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ÈܼÁCDCl3 13C NMR (101 MHz, CDCl3) ¦Ä 10.90, 13.17 ,17.76 ,18.01 , 18.38 ,18.76 ,20.06 ,21.65 ,22.04 , 23.28 ,24.04 ¨C 23.54 ,25.02 ,26.20 ,26.96 ,27.24 , 28.84 ¨C 27.91 , 30.52 ¨C 30.27,30.73 ,31.78 ,32.96 ,33.39 ,35.13,35.48 ,35.96 ,36.22 ,38.35 ,38.75 ,41.24 ,44.80 ,49.10 ,55.02 ,55.74,70.84 ,75.69 ,76.00 ,76.32,120.74 ,128.71,129.00 ,178.65 1H NMR (400 MHz, CDCl3) ¦Ä 0.08 ¨C -0.07,1.61 ¨C 1.10,4.09 ¨C 3.86,4.12,6.62,7.02,7.27,7.42,7.57 ,7.87 |
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ym633: ½ð±Ò+30 2014-05-25 19:11:15
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ym633: ½ð±Ò+30 2014-05-25 19:11:15
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1 . (6R,E)-6-((3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-3-(palmitoyloxy)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)-3-ethyl-2-methylhept-4-enoic acid C45H78O4 ÏàËÆ¶È:75.5% Life Sciences 2013 92 202-210 Antiulcer and antioxidant activities of a new steroid from Morus alba Aftab Ahmad, Gaurav Gupta, Muhammad Afzal, Imran Kazmi, Firoz Anwar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . ¦Â-sitosterol palmitate ÏàËÆ¶È:74.4% Modern Chinese Medicine 2013 15 175-177 Isolation and Identification of Non-alkaloid Constituents from Fritillaria pallidiflora Schrenk Li Wen-ling, Bu Ren, Chen Chao-jun, Yu Teng-fei, Wang Jin-hui Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . sitosterol-3-O-6-palmityl-¦Â-D-glucopyranoside ÏàËÆ¶È:72.0% Lishizhen Medicine and Materia Medica Research 2013 24 2859-2860 Study on Chemical Constituents of Alocasia macrorrhiza ZHU Ling-hua, MENG Ling-jie, YE Wen-cai, ZHOU Guang-xiong* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . ¦Â-sitosteryl-3-O-¦Â-D-glucopyr-anoside-2'-O-palmitate C51H90O7 ÏàËÆ¶È:72.0% Natural Product Research and Development 2014 26 197-201 Chemical Constituents from the Roots of Nothapodytes pittosporoides BAI Yong-hua, SONG Qi-shi* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 24-ethylcholest-5-en-3¦Â-O-¦Â-D-pyranoglucosyl-6'-O-palmitat ÏàËÆ¶È:69.7% Phytochemical Analysis 1992 3 38-41 Characterization of acylated steryl glycosides from Euryale ferox by nuclear magnetic resonance spectroscopy Zhao Haoru and Zhao Shoushun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . Klainedoxasterol C79H146O7 ÏàËÆ¶È:69.7% Fitoterapia 2013 86 108-114 Lanostane-type triterpenoid and steroid from the stem bark of Klainedoxa gabonensis Eric Ren¨¦ Sieliatchom Nkanwen, Anar Sahib Gojayev, Hippolyte Kamdem Wabo, Jean Jules Kezetas Bankeu, Muhammad Choudhary Iqbal, Akif Alakbar Guliyev, Pierre Tane Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 5,6¦Â-Epoxycholesteryl-9,10-di-tertbutyldimethylsilyloxystearate C57H108O5Si2 ÏàËÆ¶È:69.5% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . ¦Â-Sitosteryl linoleate ÏàËÆ¶È:69.5% Zeitschrift f¨¹r Naturforschung C 2012 67 172-180 Anti-Helicobacter pylori Activity of the Methanolic Extract of Geum iranicum and its Main Compounds Somayeh Shahani, Hamid R. Monsef-Esfahani, Soodabeh Saeidnia, Parastoo Saniee, Farideh Siavoshi, Alireza Foroumadi, Nasrin Samadi, and Ahmad R. Gohari Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 7-Ketocholesteryl-9,10-di-tertbutyldimethylsilyloxystearate C57H106O5Si2 ÏàËÆ¶È:68.0% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 4-Benzyl-5-N-cyclohexylcarboxamido-4-aza-5¦Á-cholestan-3-one C40H62N2O2 ÏàËÆ¶È:67.4% Steroids 2008 73 1270-1276 Synthesis of 4-azasteroids by an intramolecular Ugi reaction Fernando Alonso, Sof¨ªa L. Acebedo, Andrea C. Bruttomesso, Javier A. Ram¨ªrez Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . (3¦Â,5¦Á,6¦Â,22E)-ergosta-7,22-diene-3,5,6-triol 6-linoleate ÏàËÆ¶È:66.6% Helvetica Chimica Acta 2007 Vol. 90 1165 New Steryl Esters of Fatty Acids from the Mangrove Fungus Aspergillus awamori Hao Gao, Kui Hong, Xue Zhang, Hong-Wei Liu, Nai-Li Wang, Ling Zhuang, and Xin-Sheng Yao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . cholestery 9,12-octadecadienoate ÏàËÆ¶È:66.6% Chinese Pharmaceutical Journal 2011 46 17-20 Studies on Chemical Constituents of Sarcopyramis nepdensis ZHANG Jin-wen, CHEN Hua-dong, LIAO Mei, ZHANG Yong-hui Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 6'-linoleic-¦Â-daucosterol C30H50O ÏàËÆ¶È:66.6% Natural Product Research and Development 2009 21 776-778 Chemical Constituents of the Roots of Ligularia fischeri DENG Mei-cai; JIAO Wei; DONG Wei-wei; LU Run-hua Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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