| ²é¿´: 208 | »Ø¸´: 1 | |||
bravexueli½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
Çó΢Æ×£¬²»Ê¤¸Ð¼¤ÌéÁã
|
|
15.4,15.6,15.7,17.4,17.8,21.5,21.6,25.3,25.4,25.5,25.9,26.2,28.1,28.3,29.9,30.5,33.2,35.2,35.3,36.9,43.1,46.9,47.3,47.4,48.8,48.9,76.7,133.3,134.2,176.9 Çó΢Æ× |
» ²ÂÄãϲ»¶
ÍÁľˮÀûר˶276·ÖÇóµ÷¼Á
ÒѾÓÐ9È˻ظ´
328Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
»¯Ñ§¹¤³Ìµ÷¼Á289
ÒѾÓÐ26È˻ظ´
331Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
²ÄÁÏÓ뻯¹¤×¨Ë¶306·ÖÕÒºÏÊʵ÷¼Á
ÒѾÓÐ24È˻ظ´
²ÄÁϹ¤³Ìµ÷¼Á
ÒѾÓÐ8È˻ظ´
070300»¯Ñ§279Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
²ÄÁÏר˶µ÷¼Á
ÒѾÓÐ14È˻ظ´
334Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
²ÄÁϹ¤³Ì085601£¬270Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú13C΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
΢Æ×²é¸ö»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
¼±¼±¼±¡£¡£¡£¡£ÇóÖú΢Æ×Êý¾Ý£¨50%ÏàËÆ¶È¾ÍOKÁË£©£¬²»Ê¤¸Ðл£¡
ÒѾÓÐ8È˻ظ´
ÇóÁ½¶Î·Ò룬·Ç³£½ô¼±£¬¸Ð¼¤ÌéÁã
ÒѾÓÐ5È˻ظ´
¡¾ÇóÖú/½»Á÷¡¿¶³¸É¾úÖÖÔõô¸´»î?ÓÐûÓÐÏà¹ØµÄ×ÊÁÏ£¬²»Ê¤¸Ð¼¤¡£¡£¡£
ÒѾÓÐ12È˻ظ´
mzp-0
ľ³æ (ÕýʽдÊÖ)
- Ó¦Öú: 138 (¸ßÖÐÉú)
- ½ð±Ò: 3037.8
- ºì»¨: 3
- Ìû×Ó: 425
- ÔÚÏß: 45.1Сʱ
- ³æºÅ: 1739290
- ×¢²á: 2012-04-06
- ÐÔ±ð: MM
- רҵ: ÖÐÒ©ÖÊÁ¿ÆÀ¼Û
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
bravexueli: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-03-22 21:35:48
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
bravexueli: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-03-22 21:35:48
|
3-keto-tirucall-8,24-dien-21-oicacid ÏàËÆ¶È:76.6% Chinese Journal of Natural Medicines 2010 8 25-27 Chemical Constituents of Boswellia carterii(Frankincense) Li Fu-Shuang; YAN Dong-Lan; LIU Rang-Ru; XU Kang-Ping; TAN Gui-Shan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . trametenolicacid ÏàËÆ¶È:76.6% Natural Product Research and Development 2010 22 433-436 Chemical Constituents and Anti-inflammatory Activities of Inonotus obliquus ZHANG Xu; ZHAO Fen-qin; HAN Guang; LIU Lei; GAO Xin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 3-oxotirucallic acid C30H46O3 ÏàËÆ¶È:76.6% Zeitschrift f¨¹r Naturforschung C 2003 58 505-516 Immunomodulatory Triterpenoids from the Oleogum Resin of Boswellia carterii Birdwood F. A. Badria, B. R. Mikhaeil, G. T. Maatooq, and M. M. A. Amer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . trametenolic acid ÏàËÆ¶È:76.6% Lishizhen Medicine and Materia Medica Research 2006 17 1178-1181 Chemical Constituents of Inonotus obliquus ZHAO Fen-qin, PIAO Hui-shan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . fomitopinic acids A C30H48O5 ÏàËÆ¶È:73.3% 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . pinicolic acid A C30H46O3 ÏàËÆ¶È:73.3% Phytochemistry 1999 52 1621-1627 Steroids from the fungus Fomitopsis pinicola Joachim Rosecke, Wilfried A. Konig Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . trametenolic acid B ÏàËÆ¶È:73.3% Phytochemistry 1999 52 1621-1627 Steroids from the fungus Fomitopsis pinicola Joachim Rosecke, Wilfried