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²éѯ½á¹û£º¹²²éµ½779¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . arjunglucoside ÏàËÆ¶È:86.8% Phytochemistry 1996 41 591-594 Pentacyclic triterpenes from Combretum nigricans Akino Jossang, Mannan Seuleiman, Eric Maidou, Bernard Bodo Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 2¦Á,3¦Á,23-Trihydroxyolean-12-en-28-oic acid O-¦Â-D-glucopyranosyl ester C36H58O10 ÏàËÆ¶È:86.8% Natural Product Communications 2007 2 895-900 Flavonoids and Triterpenoid Saponins from Pimenta dioica(Merr.) L. Fatma A. Moharram, Mona A Mohamed, Mohamed SA Marzouk and Elsayed A Aboutabl Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . arjunglucoside I C36H58O11 ÏàËÆ¶È:86.8% Chromatographia 2006 64 695-699 Preparative Droplet Counter-Current Chromatography for the Separation of the New Nor-Seco-Triterpene and Pentacyclic Triterpenoids from Qualea Parviflora A. L. M. Nasser, L. P. Mazzolin, C. A. Hiruma-Lima, L. S. Santos, M. N. Eberlin, A. R. Monteiro de Souza Brito, W. Vilegas Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . bellericaside B C36H58O12 ÏàËÆ¶È:84.2% Chromatographia 2006 64 695-699 Preparative Droplet Counter-Current Chromatography for the Separation of the New Nor-Seco-Triterpene and Pentacyclic Triterpenoids from Qualea Parviflora A. L. M. Nasser, L. P. Mazzolin, C. A. Hiruma-Lima, L. S. Santos, M. N. Eberlin, A. R. Monteiro de Souza Brito, W. Vilegas Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 21-O-¦Â-D-Glucopyranosyl-2¦Á,3¦Â,21¦Â,23-tetrahydroxyolean-12-en-28-oic acid C36H58O11 ÏàËÆ¶È:81.5% Chemical Research in Chinese Universities 2009 25 404-406 Triterpene Acids from Cynoglossum amabile XU Qing-jun, ZHANG De-zhi*, DANG Li-juan and LI Kun-ping Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Hederagenic acid-28-O-¦Â-D-glucopyranoside C36H56O9 ÏàËÆ¶È:81.5% Biochemical Systematics and Ecology 2012 42 14-17 Triterpenoids and their saponins from the roots of Kalopanax septemlobus Huankai Yao, Jingyu Duan, Jianhui Wang, Yan Li Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 2¦Á,3¦Á,23-Trihydroxyolean-13(18)-en-28-oic acidO-¦Â-D-glucopyranosyl ester C36H58O10 ÏàËÆ¶È:81.5% Natural Product Communications 2007 2 895-900 Flavonoids and Triterpenoid Saponins from Pimenta dioica(Merr.) L. Fatma A. Moharram, Mona A Mohamed, Mohamed SA Marzouk and Elsayed A Aboutabl Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . prosapogenin B ÏàËÆ¶È:80.4% Planta Medica 1987 53 62-65 Triterpenoid Glycosides from the Roots of Patrinia scab iosaefolia Jae Sue Choi and Won Sick Woo Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . gamboukokoenside A C35H56O11 ÏàËÆ¶È:78.9% Phytochemistry 2003 845-849 Pentacyclic triterpenoid and saponins from Gambeya boukokoensis Jean Wandji, François Tillequin, Dulcie A. Mulholland, Jovita Chi Shirri,Nole Tsabang, ElisabethSeguin, Philippe Verite, Francine Libotb, Z.T. Fomum Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . glinoside B C35H58O8 ÏàËÆ¶È:78.9% Planta Medica 2000 66 368-371 Structure and Antiprotozoal Activity of Triterpenoid Saponins from Glinus oppositifolius Fanta Traore,Robert Faure,Evelyne Ollivier,Monique Gasquet,Nadine Azas,Laurent Debrauwer,Arouna Keita,Pierre Timon-David,Guy Balansard Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . sericoside ÏàËÆ¶È:78.9% Chinese Pharmaceutical Journal 2003 38 336-338 Studies on the constituents of Rosa multiflora LI Yan fang, HU Li hong, LOU Feng chang Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . hederagenin-3-O-¦Â-glucuronopyranoside ÏàËÆ¶È:78.9% Journal of Shenyang Pharmaceutical University 2005 22 181-182 Chemical constituents of the seeds of Acanthopanax senticosus(Rupr. et