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Ly-10 13C NMR (126 MHz, cd3od) ¦Ä15.98,16.88, 17.74, 19.32, 23.96, 24.01, 24.56, 26.30, 27.07, 28.43, 28.91, 31.53, 33.49, 37.87, 40.39, 40.72, 42.61, 42.94, 48.03, 49.28, 49.46, 50.38, 52.81, 56.97, 62.42, 63.11, 68.74, 71.12, 71.92, 73.01, 73.93, 76.27, 76.52, 77.69, 77.86, 78.31, 78.35, 78.69, 80.46, 91.81, 95.71, 104.45, 105.58, 123.81, 130.56, 144.83, 171.13, 178.06. Ly-9 13C NMR (126 MHz, cd3od) ¦Ä16.11, 17.12, 17.64, 17.82, 17.96, 22.83, 24.23, 25.87, 27.24, 27.58, 30.95, 31.38, 31.53, 36.63, 40.18, 40.36, 40.48, 41.86, 45.28, 49.41, 50.59, 52.43, 53.12, 61.77, 62.52, 62.90, 71.19, 71.69, 71.86, 75.37, 75.48, 77.64, 77.91, 78.21, 79.05, 79.85, 80.93, 84.92, 98.28, 105.54, 125.83, 132.29. Ly-7 13C NMR (126 MHz, cd3od) ¦Ä16.28,16.76, 17.30, 17.97, 19.24, 22.86, 24.21, 25.89, 27.19, 27.23, 28.43, 30.99, 31.63, 35.88, 36.63, 37.89, 40.57, 40.96, 49.73, 51.03, 52.47, 53.08, 57.53, 62.48, 62.77, 63.07, 71.15, 71.47, 71.87, 75.31, 76.26, 77.63, 77.85, 78.18, 78.26, 78.42, 81.03, 84.90, 91.31, 98.22, 104.43, 105.36, 125.81, 132.27. Ly-4 13C NMR (126 MHz, cd3od) ¦Ä15.92,16.12, 16.86, 17.05, 17.64, 17.82, 23.88, 24.08, 26.26, 26.46, 27.00, 31.53, 37.88, 40.16, 40.71, 42.92, 48.01, 49.00, 52.73, 52.90, 56.91, 57.08, 62.40, 73.07, 76.52, 76.68, 91.09, 91.15, 95.61, 95.76, 106.92, 107.12, 123.62, 123.95, 144.82, 171.38, 178.04. |
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libinoook: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-12-25 17:28:00
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libinoook: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-12-25 17:28:00
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ly-10 ²éѯ½á¹û£º¹²²éµ½790¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ¦Â-D-Glucopyranosyl 3-(O-¦Â-D-glactopyranosyl (1¡ú2)(O-¦Â-D-glucopyranosyloxy))-oleanolate C48H76O19 ÏàËÆ¶È:87.5% Monatshefte f¨¹r Chemie 2000 131 195-204 Three Saponins, a Steroid, and a Flavanol Glycoside from Achyrantes aspera Olaf Kunert, Ernst Haslinger, Martin G. Schmid, Josef Reiner, Franz Bucar, Efrem Mulatu, Dawit Abebe, and Asfaw Debella Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3-O-¦Â-D-glucopyranosyl(1¡ú3)-¦Â-D-glucuronopyranoside-28-O-¦Â-D-glucopyranosyl oleanolic acid methyl ester ÏàËÆ¶È:83.6% Bioorganic & Medicinal Chemistry Letters 2010 20 7110-7115 Oleanane-type triterpenoids from Panax stipuleanatus and their anticancer activities Chun Liang, Yan Ding, Huu Tung Nguyen, Jeong-Ah Kim, Hye-Jin Boo, Hee-Kyoung Kang, Mahn Cuong Nguyen, Young Ho Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Sandrosaponin X ÏàËÆ¶È:83.3% Journal of Natural Products 2000 63 1479-1482 Four New Triterpenoid Saponins from the Roots of Bupleurum rigidum Sandra Svnchez-Contreras, Ana Mar¨ªa Dvaz-Lanza, and Manuel Bernab¨¦ Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . spinasaponin A 28-O-glucoside ÏàËÆ¶È:83.3% Bioorganic & Medicinal Chemistry Letters 2010 20 7110-7115 Oleanane-type triterpenoids from Panax stipuleanatus and their anticancer activities Chun Liang, Yan Ding, Huu Tung Nguyen, Jeong-Ah Kim, Hye-Jin Boo, Hee-Kyoung Kang, Mahn Cuong Nguyen, Young Ho Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . pseudoginsenoside RT1 methyl ester ÏàËÆ¶È:83.3% Bioorganic & Medicinal Chemistry Letters 2010 20 7110-7115 Oleanane-type triterpenoids from Panax stipuleanatus and their anticancer activities Chun Liang, Yan Ding, Huu Tung Nguyen, Jeong-Ah Kim, Hye-Jin Boo, Hee-Kyoung Kang, Mahn Cuong Nguyen, Young Ho Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ¦Â-D-glucopyranosyl 3¦Â-[O-¦Â-D-galactopyranosyl-(1¡ú2)-O-¦Á-D-glucopyranuronosyloxy]machaerinate C40H75O20 ÏàËÆ¶È:81.2% Helvetica Chimica Acta 2000 Vol. 83 359 New Triterpenoid Saponins from Achyrantes aspera Linn. G¨¹nter Michl,Dawit Abebe,Franz Bucar,Asfaw Debella), Olaf Kunert, Martin G. Schmid, Efrem Mulatu, and Ernst Haslinger Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . ecliptasaponin B C48H47O19 ÏàËÆ¶È:81.2% Journal of Chinese Pharmaceutical Sciences 1996 5 177-181 Isolation and Identification of Ecliptasaponin A and Ecliptasaponin B from Eclipta alba (L.) Hasssk Mei Zhang and Ya-Yan Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . ecliptasaponin B ÏàËÆ¶È:81.2% Acta Pharmaceutica Sinica 1996 31 196-199 ISOLATION AND IDENTIFICATION OF ECLIPTASAPONIN A AND ECLIPTASAPONIN B FROM ECLIPTA ALBA(L.)HASSK M Zhang and YY Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . pseudoginsenoside RT1 ÏàËÆ¶È:81.2% Bioorganic & Medicinal Chemistry Letters 2010 20 7110-7115 Oleanane-type triterpenoids from Panax stipuleanatus and their anticancer activities Chun Liang, Yan Ding, Huu Tung Nguyen, Jeong-Ah Kim, Hye-Jin Boo, Hee-Kyoung Kang, Mahn Cuong Nguyen, Young Ho Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 3-O-¦Â-D-xylopyranosyl(1¡ú2)-¦Â-D-glucopyranosyl-28-O-¦Â-D-glucopyranosyl oleanolic acid ÏàËÆ¶È:81.2% Bioorganic & Medicinal Chemistry Letters 2010 20 7110-7115 Oleanane-type triterpenoids from Panax stipuleanatus and their anticancer activities Chun Liang, Yan Ding, Huu Tung Nguyen, Jeong-Ah Kim, Hye-Jin Boo, Hee-Kyoung Kang, Mahn Cuong Nguyen, Young Ho Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Bifinoside C C53H85O22 ÏàËÆ¶È:79.2% Chemical & Pharmaceutical Bulletin 2011 59 1417-1420 Oleanolic Triterpene Saponins from the Roots of Panax bipinnatifidus Nguyen Huu TUNG, Tran Hong QUANG, Nguyen Thi Thanh NGAN, Chau Van MINH, Bui Kim ANH, Pham Quoc LONG, Nguyen Manh CUONG, and Young Ho KIM Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . guaiacin