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listentomeгæ (³õÈëÎÄ̳)
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[ÇóÖú]
2014-10.17΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
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»¯ºÏÎï70-1 13C NMR (101 MHz, Acetone) ¦Ä 217.91, 213.58, 185.19, 170.22, 150.90, 137.28, 132.75, 108.16, 80.51, 78.32, 71.96, 71.82, 69.41, 55.16, 49.26, 47.86, 46.45, 40.43, 39.26, 36.92, 34.80, 33.77, 33.46, 33.13, 30.33, 27.27, 26.77, 25.95, 24.71, 24.01, 23.11, 19.86, 19.70, 19.52, 17.64 »¯ºÏÎï1-4-1 13C NMR (101 MHz, Acetone) ¦Ä 159.44, 141.48, 120.66, 70.83, 56.78, 56.05, 50.34, 45.85, 44.24, 42.46, 39.78, 37.36, 36.43, 36.04, 33.83, 31.91, 31.74, 31.65, 28.05, 24.05, 20.91, 19.18, 18.90, 18.45, 11.33 »¯ºÏÎï80-6 13C NMR (101 MHz, MeOD) ¦Ä 171.32, 171.02, 169.06, 138.18, 134.93, 134.67, 124.82, 79.57, 78.25, 72.52, 72.05, 71.45, 69.10, 68.47, 56.88, 49.21, 40.59, 40.39, 39.81, 37.95, 36.79, 33.98, 33.64, 33.26, 30.59, 30.24, 28.82, 28.46, 28.04, 25.85, 25.38, 25.27, 24.60, 23.02, 22.91, 22.31, 22.05, 20.00, 19.66, 19.37, 19.16, 19.08, 19.03. |
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»¯ºÏÎï70-1 1 . alisol F 24-acetate ÏàËÆ¶È:74.2% Chinese Traditional and Herbal Drugs 2012 43 841-843 A new triterpene in rhizome of Alisma orientale XU Nan; ZHANG Hong-da; XIE Xue Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 16,23-oxidoalisol B C30H46O4 ÏàËÆ¶È:71.4% Phytochemistry 1994 36 119-127 Terpenoids of Alisma orientale rhizome and the crude drug alismatis rhizoma Yoshijiro Nakajima, Yohko Satoh, Masumi Katsumata (nee Ohtsuka), Kazuko Tsujiyama (nee Mikoshiba), Yoshiteru Ida, Junzo Shoji Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . alisol F 24-acetate ÏàËÆ¶È:71.4% Natural Product Research and Development 2001 13(4) 1-4 TERPENOIDS OF ALISMA ORIENTALIS JUZEP. PENG Guo ping; LOU Feng chang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . alisol F C30H48O5 ÏàËÆ¶È:65.7% Chemical & Pharmaceutical Bulletin 1993 41 1948-1954 Crude Drugs from Aquatic Plants. I. On the Constituents of Alismatis Rhizoma. (1). Absolute Stereostructures of Alisols E 23-Acetate, F, and G, Three New Protostane-Type Triterpenes from Chinese Alismatis Rhizoma Masayuki YOSHIKAWA,Shoko HATAKEYAMA,Nobumitsu TANAKA,Youichi FUKUDA,Johji YAMAHARA and Nobutoshi MURAKAMI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . alisol F ÏàËÆ¶È:65.7% Chinese Chemical Letters 2008 19 438-440 A new triterpenoid from Alisma orientalis Xue Yan Hu, Yuan Qiang Guo, Wen Yuan Gao, Hai Xia Chen, Tie Jun Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . Alisol F ÏàËÆ¶È:65.7% Journal of Asian Natural Products Research 2008 10 487-490 Two new triterpenes from the rhizomes of Alisma orientalis Xue-Yan Hu, Yuan-Qiang Guo, Wen-Yuan Gao, Tie-Jun Zhang and Hai-Xia Chen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 16,23-oxidoalisol B C30H46O4 ÏàËÆ¶È:65.7% China Journal of Chinese Materia Medica 2005 30 1263-1265 Studies on triterpenes chemical constituents in rhizome of Alixma gramineum WO