A. Konig Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 3-oxo-5¦Á-lanosta-8,24-dien-21-oic acid ÏàËÆ¶È:73.3% Phytochemistry 1997 46 1143-1146 Steroids of formosan Ganoderma tsugae Chun-Nan Lin, Yih-Fen Fann, Mei-Ing Chung Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . pinnicolic acid A ÏàËÆ¶È:73.3% Chinese Traditional and Herbal Drugs 2007 38 20-23 Chemical constituents of Stenoloma chusanum REN Bing-ru; XIA Bing; LI Wei-lin; WU Ju-lan; ZHANG Han-qing Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 3-Ñõ´úÑòëçÞ-8,24-¶þÏ©-21-ôÈËá ÏàËÆ¶È:73.3% Chinese Journal of Medicinal Chemistry 2003 13 34-37 Isolation and identification of the chemical constituent of Hemerocallis fulva(L.)L. YANG Zhong-duo, LI Yuan-chao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 3-oxotirucalla-8,24-dien-21-oicacid ÏàËÆ¶È:73.3% Natural Product Communications 2010 5 1181-1182 Triterpenes from Protium hebetatum Resin Delcio Dias Marques, Ilmar Bernardo Graebner, Telma Leda Gomes de Lemos,Luciana Lucas Machado, Jõao Carlos Costa Assunção and Francisco Jos¨¦ Queiroz Monte Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . methyl 3¦Á,24S-dihydroxytirucalla-8,25-dien-21-oate C31H50O4 ÏàËÆ¶È:70.9% Phytochemistry 2006 67 1309-1315 Tirucallane triterpenes from the roots of Ozoroa insignis Yonghong Liu , Pedro Abreu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . methyl trametenolate ÏàËÆ¶È:70.9% Planta Medica 1984 50 197-198 3¦Â-Hydroxy-lanosra-8,24-dien-21-al, a New Triterpene from Inonotus obliquus Kirsti Kahlos, R. Hiltunen and M. v. Schantz Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 10¦Á-cucurbita-5,24-dien-3-ol ÏàËÆ¶È:70% Helvetica Chimica Acta 2000 Vol. 83 3191 New Terpenoids from Basidiomycetes Russula lepida Tan Jian-Wen, Dong Ze-Jun, and Liu Ji-Kai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . trematenolic acid ÏàËÆ¶È:70% Chemical & Pharmaceutical Bulletin 2002 50(12) 1603-1606 New Triterpenoids from Tricholoma saponaceum Kazuko YOSHIKAWA,Mina KUROBOSHI, Shigenobu ARIHARA,Naoko MIURA, Noriyuki TUJIMURA,and Kenji SAKAMOTO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . trametenolic acid ÏàËÆ¶È:70% 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 3-epicotillol ÏàËÆ¶È:70% Chemistry of Natural Compounds 1986 22 415-420 GLYCOSYLATION OF TRITERPENOIDS OF THE DAMMARANE SERIES.V. ¦Â-D-GLUCOPYRANOSIDES OF 12¦Â-ACETOXY-20(S),24(R)-EPOXYDAMMARANE- 3¦Á,25-DIOL AND OF 3-EPIOCOTILLOL L. N. Atopkina, N. F. Samoshina,V. A. Denisenko, N. D. Pokhiio, and N. I. Uvarova Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 3-epiocotillol ÏàËÆ¶È:70% Chemistry of Natural Compounds 1981 17 249-253 TRITERPENOIDS FROM THE LEAVES OF FAR EASTERN SPECIES OF THE SHRUBBIRCHES Betula ovalifolia AND B. middendorfii G. V. Malinovskaya, N. D. Pokhilo, V. V. Makhan'kov, V. L. Novikov, and N. I. Uvarova Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . 10-cucurbitadienol ÏàËÆ¶È:70% Chinese Chemical Letters 1999 10 297-298 Lepida Acid A from Basidiomycetes Russula lepida Jian Wen TAN Ji Kai LIU Ze Jun DONG, Pei Gui LIU, Da Gan JI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 10¦Á-cucurbitadienol ÏàËÆ¶È:70% Acta Pharmaceutica Sinica 1994 29 39-43 CHEMICAL STUDIES ON RUSSULA ROSACEA HB Wang; GH Yang; SH Wu; SF; Wang; GY Li; WK Xu; LS Meng and zY Li Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . pinicolic acid E ÏàËÆ¶È:70% Phytochemistry 2000 54 603-610 Constituents of various wood-rotting basidiomycetes Joachim Rösecke, Wilfried A. König Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . cabraleadiol ÏàËÆ¶È:70% Phytochemistry 1997 46 1139-1141 Dammarane-type triterpenes from Cordia spinescens Norio Nakamura, Shiho Kojima, Yasmina Aura Lim, Meselhy R. Meselhy, Masao Hattori, Mahabir P. Gupta, Mireya Correa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . cycloeucalenol ÏàËÆ¶È:70% Phytochemistry 1997 44 1449-1454 Sesquiterpenes, triterpenoids, limonoids and flavonoids of Cedrela odorata graft and speculations on the induced resistance against Hypsipyla grandella Jos¨¦R. de Paula, Ivo J. C. Vieira, M. F¨¢tima das G. F. da Silva, Edson Rodrigues Fo, João B. Fernandes, Paulo C. Vieira, Antônio L. Pinheiro, Evaldo F. Vilela Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . 4¦Á,14¦Á-dimethyl-cholesta-8,24-dien-3¦Â-ol ÏàËÆ¶È:70% Phytochemistry 1996 41 1191-1195 Antibacterial hydroperoxysterols from Xanthosoma robustum Takeshi Kato, Barbara Frei, Michael Heinrich, Otto Sticher Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . 21-hydroxylanosta-8,24-dien-3-one ÏàËÆ¶È:70% Phytochemistry 1996 41 1041-1046 Antimicrobial steroids from the fungus Fomitopsis pinicola Anne Caroline Keller, Marc P. Maillard, Kurt Hostettmann Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . pinicolic acid A ÏàËÆ¶È:70% Phytochemistry 1996 41 1041-1046 Antimicrobial steroids from the fungus Fomitopsis pinicola Anne Caroline Keller, Marc P. Maillard, Kurt Hostettmann Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . trametenolic acid B ÏàËÆ¶È:70% Phytochemistry 1996 41 1041-1046 Antimicrobial steroids from the fungus Fomitopsis pinicola Anne Caroline Keller, Marc P. Maillard, Kurt Hostettmann Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . inonotsutriol D C30H50O3 ÏàËÆ¶È:70% Phytochemistry Letters 2011 4 328-332 New lanostane-type triterpenoids, inonotsutriols D, and E, from Inonotus obliquus Reiko Tanaka, Misaki Toyoshima, Takeshi Yamada Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . astrahygrol C30H48O ÏàËÆ¶È:70% Phytochemistry 1987 26 2341-2344 Three triterpenes from Astraeus hygrometricus Yoshihisa Takaishi,Yoshito Murakami,Takashi Ohashi,Kimiko Nakano,Ko¯tarou Murakami,Toshiaki Tomimatsu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . 3-epi-astrahygrol C30H48O ÏàËÆ¶È:70% Phytochemistry 1987 26 2341-2344 Three triterpenes from Astraeus hygrometricus Yoshihisa Takaishi,Yoshito Murakami,Takashi Ohashi,Kimiko Nakano,Ko¯tarou Murakami,Toshiaki Tomimatsu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . astrahygrone C30H46O6 ÏàËÆ¶È:70% Phytochemistry 1987 26 2341-2344 Three triterpenes from Astraeus hygrometricus Yoshihisa Takaishi,Yoshito Murakami,Takashi Ohashi,Kimiko Nakano,Ko¯tarou Murakami,Toshiaki Tomimatsu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . Cabraleadiol C30H52O3 ÏàËÆ¶È:70% Phytochemistry 1985 24 2925-2928 Dammarane Triterpenes from the stem bark of Commiphora Dalzielii Peter G. Waterman, Stephen Ampofo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 33 . betulafolienetriol ÏàËÆ¶È:70% Phytochemistry 2010 71 877-894 Fatty acid derivatives and dammarane triterpenes from the glandular trichome exudates of Ibicella lutea and Proboscidea louisiana Teigo Asai, Noriyuki Hara, Yoshinori Fujimoto Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 34 . cabraleadiol C30H52O3 ÏàËÆ¶È:70% Chinese Journal of Natural Medicines 2010 8 270-273 Chemical Constituents from the Roots of Dysoxylum densiflorum LI Chang-Song; YU Hong-Wei; LI Guo-You; ZHANG Guo-Lin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 35 . cabraleahydroxylactone C27H44O3 ÏàËÆ¶È:70% Chinese Journal of Natural Medicines 2010 8 270-273 Chemical Constituents from the Roots of Dysoxylum densiflorum LI Chang-Song; YU Hong-Wei; LI Guo-You; ZHANG Guo-Lin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 36 . 25-Hydroperoxycycloart-23-en-3¦Â-ol ÏàËÆ¶È:70% Archives of Pharmacal Research 2002 25 628-635 Phytochemical constituens of Cirsium setidens Nakai and their cytotoxicity against human cancer cell lines Won Bin Lee, Hak Cheol Kwon, Ock Ryun Cho, Kang Choon Lee and Sang Un Choi, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 37 . Cabraleadiol ÏàËÆ¶È:70% Archives of Pharmacal Research 2008 31 21-27 A new sesquiterpene and other terpenoid constituents of Chisocheton penduliflorus Jarinporn Phongmaykin, Takuya Kumamoto, Tsutomu Ishikawa, Rutt Suttisri and Ekarin Saifah Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 38 . Epilupeol ÏàËÆ¶È:70% Journal of Chinese Pharmaceutical Sciences 2010 19 387-392 Assignment of the absolute stereochemistry of an unusual diterpenoid from the mangrove plant Excoecaria agallocha L. Zhen Liu; Wei Jiang; Zhi-Wei Deng; Wen-Han Lin* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 39 . lupeol C30H50O ÏàËÆ¶È:70% Chinese Traditional and Herbal Drugs 2012 43 1471-1474 Chemical constituents from Glochidion lanceolarium YANG Cai-xia; ZHANG Zheng-kai; LIU Ning; WEI Bin; SU Xiao-long Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 40 . 3-epi-lupeol C30H50O ÏàËÆ¶È:70% Chinese Traditional and Herbal Drugs 2012 43 1471-1474 Chemical constituents from Glochidion lanceolarium YANG Cai-xia; ZHANG Zheng-kai; LIU Ning; WEI Bin; SU Xiao-long Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 41 . cabraleahydroxylactone ÏàËÆ¶È:70% China Journal of Chinese Materia Medica 2012 37 1237-1240 Chemical constituents from stems of Dysoxylum laxiracemosum TANG Ting; ZUO Laifu; NA Zhi; XU Youkai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 42 . 