)
Ha®z Rub Nawaz, Abdul Malik , Muhammad Shaiq Ali
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

7 .     glucinoprenyl 7
C35H64O     ÏàËÆ¶È:71.4%
Phytochemistry          1997          46          715-720
Arachisprenols: Polyprenols possessing a geranyl residue from Arachis hypogaea
Tadashi Aoki, Kazuhiko Matsuo, Takayuki Suga, Shinji Ohta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

8 .     trianthenol
    ÏàËÆ¶È:71.4%
Natural Product Research and Development          2010          22          245-247
Chemical Constituents from Reineckia carnea Kunth
YANG Jian-qiong; WANG Ye; YAN Chen; WANG Nan-nan; HAO Xiao-yan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

9 .     phytyl palmitate
    ÏàËÆ¶È:71.4%
Natural Product Research and Development          2007          19          944-947
Chemical Constituents of Chondria crassicaulis
YIN Shuai-wen;SHI Yan-ping; LI Xiao-ming; WANG Bin-gui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

10 .     Pakistano1
C30H50O     ÏàËÆ¶È:70%
Journal of Natural Products          1990          Vol 53          1342
A New Pentacyclic Triterpene from Abutilon pakistanicum
Zaheer Ahmed, Syed Najam-ul-Hussain Kazmi, Abdul Malik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

11 .     3b(2-hydroxy)-ethoxycholest-5-ene
    ÏàËÆ¶È:68.9%
Bioorganic & Medicinal Chemistry Letters          2010          20          2872-2875
Irina A. Nikolaeva, Alexander Yu. Misharin, Gelii V. Ponomarev, Vladimir P. Timofeev, Yaroslav V. Tkachev
Irina A. Nikolaeva, Alexander Yu. Misharin, Gelii V. Ponomarev, Vladimir P. Timofeev, Yaroslav V. Tkachev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

12 .     phytyl-1-hexanoate
C26H50O2     ÏàËÆ¶È:67.8%
Natural Product Research          2006          20          665-670
Potent tyrosinase inhibitors from Trifolium balansae
Temine Şabudak; Mahmut Tareq Hassan Khan; M Iqbal Choudhary; Sevil Oksuz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

13 .     dihydroxylycopaene
C40H60O2     ÏàËÆ¶È:67.8%
Phytochemistry          1997          44          671-678
Four polymethylsqualene epoxides and one acyclic tetraterpene epoxide from Botryococcus braunii
V. Delahais, P. Metzger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

14 .     5¦Á-(17R,20R)-14,15-secochoiestane
    ÏàËÆ¶È:67.8%
Steroids          1990          55          263-265
Studies of the synthesis of biomarkers. VII. Synthesis of 5¦Á-(17R,20R)-14,15-secocholestane
Tong-Shuang Li, Yu-Lin Li, Xiao-Tian Liangt
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

15 .     compound 3
C27H44O2     ÏàËÆ¶È:67.8%
Tetrahedron Letters          2003          44          237-239
Efficient two-step synthesis of methylphytylbenzoquinones: precursor intermediates in the biosynthesis of vitamin E
Satyamaheshwar Peddibhotla, Zigang Cheng, Dean DellaPenna, Jetze J. Tepe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

16 .     Cholest-5-en-3¦Â-ol cholesterol
C27H46O     ÏàËÆ¶È:67.8%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

17 .     Cholest-5-en-3¦Â-ol cholesterol
C27H46O     ÏàËÆ¶È:67.8%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

18 .     Cholest-5-en-3¦Â-yl acetate
C29H48O2     ÏàËÆ¶È:67.8%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

19 .     3-epilycoclavanol
    ÏàËÆ¶È:66.6%
Chinese Traditional and Herbal Drugs          2010          41          1960-1963
Éì½î²ÝµÄ»¯Ñ§³É·ÖÑо¿
ëø´ä´ä;ºÎÓÀÖ¾;·ë½ðÀÚ;°ÍÏþÓê;Àî¶«Ó°
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

20 .     5-Cholesten-3¦Â-yl formate (3¦Â-cholesterylformate
C28H46O2     ÏàËÆ¶È:65.5%
Steroids          2006          71          632-638
A simple, convenient and chemoselective formylation of sterols by Vilsmeier reagent
Vandana Srivastava, Arvind Singh Negi, J.K. Kumar, M.M. Gupta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