Lianqun, LUO Guangming, WANG Baoxiu, ZHU Weifeng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . alisol F C30H48O5 ÏàËÆ¶È:65.7% China Journal of Chinese Materia Medica 2005 30 1263-1265 Studies on triterpenes chemical constituents in rhizome of Alixma gramineum WO Lianqun, LUO Guangming, WANG Baoxiu, ZHU Weifeng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . Alisol A Triacetate ÏàËÆ¶È:63.8% Phytochemistry 1994 36 119-127 Terpenoids of Alisma orientale rhizome and the crude drug alismatis rhizoma Yoshijiro Nakajima, Yohko Satoh, Masumi Katsumata (nee Ohtsuka), Kazuko Tsujiyama (nee Mikoshiba), Yoshiteru Ida, Junzo Shoji Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . alizexol A ÏàËÆ¶È:62.8% Chinese Chemical Letters 1995 6 675-678 ALIZEXOL A.A NOVEL PROTOSTANE TYPE OF TRTTERPENE FROM ALISMA ORIENTALIS JUZEP LU ZENG,XIAN PEN AND RU YI ZHANG Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . alismalactone-A 23-acetate C32H50O6 ÏàËÆ¶È:62.8% Chemical & Pharmaceutical Bulletin 1997 45 756-758 ABSOLUTE STEREOSTRUCTURES OF ALISMALACTONE 23-ACETATE AND ALISMAKETONE-A 23-ACETATE, NEW SECO-PROTOSTANE AND PROTOSTANE-TYPE TRITERPENES WITH VASORELAXANT EFFECTS FROM CHINESE ALISMATIS RHIZOMA Masayuki YOSHIKAWA,Toshiyuki MURAKAMI,Akira IKEBATA,Atsushi ISHIKADO,Nobutoshi MURAKAMI,Johji YAMAHARA and Hisashi MATSUDA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 16,23-oxidoalisol B C30H46O4 ÏàËÆ¶È:62.8% Chinese Traditional and Herbal Drugs 2008 39 1788-1790 Ôóк»¯Ñ§³É·ÖµÄÑо¿ ºúÑ©ÑÞ;³Âº£Ï¼;¸ßÎÄÔ¶;ÁõÐÂÇÅ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . dihydrocucurbitacin E ÏàËÆ¶È:62.8% Archives of Pharmacal Research 1994 17 348-353 Antitumor activity of Trichosanthes kirilowii Shi Yong Ryu, Seung Ho Lee, Sang Un Choi, Chong Ock Lee and Zaesung No, et al. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 39 C32H46O7 ÏàËÆ¶È:62.8% Bioorganic & Medicinal Chemistry 2012 20 3016-3030 Synthesis and cytotoxic activity evaluation of dihydrocucurbitacin B and cucurbitacin B derivatives Karen Luise Lang, Izabella Tha¨ªs Silva, Lara Almida Zimmermann, Vanessa Rocha Machado, Marina Rodrigues Teixeira, Mar¨ªa Ivana Lapuh, Mariana Alejandra Galetti, Jorge Alejandro Palermo, Gabriela Myriam Cabrera, L¨ªlian Sibelle Campos Bernardes, Cl¨¢udia Mari Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . alisol F ÏàËÆ¶È:62.8% Natural Product Research and Development 2001 13(4) 1-4 TERPENOIDS OF ALISMA ORIENTALIS JUZEP. PENG Guo ping; LOU Feng chang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . alisol B 23-acetate ÏàËÆ¶È:62.8% Natural Product Sciences 2012 18 121-129 Protective Effects of Methanol Extract and Alisol B 23-acetate of Alisma orientale on Acetaminophen-Induced Hepatotoxicity in Rats Yang, Ki-Ho; Choi, Seong-Hee; Park, Jong-Cheol Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . alisol F ÏàËÆ¶È:62.8% Chinese Traditional and Herbal Drugs 2012 43 841-843 A new triterpene in rhizome of Alisma orientale XU Nan; ZHANG Hong-da; XIE Xue Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . 3-O-(3'-O-Acetyl)-¦Á-L-arabinopyranosyloleanolic acid C37H58O8 ÏàËÆ¶È:62.1% Journal of Asian Natural Products Research 2014 16 20-28 Four new triterpenoids isolated from the resin of Garcinia hanburyi Hong-Min Wang, Qun-Fang Liu, Yi-Wu Zhao, Shuang-Zhu Liu, Zhen-Hua Chen, Ru-Jun Zhang, Zhen-Zhong Wang, Wei Xiao & Wei-Min Zhao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . fasciculic acid B C36H60O9 ÏàËÆ¶È:61.1% Chemical & Pharmaceutical Bulletin 1989 37 3247-3250 Fasciculic Acids A, B and C as Calmodulin Antagonists from the Mushroom Naematoloma fasciculare Akira TAKAHASHI,Genjiro KUSANO,Tomihisa OHTA,Yasushi OHIZUMI and Shigeo NOZOE Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . ¦Á-L-Rhamnopyranosyl oleanolate C36H58O7 ÏàËÆ¶È:61.1% Molecules 2008 13 1472-1486 Facile Synthesis of Oleanolic Acid Monoglycosides and Diglycosides Yu Sha, Mao-Cai Yan, Jiao Liu, Yang Liu and Mao-Sheng Cheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . compound 15 C38H52O7S ÏàËÆ¶È:61.1% Bioorganic & Medicinal Chemistry 2012 20 3016-3030 Synthesis and cytotoxic activity evaluation of dihydrocucurbitacin B and cucurbitacin B derivatives Karen Luise Lang, Izabella Tha¨ªs Silva, Lara Almida Zimmermann, Vanessa Rocha Machado, Marina Rodrigues Teixeira, Mar¨ªa Ivana Lapuh, Mariana Alejandra Galetti, Jorge Alejandro Palermo, Gabriela Myriam Cabrera, L¨ªlian Sibelle Campos Bernardes, Cl¨¢udia Mari Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 22 . 25-O-acetylbryoamaride C36H52O10 ÏàËÆ¶È:60.5% Chemical & Pharmaceutical Bulletin 2002 50(5) 645-648 A New Pentacyclic Cucurbitane Glucoside and a New Triterpene from the Fruits of Gymnopetalum integrifolium Toshikazu SEKINE,Hiroshi KURIHARA, Mayumi WAKU,Fumio IKEGAMI,a and Nijsiri RUANGRUNGSI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 23 . 3¦Â-acetyl-16-oxo-13¦Â, 28-epoxyoleanane C32H50O4 ÏàËÆ¶È:60% Phytochemistry 2006 67 2641-2650 Oleanane-type triterpenes of Embelia schimperi leaves Lawrence Onyango Arot Manguro, Steve Onyango Okwiri, Peter Lemmen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 24 . N-[3-oxolup-20(29)-en-28-oyl]cyclopentylamine C35H55NO2 ÏàËÆ¶È:60% Chemistry of Natural Compounds 2008 44 327-333 SYNTHESIS OF BETULONIC ACID AMIDES A. N. Antimonova, N. V. Uzenkova, N. I. Petrenko,M. M. Shakirov, E. E. Shul¡äts, and G. A. Tolstikov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ »¯ºÏÎï1-4-1 13C NMR (101 MHz, Acetone) ¦Ä 159.44, 141.48, 120.66, 70.83, 56.78, 56.05, 50.34, 45.85, 44.24, 42.46, 39.78, 37.36, 36.43, 36.04, 33.83, 31.91, 31.74, 31.65, 28.05, 24.05, 20.91, 19.18, 18.90, 18.45, 11.33 1 . ¦Â-sitosterol ÏàËÆ¶È:82.1% Chinese Joumal of Experimental Traditional Medical Fomulae 2014 20 82-85 Chemical Constituents of Gonostegia hirta HAN He-dong, HU Hai-qing, LIN Yan, LI Rong-jiao, WANG Xiao-ling Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . ¦Â-sitosterol ÏàËÆ¶È:80.7% Korean Journal of Pharmacognosy 2004 35(1) 80-87 The Chemical Structures and Their Antioxidant Activity of the Components Isolated from the Heartwood of Hemiptelea davidii