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²éѯ½á¹û£º¹²²éµ½54¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 2 ÏàËÆ¶È:55.5% Tetrahedron 1998 54 179-186 New cytotoxic sterols from the soft coral Gersemia fruticosa Reet Koljak, Annika Lopp, Tõnis Pehk, K¨¹lliki Varvas, Aleksander-Mati M¨¹¨¹risepp, Ivar Järving, Nigulas Samel Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 11-acetoxy-3¦Â,6¦Á-dihydroxy-9,11-seco-5¦Á-cholest-7-en-9-one C29H48O5 ÏàËÆ¶È:55.1% Bioorganic & Medicinal Chemistry 2009 17 4537-4541 9,11-Secosterols with antiproliferative activity from the gorgonian Eunicella cavolini Efstathia Ioannou, Ayman F. Abdel-Razik, Xanthippi Alexi, Constantinos Vagias, Michael N. Alexis, Vassilios Roussis Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (24S)-24-ethylcholesta-3¦Â,5¦Á,6¦Á-triol ÏàËÆ¶È:55.1% Chinese Journal of Applied & Environmental Biology 2009 15 615-620 Chemical Constituents from Polygonum perfoliatum LI Hongfang; MA Qingyun; LIU Yuqing; QIAN Jinfu; ZHOU Jun & ZHAO Youxing Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . dianoside I ÏàËÆ¶È:53.5% Phytochemistry 1998 47 1343-1349 Triterpenoid saponins from Vaccaria segetalis Kazuo Koike, Zhonghua Jia, Tamotsu Nikaido Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (24R)-24-ethyl-5¦Á-cholestane-3¦Â,5,6¦Â-triol C29H52O3 ÏàËÆ¶È:53.5% Journal of Natural Products 1991 Vol 54 1570 3¦Â,5¦Á,6¦Â-Trihydroxylated Sterols with a Saturated Nucleus from Two Populations of the Marine Sponge Cliona copiosa Giacomo Notaro, Vincenzo Piccialli, Donato Sica, Giuseppe Corriero Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 2¦Â,3¦Â,5¦Á and 15¦Â-O-tetraacetoxy-14-oxolathyra-12(13E)-ene-6(17)-epoxide C28H38O10 ÏàËÆ¶È:53.5% Fitoterapia 2010 81 891-893 Two new lathyrane type diterpenoids from Euphorbia aellenii Abdul Majid Ayatollahi, Mustafa Ghanadian, Suleiman Afsharypuor, Muhammad Iqbal Choudhary, Farzad Kobarfard, Mohammad Rahmati Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (22E)-2-ethoxycarbonyl-2-¦Â-hydroxy-24-methyl-Anor-cholest-5,22-diene-4-one C30H46O4 ÏàËÆ¶È:53.3% Steroids 2005 70 13-18 Steroids from the soft coral Dendronephthya sp. Guoqiang Li, Zhiwei Deng, Huashi Guan, Leen van Ofwegen, Peter Proksch, Wenhan Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (24S)-24-Ethyl-3¦Â-methoxy-8¦Á,9¦Á-epoxy-5¦Á-cholest-14-ene C30H50O2 ÏàËÆ¶È:53.3% Steroids 1994 59 181-184 Novel 3-¦Â-methoxysteroids from the senegalse sponge Microscleroderma spirophora Valeria Costantino, Ernesto Fattorusso, Alfonso Mangoni, Maurice Aknin, Emil M. Gaydou Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (22Z)-11-acetoxy-3¦Â,6¦Á-dihydroxy-24n-methyl-9,11-seco-5¦Á-cholesta-7,22-dien-9-one C30H48O5 ÏàËÆ¶È:53.3% Bioorganic & Medicinal Chemistry 2009 17 4537-4541 9,11-Secosterols with antiproliferative activity from the gorgonian Eunicella cavolini Efstathia Ioannou, Ayman F. Abdel-Razik, Xanthippi Alexi, Constantinos Vagias, Michael N. Alexis, Vassilios