21 .     ¦Á-ÉúÓý·Ó
C29H50O2     ÏàËÆ¶È:65.5%
Journal of Shenyang Pharmaceutical University          2003          20          425-427
Chemical constituents of Pyrrosia petiolosa(Christ) Ching
WANG Nan, WANG Jin-hui, CHENG Jie, LI Xian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

22 .     5,13-Dimethyl-5-heptadecen-1-ol
    ÏàËÆ¶È:65.5%
Bioscience, Biotechnology, and Biochemistry          2009          73          1618-1622
Synthesis and Field Evaluation of Methyl-branched Ketones, Sex Pheromone Components Produced by Lithosiinae Female Moths in the Family of Arctiidae
Nguyen Duc DO, Masakatsu KINJO, Tomonori TAGURI, Yasushi ADACHI, Rei YAMAKAWA and Tetsu ANDO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

23 .     N-Hydroxysuccinimidyl 5-cholesten-3¦Â-yloxy succinate
C31H50O4     ÏàËÆ¶È:64.5%
Chinese Chemical Letters          2006          17          173-176
Synthesis and Characterization of a Novel Galactosylated Cholesterol
Shao Ning WANG, Ying Kun QIU, Hui XU, Yi Hui DENG, Da Wei CHEN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

24 .     glucinoprenyl 8
C40H72O     ÏàËÆ¶È:64.5%
Phytochemistry          1997          46          715-720
Arachisprenols: Polyprenols possessing a geranyl residue from Arachis hypogaea
Tadashi Aoki, Kazuhiko Matsuo, Takayuki Suga, Shinji Ohta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

25 .     sitost-5-en-3¦Â-ol acetate
C31H52O2     ÏàËÆ¶È:64.5%
Chinese Traditional and Herbal Drugs          2010          41          1052-1056
Chemical constituents from stems of Melicope pteleifolia
LI Shuo-guo; YANG Yin; YE Wen-cai; JIANG Ren-wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

26 .     menellsteroid A
C27H48O4     ÏàËÆ¶È:64.2%
Helvetica Chimica Acta          2006          Vol. 89          813
Three New Polyoxygenated Steroids from Two Species of the South China Sea Gorgonian Muricella flexuosa and Menella verrucosa BRUNDIN
Wen Zhang, Hui Huang, Yu Ding, Margherita Gavagnin, Ernesto Mollo, Guido Cimino, and Yue-Wei Guo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

27 .     3¦Â-chlorocholest-5-ene
    ÏàËÆ¶È:64.2%
Chemistry of Natural Compounds          2000          36          595-598
13C NMR SPECTRA OF FUNCTIONALLY SUBSTITUTED 3 ¦Â-CHLORODERIVATIVES OF CHOLESTEROL AND ¦Â -SITOSTEROL
N. V. Kovganko, Zh. N. Kashkan, and E. V. Borisov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

28 .     monoacetate derivative of dihydroxylycopaene
C42H82O3     ÏàËÆ¶È:64.2%
Phytochemistry          1997          44          671-678
Four polymethylsqualene epoxides and one acyclic tetraterpene epoxide from Botryococcus braunii
V. Delahais, P. Metzger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

29 .     cholesterol
    ÏàËÆ¶È:64.2%
China Journal of Chinese Materia Medica          2010          35          2416-2419
Chemical constituents of bear bile
LUO Qiang; CHEN Quancheng; WU Yao; JIANG Miaomiao; CHEN Zhihong; ZHANG Xiaokun; CHEN Haifeng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

30 .     29,30-nordimethyl lanost-2-en
    ÏàËÆ¶È:64.2%
Indian Journal of Chemistry          2007          46B          173-176
Two new terpenes from the lichen Parmelia perlata
Abdullah,S Tarique; Hamid,Hinna; Ali,Mohammad; Ansari,S H; Alam,M Sarwar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

31 .     Cholestane-3¦Â,5¦Á,6¦Â,11b-tetrol
C27H48O4     ÏàËÆ¶È:64.2%
Pharmazie          2006          61          645-647
New polyoxygenated steroids from the South China Sea gorgonian Echinogorgia aurantiaca
Yunqi Qiu, Shuhua Qi, Si Zhang, Jin Yang and Zhihui Xiao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

32 .     ¦Ä-tocopherol
    ÏàËÆ¶È:64.2%
Journal of Shenyang Pharmaceutical University          2007          24          679-681
Chemical constituents from Canavalia gladiata
LI Ning, LI Xian, FENG Zhi-guo, MASAYUKI Yoshikawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