A C46H72O19 ÏàËÆ¶È:79.1% Planta Medica 1989 55 307-308 Guaiacin A and B from the Leaves of Guaiacum officinale Viqar Uddin Ahmad, Shaista Perveen, and Shaheen Bano Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . tauroside I ÏàËÆ¶È:79.1% Chemistry of Natural Compounds 1992 28 593-596 TRITERPENE GLYCOSIDES OF Hedera taurica X. STRUCTURES OF COMPOUNDS F 4, I, AND J FROM THE LEAVES OF CRIMEAN IVY V. I. Grishkovets, N. V. Tolkacheva,A. S. Shashkov, and V. Ya. Chirva Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . guaiacin B ÏàËÆ¶È:79.1% Phytochemistry 1999 51 1049-1053 Triterpenoid saponins from Fagonia indica Kamel H. Shaker, Mirko Bernhardt, M. Hani A. Elgamal, Karlheinz Seifert Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . oleanolic acid-3-O-[¦Â-D-galactopyranosyl-(1¡ú3)-¦Â-D-glucuronopyranosyl]-28-O-¦Â-D-glucopyranoside C48H76O19 ÏàËÆ¶È:79.1% Food Chemistry 2009 113 411-419 Saponins in Ipomoea batatas tubers: Isolation, characterization, quantification and antioxidant properties Irene Dini, Gian Carlo Tenore, Antonio Dini Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . oleanolic acid 3-O-[2'-4'-di-O-(¦Â-D-glucopyranosyl)-¦Â-D-glucopyranosyl]-28-O-¦Â-D-glucopyranoside C54H88O23 ÏàËÆ¶È:79.1% Journal of Agricultural and Food Chemistry 1996 44 3528-3533 Constituents of Chenopodium pallidicaule (Cañihua) Seeds: Isolation and Characterization of New Triterpene Saponins Luca Rastrelli, Francesco De Simone, Oreste Schettino, and Antonio Dini Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . Tuberoside A C48H76O19 ÏàËÆ¶È:79.1% European Journal of Organic Chemistry 1996 1996 781-784 Tuberosides A, B, and C, Novel Triterpenoid Saponins from the Hypoglucaemic Fraction of Ullucus tuberosus Alfonso Espada, Carlos Jim¨¦nez, Jose Dopeso and Ricardo Riguera Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 3-O-{[¦Â-D-glucopyranosyl-(1¡ú2)-O]-¦Â-D-galactopyranoside}-16-O-¦Â-D-glucopyranosyl-3¦Â,6¦Â,16¦Â-trihydroxyolean-12-ene C48H80O18 ÏàËÆ¶È:79.1% Phytochemistry 2014 97 70-80 Saponins with highly hydroxylated oleanane-type aglycones from Silphium asteriscus L. Milena Masullo, Lalita Calabria, Dario Gallotta, Cosimo Pizza, Sonia Piacente Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . phytolaccagenic acid 3-O-[¦Â-D-glucopyranosyl-(1¡ú4)-¦Â-D-glucopyranosyl]-28-O-¦Â-D-glucopyranoside C49H78O21 ÏàËÆ¶È:77.5% Journal of Agricultural and Food Chemistry 1996 44 3528-3533 Constituents of Chenopodium pallidicaule (Cañihua) Seeds: Isolation and Characterization of New Triterpene Saponins Luca Rastrelli, Francesco De Simone, Oreste Schettino, and Antonio Dini Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . phytolaccagenic acid 3-O-[¦Â-D-glucopyranosyl-(1¡ú4)-¦Â-D-glucopyranosyl-(1¡ú4)-¦Â-D-glucopyranosyl]-28-O-¦Â-D-glucopyranoside C55H88O26 ÏàËÆ¶È:77.5% Journal of Agricultural and Food Chemistry 1996 44 3528-3533 Constituents of Chenopodium pallidicaule (Cañihua) Seeds: Isolation and Characterization of New Triterpene Saponins Luca Rastrelli, Francesco De Simone, Oreste Schettino, and Antonio Dini Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 3‑O-2-(acetylamino)-2-deoxy-¦Â-D-glucopyranosylentagenicacid-28-O-¦Â-D-xylopyranosyl-(1¡ú2)-¦Â-D-glucopyranoside C49H79NO19 ÏàËÆ¶È:77.5% Planta Medica 2014 80 710-718 Triterpene Saponins from the Stems of Entada phaseoloides Xiong, Hui; Ding, Xin; Yang, Xin-zhou; Yang, Guang-zhong; Mei, Zhi-nan Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 3-O-(¦Â-D-glucopyranosyl-(1-2)-¦Â-D-glucopyranosyl)-28-O-(¦Â-D-xylopyranosyl(1-6)-¦Â-D-glucopyranosyl)-oleanolic acid C53H86O22 ÏàËÆ¶È:77.3% Phytochemistry Letters 2012 5 188-193 Saponins and alkaloids from Abuta grandifolia Charlotte Sayagh,Christophe Long,Christian Moretti,Catherine Lavaud Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2014-12-24 23:49:50
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- Ó¦Öú: 1309 (½²Ê¦)
- ½ð±Ò: 12672.8
- ºì»¨: 15
- Ìû×Ó: 1490
- ÔÚÏß: 299.5Сʱ
- ³æºÅ: 2542465
- ×¢²á: 2013-07-12
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libinoook: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-12-25 17:28:11
libinoook: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-12-25 17:28:11
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ly-9 ²éѯ½á¹û£º¹²²éµ½523¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ginsenoside Rg1 ÏàËÆ¶È:97.6% Chinese Traditional and Herbal Drugs 1996 27 647-649 Isolation and Identification of Ginsenoside from the Leaves of Wild Ginseng(Panax ginseng) Li Jing; Wei Yongdi(Berhune Medical University; Changchun); Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . ginsenoside-Rg1 C42H72O14 ÏàËÆ¶È:92.8% Chinese Traditional and Herbal Drugs 2012 43 1462-1470 Studies on chemical constituents from Aidi Injection ZHANG Miao-miao; LIU Yan-li; CHEN Zhong; LI Xiao-ran; XU Qiong-ming; YANG Shi-lin Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ginsenoside Rf ÏàËÆ¶È:88.0% Chinese Joumal of Experimental Traditional Medical Fomulae 2012 18 78-81 Study of Chemical Components from Qili Qiangxin Capsule (¢ò) QIAO Li, WANG Zong-quan, MENG Zuo-huan, JIANG Xin-gang, JIA Ji-ming, SONG Jian Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . ginsenoside Rd ÏàËÆ¶È:76.5% Journal of Industrial Microbiology & Biotechnology 2009 36 721-726 Highly selective biotransformation of ginsenoside Rb1 to Rd by the phytopathogenic fungus Cladosporium fulvum (syn.Fulvia fulva) Xuesong Zhao, Juan Wang, Jie Li, Ling Fu, Juan Gao, Xiuli Du, Hongtao Bi, Yifa Zhou, Guihua Tai Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 