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΢Æ×ÇóÖú£º 13C NMR (125 MHz, CDCl3) 10.00,14.82,15.52,17.54,18.10,21.02,21.38,23.08,26.44,27.24,30.32,31.22,34.08,35.78,36.83,38.11,38.40,39.26,40.25,42.77,43.73,44.56,46.69,46.98,47.34,49.31,52.07,64.44,73.99,217.26 лл |
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½á¹û£º¹²²éµ½20793¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . compound 346 ÏàËÆ¶È:90% 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 -------------------------------------------------------------------------------- 2 . 7¦Â-hydroxylup-20(29)-en-3-one C30H48O2 ÏàËÆ¶È:90% Phytochemistry 1989 28 2206-2208 A lupeol derivative from Salvia pratensis J. Anaya,MC. Caballero,M. Grande,J.J. Navarro,I. Tapia,J.F. Almeida Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . glochidiol ÏàËÆ¶È:86.6% Planta Medica 2005 71 208-213 Cytotoxic Activity of Lupane-Type Triterpenes from Glochidion sphaerogynum and Glochidion eriocarpum Two of which Induce Apoptosis Puapairoj, Prapawadee; Naengchomnong, Waree; Kijjoa, Anake; Pinto, Madalena M.; Pedro, Madalena; Nascimento, Maria São Jos¨¦; Silva, Artur M. S.; Herz, Werner Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . glochidonol C30H48O2 ÏàËÆ¶È:86.6% China Journal of Chinese Materia Medica 2003 28 1042-1044 Studies on Chemical Constituents in OF Clerodendrum bungei GAO Liming, WEI Xiaomei, HE Yangqing Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 6¦Á-acetoxy-16¦Â,22-dihydroxy-3-ketoisohopane C32H52O5 ÏàËÆ¶È:86.6% Fitoterapia 2002 73 363-368 Triterpenes from Adiantum lunulactum G. Brahmachari , D. Chatterjee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 20-hydroxy-lupan-3-one ÏàËÆ¶È:86.6% Phytochemistry 1982 21 2065-2068 A lupane derivative and the 13C NMR chemical shifts of some lupanols from Pleurostylia opposita Anura P. Dantanarayana, N.Savitri Kumar, P.Mangala Muthukuda, Mohamed I, M. Wazeer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 6¦Â,20-dihydroxy-lupan-3-one ÏàËÆ¶È:86.6% Phytochemistry 1982 21 2065-2068 A lupane derivative and the 13C NMR chemical shifts of some lupanols from Pleurostylia opposita Anura P. Dantanarayana, N.Savitri Kumar, P.Mangala Muthukuda, Mohamed I, M. Wazeer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . compound 10 ÏàËÆ¶È:86.6% Phytochemistry 1982 21 2065-2068 A lupane derivative and the 13C NMR chemical shifts of some lupanols from Pleurostylia opposita Anura P. Dantanarayana, N.Savitri Kumar, P.Mangala Muthukuda, Mohamed I, M. Wazeer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 3-O-[¦Â-D-ßÁà«ÆÏÌÑÌÂ(1¡ú3)-¦Â-D-ßÁà«ÆÏÌÑÌÇÈ©Ëá¼×õ¥ÜÕ]-3¦Â,15¦Á,23-ÈýôÇ»ùÆë¶Õ¹û-12-Ï©-16-ͪ ÏàËÆ¶È:86.6% Chinese Traditional and Herbal Drugs 2002 33 11-14 Chemical Constituents of Pueraria peduncularis ZHANG Xiao-rong; WANG Ming-kui; PENG Shu-lin; LIU Fa-qiang; DING Li-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 6¦Á,15¦Á,22-trihydroxyhopane C30H52O3 ÏàËÆ¶È:86.6% Phytochemistry Letters 2012 5 734-737 Hopane triterpenes from the scale insect pathogenic fungus Aschersonia calendulina BCC 23276 Masahiko Isaka, Panida Chinthanom, Sumalee Supothina, Suchada Mongkolsamrit Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . hopan-7¦Â-ol C30H52O ÏàËÆ¶È:86.6% Indian Journal of Chemistry 2004 43B 2223-2227 Phytochemical investigation of Gomphrena globosa aerial parts Biswanath Dinda*, Biplab Ghosh, Shiho Arima, Nariko Sato & Yoshihiro Harigaya Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 20-hydroxylupane C30H52O ÏàËÆ¶È:86.6% Natural Medicines 2000 54 186-189 Fern Constituents : Triterpenoids of Polypodiodes amoena HIROHARA Masayoshi,ONO Misao, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 3-oxo-monogynol A C30H48O ÏàËÆ¶È:86.6% Shoyakugaku Zasshi 1987 41 80-83 Comparative Studies on the Constituents of the Parasitic Plant and Its Host (II) : On the Constituents of the Root of Alnus maximowiczii CALLIER (1) SANADA SHUICHI, INABA KYOKO (USUI), IDA YOSHITERU, SHOJI JUNZO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 7¦Â-hydroxylup-20(29)-en-3-one monoacetae ÏàËÆ¶È:84.3% Phytochemistry 1989 28 2206-2208 A lupeol derivative from Salvia pratensis J. Anaya,MC. Caballero,M. Grande,J.J. Navarro,I. Tapia,J.F. Almeida Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . oxandran-3-one C31H52O2 ÏàËÆ¶È:83.8% Journal of Natural Products 1992 Vol 55 701 Terpenoid Constituents of Oxandra asbeckii Winston F. Tinto, Lynn C. Blair, William F. Reynolds, Stewart McLean Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 3-oxolup-20(30)-en-29-al C30H46O2 ÏàËÆ¶È:83.3% Helvetica Chimica Acta 2005 Vol. 88 1102 Lupane Pentacyclic Triterpenes Isolated from Stems and Branches of Maytenus imbricata (Celastraceae) Silvia Ribeiro de Souza e Silva, Gracia Divina de F¨¢tima Silva, Luiz Cl¨¢udio de Almeida Barbosa, Lucienir Pains Duarte, Sidney Augusto Vieira Filho Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 30-hydroxylup-20(29)-en-3-one C30H48O2 ÏàËÆ¶È:83.3% Helvetica Chimica Acta 2005 Vol. 88 1102 Lupane Pentacyclic Triterpenes Isolated from Stems and Branches of Maytenus imbricata (Celastraceae) Silvia Ribeiro de Souza e Silva, Gracia Divina de F¨¢tima Silva, Luiz Cl¨¢udio de Almeida Barbosa, Lucienir Pains Duarte, Sidney Augusto Vieira Filho Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 12¦Â,20R-dihydroxydammaran-3-one C30H52O3 ÏàËÆ¶È:83.3% Journal of Natural Products 1997 60 1236-1241 Microbial Transformation of Protopanaxadiol and Protopanaxatriol Derivatives with Mycobacterium sp. (NRRL B-3805) K. C. Wang, Perng-Haur Wang, and Shoei-Sheng Lee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . 12¦Â,20R,25-trihydroxydammaran-3-one C30H52O4 ÏàËÆ¶È:83.3% Journal of Natural Products 1997 60 1236-1241 Microbial Transformation of Protopanaxadiol and Protopanaxatriol Derivatives with Mycobacterium sp. (NRRL B-3805) K. C. Wang, Perng-Haur Wang, and Shoei-Sheng Lee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . glochidonol ÏàËÆ¶È:83.3% Planta Medica 2005 71 208-213 Cytotoxic Activity of Lupane-Type Triterpenes from Glochidion sphaerogynum and Glochidion eriocarpum Two of which Induce Apoptosis Puapairoj, Prapawadee; Naengchomnong, Waree; Kijjoa, Anake; Pinto, Madalena M.; Pedro, Madalena; Nascimento, Maria São Jos¨¦; Silva, Artur M. S.; Herz, Werner Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . monogynol A ÏàËÆ¶È:83.3% Chemical & Pharmaceutical Bulletin 1995 43 1937-1942 Chemical Evaluation of Betula Species in Japan. I.Constituents of Betula ermanii Hiroyuki FUCHINO,Tetsuya SATOH and Nobutoshi TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . 28,29-Diacetoxy-3-oxoolean-12-ene ÏàËÆ¶È:83.3% Chemistry of Natural Compounds 1992 28 1-23 13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES A. I. Kalinovskii Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . Avenestergenin B-2 ÏàËÆ¶È:83.3% Chemistry of Natural Compounds 1992 28 1-23 13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES A. I. Kalinovskii Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . Avenestergenin A-2 ÏàËÆ¶È:83.3% Chemistry of Natural Compounds 1992 28 1-23 13C NMR SPECTROSCOPY OF OLEANANE DERIVATIVES A. I. Kalinovskii Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . 15¦Á-hydroxylup-20(29)-en-3-one C30H48O2 ÏàËÆ¶È:83.3% Helvetica Chimica Acta 2009 92 2762-2768 Three Terpenoids and a Tocopherol-Related Compound from Ricinus communis Qin-Gang Tan, Xiang-Hai Cai, Zhi-Zhi Du, Xiao-Dong Luo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . lupenone C30H48O ÏàËÆ¶È:83.3% Acta Botanica Sinica 2002 44 354-358 Triterpenoids from the Dai Medicinal Plant Winchia calophylla ZHU Wei-Ming, SHEN Yue-Mao, HONG Xin, ZUO Guo-Ying, YANG Xiao-Sheng, HAO Xiao-Jiang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . compound 7a ÏàËÆ¶È:83.3% Natural Product Research 2008 22 305-319 Novel class of hybrid natural products derived from lupeol as antimalarial agents Satish Kumar; Namita Misra; Kanwal raj; Kumkum Srivastava; S. K. Puri Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . epishionol ÏàËÆ¶È:83.3% Chemical & Pharmaceutical Bulletin 1998 46 1824-1826 Astertarone A : A Triterpenoid Ketone Isolated from the Roots of Aster tataricus L. Toshihiro AKIHISA,Yumiko KIMURA,Kazuo KOIKE,takaaki TAI,Ken YASUKAWA,Koichi ARAI,Yasuhiro SUZUKI and Tamotsu NIKAIDO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . lupeone ÏàËÆ¶È:83.3% China Journal of Chinese Materia Medica 2006 31 1168-1171 Compounds from marine mangrove plant Bruguiera sexangula var. rhynchopetala BAO Shuyun, LIN Wenhan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . monogynol A ÏàËÆ¶È:83.3% China Journal of Chinese Materia Medica 2006 31 1798-1800 Studises on chemical constituents of Balanophora spicata DAI Zhong, WANG Feng, WANG Gangli, LIN Ruichao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . lupenone ÏàËÆ¶È:83.3% China Journal of Chinese Materia Medica 2006 31 1953-1955 Chemical constitutents of Bauhinia aurea SHANG Xiaoya, LI Shuai, WANG Yinghong, WANG Sujuan, YANG Yongchun, SHI Jiangong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . 22,28-epoxyhopane ÏàËÆ¶È:83.3% Chemical & Pharmaceutical Bulletin 1997 45 590-594 Fern Constituents : Triterpenoids Isolated from Rhizomes of Pyrrosia lingua. I Kazuo MASUDA,Hiroshi YAMASHITA,Kenji SHIOJIMA,Toshihiro ITOH and Hiroyuki AGETA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 33 . 3-oxo-taraxastane-20(R or S)-ol C30H50O2 ÏàËÆ¶È:83.3% Phytochemistry 1999 50 1229-1236 Triterpenoids from Mangifera indica V. Anjaneyulu , P. Satyanarayan¦Á, K.N. Viswanadham, V.G. Jyothi, K. Nageswara Rao, P. Radhika Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 34 . 3¦Â,20-dihvdroxylupane ÏàËÆ¶È:83.3% Phytochemistry 1998 48 863-866 Triterpenes from Rhus taitensis Aysen Y¨¹r¨¹ker, Jimmy Orjala, Otto Sticher, Topul Rali Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 35 . ochraceolide B C30H44O4 ÏàËÆ¶È:83.3% Journal of Natural Products 1991 Vol 54 1353 New Cytotoxic Lupane Lactones from Kokoona ochracea Olipa D. Ngassapa, Djaja D. Soejarto, Chun-Tao Che, John M. Pezzuto, Norman R. Farnsworth Structure 13C NMR ̼Æ×Ä£Äâͼ |
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