Chang, Bok-Sim; Kwon, Yong-Soo; Kim, Chang-Min Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . (3¦Á,8¦Á,9¦Â,10¦Á,13¦Á,14¦Â,17¦Â,20S)-3-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]chol-5-en-24-ol ÏàËÆ¶È:80% Steroids 2003 68 159-166 First synthesis of ent-desmosterol and its conversion to ent-deuterocholesterol Emily J. Westover, Douglas F. Covey Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 3¦Â-Hydroxy-24-norchol-5-en-23-oic acid ÏàËÆ¶È:80% Steroids 2005 70 873-878 Isolation and absolute configuration of new bioactive marine steroids from Euryspongia n. sp. Anne Mandeau, Cecile Debitus, Marie-Françoise Ari¨¨s, Bruno David Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . (3¦Á,8¦Á,9¦Â,10¦Á,13¦Á,14¦Â,17¦Á,20S)-Chol-5-en-24-oic acid,methyl ester ÏàËÆ¶È:80% Steroids 2006 71 484-488 Synthesis of ent-25-hydroxycholesterol Emily J. Westover, Douglas F. Covey Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (3¦Á,8¦Á,9¦Â,10¦Á,13¦Á,14¦Â,17¦Á,20S)-27-Norcholest-5-en-25-one C26H42O2 ÏàËÆ¶È:80% Steroids 2006 71 484-488 Synthesis of ent-25-hydroxycholesterol Emily J. Westover, Douglas F. Covey Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . (20R)-25-thia-27-norcholest-5-en-3¦Â-ol C28H50OSiS ÏàËÆ¶È:80% Bioorganic & Medicinal Chemistry 2012 20 4064-4081 Substrate analog studies of the ¦Ø-regiospecificity of Mycobacterium tuberculosis cholesterol metabolizing cytochrome P450 enzymes CYP124A1, CYP125A1 and CYP142A1 Jonathan B. Johnston, Arti A. Singh, Anaelle A. Clary, Chiung-Kuan Chen, Patricia Y. Hayes, Sharon Chow, James J. De Voss, Paul R. Ortiz de Montellano Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 6 ÏàËÆ¶È:80% Magnetic Resonance in Chemistry 1993 31 421-424 Carbon-13 NMR spectra of bile acid derivatives. Part III. Unsaturated 5¦Â-cholanoic acids Takashi Iida, Junichi Goto and Toshio Nambara Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . ¦Â-sitosterol ÏàËÆ¶È:79.3% Natural Product Research and Development 2011 23 1017-1020 Chemical Constituents of Phyllanthus niruri L. ZHU, Hong-lin, WEI, Wan-xing, ZHOU, Min, YANG, Dan, FAN, Xi-wang, LIU, Jian-xiong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . ¦Â-sitosterol ÏàËÆ¶È:79.3% South African Journal of Botany 2013 88 341-351 Phytotoxic activity of Cleome arabica L. and its principal discovered active compounds Afef Ladhari, Faten Omezzine, Marina DellaGreca, Armando Zarrelli, Simona Zuppolini, Rabiaa Haouala Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . campesterol C28H48O ÏàËÆ¶È:78.5% Natural Product Research 2014 28 1134-1141 Dragmacidoside: a new nucleoside from the Red Sea sponge Dragmacidon coccinea Dina R. Abou-Hussein, Jihan M. Badr & Diaa T.A. Youssef Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . (20S)-verazine ÏàËÆ¶È:77.7% Planta Medica 1992 58 449-453 Epimeric (20R,20S)-Verazine Isolated from Veratrum maackii: Two-Dimensional NMR Studies and Total Assignment of 1H- and 13C-Resonances Xiuwen Han and heinz Ruegger Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ »¯ºÏÎï80-6 13C NMR (101 MHz, MeOD) ¦Ä 171.32, 171.02, 169.06, 138.18, 134.93, 134.67, 124.82, 79.57, 78.25, 72.52, 72.05, 71.45, 69.10, 68.47, 56.88, 49.21, 40.59, 40.39, 39.81, 37.95, 36.79, 33.98, 33.64, 33.26, 30.59, 30.24, 28.82, 28.46, 28.04, 25.85, 25.38, 25.27, 24.60, 23.02, 22.91, 22.31, 22.05, 20.00, 19.66, 19.37, 19.16, 19.08, 19.03. 