20S-sanchirhinoside A1 C40H66O10 ÏàËÆ¶È:76.1% Molecules 2013 18 10352-10366 Bioactive Protopanaxatriol Type Saponins Isolated from the Roots of Panax Notoginseng (Burk.) F. H. Chen Yi Zhang, Li-Feng Han, Kaunda Joseph Sakah, Zhi-Zhen Wu, Li-Li Liu, Kojo Agyemang, Xiu-Mei Gao and Tao Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . gypenoside L C42H72O14 ÏàËÆ¶È:73.8% Bioorganic & Medicinal Chemistry Letters 2014 24 186-191 Cytotoxic activity of gypenosides and gynogenin against non-small cell lung carcinoma A549 cells Dao-Jin Chen, Hui-Min Liu, Shao-Fang Xing, Xiang-Lan Piao Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . gypenoside LI ÏàËÆ¶È:73.8% Bioorganic & Medicinal Chemistry Letters 2014 24 186-191 Cytotoxic activity of gypenosides and gynogenin against non-small cell lung carcinoma A549 cells Dao-Jin Chen, Hui-Min Liu, Shao-Fang Xing, Xiang-Lan Piao Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Gypenoside L C42H72O14 ÏàËÆ¶È:73.8% Archives of Pharmacal Research 2013 36 874-879 Dammarane-type saponins from heat-processed Gynostemma pentaphyllum show fortified activity against A549 cells Xiang-Lan Piao, Qian Wu, Jing Yang, Seo Young Park, Dao-Jin Chen, Hui-Min Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Gypenoside LI C42H72O14 ÏàËÆ¶È:73.8% Archives of Pharmacal Research 2013 36 874-879 Dammarane-type saponins from heat-processed Gynostemma pentaphyllum show fortified activity against A549 cells Xiang-Lan Piao, Qian Wu, Jing Yang, Seo Young Park, Dao-Jin Chen, Hui-Min Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . gypenoside L C42H72O14 ÏàËÆ¶È:73.8% Chinese Joumal of Experimental Traditional Medical Fomulae 2013 19 106-111 Saponins from Zhuang-medicine Gocaekmbaw before and after Heat-processing LIU Hui-min, CHEN Dao-jin, PIAO Xiang-lan Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . gypenoside LI C42H72O14 ÏàËÆ¶È:73.8% Chinese Joumal of Experimental Traditional Medical Fomulae 2013 19 106-111 Saponins from Zhuang-medicine Gocaekmbaw before and after Heat-processing LIU Hui-min, CHEN Dao-jin, PIAO Xiang-lan Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . ginsenoside Rg2 ÏàËÆ¶È:71.4% Chinese Traditional and Herbal Drugs 1996 27 647-649 Isolation and Identification of Ginsenoside from the Leaves of Wild Ginseng(Panax ginseng) Li Jing; Wei Yongdi(Berhune Medical University; Changchun); Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . yesanchinoside R2 C41H70O14 ÏàËÆ¶È:71.4% Helvetica Chimica Acta 2011 94 2010-2019 New Dammarane-Type Saponins from the Rhizomes of Panax japonicus (pages 2010¨C2019) Min Zhou, Min Xu, Dong Wang, Hong-Tao Zhu, Chong-Ren Yang and Ying-Jun Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . sapinmusaponin O C42H72O12 ÏàËÆ¶È:69.0% Phytochemistry 2008 69 1609-1616 Triterpenoid saponins from the fruits and galls of Sapindus mukorossi Hui-Chi Huang,Ming-Der Wub,Wei-Jern Tsai,Sin-Chung Liao,Chia-Ching Liaw,Li-Chuan Hsu,Yang-Chang Wua,Yao-Haur Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . ginsenoside Rg5 ÏàËÆ¶È:69.0% Archives of Pharmacal Research 1996 19 551-553 High performance liquid chromatographic assay of a new fluoroquinolone, LB20304, in the plasma of rats and dogs Mi-Kyeong Seo, Yi-Na Jeong, Hoon-Joo Kim, In-Chull Kim and Yong-Hee Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 3-O-¦Â-D-glucopyranosyl-29-O-¦Â-D-glucopyranosyl-3¦Â,6¦Â,16¦Â,29-tetrahydroxyolean-12-en-23-oic C42H68O16 ÏàËÆ¶È:69.0% Phytochemistry 2014 97 70-80 Saponins with highly hydroxylated oleanane-type aglycones from Silphium asteriscus L. Milena Masullo, Lalita Calabria, Dario Gallotta, Cosimo Pizza, Sonia Piacente Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . ursan-3¦Â,19¦Á,22¦Â-triol-3-O-¦Â-D-glucopyranosyl (2'¡ú1'')-¦Â-D-glucopyranoside C42H72O13 ÏàËÆ¶È:69.0% Bioorganic & Medicinal Chemistry Letters 2014 24 4203-4208 Triterpene glycosides from red ginseng marc and their anti-inflammatory activities Ill-Min Chung, Young-Ock Kim, Mohammed Ali, Seung-Hyun Kim, Inmyoung Park, Eun-Hye Kim, Ye-Sul Yang, Hye-Ran Park, Eun-Suk Son, Ateeque Ahmad Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . glinuside F C45H76O16 ÏàËÆ¶È:68.8% Journal of Natural Products 2005 68 443-446 Hopane-Type Saponins from the Seeds of Glinus lotoides Abebe Endale, Victor Wray, Renato Murillo, Peter C. Schmidt, and Irmgard Merfort Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 3¦Â,6¦Â,16¦Â-trihydroxyolean-12-en-23-oic acid-3-O-¦Â-glucopyranosyl-16-O-¦Â-glucopyranoside C42H68O15 ÏàËÆ¶È:66.6% Phytochemistry 2008 69 961-972 Triterpene saponins from Silphium radula Lalita M. Calabria, Sonia Piacente, Ireneusz Kapusta,Suranganie F. Dharmawardhane, Frances M. Segarra, Peter J. Pessiki f, Tom J. Mabry Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 16-O-¦Á-L-arabinopyranosyl-20-O-¦Â-D-glucopyranosyl-6¦Á,16¦Á,20¦Â,21¦Á-tetrahydroxytetrahymanol C41H70O14 ÏàËÆ¶È:66.6% Journal of Natural Products 2014 77 657-662 Unusual Fernane and Gammacerane Glycosides from the Aerial Parts of Spergula fallax Arafa I. Hamed, Milena Masullo, Lukasz Pecio, Dario Gallotta, Usama A. Mahalel, Sylwia Pawelec, Anna Stochmal, and Sonia Piacente Structure 13C NMR ̼Æ×Ä£Äâͼ |

3Â¥2014-12-24 23:50:29
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- Ó¦Öú: 1309 (½²Ê¦)
- ½ð±Ò: 12672.8
- ºì»¨: 15
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libinoook: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-12-25 17:28:21
libinoook: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-12-25 17:28:21