3¦Á-hydroxy-5¦Á-lanosta-8,24-dien-21-oic acid C32H50O4 ÏàËÆ¶È:68.7% Phytochemistry 1997 46 1143-1146 Steroids of formosan Ganoderma tsugae Chun-Nan Lin, Yih-Fen Fann, Mei-Ing Chung Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 43 . 31¦Â-acetoxy-5¦Á-lanosta-8,24-dien-21-oic acid C32H50O4 ÏàËÆ¶È:68.7% Phytochemistry 1997 46 1143-1146 Steroids of formosan Ganoderma tsugae Chun-Nan Lin, Yih-Fen Fann, Mei-Ing Chung Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 44 . fomefficinic acid A C31H48O3 ÏàËÆ¶È:67.7% Chemical & Pharmaceutical Bulletin 2004 52(11) 1375-1377 New Lanostane-Type Triterpenes from Fomes officinalis Xia WU, JunShan YANG,Liang ZHOU, and YueSheng DONG Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 45 . 3¦Á-hydroxy-tirucalla-8,24-dien-21-oate C31H50O3 ÏàËÆ¶È:67.7% Phytochemistry 2006 67 1309-1315 Tirucallane triterpenes from the roots of Ozoroa insignis Yonghong Liu , Pedro Abreu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 46 . methyl 3¦Á,25-dihydroxy-tirucalla-8-ene-21-oate C31H52O4 ÏàËÆ¶È:67.7% Phytochemistry 2006 67 1309-1315 Tirucallane triterpenes from the roots of Ozoroa insignis Yonghong Liu , Pedro Abreu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 47 . monocarpinine C31H48O3 ÏàËÆ¶È:67.7% Journal of Natural Products 2008 71(6) 1104-1106 A Cycloartane Incorporating a Fused Tetrahydrofuran Ring and a Cytotoxic Lactam from Monocarpia marginalis Siew-Huah Lim, Kamaliah Mahmood, Kanki Komiyama, and Toh-Seok Kam Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 48 . methyl 3¦Á-hydroxyolean-18-en-28-oate C31H40O3 ÏàËÆ¶È:67.7% Phytochemistry 1995 39 99-103 Terpenoids from the liverworts Symphyogyna brasiliensis and unidentified Frullania species Motoo Tori, Mamiko Aoki, Katsuyuki Nakashima, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 49 . 3-Oxo-24-methyl-5¦Á-lanost-8,25-dien-21-oic acid C31H48O3 ÏàËÆ¶È:67.7% Planta Medica 2010 76 464-466 Antibacterial Compounds from Mushrooms II: Lanostane Triterpenoids and an Ergostane Steroid with Activity Against Bacillus cereus Isolated from Fomitopsis pinicola Liu, Xue-Ting; Winkler, Abby L.; Schwan, William R.; Volk, Thomas J.; Rott, Marc; Monte, Aaron Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 50 . compound 1 C31H50O3 ÏàËÆ¶È:67.7% Chinese Journal of Chemistry 2001 19 702-704 A Novel Lanostanoid Lactone From the Alga Hypnea cerricornis Xiao-Hua Xu, Xiao Chen, Jian-Hua Lu, Guang-Min Yao, Yan-Ming Li and Long-Mei Zeng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 51 . 3¦Á,20(S)-Dihydroxy-25-methoxy-dammar-23-ene C31H54O3 ÏàËÆ¶È:67.7% Journal of Natural Medicines 2011 65 217-223 Seven new dammarane triterpenes from the floral spikes of Betula platyphylla var. japonica Juan Xiong ,Masatoshi Taniguchi ,Yoshiki Kashiwada ,Takashi Yamagishi ,Yoshihisa Takaishi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- |
2Â¥2013-03-18 17:49:11














»Ø¸´´ËÂ¥