33 .     17-hydroxyeujindole
C28H39NO     ÏàËÆ¶È:64.2%
Heterocycles          2011          83          351-356
New Type Indole Diterpene, Eujindoles, from Eupenicillium javanicum
Shou Nakadate, Koohei Nozawa,* Hitoshi Horie, Yuichi Fujii, and Takashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

34 .     phylloquinone-d7
C31H39D7O2     ÏàËÆ¶È:64.2%
Bioorganic & Medicinal Chemistry          2010          18          3116-3124
Structure¨Cactivity relationships in the conversion of vitamin K analogues into menaquinone-4. Substrates essential to the synthesis of menaquinone-4 in cultured human cell lines
Yoshitomo Suhara, Akimori Wada, Yoji Tachibana, Masato Watanabe, Kanae Nakamura, Kimie Nakagawa, Toshio Okano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

35 .     compound 7
C27H38N2O4     ÏàËÆ¶È:64.2%
Chinese Chemical Letters          2011          22          757-760
Synthesis and VEGF inhibitory activity of 16,17-pyrazo-annulated steroids
Hong Shan Liu, Hu Ling Zheng, Mei Ge, Peng Xia, Ying Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

36 .     5¦Á-Cholestane
C27H48     ÏàËÆ¶È:64.2%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

37 .     3¦Â-Chlorocholest-5-ene
C27H45Cl     ÏàËÆ¶È:64.2%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

38 .     Cholest-5-en-3¦Â-ol cholesterol
C27H46O     ÏàËÆ¶È:64.2%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

39 .     Cholest-5-en-3¦Â-ol cholesterol
C27H46O     ÏàËÆ¶È:64.2%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

40 .     Cholest-5-en-3¦Â-ol cholesterol
C27H46O     ÏàËÆ¶È:64.2%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

41 .     compound 5
C35H53O6N     ÏàËÆ¶È:63.6%
Chinese Chemical Letters          2006          17          173-176
Synthesis and Characterization of a Novel Galactosylated Cholesterol
Shao Ning WANG, Ying Kun QIU, Hui XU, Yi Hui DENG, Da Wei CHEN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

42 .     Phytyl (9Z,12Z,15Z)-linolenate
C38H68O2     ÏàËÆ¶È:63.6%
Natural Product Communications          2011          6          767-772
Lipophilic Components from the Ecuadorian Plant Schistocarpha eupatorioides
Gianluca Gilardoni, Solveig Tosi, Giorgio Mellerio, Maria Elena Maldonado, Ximena Chiriboga and Giovanni Vidari
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

43 .     yunnandaphninine H
    ÏàËÆ¶È:63.3%
Helvetica Chimica Acta          2008          Vol. 91          838
Yunnandaphninines F and G, New C30 Alkaloids from Daphniphyllum yunnanense
Ying-Tong Di, Ling-Li Liu, Chun-Shun Li, Yu Zhang, Qiang Zhang, Shu-Zhen Mu, Qian-Yun Sun, Fu-Mei Yang, Hai-Yang Liu, and Xiao-Jiang Hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

44 .     lycernuic acid A
    ÏàËÆ¶È:63.3%
Journal of Natural Products          2002          65          979-985
Natural Products Inhibiting Candida albicans Secreted Aspartic Proteases from Lycopodium cernuum
Zhizhen Zhang, Hala N. ElSohly, Melissa R. Jacob, David S. Pasco,Larry A. Walker, and Alice M. Clark
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

45 .     3¦Â-hydroxy-urs-5(6)-en-28-oic acid
C30H48O3     ÏàËÆ¶È:63.3%
Chinese Chemical Letters          1998          9          737-738
A New Triterpenoid from teucrium Integrifolium
Xing Liang CHEN,Tian En WANG,Bei JIANG,Zhong Wen LIN,Han Dong SUN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

46 .     integrifolin
C30H48O3     ÏàËÆ¶È:63.3%
Natural Product Research          2000          14          459-462
A New Fernane-Type Triterpenoid from Teucrium integrifolium
Xing-Liang Chen; Tian-En Wang; Bei Jiang; Zhong-Wen Lin; Yang Lu; Qi-Tai Zheng; Han-Dong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

47 .     serrat-14-en-3¦Â,21¦Â,24-triol
    ÏàËÆ¶È:63.3%
Natural Product Research          2004          18          453-459
Serratane-type Triterpenoids from Huperzia Serrata
Hui Zhou; Yun-Sen Li; Xiao-Tian Tong; Hui-Qing Liu; Shan-Hao Jiang; Da-Yuan Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