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ly-7 ²éѯ½á¹û£º¹²²éµ½823¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ginsenoside Rd ÏàËÆ¶È:91.4% Journal of Industrial Microbiology & Biotechnology 2009 36 721-726 Highly selective biotransformation of ginsenoside Rb1 to Rd by the phytopathogenic fungus Cladosporium fulvum (syn.Fulvia fulva) Xuesong Zhao, Juan Wang, Jie Li, Ling Fu, Juan Gao, Xiuli Du, Hongtao Bi, Yifa Zhou, Guihua Tai Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . gypenosideXLVI C48H82O19 ÏàËÆ¶È:87.5% Bioorganic & Medicinal Chemistry Letters 2014 24 186-191 Cytotoxic activity of gypenosides and gynogenin against non-small cell lung carcinoma A549 cells Dao-Jin Chen, Hui-Min Liu, Shao-Fang Xing, Xiang-Lan Piao Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . gypenoside XLVI C48H82O19 ÏàËÆ¶È:87.5% Chinese Joumal of Experimental Traditional Medical Fomulae 2013 19 106-111 Saponins from Zhuang-medicine Gocaekmbaw before and after Heat-processing LIU Hui-min, CHEN Dao-jin, PIAO Xiang-lan Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . gypenoside XVII ÏàËÆ¶È:83.3% China Journal of Chinese Materia Medica 1992 17 611-613 Studies on the Saponins in the Fruit Pedicels of Panax notoginseng(Burk.)F.H.Chen(continue) Wei Junxian, Chen Yegao and Cao Shuming Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . vina-ginsenoside-R9 C48H82O19 ÏàËÆ¶È:81.2% Chemical & Pharmaceutical Bulletin 1994 42 115-122 Saponins from Vietnamese Ginseng, Panax vietnamensis HA et GRUSHV. Collected in Central Vietnam. II Nguyen MINH DUC,Ryoji KASAI,Kazuhiro OHTANI,Aiko ITO,Nguyen THOI NHAM,Kazuo YAMASAKI and Osamu TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ginsenoside Rg1 ÏàËÆ¶È:79.5% Chinese Traditional and Herbal Drugs 1996 27 647-649 Isolation and Identification of Ginsenoside from the Leaves of Wild Ginseng(Panax ginseng) Li Jing; Wei Yongdi(Berhune Medical University; Changchun); Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . gypenoside L C42H72O14 ÏàËÆ¶È:79.5% Bioorganic & Medicinal Chemistry Letters 2014 24 186-191 Cytotoxic activity of gypenosides and gynogenin against non-small cell lung carcinoma A549 cells Dao-Jin Chen, Hui-Min Liu, Shao-Fang Xing, Xiang-Lan Piao Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Gypenoside L C42H72O14 ÏàËÆ¶È:79.5% Archives of Pharmacal Research 2013 36 874-879 Dammarane-type saponins from heat-processed Gynostemma pentaphyllum show fortified activity against A549 cells Xiang-Lan Piao, Qian Wu, Jing Yang, Seo Young Park, Dao-Jin Chen, Hui-Min Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . gypenoside L C42H72O14 ÏàËÆ¶È:79.5% Chinese Joumal of Experimental Traditional Medical Fomulae 2013 19 106-111 Saponins from Zhuang-medicine Gocaekmbaw before and after Heat-processing LIU Hui-min, CHEN Dao-jin, PIAO Xiang-lan Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . gypenoside LI ÏàËÆ¶È:77.2% Bioorganic & Medicinal Chemistry Letters 2014 24 186-191 Cytotoxic activity of gypenosides and gynogenin against non-small cell lung carcinoma A549 cells Dao-Jin Chen, Hui-Min Liu, Shao-Fang Xing, Xiang-Lan Piao Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ginsenoside-Rg1 C42H72O14 ÏàËÆ¶È:77.2% Chinese Traditional and Herbal Drugs 2012 43 1462-1470 Studies on chemical constituents from Aidi Injection ZHANG Miao-miao; LIU Yan-li; CHEN Zhong; LI Xiao-ran; XU Qiong-ming; YANG Shi-lin Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Gypenoside LI C42H72O14 ÏàËÆ¶È:77.2% Archives of Pharmacal Research 2013 36 874-879 Dammarane-type saponins from heat-processed Gynostemma pentaphyllum show fortified activity against A549 cells Xiang-Lan Piao, Qian Wu, Jing Yang, Seo Young Park, Dao-Jin Chen, Hui-Min Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . gypenoside LI C42H72O14 ÏàËÆ¶È:77.2% Chinese Joumal of Experimental Traditional Medical Fomulae 2013 19 106-111 Saponins from Zhuang-medicine Gocaekmbaw before and after Heat-processing LIU Hui-min, CHEN Dao-jin, PIAO Xiang-lan Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . lanost-5,24-dien-3¦Â-ol-3-O-¦Â-D-glucopyranosyl-(6'¡ú1'')-¦Â-D-glucopyranosyl-(6''¡ú1''')-¦Â-D-glucopyranoside C48H80O16 ÏàËÆ¶È:72.9% Bioorganic & Medicinal Chemistry Letters 2014 24 4203-4208 Triterpene glycosides from red ginseng marc and their anti-inflammatory activities Ill-Min Chung, Young-Ock Kim, Mohammed Ali, Seung-Hyun Kim, Inmyoung Park, Eun-Hye Kim, Ye-Sul Yang, Hye-Ran Park, Eun-Suk Son, Ateeque Ahmad Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . ginsenoside Rg5 ÏàËÆ¶È:72.7% Archives of Pharmacal Research 1996 19 551-553 High performance liquid chromatographic assay of a new fluoroquinolone, LB20304, in the plasma of rats and dogs Mi-Kyeong Seo, Yi-Na Jeong, Hoon-Joo Kim, In-Chull Kim and Yong-Hee Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . ginsenoside Rf ÏàËÆ¶È:72.7% Chinese Joumal of Experimental Traditional Medical Fomulae 2012 18 78-81 Study of Chemical Components from Qili Qiangxin Capsule (¢ò) QIAO Li, WANG Zong-quan, MENG Zuo-huan, JIANG Xin-gang, JIA Ji-ming, SONG Jian Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (25R)-26-O-¦Â-D-glucopyranosyl-5¦Â-furostan-3¦Â,22¦Á,26-triol 3-O-[¦Â-D-glucopyranosyl-(1¡ú2)-O-¦Â-D-glucopyranoside] C45H76O19 ÏàËÆ¶È:71.1% Biochemical Systematics and Ecology 2006 34 809-814 Furostanol saponins from Yucca gloriosa L. rhizomes Alexandre Skhirtladze, Alberto Plaza, Paola Montoro, Mariam Benidze, Ether Kemertelidze, Cosimo Pizza, Sonia Piacente Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . ecliptasaponin B C48H47O19 ÏàËÆ¶È:70.8% Journal of Chinese Pharmaceutical