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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 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 ÈܼÁÑ¡Ï È«²¿ CDCl3 CD3CD2OD CD2Cl2 C5D5N C3D7NO CD3SOCD3 C4D8O (CH3)4Si C4D8O2 CD3COOD C4D8O2 H2O D2O CF3COOD CD3OD ND3 CD3COCD3 C6D6 CD3CN ²éѯ¿ÕÖµ Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½4231¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |
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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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

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