1 . fomitoside H C42H66O11 ÏàËÆ¶È:60.4% Journal of Natural Products 2005 68 69-73 Lanostane Triterpenoids and Triterpene Glycosides from the Fruit Body of Fomitopsis pinicola and Their Inhibitory Activity against COX-1 and COX-2 Kazuko Yoshikawa, Megumi Inoue, Yuki Matsumoto, Chika Sakakibara,Hideki Miyataka, Hitoshi Matsumoto, and Shigenobu Arihara Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . spinasteryl glucosyl peracetate ÏàËÆ¶È:60.4% Planta Medica 1985 51 322-325 Isolation of Spinasterol and its Glucoside from Cell Suspension Cultures of Saponaria officinalis: 13CNMR Spectral Data and Batch Culture Production Max Henry and Isabelle Chantalat-Dublanche Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . betulamaximoside B C40H66O12 ÏàËÆ¶È:60.4% Chemical & Pharmaceutical Bulletin 1996 44 1748-1753 Chemical Evaluation of Betula Species in Japan. III. Constiutents of Betula maximowicziana Hiroyuki FUCHINO,Tetsuya SATOH and Nobutoshi TANAKA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 22-dihydro-¦Á-spinasterol ¦Â-D-glucopyranoside tetraacetate ÏàËÆ¶È:60.4% Phytochemistry 1990 29 2539-2543 Caffeine and theanine from cultured cells of Camellia sinensis Tsutomu Furuya,Yutaka Orihara,Yumiko Tsuda Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . catalyrique de A C56H82O17 ÏàËÆ¶È:59.0% Phytochemistry 1980 19 615-622 Triterpenoïdes nouveaux de Napoleonaea imperialis Mpuza Kapundu, Roger Warin, Clement Delaude, Robert Huls Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 3¦Á-acetoxy-12¦Â-O-(2',3',4',6'-tetra-O-acetyl-¦Â-D-glucopyranosyloxy)-20S,24R-epoxydammarane C46H72O14 ÏàËÆ¶È:58.6% Chemistry of Natural Compounds 2014 49 1076-1081 Structures of Side Products from Helferich Reaction Synthesis of 3¦Á,12¦Â,25-Trihydroxy-20S,24R-Epoxydammarane Glucosides L. N. Atopkina, V. A. Denisenko Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . fomitoside G C38H60O8 ÏàËÆ¶È:58.1% Journal of Natural Products 2005 68 69-73 Lanostane Triterpenoids and Triterpene Glycosides from the Fruit Body of Fomitopsis pinicola and Their Inhibitory Activity against COX-1 and COX-2 Kazuko Yoshikawa, Megumi Inoue, Yuki Matsumoto, Chika Sakakibara,Hideki Miyataka, Hitoshi Matsumoto, and Shigenobu Arihara Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . betulamaximoside A C38H64O11 ÏàËÆ¶È:58.1% Chemical & Pharmaceutical Bulletin 1996 44 1748-1753 Chemical Evaluation of Betula Species in Japan. III. Constiutents of Betula maximowicziana Hiroyuki FUCHINO,Tetsuya SATOH and Nobutoshi TANAKA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 3-isobutyryl-7-deacetylglabretal ÏàËÆ¶È:58.1% Phytochemistry 1992 31 4163-4166 Limonoids from Australian members of the meliaceae Dulcie A. Mulholland, David