Sciences 1996 5 177-181 Isolation and Identification of Ecliptasaponin A and Ecliptasaponin B from Eclipta alba (L.) Hasssk Mei Zhang and Ya-Yan Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . ecliptasaponin B ÏàËÆ¶È:70.8% Acta Pharmaceutica Sinica 1996 31 196-199 ISOLATION AND IDENTIFICATION OF ECLIPTASAPONIN A AND ECLIPTASAPONIN B FROM ECLIPTA ALBA(L.)HASSK M Zhang and YY Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . ginsenoside Re ÏàËÆ¶È:70.8% Chinese Joumal of Experimental Traditional Medical Fomulae 2012 18 78-81 Study of Chemical Components from Qili Qiangxin Capsule (¢ò) QIAO Li, WANG Zong-quan, MENG Zuo-huan, JIANG Xin-gang, JIA Ji-ming, SONG Jian Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . damulin B C42H70O13 ÏàËÆ¶È:70.4% Bioorganic & Medicinal Chemistry 2011 19 6254-6260 New dammarane-type glucosides as potential activators of AMP-activated protein kinase (AMPK) from Gynostemma pentaphyllum Phi Hung Nguyen, Rehman Gauhar, Seung Lark Hwang, Trong Tuan Dao, Dong Chan Park, Ji Eun Kim, Hebok Song, Tae Lin Huh, Won Keun Oh Structure 13C NMR ̼Æ×Ä£Äâͼ |

4Â¥2014-12-24 23:58:07
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libinoook: ½ð±Ò+10 2014-12-25 17:28:30
libinoook: ½ð±Ò+10 2014-12-25 17:28:30
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ly-4 ²éѯ½á¹û£º¹²²éµ½823¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ginsenoside Rd ÏàËÆ¶È:91.4% Journal of Industrial Microbiology & Biotechnology 2009 36 721-726 Highly selective biotransformation of ginsenoside Rb1 to Rd by the phytopathogenic fungus Cladosporium fulvum (syn.Fulvia fulva) Xuesong Zhao, Juan Wang, Jie Li, Ling Fu, Juan Gao, Xiuli Du, Hongtao Bi, Yifa Zhou, Guihua Tai Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . gypenosideXLVI C48H82O19 ÏàËÆ¶È:87.5% Bioorganic & Medicinal Chemistry Letters 2014 24 186-191 Cytotoxic activity of gypenosides and gynogenin against non-small cell lung carcinoma A549 cells Dao-Jin Chen, Hui-Min Liu, Shao-Fang Xing, Xiang-Lan Piao Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . gypenoside XLVI C48H82O19 ÏàËÆ¶È:87.5% Chinese Joumal of Experimental Traditional Medical Fomulae 2013 19 106-111 Saponins from Zhuang-medicine Gocaekmbaw before and after Heat-processing LIU Hui-min, CHEN Dao-jin, PIAO Xiang-lan Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . gypenoside XVII ÏàËÆ¶È:83.3% China Journal of Chinese Materia Medica 1992 17 611-613 Studies on the Saponins in the Fruit Pedicels of Panax notoginseng(Burk.)F.H.Chen(continue) Wei Junxian, Chen Yegao and Cao Shuming Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . vina-ginsenoside-R9 C48H82O19 ÏàËÆ¶È:81.2% Chemical & Pharmaceutical Bulletin 1994 42 115-122 Saponins from Vietnamese Ginseng, Panax vietnamensis HA et GRUSHV. Collected in Central Vietnam. II Nguyen MINH DUC,Ryoji KASAI,Kazuhiro OHTANI,Aiko ITO,Nguyen THOI NHAM,Kazuo YAMASAKI and Osamu TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ginsenoside Rg1 ÏàËÆ¶È:79.5% Chinese Traditional and Herbal Drugs 1996 27 647-649 Isolation and Identification of Ginsenoside from the Leaves of Wild Ginseng(Panax ginseng) Li Jing; Wei Yongdi(Berhune Medical University; Changchun); Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . gypenoside L C42H72O14 ÏàËÆ¶È:79.5% Bioorganic & Medicinal Chemistry Letters 2014 24 186-191 Cytotoxic activity of gypenosides and gynogenin against non-small cell lung carcinoma A549 cells Dao-Jin Chen, Hui-Min Liu, Shao-Fang Xing, Xiang-Lan Piao Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Gypenoside L C42H72O14 ÏàËÆ¶È:79.5% Archives of Pharmacal Research 2013 36 874-879 Dammarane-type saponins from heat-processed Gynostemma pentaphyllum show fortified activity against A549 cells Xiang-Lan Piao, Qian Wu, Jing Yang, Seo Young Park, Dao-Jin Chen, Hui-Min Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . gypenoside L C42H72O14 ÏàËÆ¶È:79.5% Chinese Joumal of Experimental Traditional Medical Fomulae 2013 19 106-111 Saponins from Zhuang-medicine Gocaekmbaw before and after Heat-processing LIU Hui-min, CHEN Dao-jin, PIAO Xiang-lan Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . gypenoside LI ÏàËÆ¶È:77.2% Bioorganic & Medicinal Chemistry Letters 2014 24 186-191 Cytotoxic activity of gypenosides and gynogenin against non-small cell lung carcinoma A549 cells Dao-Jin Chen, Hui-Min Liu, Shao-Fang Xing, Xiang-Lan Piao Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ginsenoside-Rg1 C42H72O14 ÏàËÆ¶È:77.2% Chinese Traditional and Herbal Drugs 2012 43 1462-1470 Studies on chemical constituents from Aidi Injection ZHANG Miao-miao; LIU Yan-li; CHEN Zhong; LI Xiao-ran; XU Qiong-ming; YANG Shi-lin Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Gypenoside LI C42H72O14 ÏàËÆ¶È:77.2% Archives of Pharmacal Research 2013 36 874-879 Dammarane-type saponins from heat-processed Gynostemma pentaphyllum show fortified activity against A549 cells Xiang-Lan Piao, Qian Wu, Jing Yang, Seo Young Park, Dao-Jin Chen, Hui-Min Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . gypenoside LI C42H72O14 ÏàËÆ¶È:77.2% Chinese Joumal of Experimental Traditional Medical Fomulae 2013 19 106-111 Saponins from Zhuang-medicine Gocaekmbaw before and after Heat-processing LIU Hui-min, CHEN Dao-jin, PIAO Xiang-lan Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . lanost-5,24-dien-3¦Â-ol-3-O-¦Â-D-glucopyranosyl-(6'¡ú1'')-¦Â-D-glucopyranosyl-(6''¡ú1''')-¦Â-D-glucopyranoside C48H80O16 ÏàËÆ¶È:72.9% Bioorganic & Medicinal Chemistry Letters 2014 24 4203-4208 Triterpene glycosides from red ginseng marc and their