Roussis Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . sphenasin A C27H38O4 ÏàËÆ¶È:51.8% Phytochemistry 2008 69 2862-2866 Nortriterpenoids and lignans from Schisandra sphenanthera Wei-Lie Xiao, Sheng-Xiong Huang, Rui-Rui Wang, Jia-Liang Zhong, Xue-Mei Gao, Fei He,Jian-Xin Pu, Yang Lu, Yong-Tang Zheng, Qi-Tai Zheng, Han-Dong Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Âó½ÇçÞ-3¦Â,5¦Á,6¦Â-Èý´¼ ÏàËÆ¶È:51.8% Chinese Journal of Marine Drugs 2010 29(2) 6-9 Secondary metabolites from marine actinomycete Strep tomyces sp. ( No. 172221) MA Jing-jing, T ANG Jin-shan, GAO Hao, HONG Kui, ZHOU Guang-xiong, YAO Xin-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . methyl 6¦Á-hydroxy-17-(¦Á-methylbutyroxy)grindelate ÏàËÆ¶È:51.8% Phytochemistry 1987 26 467-470 Five grindelane diterpenoids from Grindelia acutifolia Barbara N. Timmermann,Joseph J. Hoffmann,Shivanand D. Jolad,Robert B. Bates,Teruna J. Siahaan Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 3¦Â,6¦Á,11-trihydroxy-9,11-seco-5¦Á-cholest-7-ene-9-one C28H46O4 ÏàËÆ¶È:51.8% Steroids 1998 63 575-578 New 9,11-secosterols from gorgonia Subergorgia suberosa of the Indian Ocean M. Aknin, V. Costantino, A. Mangoni, E. Fattorusso, E. M. Gaydou Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . µ¨çÞ-5-Ï©-3¦Â-´¼ ÏàËÆ¶È:51.8% Chinese Journal of Medicinal Chemistry 2007 17 95-100 Chemical constituents from soft coral Sinularia dissecta in south China sea JIN Peng-fei, LIN Wen-han, DENG Zhi-wei, PEI Yue-hu, SUN Chun-hua, Hu Xin Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . Chabamide K C28H50N2O2 ÏàËÆ¶È:51.8% Tetrahedron 2011 67 1885-1892 Novel dimeric amide alkaloids from Piper chaba Hunter: isolation, cytotoxic activity, and their biomimetic synthesis V. Rama Subba Rao, G. Suresh, K. Suresh Babu, S. Satyanarayana Raju, M.V.P.S. Vishnu vardhan, Sistla Ramakrishna, J. Madhusudana Rao Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . Chabamide K C28H50N2O2 ÏàËÆ¶È:51.8% Tetrahedron 2011 67 1885-1892 Novel dimeric amide alkaloids from Piper chaba Hunter: isolation, cytotoxic activity, and their biomimetic synthesis V. Rama Subba Rao, G. Suresh, K. Suresh Babu, S. Satyanarayana Raju, M.V.P.S. Vishnu vardhan, Sistla Ramakrishna, J. Madhusudana Rao Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 9 C28H39NO6 ÏàËÆ¶È:51.8% The Journal of Antibiotics 2002 55 239-248 Novel Stachyflin Derivatives from Stachybotrys sp. RF-7260 Fermentation, Isolation, Structure Elucidation and Biological Activities KAZUYUKI MINAGAWA,SHUICHI KOUZUKI,HIROYOSHI TANI,KIKUO ISHII,TATSUO TANIMOTO,YOSHIHIRO TERUI and TOSHIYUKI KAMIGAUCHI Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . stigmasta-3,5-dien-7-one ÏàËÆ¶È:51.7% Planta Medica 2000 66 67-69 Steroids from Harrisonia abyssinica Aliou M.Bald¨¦,Sandra Apers,Tess E.De Bruyne,Hilde Van Den Heuve,Magda Claeys, Arnold J.Vlietinck Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . (24R)-3¦Â -chlorostigmast-5-en-7-one