48 .     hexadecanoyl choleserol esterol
C43H76O2     ÏàËÆ¶È:63.3%
China Journal of Chinese Materia Medica          2002          27          435-436
The Studies on the Chemical Componensts of Trutleback
JIANG Dacheng, WANG Yongsheng, XIU Yanmei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

49 .     28,29dihydroxyfriedelan-3-one
    ÏàËÆ¶È:63.3%
Journal of Natural Products          1990          Vol 53          1039
Antitumor Agents, 116. Cytotoxic Triterpenes from Maytenus diversifolia
Hiroshi Nozaki, Yukinaga Matsuura, Satomi Hirono, Ryoji Kasai, Jer-Jang Chang, Kuo-Hsiung Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

50 .     rubiprasin C
    ÏàËÆ¶È:63.3%
Phytochemistry          1994          37          1517-1575
13C NMR Spectra of pentacyclic triterpenoids¡ªa compilation and some salient features
Shashi B. Mahato, Asish P. Kundu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3Â¥2012-06-23 18:09:26
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1 .     trans-phytyl palmitate
C16H31O     ÏàËÆ¶È:83.8%
Journal of Natural Products          1991          Vol 54          1444
Diterpene Fatty Acid Ester from Leucas nutans
Mashooda Hasan, Dadu Khan Burdi, Viqar Uddin Ahmad
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     phytyl-1-hexanoate
    ÏàËÆ¶È:75%
Natural Product Research          2007          21          828-833
Lipid constituents of Trifolium resupinatum var. microcephalum
Temine Sabudak; Emel Isik; Sevil Oksuz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     epoxylycopaene
C40H78O     ÏàËÆ¶È:75%
Phytochemistry          1997          44          671-678
Four polymethylsqualene epoxides and one acyclic tetraterpene epoxide from Botryococcus braunii
V. Delahais, P. Metzger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     balansenate I
C32H62O2     ÏàËÆ¶È:73.3%
Helvetica Chimica Acta          2003          Vol. 86          2452
New Long-Chain Esters and Adenine Analogs from the Leaves of Formosan Bridelia balansae
Yeh-Hsin Tsai, Ih-Sheng Chen, and Ian-Lih Tsai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     palmitate
C36H70O2     ÏàËÆ¶È:72.4%
Natural Product Communications          2011          6          767-772
Lipophilic Components from the Ecuadorian Plant Schistocarpha eupatorioides
Gianluca Gilardoni, Solveig Tosi, Giorgio Mellerio, Maria Elena Maldonado, Ximena Chiriboga and Giovanni Vidari
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     trianthenol
C40H78O     ÏàËÆ¶È:71.4%
Phytochemistry          2001          56          99-102
Trianthenol: an antifungal tetraterpenoid from Trianthema portulacastrum (Aizoaceae)
Ha?z Rub Nawaz, Abdul Malik , Muhammad Shaiq Ali
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     glucinoprenyl 7
C35H64O     ÏàËÆ¶È:71.4%
Phytochemistry          1997          46          715-720
Arachisprenols: Polyprenols possessing a geranyl residue from Arachis hypogaea
Tadashi Aoki, Kazuhiko Matsuo, Takayuki Suga, Shinji Ohta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     trianthenol
    ÏàËÆ¶È:71.4%
Natural Product Research and Development          2010          22          245-247
Chemical Constituents from Reineckia carnea Kunth
YANG Jian-qiong; WANG Ye; YAN Chen; WANG Nan-nan; HAO Xiao-yan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     phytyl palmitate
    ÏàËÆ¶È:71.4%
Natural Product Research and Development          2007          19          944-947
Chemical Constituents of Chondria crassicaulis
YIN Shuai-wen;SHI Yan-ping; LI Xiao-ming; WANG Bin-gui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     Pakistano1
C30H50O     ÏàËÆ¶È:70%
Journal of Natural Products          1990          Vol 53          1342
A New Pentacyclic Triterpene from Abutilon pakistanicum
Zaheer Ahmed, Syed Najam-ul-Hussain Kazmi, Abdul Malik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     3b(2-hydroxy)-ethoxycholest-5-ene
    ÏàËÆ¶È:68.9%
Bioorganic & Medicinal Chemistry Letters          2010          20          2872-2875