A.H. Taylor Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . ¦Â-sitosterol-¦Â-D-ghcopyranoside ÏàËÆ¶È:58.1% Phytochemistry 1991 30 1026-1029 A butyrolactone lignan disaccharide from Flacourtia ramontchi V. Satyanarayana, G.L.David Krupadanam, G. Srimannarayana Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . stigmasta-3¦Á,5¦Á-diol-3-O-¦Â-D-glucopyranoside tetraacetate ÏàËÆ¶È:58.1% Phytochemistry 1991 30 3383-3387 Steroids and triterpenoids from Rosa laevigata Jim-Min Fang, Kuang-Chaun Wang, Yu-Shia Cheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 6a ÏàËÆ¶È:58.1% Phytochemistry 1990 29 2351-2355 Sterol glucosides from Prunella vulgaris Hisashi Kojima,Noriko Sato,Akiko Hatano,Haruo Ogura Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 6b ÏàËÆ¶È:58.1% Phytochemistry 1990 29 2351-2355 Sterol glucosides from Prunella vulgaris Hisashi Kojima,Noriko Sato,Akiko Hatano,Haruo Ogura Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 5a C30H52O3 ÏàËÆ¶È:58.1% Phytochemistry 1985 24 2359-2367 Triterpenoids from Mangifera indica V. Anjaneyulu, K. Harischandra Prasad, K. Ravi, J.D. Connolly Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 3¦Â-[(¦Á-L-arabinopyranosyl)oxy]-urs-12,18-dien-28-oic acid-¦Â-D-glucopyranosyl ester ÏàËÆ¶È:58.1% Chinese Journal of Medicinal Chemistry 2008 18 138-141 Triterpenoid saponins of Sanguisorba off icinalis and their anti-inflammatory activity LUO Yan, WANG Han, YUAN Zhong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 3¦Â,24(S),25-trihydroxycycloartane and 3¦Â,24(R),25-trihydroxycycloartane ÏàËÆ¶È:58.1% Zeitschrift f¨¹r Naturforschung C 2004 59 15-18 Chemical Constituents of Euphorbia marschalliana Boiss. A. R. Jassbi, S. Zamanizadehnajari, and S. Tahara Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . rivaloside A C44H68O16 ÏàËÆ¶È:56.8% Journal of Natural Products 2000 63 1012-1014 Rivalosides A and B, Two 19-Oxo Triterpenoid Saponins from Galium rivale Salvatore De Rosa,Maya Mitova, Nedyalka Handjieva, Simeon Popov, and Mincho Anchev Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . artemisterol B C44H72O4 ÏàËÆ¶È:56.8% Journal of Natural Products 1996 59 181-184 New 9¦Â-Lanostane-Type Triterpenic and 13, 14-seco-Steroidal Esters from the Roots of Artemisia scoparia Surendra Kumar Sharma and Mohammad Ali Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . amphiphilic hexasubstituted [60]fullerene C412H576O38 ÏàËÆ¶È:56.8% Tetrahedron Letters 2005 46 6507-6510 Interfacial behavior and film-forming properties of an amphiphilic hexasubstituted [60]fullerene Delphine Felder-Flesch, Cyril Bourgogne, Jean-Louis Gallani, Daniel Guillon Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . Didemnaketal A C44H72O14 ÏàËÆ¶È:56.8% Journal of the American Chemical Society 1991 113 6321-6322 Didemnaketals A and B, HIV-1 protease inhibitors from the ascidian Didemnum sp Barbara C. M. Potts, D. John Faulkner, James A. Chan, Gerald C. Simolike, Priscilla Offen, Mark E. Hemling, Terry A. Francis Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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