oxime ÏàËÆ¶È:51.7% 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 ̼Æ×Ä£Äâͼ 20 . compound 3b ÏàËÆ¶È:51.7% Chemistry of Natural Compounds 1999 35 646-649 13C NMR SPECTRA OF II-SITOSTEROL DERIVATIVES WITH OXIDIZED RINGS A AND B N. V. Kovganko, Zh. N. Kashkan,E. V. Borisov, and E. V. Batura Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 24-ethyl-5¦Á-cholestane-3¦Â,5,6¦Â-triol ÏàËÆ¶È:51.7% China Journal of Chinese Materia Medica 2008 33 1035-1038 Study on Steroids of Cacalia tangutica LIU Qing, LIU Zhenling, TIAN Xuan Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . (24S)-24-ethyl-5¦Á-cholestane-3¦Â,5,6¦Â-triol C29H52O3 ÏàËÆ¶È:51.7% Journal of Natural Products 1991 Vol 54 1570 3¦Â,5¦Á,6¦Â-Trihydroxylated Sterols with a Saturated Nucleus from Two Populations of the Marine Sponge Cliona copiosa Giacomo Notaro, Vincenzo Piccialli, Donato Sica, Giuseppe Corriero Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . Stigmast-4-en-3-one ÏàËÆ¶È:51.7% Natural Product Sciences 2008 14 100-106 Phytochemical Constituents of Schizonepeta tenuifolia Briquet Lee, Il-Kyun; Kim, Min-Ah; Lee, Seung-Young; Hong, Jong-Ki; Lee, Jei-Hyun; Lee, Kang-Ro Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 5¦Á,6¦Â-Dihydroxysitosterol ÏàËÆ¶È:51.7% Korean Journal of Pharmacognosy 2008 39(3) 186-193 Phytochemical Studies on Astragalus Root (3);Triterpenoids and Sterols Jung, Hye-Sil; Lee, Eun-Ju; Lee, Je-Hyun; Kim, Ju-Sun; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . (24S)-24-Ethyl-5¦Á-cholest-7-en-3¦Â-ol ÏàËÆ¶È:51.7% Phytochemistry 1981 20 2403-2405 Minor and trace sterols of Dunaliella tertiolecta Jeffrey L. C. Wright Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . 3¦Â,5¦Á,6¦Â-ÈýôÇ»ù¶¹çÞÍé ÏàËÆ¶È:51.7% Chinese Traditional and Herbal Drugs 2010 41 1782-1785 ¹óÖÝ´ó·½ÁÖÏÂÔÔÅàÌìÂéµÄ»¯Ñ§³É·ÖÑо¿ ÕÅΰ;ËÎÆôʾ Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . sitosterone C29H48O ÏàËÆ¶È:51.7% Chinese Journal of Natural Medicines 2005 3 181-183 Chemical Constituents of Nauclea officinalis XUAN Wei-Dong; CHEN Hai-Sheng); YUAN Zhi-Xian; ZHU Ping Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . stigmasta-4-en-3-one C29H46O ÏàËÆ¶È:51.7% Chinese Journal of Natural Medicines 2008 6 271-274 Chemical Constituents from the Roots and Stems of Ervatamia hainanensis JIN Li; LU Jia; JIN Yong-Sheng; YANG Xiang-Nan; CHEN Hai-Sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . sitosterone ÏàËÆ¶È:51.7% Chinese Pharmaceutical Journal 2009 44 576-580 Studies on Antitumor Steroids and Flavonoids from Tamarix chinensis Lour. WANG Bin, REN Shu-wen, LI Guo-qiang, GUAN Hua-shi Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . stigmast-4-ene-3-one ÏàËÆ¶È:51.7% Turkish Journal of Chemistry 2006 30 325-332 Secondary Metabolites from Euphorbia helioscopia and Their Vasodepressor Activity ASLI BARLA, H¨¹SNİYE BİRMAN, ި¹KRAN K¨¹LT¨¹R, SEVİL ÖKS¨¹Z Structure 13C NMR ̼Æ×Ä£Äâͼ |

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