anti-inflammatory activities Ill-Min Chung, Young-Ock Kim, Mohammed Ali, Seung-Hyun Kim, Inmyoung Park, Eun-Hye Kim, Ye-Sul Yang, Hye-Ran Park, Eun-Suk Son, Ateeque Ahmad Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . ginsenoside Rg5 ÏàËÆ¶È:72.7% Archives of Pharmacal Research 1996 19 551-553 High performance liquid chromatographic assay of a new fluoroquinolone, LB20304, in the plasma of rats and dogs Mi-Kyeong Seo, Yi-Na Jeong, Hoon-Joo Kim, In-Chull Kim and Yong-Hee Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . ginsenoside Rf ÏàËÆ¶È:72.7% Chinese Joumal of Experimental Traditional Medical Fomulae 2012 18 78-81 Study of Chemical Components from Qili Qiangxin Capsule (¢ò) QIAO Li, WANG Zong-quan, MENG Zuo-huan, JIANG Xin-gang, JIA Ji-ming, SONG Jian Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (25R)-26-O-¦Â-D-glucopyranosyl-5¦Â-furostan-3¦Â,22¦Á,26-triol 3-O-[¦Â-D-glucopyranosyl-(1¡ú2)-O-¦Â-D-glucopyranoside] C45H76O19 ÏàËÆ¶È:71.1% Biochemical Systematics and Ecology 2006 34 809-814 Furostanol saponins from Yucca gloriosa L. rhizomes Alexandre Skhirtladze, Alberto Plaza, Paola Montoro, Mariam Benidze, Ether Kemertelidze, Cosimo Pizza, Sonia Piacente Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . ecliptasaponin B C48H47O19 ÏàËÆ¶È:70.8% Journal of Chinese Pharmaceutical Sciences 1996 5 177-181 Isolation and Identification of Ecliptasaponin A and Ecliptasaponin B from Eclipta alba (L.) Hasssk Mei Zhang and Ya-Yan Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . ecliptasaponin B ÏàËÆ¶È:70.8% Acta Pharmaceutica Sinica 1996 31 196-199 ISOLATION AND IDENTIFICATION OF ECLIPTASAPONIN A AND ECLIPTASAPONIN B FROM ECLIPTA ALBA(L.)HASSK M Zhang and YY Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . ginsenoside Re ÏàËÆ¶È:70.8% Chinese Joumal of Experimental Traditional Medical Fomulae 2012 18 78-81 Study of Chemical Components from Qili Qiangxin Capsule (¢ò) QIAO Li, WANG Zong-quan, MENG Zuo-huan, JIANG Xin-gang, JIA Ji-ming, SONG Jian Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . damulin B C42H70O13 ÏàËÆ¶È:70.4% Bioorganic & Medicinal Chemistry 2011 19 6254-6260 New dammarane-type glucosides as potential activators of AMP-activated protein kinase (AMPK) from Gynostemma pentaphyllum Phi Hung Nguyen, Rehman Gauhar, Seung Lark Hwang, Trong Tuan Dao, Dong Chan Park, Ji Eun Kim, Hebok Song, Tae Lin Huh, Won Keun Oh Structure 13C NMR ̼Æ×Ä£Äâͼ |

5Â¥2014-12-24 23:58:30
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6Â¥2014-12-25 08:01:47
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7Â¥2014-12-25 10:06:12
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libinoook: ½ð±Ò+10 2014-12-25 17:28:39
libinoook: ½ð±Ò+10 2014-12-25 17:28:39
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²»ºÃÒâ˼£¬ÊÇly-4Ū´íÁË£¬ÖØÐ²éÁËÒ»±é ly-4 ²éѯ½á¹û£º¹²²éµ½149¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 3-O-¦Â-D-Glucuronopyranosyl-oleanolic acid methylester C37H58O9 ÏàËÆ¶È:67.5% Archives of Pharmacal Research 2003 26 132-137 Cerebrosides and terpene glycosides from the root of aster scaber Kwon Hak Cheol, Cho Ock Ryun, Lee Kang Choon and Lee Kang Ro Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (3¦Â)-3-hydroxy-30-noroleana-12,20(29)-dien-28-oic acid 3-(¦Â-D-glucopyranosiduronic acid 6-methyl ester) C36H54O9 ÏàËÆ¶È:67.5% Helvetica Chimica Acta 2012 95 1395-1400 A New 30-Noroleanane Saponin from Wedelia chinensis Xing Li, Yu-Fang Wang, Qing-Wen Shi and Françoise Sauriol Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . philoxeroideside D C42H64O14 ÏàËÆ¶È:66.6% Journal of Asian Natural Products Research 2009 11 261-266 Cytotoxic triterpene saponins from Alternanthera philoxeroides Jin-Bo Fang , Zhi Yao , Jia-Chun Chen , Yan-Wen Liu , Yoshihisa Takaishi and Hong-Quan Duana Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . oleanolic acid 3-O-¦Â-D-glucuronopyranoside-6'-O-methyl ester ÏàËÆ¶È:64.8% China Journal of Chinese Materia Medica 2009 34 2473-2476 Constituents from Alternanthera philoxeroides and their antitumor activity FANG Jinbo, CHEN Jiachun, LIU Yanwen, DUAN Hongquan Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Æë¶Õ¹ûËá-3-O-¦Â-D-ßÁà«ÆÏÌÑÌÇÈ©ËáÜÕ-6'-O-¼×õ¥ C37H58O9 ÏàËÆ¶È:64.8% Journal of Tropical and Subtropical Botany 2013 21 57-62 Chemical Constituents from Roots of Achyranthes bidentata TANG Xin, PEI Gang, ZHOU Zhong-yu, TAN Jian-wen Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Longispinogenin 3,16-di-O-¦Â-D-glucopyranosid(corchorusin A) C42H70O13 ÏàËÆ¶È:62.1% Phytochemistry 1995 39 251-253 Triterpenoid diglucoside of Enterospermum pruinosum P. Rasoanaivo, G. Multari, E. Federici, C. Galeffi Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . impatiprin A C38H60O10 ÏàËÆ¶È:60.5% Journal of Asian Natural Products Research 2007 9 379-385 Three new triterpenoid saponins from the rhizomes of Impatiens pritzellii var. hupehensis X.-F. ZHOU, X.-Y. ZHAO, L. TANG, H.-L. RUAN, Y.-H. ZHANG, H.-F. PI,W.-L. XIAO, H.-D. SUN and J.