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| ¦Ä13C(75 MHz, CDCl3): 12.57, 17.03, 20.61, 21.25, 21.30, 22.21, 22.56, 24.28, 29.52, 30.36, 30.97, 32.51, 34.66, 38.46, 39.97, 40.53, 40.85, 42.94, 46.02, 56.11, 56.18, 67.79, 76.17, 76.25, 109.75, 129.32, 136.15, 153.17. |
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²éѯ½á¹û£º¹²²éµ½12110¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (20R,22E,24R)-Stigmasta-22,25-dien-3¦Â,6¦Â,9¦Á-triol C29H48O3 ÏàËÆ¶È:89.6% Steroids 2013 78 711-716 New cytotoxic steroids from the leaves of Clerodendrum trichotomum Rui-Lan Xu, Rui Wang, Lan Ding, Yan-Ping Shi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 3a ÏàËÆ¶È:85.7% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . compound 16 C27H44O2 ÏàËÆ¶È:85.7% Steroids 2007 72 643-652 Atypical regioselective biohydrolysis on steroidal oxiranes by Aspergillus niger whole cells: Some stereochemical features Fabricio R. Bisogno, Alejandro A. Orden, Celeste Aguirre Pranzoni, Diego A. Cifuente, Oscar S. Giordano, Marcela Kurina Sanz Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 5¦Á-ergosta-7,22-diene-3¦Â,5,6¦Â-triol ÏàËÆ¶È:85.7% Journal of Natural Products 1988 Vol 51 1098 Polar Steroids from the Marine Scallop Patinopecten yessoensis Maria Iorizzi, Luigi Minale, Raffaele Riccio, Jong-Soo Lee, Takeshi Yasumoto Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 5¦Á-cholestane-3¦Â,5,6¦Â-triol C27H4HO3 ÏàËÆ¶È:85.7% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (22E,24R)-Âó½ÇçÞ-7,22-¶þÏ©-3¦Â,5¦Á,6¦Â-Èý´¼ ÏàËÆ¶È:85.7% Chemical Journal of Chinese Universities 2005 26 81-83 Two New Steroidal Saponins from the Soft Coral Cladiella sp. ZHANG Guang-Wen,MA Xiang-Quan, YAN Su-Jun,ZENG Long-Mei,SU Jing-Yu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . bebryceoid A C26H44O3 ÏàËÆ¶È:85.7% Chemical & Pharmaceutical Bulletin 2010 58 1240-1242 New 3¦Â,5¦Á,6¦Â-Trihydroxysteroids from the Octocorals Bebryce sp. (Plexauridae) and Carijoa sp. (Clavulariidae) Ping-Jyun Sung and Chih-Yang Liu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . cholest-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:85.7% Journal of Shenyang Pharmaceutical University 2010 27 191-194 Steroids from marine spongeSpheciospongia sp. from the South China Sea LIU Dong, LIN Wen-han, DENG Zhi-wei, WU Li-jun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . (22E,24R)-rgosta-7,22-diene-3¦Â,5¦Á,6¦Â-triol ÏàËÆ¶È:85.7% Natural Product Research and Development 2007 19 610-613 Chemical Constituents from Schizophyllum commune MAO Shao-chun; LI Zhu-ying; LI Cong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . muriflasteroid A C28H46O4 ÏàËÆ¶È:85.7% Steroids 2013 78 108-114 3¦Â,5¦Á,6¦Â-Oxygenated sterols from the South China Sea gorgonian Muriceopsis flavida and their tumor cell growth inhibitory activity and apoptosis-inducing function Tao-Fang Liu, Xin Lu, Hua Tang, Min-Min Zhang, Pan Wang, Peng Sun, Zhi-Yong Liu, Zeng-Lei Wang, Ling Li, Yao-Cheng Rui, Tie-Jun Li, Wen Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 3¦Â,5¦Á,6¦Â-ÈýôÇ»ùµ¨çÞÍé´¼ ÏàËÆ¶È:85.7% Acta Scientiarum Naturalium Universitatis Sunyatseni 1988 27(2) 69-76 Studies on the Chemical Constituents of the Chinese Soft Coral Lobophytum chevalieri(XVII) Li Ruisheng Di Li Long Kanghou Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 5¦Á-Cholestane-3¦Â,5,6¦Â-triol