Irina A. Nikolaeva, Alexander Yu. Misharin, Gelii V. Ponomarev, Vladimir P. Timofeev, Yaroslav V. Tkachev
Irina A. Nikolaeva, Alexander Yu. Misharin, Gelii V. Ponomarev, Vladimir P. Timofeev, Yaroslav V. Tkachev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     phytyl-1-hexanoate
C26H50O2     ÏàËÆ¶È:67.8%
Natural Product Research          2006          20          665-670
Potent tyrosinase inhibitors from Trifolium balansae
Temine ?abudak; Mahmut Tareq Hassan Khan; M Iqbal Choudhary; Sevil Oksuz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     dihydroxylycopaene
C40H60O2     ÏàËÆ¶È:67.8%
Phytochemistry          1997          44          671-678
Four polymethylsqualene epoxides and one acyclic tetraterpene epoxide from Botryococcus braunii
V. Delahais, P. Metzger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     compound 3
C27H44O2     ÏàËÆ¶È:67.8%
Tetrahedron Letters          2003          44          237-239
Efficient two-step synthesis of methylphytylbenzoquinones: precursor intermediates in the biosynthesis of vitamin E
Satyamaheshwar Peddibhotla, Zigang Cheng, Dean DellaPenna, Jetze J. Tepe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     Cholest-5-en-3¦Â-ol cholesterol
C27H46O     ÏàËÆ¶È:67.8%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     Cholest-5-en-3¦Â-ol cholesterol
C27H46O     ÏàËÆ¶È:67.8%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     Cholest-5-en-3¦Â-yl acetate
C29H48O2     ÏàËÆ¶È:67.8%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     3-epilycoclavanol
    ÏàËÆ¶È:66.6%
Chinese Traditional and Herbal Drugs          2010          41          1960-1963
Éì½î²ÝµÄ»¯Ñ§³É·ÖÑо¿
ëø´ä´ä;ºÎÓÀÖ¾;·ë½ðÀÚ;°ÍÏþÓê;Àî¶«Ó°
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     5-Cholesten-3¦Â-yl formate (3¦Â-cholesterylformate
C28H46O2     ÏàËÆ¶È:65.5%
Steroids          2006          71          632-638
A simple, convenient and chemoselective formylation of sterols by Vilsmeier reagent
Vandana Srivastava, Arvind Singh Negi, J.K. Kumar, M.M. Gupta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     ¦Á-ÉúÓý·Ó
C29H50O2     ÏàËÆ¶È:65.5%
Journal of Shenyang Pharmaceutical University          2003          20          425-427
Chemical constituents of Pyrrosia petiolosa(Christ) Ching
WANG Nan, WANG Jin-hui, CHENG Jie, LI Xian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     5,13-Dimethyl-5-heptadecen-1-ol
    ÏàËÆ¶È:65.5%
Bioscience, Biotechnology, and Biochemistry          2009          73          1618-1622
Synthesis and Field Evaluation of Methyl-branched Ketones, Sex Pheromone Components Produced by Lithosiinae Female Moths in the Family of Arctiidae
Nguyen Duc DO, Masakatsu KINJO, Tomonori TAGURI, Yasushi ADACHI, Rei YAMAKAWA and Tetsu ANDO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     N-Hydroxysuccinimidyl 5-cholesten-3¦Â-yloxy succinate
C31H50O4     ÏàËÆ¶È:64.5%
Chinese Chemical Letters          2006          17          173-176
Synthesis and Characterization of a Novel Galactosylated Cholesterol
Shao Ning WANG, Ying Kun QIU, Hui XU, Yi Hui DENG, Da Wei CHEN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     glucinoprenyl 8
C40H72O     ÏàËÆ¶È:64.5%
Phytochemistry          1997          46          715-720
Arachisprenols: Polyprenols possessing a geranyl residue from Arachis hypogaea
Tadashi Aoki, Kazuhiko Matsuo, Takayuki Suga, Shinji Ohta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     sitost-5-en-3¦Â-ol acetate
C31H52O2     ÏàËÆ¶È:64.5%
Chinese Traditional and Herbal Drugs          2010          41          1052-1056
Chemical constituents from stems of Melicope pteleifolia
LI Shuo-guo; YANG Yin; YE Wen-cai; JIANG Ren-wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     3¦Â-chlorocholest-5-ene
    ÏàËÆ¶È:64.2%
Chemistry of Natural Compounds          2000          36          595-598
13C NMR SPECTRA OF FUNCTIONALLY SUBSTITUTED 3 ¦Â-CHLORODERIVATIVES OF CHOLESTEROL AND ¦Â -SITOSTEROL