-Z. WU† Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . ecliptasaponin A ÏàËÆ¶È:59.4% Acta Pharmaceutica Sinica 1996 31 196-199 ISOLATION AND IDENTIFICATION OF ECLIPTASAPONIN A AND ECLIPTASAPONIN B FROM ECLIPTA ALBA(L.)HASSK M Zhang and YY Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . philoxeroideside B C37H58O10 ÏàËÆ¶È:59.4% Journal of Asian Natural Products Research 2009 11 261-266 Cytotoxic triterpene saponins from Alternanthera philoxeroides Jin-Bo Fang , Zhi Yao , Jia-Chun Chen , Yan-Wen Liu , Yoshihisa Takaishi and Hong-Quan Duana Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . philoxeroideside C C36H56O10 ÏàËÆ¶È:59.4% Journal of Asian Natural Products Research 2009 11 261-266 Cytotoxic triterpene saponins from Alternanthera philoxeroides Jin-Bo Fang , Zhi Yao , Jia-Chun Chen , Yan-Wen Liu , Yoshihisa Takaishi and Hong-Quan Duana Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . oleanolic acid 3-O-¦Â-D-glucuropyranoside ÏàËÆ¶È:59.4% China Journal of Chinese Materia Medica 2009 34 2473-2476 Constituents from Alternanthera philoxeroides and their antitumor activity FANG Jinbo, CHEN Jiachun, LIU Yanwen, DUAN Hongquan Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . oleanolic acid 3-O-¦Â-D-glucuronopyranoside ÏàËÆ¶È:59.4% Chinese Traditional and Herbal Drugs 2007 38 976-979 Antivirus constituents from Alternanthera philoxeroides FANG Jin-bo; LIU Yan-wen; ZHANG Yan-wen; TENG Jie; DUAN Hong-quan Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . ecliptasaponin A ÏàËÆ¶È:59.4% Chinese Joumal of Experimental Traditional Medical Fomulae 2011 17 103-105 Studies on Chemical Constituents of Herba Ecliptae YUAN Hong-xia, ZHAO Yun-li, YAN Yan, YU Zhi-guo Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . chikusetsusaponin Iva ÏàËÆ¶È:58.5% Chinese Traditional and Herbal Drugs 2014 45 765-769 Chemical constituents of Sabia fasciculata HUANG Yan, LI Qi-xiu, LIU Yuan, SONG Zhi-zhao, WEN Zhi-yun, LIU Bu-ming, Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . impatiprin B C40H64O10 ÏàËÆ¶È:57.5% Journal of Asian Natural Products Research 2007 9 379-385 Three new triterpenoid saponins from the rhizomes of Impatiens pritzellii var. hupehensis X.-F. ZHOU, X.-Y. ZHAO, L. TANG, H.-L. RUAN, Y.-H. ZHANG, H.-F. PI,W.-L. XIAO, H.-D. SUN and J.-Z. WU† Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . quinovic acid 3-O-[¦Â-D-quinovopyranoside]-27-O-[¦Â-D-glucopyranosyl] ester C42H66O14 ÏàËÆ¶È:57.1% Natural Product Research 2002 16 389-393 Quinovic Acid Glycosides From MitraGyna Stipulosa - First Examples of Natural Inhibitors of Snake Venom Phosphodiesterase I Naheed Fatima; Leon Azefack Tapondjou; David Lontsi; B. L. Sondengam; Atta-Ur-Rahman; M. Iqbal Choudhary Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 4 ÏàËÆ¶È:57.1% Journal of Natural Products 1990 Vol 53 1193 Saponins from Zygophyllum propinquum Viqar Uddin Ahmad, Ghazala, Shafi Uddin, Shaheen Bano Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . pesudoginsenoside RP1 methyl ester ÏàËÆ¶È:57.1% Bioorganic & Medicinal Chemistry Letters 2010 20 7110-7115 Oleanane-type triterpenoids from Panax stipuleanatus and their anticancer activities Chun Liang, Yan Ding, Huu Tung Nguyen, Jeong-Ah Kim, Hye-Jin Boo, Hee-Kyoung Kang, Mahn Cuong Nguyen, Young Ho Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . chikusetsusaponin IVa ÏàËÆ¶È:57.1% Bioorganic & Medicinal Chemistry Letters 2010 20 7110-7115 Oleanane-type triterpenoids from Panax stipuleanatus and their anticancer activities Chun Liang, Yan Ding, Huu Tung Nguyen, Jeong-Ah Kim, Hye-Jin Boo, Hee-Kyoung Kang, Mahn Cuong Nguyen, Young Ho Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . chikusetsusaponin Iva ÏàËÆ¶È:57.1% Journal of Agricultural and Food Chemistry 1997 45 1027-1031 Saponins from Ilex dumosa, an Erva-mat¨¦ (Ilex paraguariensis) Adulterating Plant Viviane S. Pires, Dominique Guillaume, Grace Gosmann, and Eloir P. Schenkel Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . ¦Â-D-Glucopyranosyl 3-(O-¦Â-D-glucopyranosyloxy)-oleanolate C42H66O14 ÏàËÆ¶È:57.1% Monatshefte f¨¹r Chemie 2000 131 195-204 Three Saponins, a Steroid, and a Flavanol Glycoside from Achyrantes aspera Olaf Kunert, Ernst Haslinger, Martin G. Schmid, Josef Reiner, Franz Bucar, Efrem Mulatu, Dawit Abebe, and Asfaw Debella Structure 13C NMR ̼Æ×Ä£Äâͼ |

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ly-7 ²éѯ½á¹û£º¹²²éµ½823¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ginsenoside Rd ÏàËÆ¶È:91.4% Journal of Industrial Microbiology & Biotechnology 2009 36 721-726 Highly selective biotransformation of ginsenoside Rb1 to Rd by the phytopathogenic fungus Cladosporium fulvum (syn.Fulvia fulva) Xuesong Zhao, Juan Wang, Jie Li, Ling Fu, Juan Gao, Xiuli Du, Hongtao Bi, Yifa Zhou, Guihua Tai Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . gypenosideXLVI C48H82O19 ÏàËÆ¶È:87.5% Bioorganic & Medicinal Chemistry Letters 2014 24 186-191 Cytotoxic activity of gypenosides and gynogenin against non-small cell lung carcinoma A549 cells Dao-Jin Chen, Hui-Min Liu, Shao-Fang Xing, Xiang-Lan Piao Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . gypenoside XLVI C48H82O19 ÏàËÆ¶È:87.5% Chinese Joumal of Experimental Traditional Medical Fomulae 2013 19 106-111 Saponins from Zhuang-medicine Gocaekmbaw before and after Heat-processing LIU Hui-min, CHEN Dao-jin, PIAO Xiang-lan Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . gypenoside XVII ÏàËÆ¶È:83.3% China Journal of Chinese Materia Medica 1992 17 611-613 Studies on the Saponins in the Fruit Pedicels of Panax notoginseng(Burk.)F.H.Chen(continue) Wei Junxian, Chen Yegao and Cao Shuming Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . vina-ginsenoside-R9 C48H82O19 ÏàËÆ¶È:81.2% Chemical & Pharmaceutical Bulletin 1994 42 115-122 Saponins from Vietnamese Ginseng, Panax vietnamensis HA et GRUSHV. Collected in Central Vietnam. II Nguyen MINH DUC,Ryoji KASAI,Kazuhiro OHTANI,Aiko ITO,Nguyen THOI NHAM,Kazuo YAMASAKI and Osamu TANAKA Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ginsenoside Rg1 ÏàËÆ¶È:79.5% Chinese Traditional and Herbal Drugs 1996 27 647-649 Isolation and Identification of Ginsenoside from the