C27H48O3 ÏàËÆ¶È:85.7% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . cholestan-3¦Â,5¦Á,6¦Â-triol C27H48O3 ÏàËÆ¶È:85.7% Journal of Tropical Oceanography 2013 32 55−59 Steroids from South China Sea sponge Halichondria sp. SUN Jian-fan, LI Yun-qiu, YANG Bin, HU Jing, DONG Guang, LIU Yong-hong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . cholestan-3¦Â,5¦Á,6¦Â-triol C27H48O3 ÏàËÆ¶È:85.7% Tropic Oceanology 2013 32 55-59 Steroids from South China Sea sponge Halichondria sp. SUN Jian-fan, LI Yun-qiu, YANG Bin, HU Jing, DONG Guang, LIU Yong-hong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . cerevisterol ÏàËÆ¶È:85.7% Chinese Joumal of Experimental Traditional Medical Fomulae 2014 20 42-46 Chemical Constituents of Laetiporus montanus LI Wei, BAO Hai-ying, BAU Tolgor Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . cerevisterol ÏàËÆ¶È:85.7% Natural Product Research 2015 29 345-348 Antimicrobial and allelopathic metabolites produced by Penicillium brasilianum Hao-Yu Tang, Qiang Zhang, He Li & Jin-Ming Gao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . (22E,24S)-11¦Á-acetoxy-ergostane-22,25-dien-3¦Â,5¦Á,6¦Â-triol C30H48O5 ÏàËÆ¶È:83.3% Marine Drugs 2013 11 775-787 Bioactive Polyoxygenated Steroids from the South China Sea Soft Coral, Sarcophyton sp. Zenglei Wang, Hua Tang, Pan Wang, Wei Gong, Mei Xue, Hongwei Zhang, Taofang Liu, Baoshu Liu, Yanghua Yi and Wen Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . 24-ethyl-5¦Á-cholestane-3¦Â,5,6¦Â-triol ÏàËÆ¶È:82.7% 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . 3,5,6-trihydroxysitostane ÏàËÆ¶È:82.7% Phytochemistry 1998 47 789-797 On the cytotoxity of oxidized phytosterols isolated from photoautotrophic cell cultures of Chenopodium rubrum tested on meal-worms Tenebrio molitor Werner Meyer, Harald Jungnickel, Markus Jandke, Konrad Dettner, Gerhard Spiteller Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . 24¦Î-methylcholestane-3¦Â,5¦Á,6¦Â,25-tetrol 25-monoacetate ÏàËÆ¶È:82.7% Journal of the Chinese Chemical Society 1991 38 397-399 Isolation of a Bioactive Sterol from the Soft Coral Lobophytum mirabile ÔSÖ¾ºê(Jyh-Horng Sheu);È~´äÈA(Tsuey-Hua Yeh) Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . compound 4a ÏàËÆ¶È:82.7% Magnetic Resonance in Chemistry 1988 26 104-107 Nuclear magnetic resonance and infrared spectral characterization of some peroxysterols Krzysztof Jaworski and Leland L. Smith Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 22 . (23S,24R)-dimethylcholest-7-ene-3¦Â,5¦Á,6¦Â-triol C29H50O3 ÏàËÆ¶È:82.7% Phytochemistry Letters 2014 9 1-6 New 3¦Â,6¦Â-dihydroxy and 3¦Â,5¦Á,6¦Â-trihydroxy sterols from marine bryozoan Bugula neritina in South China Sea and their cytotoxicity Xiang-Rong Tian, Hai-Feng Tang, Yu-Shan Li, Hou-Wen Lin, Xiao-Pei Fan, Jun-Tao Feng, Xing Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 23 . 6¦Â-acetoxycholest-22E-ene-3¦Â,5¦Á,18-triol C29H48O5 ÏàËÆ¶È:82.7% Marine Drugs 2014 12 5864-5880 Polyoxygenated Steroids from the Octocoral Leptogorgia punicea and in Vitro Evaluation of Their Cytotoxic Activity Maria Izabel G. Moritz, Lucas Lourenço Marostica, ¨¦verson M. Bianco, Maria Tereza R. Almeida, João L. Carraro, Gabriela M. Cabrera, Jorge A. Palermo, Cl¨¢udia M. O. Simões and Eloir P. Schenkel Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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