Maxim) Harms ZHANG Jie, LI Wen, GAO Hui-Yuan, WU Bin, WU Li-jun Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 2¦Á,19¦Á-dihydroxy-3-oxo-olean-12-en-oic acid 28-¦Â-D-glucopyranoside C36H56O10 ÏàËÆ¶È:78.9% Indian Journal of Chemistry Section B 2001 40B 354-356 New constituent from the roots of Terminalia arjuna: antifungal agent B K Chouksey, S K Srivastava Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . PJS-1 ÏàËÆ¶È:78.9% Jiangsu Pharmacertical and Clinical Research 2004 12 18-19 Studies on the Chemical Constituents of Achyranthes bidentata Hu An-ming, Bi Zhi-ming, Li Ping Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . oleanolic acid 28-O-¦Â-D-glucopyranosyl ester C36H58O8 ÏàËÆ¶È:78.9% Chinese Joumal of Experimental Traditional Medical Fomulae 2012 18 83-85 Studies on Chemical Constituents of Lycopus lucidus Turcz.var.hirtus Regel. WANG Tao, LI Chao, PU She-ban, QIAN Shi-hui Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . collinsonidin C41H66O13 ÏàËÆ¶È:78.0% Journal of Natural Products 1992 Vol 55 1468 Saponins from Collinsonia canadensis Balawant S. Joshi, Kristi M. Moore, S. William Pelletier, Mohindar S. Puar, B. N. Pramanik Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . hederagenin 3-O-¦Á-L-arabinopyranosyl(1e¡ú2)-¦Á-L-arabinopyranoside ÏàËÆ¶È:78.0% Korean Journal of Pharmacognosy 1997 28(2) 93-98 Studies on Components of Patrinia scabiosaefolia Kim, Young-Hee Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . hederagenin-3-O-¦Â-D-glucopyranosyl-(1¡ú2)-¦Á-L-arabinopyranoside C41H66O13 ÏàËÆ¶È:78.0% Journal of Anhui Agricultural Sciences 2012 40 745-747 Study on the Chemical Constitutes of C. robustum root MA Yang-min et al Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . chikusetsusaponin IVa methyl ester ÏàËÆ¶È:78.0% Chemistry of Natural Compounds 2012 48 258-261 A new triterpenoid saponin and other saponins from Salicornia europaea Min Yin, Xiangyun Wang, Ming Wang, Yu Chen and Yunfa Dong, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . cauloside C C41H66O13 ÏàËÆ¶È:78.0% Journal of Agricultural and Food Chemistry 2001 49 5969-5974 Characterization of the Triterpene Saponins of the Roots and Rhizomes of Blue Cohosh (Caulophyllum Thalictroides) Jin-Woo Jhoo, Shengmin Sang, Kan He, Xiaofang Cheng, Nanqun Zhu, Ruth E. Stark, Qun Yi Zheng, Robert T. Rosen, and Chi-Tang Ho Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . prosapogenin A ÏàËÆ¶È:76.3% Planta Medica 1987 53 62-65 Triterpenoid Glycosides from the Roots of Patrinia scab iosaefolia Jae Sue Choi and Won Sick Woo Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . sigmoiside A C36H60O7 ÏàËÆ¶È:76.3% Journal of Natural Products 1991 Vol 54 1288 Two New Triterpenoid Saponins from Erythrina sigmoidea J. Kouam, A. Ephrem Nkengfack, Z. Tanee Fomum, Rosa Ubillas, Michael S. Tempesta, Mich¨¨le Meyer Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . sigmoiside B ÏàËÆ¶È:76.3% Journal of Natural Products 1991 Vol 54 1288 Two New Triterpenoid Saponins from Erythrina sigmoidea J. Kouam, A. Ephrem Nkengfack, Z. Tanee Fomum, Rosa Ubillas, Michael S. Tempesta, Mich¨¨le Meyer Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . trachelosperoside D-1 ÏàËÆ¶È:76.3% Chinese Traditional and Herbal Drugs 2006 37 171-174 Triterpenoids from canes with leaves of Trachelospermum jasminoides TAN Xing-qi; CHEN Hai-sheng; ZHOU Mi; ZHANG Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . niga-ichigoside F1 C36H58O11 ÏàËÆ¶È:76.3% Chinese Journal of Natural Medicines 2005 3 17-20 Isolation and Identification of Chemical Constituents from Rubus Parvifolius L. DU Shu-Hu; FENG Fang; LIU Wen-Ying; RAO Jin-Hua; BAI Juan Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . niga-ichigosideF1 ÏàËÆ¶È:76.3% Natural Product Research and Development 2014 26 215-217 Chemical Constituents from the Water-soluble Fraction of Rabdosia excisa TANG Jian, MA Rui-li, LIU Hong-chuan, OUYANG Zhen, CHEN Hai-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . 3¦Â,21¦Á-dihydroxyl-ursolic acid-28-O-¦Â-D-glucopyranoside C36H58O9 ÏàËÆ¶È:76.3% Chinese Traditional and Herbal Drugs 2014 45 1043-1046 Microbial transformation of ursolic acid by Penicillium adametzi WANG Zhi-ping, LIU Dai-lin, YAN Hui-jun, MA Wei-jun Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . pulsatilla saponin A ÏàËÆ¶È:75.6% Chinese Traditional and Herbal Drugs 2013 44 1086-1090 Chemical constituents from berries of Physalis pubescens JIA Yuan-min, CHEN Zhong, XU Qiong-ming, LI Xiao-ran, YANG Shi-lin Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . bidentatoside II C40H62O13 ÏàËÆ¶È:75% Chemical & Pharmaceutical Bulletin 2001 49(11) 1492-1494 Two Triterpene Saponins from Achyranthes bidentata Anne-Claire MITAINE-OFFER, Abderrazak MAROUF,Bernard HANQUET,Nicolas BIRLIRAKIS,and Marie-Aleth LACAILLE-DUBOIS Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . [¦Á-L-rhamnopyranosyl(1¡ú4)-¦Â-D-glucopyranosyl(1¡ú3)]-3,23¦Â-di-hydroxy-olean-12-en-28-oic acid ÏàËÆ¶È:73.8% Phytochemistry 1992 31 1427-1428 Triterpenoid saponins from roots of Clematis grata Sudhir K Uniyal, O.P Sati Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . gamboukokoenside B C35H54O10 ÏàËÆ¶È:73.6% Phytochemistry 2003 845-849 Pentacyclic triterpenoid and saponins from Gambeya boukokoensis Jean Wandji, François Tillequin, Dulcie A. Mulholland, Jovita Chi Shirri,Nole Tsabang, ElisabethSeguin, Philippe Verite, Francine Libotb, Z.T. Fomum Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . compound 2a ÏàËÆ¶È:73.6% Journal of Natural Products 2000 63 1497-1502 Two New Biologically Active Triterpene Saponins from Acanthophyllum squarrosum Ghezala Gaidi,Tomofumi Miyamoto, Abdolhossein Rustaiyan, V¨¦ronique Laurens,and Marie-Aleth Lacaille-Dubois Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . glinoside A C35H58O9 ÏàËÆ¶È:73.6% Planta Medica 2000 66 368-371 Structure and Antiprotozoal Activity of Triterpenoid Saponins from Glinus oppositifolius Fanta Traore,Robert Faure,Evelyne Ollivier,Monique Gasquet,Nadine Azas,Laurent Debrauwer,Arouna Keita,Pierre Timon-David,Guy Balansard Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . ¦Â-amyrin-3-O-(2'-acetyl(glucoside)) ÏàËÆ¶È:73.6% Natural Product Research 2012 26 619-629 Chemical and biological study of the seeds of Eragrostis tef (Zucc.) Trotter Taha S. El-Alfy, Shahira M. Ezzat and Amani A. Sleem Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . 22¦Á-hydroxyolean-12-en-3¦Â-yl-¦Â-D-galactopyra-noside C36H60O7 ÏàËÆ¶È:73.6% Chemical & Pharmaceutical Bulletin 2010 58 1093-1095 Two New Aristolochic Acid Derivatives from the Roots of Aristolochia fangchi and Their Cytotoxicities Yu Cai and Tian-Ge Cai Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . compound 9 ÏàËÆ¶È:73.6% Phytochemistry 1984 23 2893-2898 Further triterpenoids and 13C NMR spectra of oleanane derivatives from Phytolacca acinosa S. Harkar, T.K. Razdan, E.S. Waight Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . Junceoside D ÏàËÆ¶È:73.6% Pharmazie 2005 60 635-637 An unusual new sulfated triterpene saponin from Arenaria juncea G. Gaidi, T. Miyamoto and M. A. Lacaille-Dubois Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . 9¦Â,25-cyclo 3¦Â-O-(¦Â-D-glucopyranosyl)echynocystic acid C36H56O9 ÏàËÆ¶È:73.6% Journal of Ethnopharmacology 2011 135 78-87 Chemical constituents from the stem bark of Symplocos paniculata Thunb. with antimicrobial, analgesic and anti-inflammatory activities Ruchi Badoni Semwal, Deepak Kumar Semwal, Ravindra Semwal, Randhir Singh, Mohan Singh Maniyari Rawat Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . 3¦Â,19¦Á-hydroxyolean-12-en-28-oic acid 28-¦Â-D-glucopyranoside C36H58O9 ÏàËÆ¶È:73.6% Molecules 2012 17 7629-7636 Terpene Glycosides from the Roots of Sanguisorba officinalis L. and Their Hemostatic Activities Wei Sun, Zi-Long Zhang, Xin Liu, Shuang Zhang, Lu He, Zhe Wang and Guang-Shu Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . 16¦Á,23,28-trihydroxy-olean-12-en-3-O-¦Á-L-arabinopyranoside C35H58O8 ÏàËÆ¶È:73.6% Journal of Anhui Agricultural Sciences 2012 40 745-747 Study on the Chemical Constitutes of C. robustum root MA Yang-min et al Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . hederagenin-3-O-¦Á-L-arabinopyranoside C35H56O8 ÏàËÆ¶È:73.6% Journal of Anhui Agricultural Sciences 2012 40 745-747 Study on the Chemical Constitutes of C. robustum root MA Yang-min et al Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . caulophyllogenin-3-O-¦Á-L-arabinopyranoside C35H56O9 ÏàËÆ¶È:73.6% Journal of Anhui Agricultural Sciences 2012 40 745-747 Study on the Chemical Constitutes of C. robustum root MA Yang-min et al Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . eclalbatin C41H66O12 ÏàËÆ¶È:73.1% Journal of Asian Natural Products Research 2001 3 213-217 Eclalbatin, a Triterpene Saponin from Eclipta Alba R. K. UPADHYAY, M. B. PANDEY, R. N. JHA and V. B. PANDEY Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . 3¦Â-[(¦Á-L-arabinopyranosyl)oxy]-19¦Á-hydroxyolean-12-en-28-oic acid 28-¦Â-D-glucopyranoside C41H66O13 ÏàËÆ¶È:73.1% Molecules 2012 17 7629-7636 Terpene Glycosides from the Roots of Sanguisorba officinalis L. and Their Hemostatic Activities Wei Sun, Zi-Long Zhang, Xin Liu, Shuang Zhang, Lu He, Zhe Wang and Guang-Shu Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . 3-O-(methyl-¦Â-D-glucuronopyranosiduronoate)-28-O-¦Â-D-glucopyranosyl oleanolate C43H68O14 ÏàËÆ¶È:72.0% Phytochemistry 2001 56 93-97 Bioactive oleanolic acid saponins and other constituents from the roots of Viguiera decurrens Silvia Marquina, Nora Maldonado, Marı́a Luisa Garduño-Ramı́rez, Eduardo Aranda, Marı́a Luisa Villarreal, Vı́ctor Navarro, Robert Bye, Guillermo Delgado, Laura Alvarez Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . hederagenin-3-O-¦Á-L-rhamnopyranosyl(1¡ú4)-¦Â-D-glucopyranosyl ÏàËÆ¶È:71.4% Natural Product Research and Development 2014 26 864-867 Chemical Constituents of Clematis tangutica NIU Jiang-jin, ZHANG Ben-yin, WANG Ying, ZHANG Lin, SHAO Yun, MEI Li-juan, TAO Yan-duo Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . Oleanolic acid 3-O-¦Â-D-galactopyranoside C36H58O8 ÏàËÆ¶È:71.0% 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 ̼Æ×Ä£Äâͼ 48 . compound 10 ÏàËÆ¶È:71.0% Acta Pharmaceutica Sinica 1995 30 27-33 NEW TRTEKPENOIDAL SAPOGENINS FROM THE ROOTS OF GLYCYRRHIZA YUNNANENSIS JF Hu; ZL Ye and FJ Shen Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . Terminoside A C36H58O10 ÏàËÆ¶È:71.0% Journal of Asian Natural Products Research 2003 5 137-142 TERMINOSIDE A, A NEW TRITERPENE GLYCOSIDE FROM THE BARK OF TERMINALIA ARJUNA INHIBITS NITRIC OXIDE PRODUCTION IN MURINE MACROPHAGES ASIF ALI, GURPREET KAUR, HINNA HAMID, TARIQUE ABDULLAH,MOHAMMED ALI, M. NIWAd and M.S. ALAM Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . termiarjunoside I C36H58O11 ÏàËÆ¶È:71.0% Natural Product Research 2008 22 1279-1288 Two new bioactive oleanane triterpene glycosides from Terminalia arjuna M. Sarwar Alam; Gurpreet Kaur; Asif Ali; Hinna Hamid; Mohammad Ali; Mohammad Athar Structure 13C NMR ̼Æ×Ä£Äâͼ |
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