Leaves of Wild Ginseng(Panax ginseng) Li Jing; Wei Yongdi(Berhune Medical University; Changchun); Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . gypenoside L C42H72O14 ÏàËÆ¶È:79.5% Bioorganic & Medicinal Chemistry Letters 2014 24 186-191 Cytotoxic activity of gypenosides and gynogenin against non-small cell lung carcinoma A549 cells Dao-Jin Chen, Hui-Min Liu, Shao-Fang Xing, Xiang-Lan Piao Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Gypenoside L C42H72O14 ÏàËÆ¶È:79.5% Archives of Pharmacal Research 2013 36 874-879 Dammarane-type saponins from heat-processed Gynostemma pentaphyllum show fortified activity against A549 cells Xiang-Lan Piao, Qian Wu, Jing Yang, Seo Young Park, Dao-Jin Chen, Hui-Min Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . gypenoside L C42H72O14 ÏàËÆ¶È:79.5% Chinese Joumal of Experimental Traditional Medical Fomulae 2013 19 106-111 Saponins from Zhuang-medicine Gocaekmbaw before and after Heat-processing LIU Hui-min, CHEN Dao-jin, PIAO Xiang-lan Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . gypenoside LI ÏàËÆ¶È:77.2% Bioorganic & Medicinal Chemistry Letters 2014 24 186-191 Cytotoxic activity of gypenosides and gynogenin against non-small cell lung carcinoma A549 cells Dao-Jin Chen, Hui-Min Liu, Shao-Fang Xing, Xiang-Lan Piao Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . ginsenoside-Rg1 C42H72O14 ÏàËÆ¶È:77.2% Chinese Traditional and Herbal Drugs 2012 43 1462-1470 Studies on chemical constituents from Aidi Injection ZHANG Miao-miao; LIU Yan-li; CHEN Zhong; LI Xiao-ran; XU Qiong-ming; YANG Shi-lin Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Gypenoside LI C42H72O14 ÏàËÆ¶È:77.2% Archives of Pharmacal Research 2013 36 874-879 Dammarane-type saponins from heat-processed Gynostemma pentaphyllum show fortified activity against A549 cells Xiang-Lan Piao, Qian Wu, Jing Yang, Seo Young Park, Dao-Jin Chen, Hui-Min Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . gypenoside LI C42H72O14 ÏàËÆ¶È:77.2% Chinese Joumal of Experimental Traditional Medical Fomulae 2013 19 106-111 Saponins from Zhuang-medicine Gocaekmbaw before and after Heat-processing LIU Hui-min, CHEN Dao-jin, PIAO Xiang-lan Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . lanost-5,24-dien-3¦Â-ol-3-O-¦Â-D-glucopyranosyl-(6'¡ú1'')-¦Â-D-glucopyranosyl-(6''¡ú1''')-¦Â-D-glucopyranoside C48H80O16 ÏàËÆ¶È:72.9% Bioorganic & Medicinal Chemistry Letters 2014 24 4203-4208 Triterpene glycosides from red ginseng marc and their anti-inflammatory activities Ill-Min Chung, Young-Ock Kim, Mohammed Ali, Seung-Hyun Kim, Inmyoung Park, Eun-Hye Kim, Ye-Sul Yang, Hye-Ran Park, Eun-Suk Son, Ateeque Ahmad Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . ginsenoside Rg5 ÏàËÆ¶È:72.7% Archives of Pharmacal Research 1996 19 551-553 High performance liquid chromatographic assay of a new fluoroquinolone, LB20304, in the plasma of rats and dogs Mi-Kyeong Seo, Yi-Na Jeong, Hoon-Joo Kim, In-Chull Kim and Yong-Hee Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . ginsenoside Rf ÏàËÆ¶È:72.7% Chinese Joumal of Experimental Traditional Medical Fomulae 2012 18 78-81 Study of Chemical Components from Qili Qiangxin Capsule (¢ò) QIAO Li, WANG Zong-quan, MENG Zuo-huan, JIANG Xin-gang, JIA Ji-ming, SONG Jian Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . (25R)-26-O-¦Â-D-glucopyranosyl-5¦Â-furostan-3¦Â,22¦Á,26-triol 3-O-[¦Â-D-glucopyranosyl-(1¡ú2)-O-¦Â-D-glucopyranoside] C45H76O19 ÏàËÆ¶È:71.1% Biochemical Systematics and Ecology 2006 34 809-814 Furostanol saponins from Yucca gloriosa L. rhizomes Alexandre Skhirtladze, Alberto Plaza, Paola Montoro, Mariam Benidze, Ether Kemertelidze, Cosimo Pizza, Sonia Piacente Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . ecliptasaponin B C48H47O19 ÏàËÆ¶È:70.8% Journal of Chinese Pharmaceutical Sciences 1996 5 177-181 Isolation and Identification of Ecliptasaponin A and Ecliptasaponin B from Eclipta alba (L.) Hasssk Mei Zhang and Ya-Yan Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . ecliptasaponin B ÏàËÆ¶È:70.8% Acta Pharmaceutica Sinica 1996 31 196-199 ISOLATION AND IDENTIFICATION OF ECLIPTASAPONIN A AND ECLIPTASAPONIN B FROM ECLIPTA ALBA(L.)HASSK M Zhang and YY Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . ginsenoside Re ÏàËÆ¶È:70.8% Chinese Joumal of Experimental Traditional Medical Fomulae 2012 18 78-81 Study of Chemical Components from Qili Qiangxin Capsule (¢ò) QIAO Li, WANG Zong-quan, MENG Zuo-huan, JIANG Xin-gang, JIA Ji-ming, SONG Jian Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . damulin B C42H70O13 ÏàËÆ¶È:70.4% Bioorganic & Medicinal Chemistry 2011 19 6254-6260 New dammarane-type glucosides as potential activators of AMP-activated protein kinase (AMPK) from Gynostemma pentaphyllum Phi Hung Nguyen, Rehman Gauhar, Seung Lark Hwang, Trong Tuan Dao, Dong Chan Park, Ji Eun Kim, Hebok Song, Tae Lin Huh, Won Keun Oh Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . Damulin B C42H70O13 ÏàËÆ¶È:70.4% Archives of Pharmacal Research 2013 36 874-879 Dammarane-type saponins from heat-processed Gynostemma pentaphyllum show fortified activity against A549 cells Xiang-Lan Piao, Qian Wu, Jing Yang, Seo Young Park, Dao-Jin Chen, Hui-Min Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . damulin B C42H70O13 ÏàËÆ¶È:70.4% Chinese Joumal of Experimental Traditional Medical Fomulae 2013 19 106-111 Saponins from Zhuang-medicine Gocaekmbaw before and after Heat-processing LIU Hui-min, CHEN Dao-jin, PIAO Xiang-lan Structure 13C NMR ̼Æ×Ä£Äâͼ |

9Â¥2014-12-25 10:12:26














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