N. V. Kovganko, Zh. N. Kashkan, and E. V. Borisov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     monoacetate derivative of dihydroxylycopaene
C42H82O3     ÏàËÆ¶È:64.2%
Phytochemistry          1997          44          671-678
Four polymethylsqualene epoxides and one acyclic tetraterpene epoxide from Botryococcus braunii
V. Delahais, P. Metzger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     cholesterol
    ÏàËÆ¶È:64.2%
China Journal of Chinese Materia Medica          2010          35          2416-2419
Chemical constituents of bear bile
LUO Qiang; CHEN Quancheng; WU Yao; JIANG Miaomiao; CHEN Zhihong; ZHANG Xiaokun; CHEN Haifeng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     29,30-nordimethyl lanost-2-en
    ÏàËÆ¶È:64.2%
Indian Journal of Chemistry          2007          46B          173-176
Two new terpenes from the lichen Parmelia perlata
Abdullah,S Tarique; Hamid,Hinna; Ali,Mohammad; Ansari,S H; Alam,M Sarwar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     5¦Á-(17R,20R)-14,15-secochoiestane
    ÏàËÆ¶È:64.2%
Steroids          1990          55          263-265
Studies of the synthesis of biomarkers. VII. Synthesis of 5¦Á-(17R,20R)-14,15-secocholestane
Tong-Shuang Li, Yu-Lin Li, Xiao-Tian Liangt
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     Cholestane-3¦Â,5¦Á,6¦Â,11b-tetrol
C27H48O4     ÏàËÆ¶È:64.2%
Pharmazie          2006          61          645-647
New polyoxygenated steroids from the South China Sea gorgonian Echinogorgia aurantiaca
Yunqi Qiu, Shuhua Qi, Si Zhang, Jin Yang and Zhihui Xiao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     C-friedo-oleana-7,9(11)-diene-3¦Á,29-diol
C30H48O2     ÏàËÆ¶È:64.2%
Chinese Pharmaceutical Journal          2000          35          733-736
Studies on the chemical constituents of unsaponifiable lipids from the seeds of Trichosanthes kirilowii
CHAO Zhi mao, HE Bo, ZHANG Ying, AKIHISA Toshihiro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     karounidiol
C30H48O2     ÏàËÆ¶È:64.2%
Chinese Pharmaceutical Journal          2001          36          157-160
Study on the chemical constituents of unsaponifiable lipids from the seeds of Trichosanthes rosthornii
CHAO Zhi mao, HE Bo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     ¦Ä-tocopherol
    ÏàËÆ¶È:64.2%
Journal of Shenyang Pharmaceutical University          2007          24          679-681
Chemical constituents from Canavalia gladiata
LI Ning, LI Xian, FENG Zhi-guo, MASAYUKI Yoshikawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     phylloquinone-d7
C31H39D7O2     ÏàËÆ¶È:64.2%
Bioorganic & Medicinal Chemistry          2010          18          3116-3124
Structure¨Cactivity relationships in the conversion of vitamin K analogues into menaquinone-4. Substrates essential to the synthesis of menaquinone-4 in cultured human cell lines
Yoshitomo Suhara, Akimori Wada, Yoji Tachibana, Masato Watanabe, Kanae Nakamura, Kimie Nakagawa, Toshio Okano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     compound 7
C27H38N2O4     ÏàËÆ¶È:64.2%
Chinese Chemical Letters          2011          22          757-760
Synthesis and VEGF inhibitory activity of 16,17-pyrazo-annulated steroids
Hong Shan Liu, Hu Ling Zheng, Mei Ge, Peng Xia, Ying Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     5¦Á-Cholestane
C27H48     ÏàËÆ¶È:64.2%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     3¦Â-Chlorocholest-5-ene
C27H45Cl     ÏàËÆ¶È:64.2%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     Cholest-5-en-3¦Â-ol cholesterol
C27H46O     ÏàËÆ¶È:64.2%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     Cholest-5-en-3¦Â-ol cholesterol
C27H46O     ÏàËÆ¶È:64.2%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     compound 5
C35H53O6N     ÏàËÆ¶È:63.6%
Chinese Chemical Letters          2006          17          173-176
Synthesis and Characterization of a Novel Galactosylated Cholesterol
Shao Ning WANG, Ying Kun QIU, Hui XU, Yi Hui DENG, Da Wei CHEN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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